Re: [TMIC] update on Michael

2010-08-27 Thread Kevin Wolfthal

Kim,
Beautifully said.
Kevin




kimr1999 wrote:
God saw Michael getting tired and a cure was not to be. So He put His 
arms around him and whispered come to me. With tearful eyes we 
watched , and saw him pass away. Although we loved him dearly, we 
could not make him stay. A golden heart stopped beating, hardworking 
hands at rest. God broke our hearts to prove to us, He only takes the 
best.
May the peace which comes from the memories of love shared, comfort 
you now and in the days ahead.




*From:* Jill Hammond 3jmhamm...@clearwire.net
*To:* Anna  Jim jnawil...@roadrunner.com; Annie 
annielyman1...@yahoo.com; Becky  Steve mcsmi...@adelphia.net; 
Beth  Greg g...@comcast.net; Bob  Beverly b.doerfl...@gmail.com; 
Boyd b...@boydbryant.com; Carole Matteson 
carolematte...@hotmail.com; Char Brower charsreti...@hotmail.com; 
Cheryl Hammond i...@todaydata.com; Cindy Dunn cdunn53...@aol.com; 
Craig  Candi bur...@comcast.net; Craig Fiore 
cr...@ultra6.eskimo.com; fi...@dhs.gov; David and Patty Brooks 
blueba...@verizon.net; David Gay raega...@yahoo.com; Dennis  Pam 
burpee...@msn.com; Earl Fordham earl.ford...@gmail.com; Elaine 
Boos elaineb...@bellsouth.net; Eric  Eri 
ericshamm...@hotmail.com; Fred  Susan graceann1...@charter.net; 
Gil  Mari cdav...@dc.rr.com; James Fulmer jedi...@gmail.com; Jan 
Hlavaty-LaPosa janet.hlavaty-lap...@dhs.gov; Jim and Bobbi 
jimbobk...@msn.com; Johanna mjber...@verizon.net; Judy  Karl 
romocharlo...@hotmail.com; Keenan kee...@seattlegeek.net; Kendra 
kwa...@comcast.net; Lenny Lisa len.l...@verizon.net; Lisa 
l...@lisalundt.com; Lynn  Jade lynn.mari...@pfpa.mil; Mari 
wordfromwis...@smtel.com; marie swanson 
swansonbythe...@comcast.net; Mica Ward m...@detech.net; Mike  
Nancy mmccallis...@soundandsea.com; Nancy npurcell1...@yahoo.com; 
Noah n...@noahconrad.com; Pat Allegretti paa...@gmail.com; Pat and 
Corky pjgren...@hotmail.com; Pat Doebele grandmap...@comcast.net; 
Pat Massey patrick.mas...@dhs.gov; Paula 
paula.lazz...@attachmate.com; PJ pjn...@yahoo.com; Ron 
ron.brook...@att.net; Sally sa...@bsorenson.com; Sarah Bell-Schell 
maeb...@vandals.uidaho.edu; Scott Hamilton scotthamil...@live.com; 
Sharon  Steve pianica...@comcast.net; Sheri Meyer 
sheme...@cisco.com; Steve  Gail crescentc...@nwi.net; Steve and 
Jo stevejojohn...@msn.com; Susan  Ted Roth susanema...@mchsi.com; 
Tmic tmic-list@eskimo.com; Tom  Deb t...@ddoel.com; vanessa Quinn 
vanessa.qu...@dhs.gov; Wayne wme...@ci.everett.wa.us; Zsolt  
Patty zdor...@comcast.net

*Sent:* Thu, August 26, 2010 1:52:18 PM
*Subject:* [TMIC] update on Michael

Hello Family and Friends,

Michael slipped peacefully away yesterday evening at 9:30 p.m. He is 
now in a much better place.


Thank you for all your thoughts and prayers on his behalf.  The family 
greatly appreciates all the support and love you have all sent our way 
as we struggled through this past year.


with love and gratitude,

The Hammond Team





RE: [TMIC] update on Mike

2010-08-27 Thread Alle111
Jill and the Hammond  Team,
My deepest condolences to all of  you. You will always be a part of TMIC 
and we'll always be here to listen and  support. R.I.P MikeElla

Re: [TMIC] update on Michael

2010-08-26 Thread rn11...@yahoo.com
I am so sorry for your loss.
  Cheryl

--- On Thu, 8/26/10, Jill Hammond 3jmhamm...@clearwire.net wrote:


From: Jill Hammond 3jmhamm...@clearwire.net
Subject: [TMIC] update on Michael
To: Anna  Jim  jnawil...@roadrunner.com, Annie  
annielyman1...@yahoo.com, Becky  Steve mcsmi...@adelphia.net, Beth  
Greg g...@comcast.net, Bob  Beverly  b.doerfl...@gmail.com, 'Boyd' 
b...@boydbryant.com, Carole Matteson carolematte...@hotmail.com, Char 
Brower charsreti...@hotmail.com, Cheryl Hammond i...@todaydata.com, 
Cindy Dunn cdunn53...@aol.com, Craig  Candi bur...@comcast.net, 
'Craig Fiore' cr...@ultra6.eskimo.com, fi...@dhs.gov, 'David and Patty 
Brooks' blueba...@verizon.net, 'David Gay' raega...@yahoo.com, Dennis  
Pam burpee...@msn.com, 'Earl Fordham' earl.ford...@gmail.com, Elaine 
Boos elaineb...@bellsouth.net, Eric  Eri ericshamm...@hotmail.com, 
Fred  Susan graceann1...@charter.net, Gil  Mari cdav...@dc.rr.com, 
'James Fulmer' jedi...@gmail.com, Jan Hlavaty-LaPosa  
janet.hlavaty-lap...@dhs.gov, Jim and Bobbi  jimbobk...@msn.com, Johanna 

 mjber...@verizon.net, Judy  Karl romocharlo...@hotmail.com, Keenan 
kee...@seattlegeek.net, Kendra  kwa...@comcast.net, Lenny Lisa 
len.l...@verizon.net, Lisa  l...@lisalundt.com, Lynn  Jade 
lynn.mari...@pfpa.mil, Mari  wordfromwis...@smtel.com, marie swanson 
swansonbythe...@comcast.net, 'Mica Ward' m...@detech.net, Mike  Nancy 
mmccallis...@soundandsea.com, Nancy npurcell1...@yahoo.com, Noah  
n...@noahconrad.com, Pat Allegretti paa...@gmail.com, Pat and Corky 
pjgren...@hotmail.com, Pat Doebele grandmap...@comcast.net, Pat Massey  
patrick.mas...@dhs.gov, Paula  paula.lazz...@attachmate.com, PJ  
pjn...@yahoo.com, Ron  ron.brook...@att.net, 'Sally' 
sa...@bsorenson.com, Sarah Bell-Schell  maeb...@vandals.uidaho.edu, 
'Scott Hamilton' scotthamil...@live.com, Sharon  Steve  
pianica...@comcast.net, 'Sheri Meyer' sheme...@cisco.com, Steve  Gail 
 crescentc...@nwi.net, Steve and Jo stevejojohn...@msn.com, Susan  Ted 
Roth susanema...@mchsi.com, Tmic tmic-list@eskimo.com, Tom  Deb  
t...@ddoel.com, 'vanessa Quinn' vanessa.qu...@dhs.gov, Wayne  
wme...@ci.everett.wa.us, Zsolt  Patty zdor...@comcast.net
Date: Thursday, August 26, 2010, 1:52 PM








Hello Family and Friends,
Michael slipped peacefully away yesterday evening at 9:30 p.m. He is now in a 
much better place.  
 
Thank you for all your thoughts and prayers on his behalf.  The family greatly 
appreciates all the support and love you have all sent our way as we struggled 
through this past year.
 
with love and gratitude,
The Hammond Team


  

Re: [TMIC] update on Michael

2010-08-26 Thread kimr1999
God saw Michael getting tired and a cure was not to be. So He put His arms 
around him and whispered come to me. With tearful eyes we watched , and saw 
him pass away. Although we loved him dearly, we could not make him stay. A 
golden heart stopped beating, hardworking hands at rest. God broke our hearts 
to 
prove to us, He only takes the best.

May the peace which comes from the memories of love shared, comfort you now and 
in the days ahead.


 




From: Jill Hammond 3jmhamm...@clearwire.net
To: Anna  Jim jnawil...@roadrunner.com; Annie annielyman1...@yahoo.com; 
Becky  Steve mcsmi...@adelphia.net; Beth  Greg g...@comcast.net; Bob  
Beverly b.doerfl...@gmail.com; Boyd b...@boydbryant.com; Carole Matteson 
carolematte...@hotmail.com; Char Brower charsreti...@hotmail.com; Cheryl 
Hammond i...@todaydata.com; Cindy Dunn cdunn53...@aol.com; Craig  Candi 
bur...@comcast.net; Craig Fiore cr...@ultra6.eskimo.com; fi...@dhs.gov; 
David and Patty Brooks blueba...@verizon.net; David Gay raega...@yahoo.com; 
Dennis  Pam burpee...@msn.com; Earl Fordham earl.ford...@gmail.com; Elaine 
Boos elaineb...@bellsouth.net; Eric  Eri ericshamm...@hotmail.com; Fred  
Susan graceann1...@charter.net; Gil  Mari cdav...@dc.rr.com; James Fulmer 
jedi...@gmail.com; Jan Hlavaty-LaPosa janet.hlavaty-lap...@dhs.gov; Jim and 
Bobbi jimbobk...@msn.com; Johanna mjber...@verizon.net; Judy  Karl 
romocharlo...@hotmail.com; Keenan kee...@seattlegeek.net; Kendra 
kwa...@comcast.net; Lenny Lisa len.l...@verizon.net; Lisa 
l...@lisalundt.com; Lynn  Jade lynn.mari...@pfpa.mil; Mari 
wordfromwis...@smtel.com; marie swanson swansonbythe...@comcast.net; Mica 
Ward m...@detech.net; Mike  Nancy mmccallis...@soundandsea.com; Nancy 
npurcell1...@yahoo.com; Noah n...@noahconrad.com; Pat Allegretti 
paa...@gmail.com; Pat and Corky pjgren...@hotmail.com; Pat Doebele 
grandmap...@comcast.net; Pat Massey patrick.mas...@dhs.gov; Paula 
paula.lazz...@attachmate.com; PJ pjn...@yahoo.com; Ron 
ron.brook...@att.net; Sally sa...@bsorenson.com; Sarah Bell-Schell 
maeb...@vandals.uidaho.edu; Scott Hamilton scotthamil...@live.com; Sharon  
Steve pianica...@comcast.net; Sheri Meyer sheme...@cisco.com; Steve  Gail 
crescentc...@nwi.net; Steve and Jo stevejojohn...@msn.com; Susan  Ted Roth 
susanema...@mchsi.com; Tmic tmic-list@eskimo.com; Tom  Deb 
t...@ddoel.com; 
vanessa Quinn vanessa.qu...@dhs.gov; Wayne wme...@ci.everett.wa.us; Zsolt  
Patty zdor...@comcast.net
Sent: Thu, August 26, 2010 1:52:18 PM
Subject: [TMIC] update on Michael


Hello Family and Friends,
Michael slipped peacefully away yesterday evening at 9:30 p.m. He is now in a 
much better place.  

 
Thank you for all your thoughts and prayers on his behalf.  The family greatly 
appreciates all the support and love you have all sent our way as we struggled 
through this past year.
 
with love and gratitude,
The Hammond Team

Re: [TMIC] update on Mike

2010-08-25 Thread Lori Biehler
Hammond Team,
You are all in my thoughts. He gave a very valiant fight and with all your 
support he knew he was very, very loved.
May you all find peace at this time and know the TM community is thinking of 
all of you.
Lori


From: Jill Hammond 
Sent: Wednesday, August 25, 2010 6:43 PM
To: d...@excellentsite.com ; Anna  Jim ; Annie ; Becky  Steve ; Beth  Greg ; 
Bob  Beverly ; 'Boyd' ; Carole Matteson ; Char Brower ; Cheryl Hammond ; Cindy 
Dunn ; Craig  Candi ; 'Craig Fiore' ; fi...@dhs.gov ; 'David and Patty Brooks' 
; 'David Gay' ; Dennis  Pam ; 'Earl Fordham' ; Elaine Boos ; Eric  Eri ; Fred 
 Susan ; Gil  Mari ; 'James Fulmer' ; Jan Hlavaty-LaPosa ; Jim and Bobbi ; 
Johanna ; Judy  Karl ; Keenan ; Kendra ; Lenny Lisa ; Lisa ; Lynn  Jade ; 
Mari ; marie swanson ; 'Mica Ward' ; Mike  Nancy ; Nancy ; Noah ; Pat 
Allegretti ; Pat and Corky ; Pat Doebele ; Pat Massey ; Paula ; PJ ; Ron ; 
'Sally' ; Sarah Bell-Schell ; 'Scott Hamilton' ; Sharon  Steve ; 'Sheri Meyer' 
; Steve  Gail ; Steve and Jo ; Susan  Ted Roth ; Tmic ; Tom  Deb ; 'vanessa 
Quinn' ; Wayne ; Zsolt  Patty 
Subject: [TMIC] update on Mike


Hello Family and Friends,

Our meeting last week with the Oncologist brought us very sad and shocking 
news.  Mike's cancer is not only back, but in the brain and spinal cord.  It is 
inoperable and the doctor's best guess was that he would have anywhere from 2 
weeks to 2 months.  The only positive thing about this news was that Mike was 
too disoriented to understand what was going on.  We came home and called in 
Hospice to help us through our ordeal.

 

Hospice came last Friday for the evaluation and to set Mike up on comfort only 
drugs.  By Sunday, I was unable to get Mike out of bed, even with help, and 
another call to Hospice brought a delivery of a hospital bed and accessories.  
By Monday, Mike was not speaking other than incoherent mumbling, except for an 
occasional name of Jill, Janel or Joel.  Today (Wednesday) Mike is unresponsive 
and it is clear from the Hospice nurse that he won't last more than 24 hours, 
if that, before he has left us for a better place.  

 

Had I known that things were going to transpire this fast, I would have sent a 
letter out sooner, but we are all still in shock that we have had barely a week 
since the news of his setback.  Too soon, we are having to say our goodbyes.

 

Please keep Mike in your hearts and prayers that he may go swiftly and easily. 

 

Love and peace,

The Hammond Team  


Re: [TMIC] Update on Mike

2010-08-18 Thread Celrods
I am so sorry to hear this.  Will keep up the prayers.
 
Jane/Splendora Tx
 
 
 
In a message dated 8/17/2010 10:17:13 A.M. Central Daylight Time,  
3jmhamm...@clearwire.net writes:

 
Hello Family and  Friends, 
Sorry to send this information  over mass email, but it’s the fastest way 
to keep everyone informed.   Over the last couple of weeks, Mike has been 
very disoriented, sleeping a lot  and losing weight. The MRI test that he had 
earlier this week indicates that  the cancer has spread to the brain.  We are 
meeting w/the Oncologist  today and hopefully get more answers and find out 
what our course of treatment  will be. I’ll keep you informed as soon as we 
can.   Keep us in your  prayers….Love, The Hammond Team  


Re: [TMIC] Update on Mike

2010-08-17 Thread L T CHERPESKI
Hello dear Jill and the Hammond Team,

I am so, so sorry to hear this latest news.  Thank you for keeping us updated - 
we really appreciate you keeping us in the loop.  Will keep all of you in my 
thoughts and prayers. 

Much love to you and the family,

Linda (Eagle, ID) previously Bothell, WA - Mike  I had talked about that some 
time ago.


  - Original Message - 
  From: Jill Hammondmailto:3jmhamm...@clearwire.net 
  To: Anna  Jim mailto:jnawil...@roadrunner.com; Annie 
mailto:annielyman1...@yahoo.com; Becky  Stevemailto:mcsmi...@adelphia.net 
; Beth  Gregmailto:g...@comcast.net ; Bob  Beverly 
mailto:b.doerfl...@gmail.com; 'Boyd'mailto:b...@boydbryant.com ; Carole 
Mattesonmailto:carolematte...@hotmail.com ; Char 
Browermailto:charsreti...@hotmail.com ; Cheryl 
Hammondmailto:i...@todaydata.com ; Cindy Dunnmailto:cdunn53...@aol.com ; 
Craig  Candimailto:bur...@comcast.net ; 'Craig 
Fiore'mailto:cr...@ultra6.eskimo.com ; fi...@dhs.govmailto:fi...@dhs.gov ; 
'David and Patty Brooks'mailto:blueba...@verizon.net ; 'David 
Gay'mailto:raega...@yahoo.com ; Dennis  Pammailto:burpee...@msn.com ; 
'Earl Fordham'mailto:earl.ford...@gmail.com ; Elaine 
Boosmailto:elaineb...@bellsouth.net ; Eric  
Erimailto:ericshamm...@hotmail.com ; Fred  
Susanmailto:graceann1...@charter.net ; Gil  Marimailto:cdav...@dc.rr.com ; 
'James Fulmer'mailto:jedi...@gmail.com ; Jan Hlavaty-LaPosa 
mailto:janet.hlavaty-lap...@dhs.gov; Jim and Bobbi 
mailto:jimbobk...@msn.com; Johanna mailto:mjber...@verizon.net; Judy  
Karlmailto:romocharlo...@hotmail.com ; Keenanmailto:kee...@seattlegeek.net 
; Kendra mailto:kwa...@comcast.net; Lenny Lisamailto:len.l...@verizon.net ; 
Lisa mailto:l...@lisalundt.com; Lynn  Jademailto:lynn.mari...@pfpa.mil ; 
Mari  Garymailto:wordfromwis...@smtel.com ; marie 
swansonmailto:swansonbythe...@comcast.net ; 'Mica 
Ward'mailto:m...@detech.net ; Mike  
Nancymailto:mmccallis...@soundandsea.com ; 
Nancymailto:npurcell1...@yahoo.com ; Noah mailto:n...@noahconrad.com; Pat 
Allegrettimailto:paa...@gmail.com ; Pat and 
Corkymailto:pjgren...@hotmail.com ; Pat 
Doebelemailto:grandmap...@comcast.net ; Pat Massey 
mailto:patrick.mas...@dhs.gov; Paula mailto:paula.lazz...@attachmate.com; 
PJ mailto:pjn...@yahoo.com; Ron mailto:ron.brook...@att.net; 
'Sally'mailto:sa...@bsorenson.com ; Sarah Bell-Schell 
mailto:maeb...@vandals.uidaho.edu; 'Scott 
Hamilton'mailto:scotthamil...@live.com ; Sharon  Steve 
mailto:pianica...@comcast.net; 'Sheri Meyer'mailto:sheme...@cisco.com ; 
Steve  Gail mailto:crescentc...@nwi.net; Steve and 
Jomailto:stevejojohn...@msn.com ; Susan  Ted 
Rothmailto:susanema...@mchsi.com ; Tmicmailto:tmic-list@eskimo.com ; Tom  
Deb mailto:t...@ddoel.com; 'vanessa Quinn'mailto:vanessa.qu...@dhs.gov ; 
Wayne mailto:wme...@ci.everett.wa.us; Zsolt  
Pattymailto:zdor...@comcast.net 
  Sent: Tuesday, August 17, 2010 9:16 AM
  Subject: [TMIC] Update on Mike


  Hello Family and Friends,

   

  Sorry to send this information over mass email, but it's the fastest way to 
keep everyone informed.  Over the last couple of weeks, Mike has been very 
disoriented, sleeping a lot and losing weight. The MRI test that he had earlier 
this week indicates that the cancer has spread to the brain.  We are meeting 
w/the Oncologist today and hopefully get more answers and find out what our 
course of treatment will be. I'll keep you informed as soon as we can.   Keep 
us in your prayers..Love, The Hammond Team  


RE: [TMIC] Update on Mike

2010-08-17 Thread j ra

I'm so sorry to hear thisall I can offer is the thoughts and prayers of me 
and my wife. I hope Mike knows how much people all over the world cares for him 
and he feels our love and prayers in his time of need.
Jeron

Date: Tue, 17 Aug 2010 10:13:55 -0700
From: rn11...@yahoo.com
Subject: Re: [TMIC] Update on Mike
To: 3jmhamm...@clearwire.net
CC: tmic-list@eskimo.com

 I'm so sorry to hear that. I will pray for your family.
 Cheryl

--- On Tue, 8/17/10, Jill Hammond 3jmhamm...@clearwire.net wrote:


From: Jill Hammond 3jmhamm...@clearwire.net
Subject: [TMIC] Update on Mike
To: Anna  Jim  jnawil...@roadrunner.com, Annie  
annielyman1...@yahoo.com, Becky  Steve mcsmi...@adelphia.net, Beth  
Greg g...@comcast.net, Bob  Beverly  b.doerfl...@gmail.com, 'Boyd' 
b...@boydbryant.com, Carole Matteson carolematte...@hotmail.com, Char 
Brower charsreti...@hotmail.com, Cheryl Hammond i...@todaydata.com, 
Cindy Dunn cdunn53...@aol.com, Craig  Candi bur...@comcast.net, 
'Craig Fiore' cr...@ultra6.eskimo.com, fi...@dhs.gov, 'David and Patty 
Brooks' blueba...@verizon.net, 'David Gay' raega...@yahoo.com, Dennis  
Pam burpee...@msn.com, 'Earl Fordham' earl.ford...@gmail.com,
 Elaine Boos elaineb...@bellsouth.net, Eric  Eri 
ericshamm...@hotmail.com, Fred  Susan graceann1...@charter.net, Gil  
Mari cdav...@dc.rr.com, 'James Fulmer' jedi...@gmail.com, Jan 
Hlavaty-LaPosa  janet.hlavaty-lap...@dhs.gov, Jim and Bobbi  
jimbobk...@msn.com, Johanna  mjber...@verizon.net, Judy  Karl 
romocharlo...@hotmail.com, Keenan kee...@seattlegeek.net, Kendra  
kwa...@comcast.net, Lenny Lisa len.l...@verizon.net, Lisa  
l...@lisalundt.com, Lynn  Jade lynn.mari...@pfpa.mil, Mari  Gary 
wordfromwis...@smtel.com, marie swanson swansonbythe...@comcast.net, 
'Mica Ward' m...@detech.net, Mike  Nancy mmccallis...@soundandsea.com, 
Nancy npurcell1...@yahoo.com, Noah  n...@noahconrad.com, Pat 
Allegretti paa...@gmail.com,
 Pat and Corky pjgren...@hotmail.com, Pat Doebele 
grandmap...@comcast.net, Pat Massey  patrick.mas...@dhs.gov, Paula  
paula.lazz...@attachmate.com, PJ  pjn...@yahoo.com, Ron  
ron.brook...@att.net, 'Sally' sa...@bsorenson.com, Sarah Bell-Schell  
maeb...@vandals.uidaho.edu, 'Scott Hamilton' scotthamil...@live.com, 
Sharon  Steve  pianica...@comcast.net, 'Sheri Meyer' 
sheme...@cisco.com, Steve  Gail  crescentc...@nwi.net, Steve and Jo 
stevejojohn...@msn.com, Susan  Ted Roth susanema...@mchsi.com, Tmic 
tmic-list@eskimo.com, Tom  Deb  t...@ddoel.com, 'vanessa Quinn' 
vanessa.qu...@dhs.gov, Wayne  wme...@ci.everett.wa.us, Zsolt  Patty 
zdor...@comcast.net
Date: Tuesday, August 17, 2010, 11:16 AM






Hello Family and Friends,
 
Sorry to send this information over mass email, but it’s the fastest way to 
keep everyone informed.  Over the last couple of weeks, Mike has been very 
disoriented, sleeping a lot and losing weight. The MRI test that he had earlier 
this week indicates that the cancer has spread to the brain.  We are meeting 
w/the Oncologist today and hopefully get more answers and find out what our 
course of treatment will be. I’ll keep you informed as soon as we can.   Keep 
us in your prayers….Love, The Hammond Team  
  

[TMIC] Update

2010-06-01 Thread Jill Hammond
Hi, everyone, I would like to give you an update on what is happening.
Last week I received the results of both my latest PET scan and CAT scan.  I
am now considered to be in remission.   Yahoo!!.All of the prayers that
you offered were heard.   Now, I can look forward to putting my energy into
getting better.   I am now volunteering once a week at the Cancer Center
where I received treatment.  Now, it is as a worker for the American Cancer
Society working with new patients.  When you have Been there, done that,
it is much easier to talk to someone about their concerns or questions.  I
am contemplating some other volunteer activities and also some work with my
last employer as a volunteer.  

 

I do not have any more tests for several months, but will keep you informed
of any changes.  On behalf of all of Team Hammond (Mike, Jill, Joel and
Janel) I want to thank you for your thoughts, prayers, emails, calls and
cards, they all meant a great deal to us.  God bless each of you and we'll
be talking to you soon.   All the best, and all our love,   Team Hammond

 



Re: [TMIC] Update

2010-06-01 Thread jrushton
 OHMYGOSH!!!  Prayers answered for sure!  What wonderful news from our dear
friends...Thank you for sharing with us!!! Loves and hugs..Jeanne
 
---Original Message---
 
From: Jill Hammond
Date: 6/1/2010 6:29:05 PM
To: Anna  Jim;  Annie;  Becky  Steve;  Beth  Greg;  Bob  Beverly;  'Boyd
;  Carole Matteson;  Char Brower;  Cheryl Hammond;  Cindy Dunn;  Craig 
Candi;  'Craig Fiore';  fi...@dhs.gov;  David Brooks;  'David Gay';  Dennis
 Pam;  'Earl Fordham';  Elaine Boos;  Eric  Eri;  Fred  Susan;  Gil 
Mari;  'James Fulmer';  Jan Hlavaty-LaPosa;  Jim and Bobbi;  Johanna;  Judy
 Karl;  Keenan;  Kendra;  Lenny Lisa;  Lisa;  Lynn  Jade;  Mari  Gary; 
marie swanson;  'Mica Ward';  Mike  Nancy;  Nancy;  Noah;  Pat Allegretti; 
Pat and Corky;  Pat Doebele;  Pat Massey;  Paula;  PJ;  Ron;  'Sally'; 
Sarah Bell-Schell;  'Scott Hamilton';  Sharon  Steve;  'Sheri Meyer'; 
Steve  Gail;  Steve and Jo;  Susan  Ted Roth;  Tmic;  Tom  Deb;  'vanessa
Quinn';  Wayne;  Zsolt  Patty
Subject: [TMIC] Update
 
Hi, everyone, I would like to give you an update on what is happening.  
Last week I received the results of both my latest PET scan and CAT scan.  I
am now considered to be in remission.   Yahoo!!.All of the prayers that
you offered were heard.   Now, I can look forward to putting my energy into
getting better.   I am now volunteering once a week at the Cancer Center
where I received treatment.  Now, it is as a worker for the American Cancer
Society working with new patients.  When you have “Been there, done that”,
it is much easier to talk to someone about their concerns or questions.  I
am contemplating some other volunteer activities and also some work with my
last employer as a volunteer.  
 
I do not have any more tests for several months, but will keep you informed
of any changes.  On behalf of all of “Team Hammond” (Mike, Jill, Joel and
Janel) I want to thank you for your thoughts, prayers, emails, calls and
cards, they all meant a great deal to us.  God bless each of you and we’ll
be talking to you soon.   All the best, and all our love,   Team Hammond
 
 01_tile.jpg01_side.gif

Re: [TMIC] Update

2010-06-01 Thread Jan Hargrove
Team Hammond,

Thank goodnesswhat a great message!!  Please know how wonderful
that makes your tm family!  Continue your trip to return of strength and we'll
keep you in our prayers..you know we have much to be thankful for,
too..our Mike is up and running (or some such),

In my opinion, your decision to get into the volunteer mode, has a lot to do
with the strength you've gained through the power of prayer and the folks
who were by your side through this long journey, the medics and the tmers.

Again, thanks for keeping us informed.  Please continue the same as time 
goes along.

Hugs to the whole team!  
janh   Stillwater, OK




Hi, everyone, I would like to give you an update on what is happening.   Last 
week I received the results of both my latest PET scan and CAT scan.  I am now 
considered to be in remission.   Yahoo!!.    All of the prayers that you 
offered were heard.   Now, I can look forward to putting my energy into getting 
better.   I am now volunteering once a week at the Cancer Center where I 
received treatment.  Now, it is as a worker for the American Cancer Society 
working with new patients.  When you have “Been there, done that”, it is much 
easier to talk to someone about their concerns or questions.  I am 
contemplating some other volunteer activities and also some work with my last 
employer as a volunteer.  
 
I do not have any more tests for several months, but will keep you informed of 
any changes.  On behalf of all of “Team Hammond” (Mike, Jill, Joel and Janel ) 
I want to thank you for your thoughts, prayers, emails, calls and cards, they 
all meant a great deal to us.  God bless each of you and we’ll be talking to 
you soon.   All the best, and all our love,   Team Hammond

Re: [TMIC] update of our travels

2010-05-12 Thread Janice Nichols
I think this is absolutely the best thing for you both!!  Email again after 
Los Vegas.  Good for you guys!
Janice



From: Barbara Alma 
Sent: Wednesday, May 12, 2010 5:07 PM
To: tmic-list@eskimo.com 
Subject: [TMIC] update of our travels


We've had our share of everything from a warm 83 degrees to a cold 45, and very 
windy and cold to so pleasantly warm.  Our trip hasn't been without it's 
problems, but if we hadn't have gone for it, we would have missed so much that 
we would have never done.  We would never have set out to see most of the 
country that we did on it's own, only because of where it all fit together in 
the big puzzle of our country.  I've needed some down time, but I do that at 
home too.  

Other than the night in the shelter, until yesterday things were going really 
well.  I woke up feeling really weak and then I was coughing up some blood 
while brushing my teeth.  Since I'm on blood thinners, I have to pay attention 
to this, and it generally means that I've got pneumonia.  So off we went to 
find a hospital for a chest x-ray and treatment.  We are in southern Colorado 
in a beautiful little town at 7,500 ft elevation called Pagosa Springs and they 
have a little hospital that opened up two years ago.  Well, of course I had 
pneumonia, my oxygen level was at 85, which is low, and with oxygen treatment I 
couldn't hold it higher, so the doc wouldn't let me go back to our condo and he 
admitted me.  I cried as I didn't ever want to be in a hospital again after 
spending 5-1/2 weeks when I got TM.  Once admitted I found out that I was the 
only patient in the hospital, so I teased them about admitting me because they 
needed the revenue.  Although none of us ever want to be in the hospital, if 
you ever get the luxury of being in the hospital all by yourself, it's the way 
to be in one.  You get so much care, you cannot believe it.  I had 3 nurses 
without too many patients to care for during the day who worked the E/R and the 
hospital ward, but nobody else came into the E/R till night time.  During the 
night, there were 2 on duty and they had 2 people come in with kidney stones so 
didn't stay too long.  They wouldn't let me go to the bathroom on my own since 
I was very weak, even with a bedside commode, so when I rang the bell, they 
were there in a minute.  Imagine that!  Well, with so much good care, a darned 
good IV antibiotic, oxygen and breathing treatments, I was able to be released 
today.  Overall, it wasn't as traumatic after I settled in as I thought it 
would be.   

So, I'm going to be taking it easy for a few days, and on Friday we're off to 
Las Vegas for a week and then home.  I'm starting to look forward to being home 
now, but it took this long, almost 6 weeks, lol. 

Hugs, Barbara A in Auburn CA

RE: [TMIC] Update

2010-04-03 Thread Patricia Cooley
Hi Mike and the rest of your team

 

I am so glad to hear your latest update.  I have been looking for an update
from you for some weeks now.  I am so very glad to hear that you received
some good news, and will continue to pray that your recovery continues.  I
hope you enjoy your retirement.  As you mentioned, volunteering at the
cancer center is a wonderful idea.  It feels good to be able to give back.
Also, now is a time to fully enjoy your family and friends that were all
praying for you these past months.

 

Please continue to keep us all informed.

 

Happy Easter to you and your family.

 

Patti - Wisconsin

 

From: Jill Hammond [mailto:3jmhamm...@clearwire.net] 
Sent: Friday, April 02, 2010 7:09 PM
To: Anna  Jim ; Annie ; Becky  Steve; Beth  Greg; Bob  Beverly ; 'Boyd';
Carole Matteson; Char Brower; Cheryl Hammond; Cindy Dunn; Craig  Candi;
'Craig Fiore'; fi...@dhs.gov; David Brooks; 'David Gay'; Dennis  Pam; 'Earl
Fordham'; Elaine Boos; Eric  Eri; Fred  Susan; Gil  Mari; 'James Fulmer';
Jan Hlavaty-LaPosa ; Jim and Bobbi ; Johanna ; Judy  Karl; Keenan; Kendra ;
Lenny Lisa; Lisa ; Lynn  Jade; Mari  Gary; marie swanson; 'Mica Ward';
Mike  Nancy; Nancy; Noah ; Pat Allegretti; Pat and Corky; Pat Doebele; Pat
Massey ; Paula ; PJ ; Ron ; 'Sally'; Sarah Bell-Schell ; 'Scott Hamilton';
Sharon  Steve ; 'Sheri Meyer'; Steve  Gail ; Steve and Jo; Susan  Ted
Roth ; Tmic; Tom  Deb ; 'vanessa Quinn'; Wayne ; Zsolt  Patty
Subject: [TMIC] Update

 

Please see the attached Update.   Mike



[TMIC] Update

2010-04-03 Thread Jan Hargrove


Jill and Mike,
 
What a special time to let us know of the prgress Mike's
made!! This is what we've all been praying for.
 
As to your retirement, I think that was smart.you need
all the energy you can muster to share life with your family,
do the volunteering at the place that's meant so much to
you and your family, and to be able to just take it easy!!!
 
Thanks for keeping us informed and on the prayer list and
please continue to keep us updated.
 
What a wonderful Easter for you and the rest of your family!
 
Hugs, janh

[TMIC] Update

2010-04-02 Thread Jill Hammond
Please see the attached Update.   Mike



UPDATE.doc
Description: MS-Word document


Re: [TMIC] Update

2010-04-02 Thread Janice Nichols
This is certainly good news!   Sounds like you want to get active again, 
which is great.But don't jump into things too fast and take a chance on 
getting down.
Activity is good for you, just don't overdo it. We are so happy for you.
Janice


From: Jill Hammond 
Sent: Friday, April 02, 2010 7:08 PM
To: Anna  Jim ; Annie ; Becky  Steve ; Beth  Greg ; Bob  Beverly ; 'Boyd' ; 
Carole Matteson ; Char Brower ; Cheryl Hammond ; Cindy Dunn ; Craig  Candi ; 
'Craig Fiore' ; fi...@dhs.gov ; David Brooks ; 'David Gay' ; Dennis  Pam ; 
'Earl Fordham' ; Elaine Boos ; Eric  Eri ; Fred  Susan ; Gil  Mari ; 'James 
Fulmer' ; Jan Hlavaty-LaPosa ; Jim and Bobbi ; Johanna ; Judy  Karl ; Keenan ; 
Kendra ; Lenny Lisa ; Lisa ; Lynn  Jade ; Mari  Gary ; marie swanson ; 'Mica 
Ward' ; Mike  Nancy ; Nancy ; Noah ; Pat Allegretti ; Pat and Corky ; Pat 
Doebele ; Pat Massey ; Paula ; PJ ; Ron ; 'Sally' ; Sarah Bell-Schell ; 'Scott 
Hamilton' ; Sharon  Steve ; 'Sheri Meyer' ; Steve  Gail ; Steve and Jo ; 
Susan  Ted Roth ; Tmic ; Tom  Deb ; 'vanessa Quinn' ; Wayne ; Zsolt  Patty 
Subject: [TMIC] Update


Please see the attached Update.   Mike


Re: [TMIC] Update

2010-01-07 Thread L T CHERPESKI
Hi Team Hammond,

Thanks for the update.  Sorry to hear that you will be going for more chemo; 
however, the results so far sound very encouraging.  Mike, you have remained so 
strong and so positive throughout all of this. And I think we all agree that 
can't be easy.

Very encouraging news and looking forward to more good news after these 
treatments are done.

Take care and know that we are thinking of you and your family
Linda
  - Original Message - 
  From: Jill Hammondmailto:3jmhamm...@clearwire.net 
  To: Anna  Jim mailto:jnawil...@roadrunner.com; Annie 
mailto:annielyman1...@yahoo.com; Becky  Stevemailto:mcsmi...@adelphia.net 
; Beth  Gregmailto:g...@comcast.net ; Bob  Beverly 
mailto:b.doerfl...@gmail.com; 'Boyd'mailto:b...@boydbryant.com ; Carole 
Mattesonmailto:carolematte...@hotmail.com ; Char 
Browermailto:charsreti...@hotmail.com ; Cheryl 
Hammondmailto:i...@todaydata.com ; Cindy Dunnmailto:cdunn53...@aol.com ; 
Craig  Candimailto:bur...@comcast.net ; 'Craig 
Fiore'mailto:cr...@ultra6.eskimo.com ; fi...@dhs.govmailto:fi...@dhs.gov ; 
David Brooksmailto:ba...@shawneelink.net ; 'David 
Gay'mailto:raega...@yahoo.com ; Denise  Pammailto:burpee...@msn.com ; 
'Earl Fordham'mailto:earl.ford...@gmail.com ; Elaine 
Boosmailto:elaineb...@bellsouth.net ; Eric  
Erimailto:ericshamm...@hotmail.com ; Fred  
Susanmailto:graceann1...@charter.net ; Gil  Marimailto:cdav...@dc.rr.com ; 
'James Fulmer'mailto:jedi...@gmail.com ; Jan Hlavaty-LaPosa 
mailto:janet.hlavaty-lap...@dhs.gov; Jim and Bobbi 
mailto:jimbobk...@msn.com; Johanna mailto:mjber...@verizon.net; Judy  
Karlmailto:romocharlo...@hotmail.com ; Keenanmailto:kee...@seattlegeek.net 
; Kendra mailto:kwa...@comcast.net; Lenny Lisamailto:len.l...@verizon.net ; 
Lisa mailto:l...@lisalundt.com; Lynn  Jademailto:lynn.mari...@pfpa.mil ; 
Mari  Garymailto:wordfromwis...@smtel.com ; marie 
swansonmailto:swansonbythe...@comcast.net ; 'Mica 
Ward'mailto:m...@detech.net ; Mike  
Nancymailto:mmccallis...@soundandsea.com ; 
Nancymailto:npurcell1...@yahoo.com ; Noah mailto:n...@noahconrad.com; Pat 
Allegrettimailto:paa...@gmail.com ; Pat and 
Corkymailto:pjgren...@hotmail.com ; Pat 
Doebelemailto:grandmap...@comcast.net ; Pat Massey 
mailto:patrick.mas...@dhs.gov; Paula mailto:paula.lazz...@attachmate.com; 
PJ mailto:pjn...@yahoo.com; Ron mailto:ron.brook...@att.net; 
Sallymailto:sa...@bsorenson.com ; Sarah Bell-Schell 
mailto:maeb...@vandals.uidaho.edu; 'Scott 
Hamilton'mailto:scotthamil...@live.com ; Sharon  Steve 
mailto:pianica...@comcast.net; 'Sheri Meyer'mailto:sheme...@cisco.com ; 
Steve  Gail mailto:crescentc...@nwi.net; Steve and 
Jomailto:stevejojohn...@msn.com ; Susan  Ted Roth 
mailto:susanema...@mchsi.com; Tmicmailto:tmic-list@eskimo.com ; Tom  Deb 
mailto:t...@ddoel.com; 'vanessa Quinn'mailto:vanessa.qu...@dhs.gov ; Wayne 
mailto:wme...@ci.everett.wa.us; Zsolt  Pattymailto:zdor...@comcast.net 
  Sent: Wednesday, January 06, 2010 9:23 AM
  Subject: [TMIC] Update


  Update # 8

   

  Hi, everyone,

   

  Team Hammond here with the results of my PET scan.   Yesterday we learned 
that I will be going back in for chemo starting today.  There were a couple of 
spots left on the scan which means at least two more chemo sessions are needed. 
 Both of the doctors we saw yesterday were very pleased with the results so 
far, and that is very encouraging.  

  The team here is very encouraged by the results and looks forward to stamping 
this out in the next sessions.  Please continue to keep us all in your prayers 
and we will keep fighting.  

   Take care,   Team Hammond

   


[TMIC] Update

2010-01-06 Thread Jill Hammond
Update # 8

 

Hi, everyone,

 

Team Hammond here with the results of my PET scan.   Yesterday we learned
that I will be going back in for chemo starting today.  There were a couple
of spots left on the scan which means at least two more chemo sessions are
needed.  Both of the doctors we saw yesterday were very pleased with the
results so far, and that is very encouraging.  

The team here is very encouraged by the results and looks forward to
stamping this out in the next sessions.  Please continue to keep us all in
your prayers and we will keep fighting.  

 Take care,   Team Hammond

 



Re: [TMIC] Update

2010-01-06 Thread Janice Nichols
Wow, that sounds wonderful.   It takes a village! Keep us posted on how 
the next 2 chemo sessions go.
Janice



From: Jill Hammond 
Sent: Wednesday, January 06, 2010 10:23 AM
To: Anna  Jim ; Annie ; Becky  Steve ; Beth  Greg ; Bob  Beverly ; 'Boyd' ; 
Carole Matteson ; Char Brower ; Cheryl Hammond ; Cindy Dunn ; Craig  Candi ; 
'Craig Fiore' ; fi...@dhs.gov ; David Brooks ; 'David Gay' ; Denise  Pam ; 
'Earl Fordham' ; Elaine Boos ; Eric  Eri ; Fred  Susan ; Gil  Mari ; 'James 
Fulmer' ; Jan Hlavaty-LaPosa ; Jim and Bobbi ; Johanna ; Judy  Karl ; Keenan ; 
Kendra ; Lenny Lisa ; Lisa ; Lynn  Jade ; Mari  Gary ; marie swanson ; 'Mica 
Ward' ; Mike  Nancy ; Nancy ; Noah ; Pat Allegretti ; Pat and Corky ; Pat 
Doebele ; Pat Massey ; Paula ; PJ ; Ron ; Sally ; Sarah Bell-Schell ; 'Scott 
Hamilton' ; Sharon  Steve ; 'Sheri Meyer' ; Steve  Gail ; Steve and Jo ; 
Susan  Ted Roth ; Tmic ; Tom  Deb ; 'vanessa Quinn' ; Wayne ; Zsolt  Patty 
Subject: [TMIC] Update


Update # 8

 

Hi, everyone,

 

Team Hammond here with the results of my PET scan.   Yesterday we learned that 
I will be going back in for chemo starting today.  There were a couple of spots 
left on the scan which means at least two more chemo sessions are needed.  Both 
of the doctors we saw yesterday were very pleased with the results so far, and 
that is very encouraging.  

The team here is very encouraged by the results and looks forward to stamping 
this out in the next sessions.  Please continue to keep us all in your prayers 
and we will keep fighting.  

 Take care,   Team Hammond

 


Re: [TMIC] Update

2010-01-06 Thread Jan Hargrove
Hey Mike,

This member of the Hammond Team is:  1.) Pleased with your report 
and 2.) Continuing my Prayers for you and your family!

This is good news!! I liked the reactions of the 2 doctors, that says 
a lot! What a great gift for the New Year!! I hope that your trip is 
almost done and soon you'll be your old self!!

Hugs, 
janh    Stillwater, OK




Update # 8
 
Hi, everyone,
 
Team Hammond here with the results of my PET scan.   Yesterday we learned that 
I will be going back in for chemo starting today.  There were a couple of spots 
left on the scan which means at least two more chemo sessions are needed.  Both 
of the doctors we saw yesterday were very pleased with the results so far, and 
that is very encouraging.  
The team here is very encouraged by the results and looks forward to stamping 
this out in the next sessions.  Please continue to keep us all in your prayers 
and we will keep fighting.  
 Take care,   Team Hammond

Re: [TMIC] Update 5

2009-11-08 Thread L T CHERPESKI
Mike, great news about the radiation treatments!  Yay - be done with those!  
Now we'll keep right on praying that those chemo treatments go well for you.  
God Bless Team Hammond

hugs,
Linda


  Sent: Saturday, November 07, 2009 1:29 PM
  Subject: [TMIC] Update 5


  Hi, Everybody, Here is an update from Team Hammond


Re: [TMIC] Update 5

2009-11-07 Thread jrushton
What a wonderful friend and family you are!  Just love hearing from you and
you are still in my prayers which couldn't be any better for getting you
better.  You Hammonds are something else!  Jeanne in Dayton, WA

---Original Message---
 
From: Jill Hammond
Date: 11/7/2009 2:30:56 PM
To: Anna  Jim;  Annie;  Becky  Steve;  Beth  Greg;  Bob  Beverly;  'Boyd
;  Carole Matteson;  Char Brower;  Cheryl Hammond;  Cindy Dunn;  Craig 
Candi;  'Craig Fiore';  fi...@dhs.gov;  David Brooks;  'David Gay';  Denise
 Pam;  'Earl Fordham';  Elaine Boos;  Eric  Eri;  Fred  Susan;  Gil 
Mari;  'James Fulmer';  Jan Hlavaty-LaPosa;  Jim and Bobbi;  Johanna;  Judy
 Karl;  Keenan;  Kendra;  Lenny Lisa;  Lisa;  Lynn  Jade;  Mari  Gary; 
marie swanson;  'Mica Ward';  Mike  Nancy;  Nancy;  Noah;  Pat Allegretti; 
Pat and Corky;  Pat Doebele;  Pat Massey;  Paula;  PJ;  Ron;  Sally;  Sarah
Bell-Schell;  'Scott Hamilton';  Sharon  Steve;  'Sheri Meyer';  Steve 
Gail;  Steve and Jo;  Susan  Ted Roth;  Tmic;  Tom  Deb;  'vanessa Quinn';
 Wayne;  Zsolt  Patty
Subject: [TMIC] Update 5
 
Hi, Everybody, Here is an update from Team Hammond
 dog_chase2.gif

Re: [TMIC] Update on Mike

2009-10-27 Thread Janice
Mike,
Am so glad the tumor is shrinking - such great news! But, as usual, nothing 
is easy.You have really paid a price for
the tumor improvement,  but this may be it for fighting extra battles. 
Hopefully, it will be a smoother sail from here 
until complete recovery. We wish the best for you and your Team.
Janice
  - Original Message - 
  From: L T CHERPESKI 
  To: Jill Hammond ; Transverse Mylitis Group ; Catherine 
  Sent: Monday, October 26, 2009 7:56 PM
  Subject: Re: [TMIC] Update on Mike


  Hello Team Hammond,

  Mike, such good news to hear your tumor is shrinking!  Remember as Catherine 
said, we are all here still praying for you and Jill.  One day at a time, Mike. 
 One day. God Bless you and Jill.

  Love, Linda
- Original Message - 
From: Catherine 
To: Jill Hammond ; Transverse Mylitis Group 
Sent: Sunday, October 25, 2009 4:16 PM
Subject: Re: [TMIC] Update on Mike


We are all here still praying for you and Jill.  God Bless Youmay He 
hold you in the palm of his hand and give you comfort, release you of pain and 
keep you safe.



Love Catherine   

Life is short, Break the rules sometimes, Forgive quickly, Kiss slowly, 
Love truly, Laugh uncontrollably, And never regret anything that made you smile







From: Jill Hammond 3jmhamm...@clearwire.net
To: Anna  Jim jnawil...@roadrunner.com; Annie 
annielyman1...@yahoo.com; Becky  Steve mcsmi...@adelphia.net; Beth  Greg 
g...@comcast.net; Bob  Beverly b.doerfl...@gmail.com; Boyd 
b...@boydbryant.com; Carole Matteson carolematte...@hotmail.com; Char 
Brower charsreti...@hotmail.com; Cheryl Hammond i...@todaydata.com; Cindy 
Dunn cdunn53...@aol.com; Craig  Candi bur...@comcast.net; Craig Fiore 
cr...@ultra6.eskimo.com; fi...@dhs.gov; David Brooks ba...@shawneelink.net; 
David Gay raega...@yahoo.com; Denise  Pam burpee...@msn.com; Earl Fordham 
earl.ford...@gmail.com; Elaine Boos elaineb...@bellsouth.net; Eric  Eri 
ericshamm...@hotmail.com; Fred  Susan graceann1...@charter.net; Gil  Mari 
cdav...@dc.rr.com; James Fulmer jedi...@gmail.com; Jan Hlavaty-LaPosa 
janet.hlavaty-lap...@dhs.gov; Jim and Bobbi jimbobk...@msn.com; Johanna 
mjber...@verizon.net; Judy  Karl romocharlo...@hotmail.com; Keenan 
kee...@seattlegeek.net; Kendra kwa...@comcast.net; Lenny Lisa 
len.l...@verizon.net; Lisa l...@lisalundt.com; Lynn  Jade 
lynn.mari...@pfpa.mil; Mari  Gary wordfromwis...@smtel.com; marie swanson 
swansonbythe...@comcast.net; Mica Ward m...@detech.net; Mike  Nancy 
mmccallis...@soundandsea.com; Nancy npurcell1...@yahoo.com; Noah 
n...@noahconrad.com; Pat Allegretti paa...@gmail.com; Pat and Corky 
pjgren...@hotmail.com; Pat Doebele grandmap...@comcast.net; Pat Massey 
patrick.mas...@dhs.gov; Paula paula.lazz...@attachmate.com; PJ 
pjn...@yahoo.com; Ron ron.brook...@att.net; Sally sa...@bsorenson.com; 
Sarah Bell-Schell maeb...@vandals.uidaho.edu; Scott Hamilton 
scotthamil...@live.com; Sharon  Steve pianica...@comcast.net; Sheri Meyer 
sheme...@cisco.com; Steve  Gail crescentc...@nwi.net; Steve and Jo 
stevejojohn...@msn.com; Susan  Ted Roth susanema...@mchsi.com; Tmic 
tmic-list@eskimo.com; Tom  Deb t...@ddoel.com; vanessa Quinn 
vanessa.qu...@dhs.gov; Wayne wme...@ci.everett.wa.us; Zsolt  Patty 
zdor...@comcast.net
Sent: Sun, October 25, 2009 5:50:23 PM
Subject: [TMIC] Update on Mike


Well, here we are for the next update on Team Hammond.  The second round of 
Chemo finished on Wednesday, October 14.  Mike, at that point was also down to 
only 12 radiation treatments left.  After the treatment on Thursday the 15th, 
we had a consultation with the Doctor and he was very positive.   The tumor is 
definitely shrinking, Yeah, way to go Team, those prayers are working.   In all 
the rest of this, I am still loosing a little weight, went under 180 for the 
first time since around third grade somewhere.  One of the worst things about 
coming down off Chemo is that they give you steroids during it.  I don’t know 
if they are like the ones that some athletes take, but they can have them, you 
feel like you are on constant edge, cannot sit still or concentrate on 
anything.  That seems to be wearing down fast today.   Well,, this all amounted 
to too much of a good thing and Sunday, October 18th I went back into the 
hospital.  Jill was finally able to spring me yesterday, Saturday and so here 
we are once again trying to figure out what train hit us.  This one seems 
mostly caused by diarrhea and dehydration accompanied by an infection and 
assorted other complaints.  



I have now found a new low.  The last time it only seemed bad, this time it 
was close to being unfathomable.  I could not seem to find a way out.  Every 
time I got to the bottom and wanted to give up I thought about all of you who 
have sent cards, emails, phone calls and kept in touch and kept up the prayers. 
 Once again

Re: [TMIC] Update on Mike

2009-10-26 Thread L T CHERPESKI
Hello Team Hammond,

Mike, such good news to hear your tumor is shrinking!  Remember as Catherine 
said, we are all here still praying for you and Jill.  One day at a time, Mike. 
 One day. God Bless you and Jill.

Love, Linda
  - Original Message - 
  From: Catherinemailto:camoa...@yahoo.com 
  To: Jill Hammondmailto:3jmhamm...@clearwire.net ; Transverse Mylitis 
Groupmailto:tmic-list@eskimo.com 
  Sent: Sunday, October 25, 2009 4:16 PM
  Subject: Re: [TMIC] Update on Mike


  We are all here still praying for you and Jill.  God Bless Youmay He hold 
you in the palm of his hand and give you comfort, release you of pain and keep 
you safe.



  Love Catherine   

  Life is short, Break the rules sometimes, Forgive quickly, Kiss slowly, Love 
truly, Laugh uncontrollably, And never regret anything that made you smile






--
  From: Jill Hammond 3jmhamm...@clearwire.net
  To: Anna  Jim jnawil...@roadrunner.com; Annie annielyman1...@yahoo.com; 
Becky  Steve mcsmi...@adelphia.net; Beth  Greg g...@comcast.net; Bob  
Beverly b.doerfl...@gmail.com; Boyd b...@boydbryant.com; Carole Matteson 
carolematte...@hotmail.com; Char Brower charsreti...@hotmail.com; Cheryl 
Hammond i...@todaydata.com; Cindy Dunn cdunn53...@aol.com; Craig  Candi 
bur...@comcast.net; Craig Fiore cr...@ultra6.eskimo.com; fi...@dhs.gov; 
David Brooks ba...@shawneelink.net; David Gay raega...@yahoo.com; Denise  
Pam burpee...@msn.com; Earl Fordham earl.ford...@gmail.com; Elaine Boos 
elaineb...@bellsouth.net; Eric  Eri ericshamm...@hotmail.com; Fred  Susan 
graceann1...@charter.net; Gil  Mari cdav...@dc.rr.com; James Fulmer 
jedi...@gmail.com; Jan Hlavaty-LaPosa janet.hlavaty-lap...@dhs.gov; Jim and 
Bobbi jimbobk...@msn.com; Johanna mjber...@verizon.net; Judy  Karl 
romocharlo...@hotmail.com; Keenan kee...@seattlegeek.net; Kendra 
kwa...@comcast.net; Lenny Lisa len.l...@verizon.net; Lisa 
l...@lisalundt.com; Lynn  Jade lynn.mari...@pfpa.mil; Mari  Gary 
wordfromwis...@smtel.com; marie swanson swansonbythe...@comcast.net; Mica 
Ward m...@detech.net; Mike  Nancy mmccallis...@soundandsea.com; Nancy 
npurcell1...@yahoo.com; Noah n...@noahconrad.com; Pat Allegretti 
paa...@gmail.com; Pat and Corky pjgren...@hotmail.com; Pat Doebele 
grandmap...@comcast.net; Pat Massey patrick.mas...@dhs.gov; Paula 
paula.lazz...@attachmate.com; PJ pjn...@yahoo.com; Ron 
ron.brook...@att.net; Sally sa...@bsorenson.com; Sarah Bell-Schell 
maeb...@vandals.uidaho.edu; Scott Hamilton scotthamil...@live.com; Sharon  
Steve pianica...@comcast.net; Sheri Meyer sheme...@cisco.com; Steve  Gail 
crescentc...@nwi.net; Steve and Jo stevejojohn...@msn.com; Susan  Ted Roth 
susanema...@mchsi.com; Tmic tmic-list@eskimo.com; Tom  Deb 
t...@ddoel.com; vanessa Quinn vanessa.qu...@dhs.gov; Wayne 
wme...@ci.everett.wa.us; Zsolt  Patty zdor...@comcast.net
  Sent: Sun, October 25, 2009 5:50:23 PM
  Subject: [TMIC] Update on Mike


  Well, here we are for the next update on Team Hammond.  The second round of 
Chemo finished on Wednesday, October 14.  Mike, at that point was also down to 
only 12 radiation treatments left.  After the treatment on Thursday the 15th, 
we had a consultation with the Doctor and he was very positive.   The tumor is 
definitely shrinking, Yeah, way to go Team, those prayers are working.   In all 
the rest of this, I am still loosing a little weight, went under 180 for the 
first time since around third grade somewhere.  One of the worst things about 
coming down off Chemo is that they give you steroids during it.  I don’t know 
if they are like the ones that some athletes take, but they can have them, you 
feel like you are on constant edge, cannot sit still or concentrate on 
anything.  That seems to be wearing down fast today.   Well,, this all amounted 
to too much of a good thing and Sunday, October 18th I went back into the 
hospital.  Jill was finally able to spring me yesterday, Saturday and so here 
we are once again trying to figure out what train hit us.  This one seems 
mostly caused by diarrhea and dehydration accompanied by an infection and 
assorted other complaints.  



  I have now found a new low.  The last time it only seemed bad, this time it 
was close to being unfathomable.  I could not seem to find a way out.  Every 
time I got to the bottom and wanted to give up I thought about all of you who 
have sent cards, emails, phone calls and kept in touch and kept up the prayers. 
 Once again that made all the difference in the world, and God bless you all 
for doing that. Jill will probably back this up, but I am a stubborn person at 
times.  At first I was hesitant, somewhat to ask for help, well, let me tell 
you that is gone.  I’m busy keeping the Lord going by turning over problems to 
Him.  



  I will tell you that I am drawing on that well of thoughts and prayers often, 
there are times when this journey is measured one day at a time. Faith

[TMIC] Update on Mike

2009-10-25 Thread Jill Hammond
Well, here we are for the next update on Team Hammond.  The second round of
Chemo finished on Wednesday, October 14.  Mike, at that point was also down
to only 12 radiation treatments left.  After the treatment on Thursday the
15th, we had a consultation with the Doctor and he was very positive.   The
tumor is definitely shrinking, Yeah, way to go Team, those prayers are
working.   In all the rest of this, I am still loosing a little weight, went
under 180 for the first time since around third grade somewhere.  One of the
worst things about coming down off Chemo is that they give you steroids
during it.  I don't know if they are like the ones that some athletes take,
but they can have them, you feel like you are on constant edge, cannot sit
still or concentrate on anything.  That seems to be wearing down fast today.
Well,, this all amounted to too much of a good thing and Sunday, October
18th I went back into the hospital.  Jill was finally able to spring me
yesterday, Saturday and so here we are once again trying to figure out what
train hit us.  This one seems mostly caused by diarrhea and dehydration
accompanied by an infection and assorted other complaints.  

 

I have now found a new low.  The last time it only seemed bad, this time it
was close to being unfathomable.  I could not seem to find a way out.  Every
time I got to the bottom and wanted to give up I thought about all of you
who have sent cards, emails, phone calls and kept in touch and kept up the
prayers.  Once again that made all the difference in the world, and God
bless you all for doing that. Jill will probably back this up, but I am a
stubborn person at times.  At first I was hesitant, somewhat to ask for
help, well, let me tell you that is gone.  I'm busy keeping the Lord going
by turning over problems to Him.  

 

I will tell you that I am drawing on that well of thoughts and prayers
often, there are times when this journey is measured one day at a time.
Faith, and knowing there are a lot of people pulling for all of team
Hammond, make it easier, to keep moving forward. I will let everyone know
when my next, and last chemo session is going to happen as soon as I know,
which should be this week.   By the way, this Tuesday may well be my last
radiation treatment, thanks, from Team Hammond, of which you are all a part.


 

 

 



Re: [TMIC] Update on Mike

2009-10-25 Thread Catherine
We are all here still praying for you and Jill.  God Bless Youmay He hold 
you in the palm of his hand and give you comfort, release you of pain and keep 
you safe.

 

Love Catherine   
Life is short, Break the rules sometimes, Forgive quickly, Kiss slowly, Love 
truly, Laugh uncontrollably, And never regret anything that made you smile





From: Jill Hammond 3jmhamm...@clearwire.net
To: Anna  Jim  jnawil...@roadrunner.com; Annie  annielyman1...@yahoo.com; 
Becky  Steve mcsmi...@adelphia.net; Beth  Greg g...@comcast.net; Bob  
Beverly  b.doerfl...@gmail.com; Boyd b...@boydbryant.com; Carole Matteson 
carolematte...@hotmail.com; Char Brower charsreti...@hotmail.com; Cheryl 
Hammond i...@todaydata.com; Cindy Dunn cdunn53...@aol.com; Craig  Candi 
bur...@comcast.net; Craig Fiore cr...@ultra6.eskimo.com; fi...@dhs.gov; 
David Brooks ba...@shawneelink.net; David Gay raega...@yahoo.com; Denise  
Pam burpee...@msn.com; Earl Fordham earl.ford...@gmail.com; Elaine Boos 
elaineb...@bellsouth.net; Eric  Eri ericshamm...@hotmail.com; Fred  Susan 
graceann1...@charter.net; Gil  Mari cdav...@dc.rr.com; James Fulmer 
jedi...@gmail.com; Jan Hlavaty-LaPosa  janet.hlavaty-lap...@dhs.gov; Jim 
and Bobbi  jimbobk...@msn.com; Johanna  mjber...@verizon.net; Judy  Karl 
romocharlo...@hotmail.com; Keenan
 kee...@seattlegeek.net; Kendra  kwa...@comcast.net; Lenny  Lisa 
len.l...@verizon.net; Lisa  l...@lisalundt.com; Lynn  Jade 
lynn.mari...@pfpa.mil; Mari  Gary wordfromwis...@smtel.com; marie swanson 
swansonbythe...@comcast.net; Mica Ward m...@detech.net; Mike  Nancy 
mmccallis...@soundandsea.com; Nancy npurcell1...@yahoo.com; Noah  
n...@noahconrad.com; Pat Allegretti paa...@gmail.com; Pat and Corky 
pjgren...@hotmail.com; Pat Doebele grandmap...@comcast.net; Pat Massey  
patrick.mas...@dhs.gov; Paula  paula.lazz...@attachmate.com; PJ  
pjn...@yahoo.com; Ron  ron.brook...@att.net; Sally sa...@bsorenson.com; 
Sarah Bell-Schell  maeb...@vandals.uidaho.edu; Scott Hamilton 
scotthamil...@live.com; Sharon  Steve  pianica...@comcast.net; Sheri Meyer 
sheme...@cisco.com; Steve  Gail  crescentc...@nwi.net; Steve and Jo 
stevejojohn...@msn.com; Susan  Ted Roth  susanema...@mchsi.com; Tmic 
tmic-list@eskimo.com; Tom
  Deb  t...@ddoel.com; vanessa Quinn vanessa.qu...@dhs.gov; Wayne   
wme...@ci.everett.wa.us; Zsolt  Patty zdor...@comcast.net
Sent: Sun, October 25, 2009 5:50:23 PM
Subject: [TMIC] Update on Mike

 
Well, here we are for the next update on Team Hammond.  The second
round of Chemo finished on Wednesday, October 14.  Mike, at that point was also
down to only 12 radiation treatments left.  After the treatment on Thursday the
15th, we had a consultation with the Doctor and he was very
positive.   The tumor is definitely shrinking, Yeah, way to go Team, those
prayers are working.   In all the rest of this, I am still loosing a little
weight, went under 180 for the first time since around third grade somewhere. 
One of the worst things about coming down off Chemo is that they give you
steroids during it.  I don’t know if they are like the ones that some athletes
take, but they can have them, you feel like you are on constant edge, cannot
sit still or concentrate on anything.  That seems to be wearing down fast
today.   Well,, this all amounted to too much of a good thing and Sunday,
October 18th I went back into the hospital.  Jill was finally able
to spring me yesterday, Saturday and so here we are once again trying to figure
out what train hit us.  This one seems mostly caused by diarrhea and
dehydration accompanied by an infection and assorted other complaints.  
 
I have now found a new low.  The last time it only seemed bad, this
time it was close to being unfathomable.  I could not seem to find a way out. 
Every time I got to the bottom and wanted to give up I thought about all of you
who have sent cards, emails, phone calls and kept in touch and kept up the
prayers.  Once again that made all the difference in the world, and God bless
you all for doing that. Jill will probably back this up, but I am a stubborn
person at times.  At first I was hesitant, somewhat to ask for help, well, let
me tell you that is gone.  I’m busy keeping the Lord going by turning over
problems to Him.  
 
I will tell you that I am drawing on that well of thoughts and prayers
often, there are times when this journey is measured one day at a time. Faith,
and knowing there are a lot of people pulling for all of team Hammond, make it
easier, to keep moving forward. I will let everyone know when my next, and last
chemo session is going to happen as soon as I know, which should be this
week.   By the way, this Tuesday may well be my last radiation treatment,
thanks, from Team Hammond, of which you are all a part.


  

[TMIC] Update from Mike

2009-10-04 Thread Jill Hammond
 

 

Hi Everyone!

 

Well, I am back from three days at the hospital.   Here is what happened in
a nutshell.  Monday I started to get a fever and it went up quick enough
that we called the Doctor and were told to make a beeline for the hospital.
My white blood cell count was in the critical area.  As it turns out, Monday
was the 10th day after the beginning on my first day of my first chemo
session.  This time frame happens to be at the worst for how low you can
get.  Also, as you may remember, I had just had a feeding tube put in and
this may have been the source of the slight infection, the Docs could never
determine just what had happened

 

Monday was the low of my experience so far, I was feeling so bad I wanted to
give up.  This is where all of team Hammond came into play, family and
friends both.  As things got feeling worse, I felt a sort of nudge and
realized I could not give up, there is too much depending on a positive
attitude.  I think what that nudge was, is that a

lot of prayers to the Good Lord prompted Him to give me one swift kick to my
spiritual butt. And, this got me to look ahead, not back.  

 

Since getting out, I have had 2 more radiation treatments, and now, we have
the weekend off.  Thanks to all of you for the cards, prayers, visits, and
whatever.  Next update when needed. 

 

Love ya all, Team Hammond

 



RE: [TMIC] Update on Mike

2009-09-28 Thread Tami Streeter
Yes I agree with Janice.  Your attitude alone is amazing.  

 

'For I know the thoughts and plans that I have for you, says the Lord,
thoughts and plans for welfare and peace and not for evil, to give you hope
in your final outcome'

Jeremiah 29:11

 

You are in our prayers,

Tami

 

  _  

From: Janice [mailto:jan...@centurytel.net] 
Sent: Sunday, September 27, 2009 10:29 PM
To: Jill Hammond; Anna  Jim ; Annie ; Becky  Steve; Beth  Greg; Bob 
Beverly ; Carole Matteson; Char Brower; Cheryl Hammond; Cindy Dunn; Craig 
Candi; David Brooks; Denise  Pam; Elaine Boos; Eric  Eri; Fred  Susan;
Gil  Mari; 'James Fulmer'; Jan Hlavaty-LaPosa ; Jim and Bobbi ; Johanna ;
Judy  Karl; Keenan; Kendra ; Lenny Lisa; Lisa ; Lynn  Jade; Mari  Gary;
marie swanson; Mike  Nancy; Nancy; Noah ; Pat Allegretti; Pat and Corky;
Pat Doebele; Pat Massey ; Paula ; PJ ; Ron ; Sally; Sarah Bell-Schell ;
Sharon  Steve ; 'Sheri Meyer'; Steve  Gail ; Steve and Jo; Susan  Ted
Roth ; Tmic; Tom  Deb ; Wayne ; Zsolt  Patty
Cc: tmic-l...@eskimo.net; ed
Subject: Re: [TMIC] Update on Mike

 

Mike,

You don't know me from Adam, but I am a TM'er and following these emails.
You have my prayers, but also

my complete respect for your courage and outlook/attitude that endears you
to all of us.I guess you realize

you have the dubious honor of being the one that I can look at and say he
is worse off than I am.You have a

lot to fight and it sounds as if you have a lot of fight in you.Don't
think that because we are not there with you

that you are not in our thoughts and prayers.   Please keep us posted -
we care - and God bless.

Janice, Missouri

- Original Message - 

From: Jill mailto:3jmhamm...@clearwire.net  Hammond 

To: Anna mailto:jnawil...@roadrunner.com   Jim ; Annie
mailto:annielyman1...@yahoo.com ; Becky  mailto:mcsmi...@adelphia.net 
Steve ; Beth mailto:g...@comcast.net   Greg ; Bob
mailto:b.doerfl...@gmail.com  Beverly ; Carole
mailto:carolematte...@hotmail.com  Matteson ; Char Brower
mailto:charsreti...@hotmail.com  ; Cheryl Hammond
mailto:i...@todaydata.com  ; Cindy Dunn mailto:cdunn53...@aol.com  ;
Craig  mailto:bur...@comcast.net  Candi ; David
mailto:ba...@shawneelink.net  Brooks ; Denise mailto:burpee...@msn.com
 Pam ; Elaine Boos mailto:elaineb...@bellsouth.net  ; Eric
mailto:ericshamm...@hotmail.com   Eri ; Fred
mailto:graceann1...@charter.net  Susan ; Gil  mailto:cdav...@dc.rr.com
 Mari ; 'James Fulmer' mailto:jedi...@gmail.com  ; Jan
mailto:janet.hlavaty-lap...@dhs.gov  Hlavaty-LaPosa ; Jim and Bobbi
mailto:jimbobk...@msn.com ; Johanna  mailto:mjber...@verizon.net ; Judy
mailto:romocharlo...@hotmail.com   Karl ; Keenan
mailto:kee...@seattlegeek.net  ; Kendra  mailto:kwa...@comcast.net ;
Lenny Lisa mailto:len.l...@verizon.net  ; Lisa
mailto:l...@lisalundt.com ; Lynn  mailto:lynn.mari...@pfpa.mil  Jade ;
Mari  mailto:wordfromwis...@smtel.com  Gary ; marie
mailto:swansonbythe...@comcast.net  swanson ; Mike
mailto:mmccallis...@soundandsea.com  Nancy ; Nancy
mailto:npurcell1...@yahoo.com  ; Noah  mailto:n...@noahconrad.com ; Pat
Allegretti mailto:paa...@gmail.com  ; Pat and Corky
mailto:pjgren...@hotmail.com  ; Pat mailto:grandmap...@comcast.net
Doebele ; Pat Massey  mailto:patrick.mas...@dhs.gov ; Paula
mailto:paula.lazz...@attachmate.com  ; PJ  mailto:pjn...@yahoo.com ; Ron
mailto:ron.brook...@att.net ; Sally mailto:sa...@bsorenson.com  ; Sarah
mailto:maeb...@vandals.uidaho.edu  Bell-Schell ; Sharon
mailto:pianica...@comcast.net  Steve ; 'Sheri Meyer'
mailto:sheme...@cisco.com  ; Steve  mailto:crescentc...@nwi.net  Gail ;
Steve and Jo mailto:stevejojohn...@msn.com  ; Susan
mailto:susanema...@mchsi.com  Ted Roth ; Tmic
mailto:tmic-list@eskimo.com  ; Tom  mailto:t...@ddoel.com  Deb ; Wayne
mailto:wme...@ci.everett.wa.us ; Zsolt  mailto:zdor...@comcast.net 
Patty 

Sent: Sunday, September 27, 2009 11:25 AM

Subject: [TMIC] Update on Mike

 

 

Hi, everyone! 

 

First a little update on what has happened since the last update a couple
weeks ago, and then the schedule for the next round..  

 

Radiation has really started to take a toll on me. Last Friday, Jill took me
in for my 12th rad treatment.  The Tomotherapy machine that they are using
is state of the art.

 

 Even thought our son took me in to have the old bowling ball shaved, now,
my eyebrows are falling out.  We think we may have the perfect Halloween
costume, Dr. really not-so-evil. All I need now is to find the hairless
cat to complete the costume. 

 

Had a feeding tube put in last Thursday   I have completely lost the sense
of smell, and most of taste.  The salivary glands are so far gone that it is
painful to swallow.   Now, I eat 8 cans a day of a liquid nutrient, and
some of my hydration.  This is accomplished by a large syringe to a port in
my stomach just below the rib cage.  Jill and I were able to pick this up
very quickly.  By the way, for the first time in many moons, today I was
able to get into a size 34 waist, yahoo

RE: [TMIC] Update on Mike

2009-09-28 Thread Patricia Cooley
Mile  Jill

 

Thanks for the update.  It sure sound like you are going through h- - l.
All of our prayers and thoughts are with you at this time.  The only choice
one has is to try and be strong for your family and keep your faith.  You
did give me a laugh when you mentioned getting into a smaller size.  I joke
all the time that the only thing that came from having TM is I lost the
40-50 pounds that I have been trying to lose forever.  So far, I have been
able to keep it off and hope to continue to do so.  In fact, I have often
said I would take the weight back if I could get rid to TM.

 

Keep us posted and I will continue to mention you both in my prayers.

 

Patti - Wisconsin 

 

From: Jill Hammond [mailto:3jmhamm...@clearwire.net] 
Sent: Sunday, September 27, 2009 11:25 AM
To: Anna  Jim ; Annie ; Becky  Steve; Beth  Greg; Bob  Beverly ; Carole
Matteson; Char Brower; Cheryl Hammond; Cindy Dunn; Craig  Candi; David
Brooks; Denise  Pam; Elaine Boos; Eric  Eri; Fred  Susan; Gil  Mari;
'James Fulmer'; Jan Hlavaty-LaPosa ; Jim and Bobbi ; Johanna ; Judy  Karl;
Keenan; Kendra ; Lenny Lisa; Lisa ; Lynn  Jade; Mari  Gary; marie swanson;
Mike  Nancy; Nancy; Noah ; Pat Allegretti; Pat and Corky; Pat Doebele; Pat
Massey ; Paula ; PJ ; Ron ; Sally; Sarah Bell-Schell ; Sharon  Steve ;
'Sheri Meyer'; Steve  Gail ; Steve and Jo; Susan  Ted Roth ; Tmic; Tom 
Deb ; Wayne ; Zsolt  Patty
Subject: [TMIC] Update on Mike

 

 

Hi, everyone! 

 

First a little update on what has happened since the last update a couple
weeks ago, and then the schedule for the next round..  

 

Radiation has really started to take a toll on me. Last Friday, Jill took me
in for my 12th rad treatment.  The Tomotherapy machine that they are using
is state of the art.

 

 Even thought our son took me in to have the old bowling ball shaved, now,
my eyebrows are falling out.  We think we may have the perfect Halloween
costume, Dr. really not-so-evil. All I need now is to find the hairless
cat to complete the costume. 

 

Had a feeding tube put in last Thursday   I have completely lost the sense
of smell, and most of taste.  The salivary glands are so far gone that it is
painful to swallow.   Now, I eat 8 cans a day of a liquid nutrient, and
some of my hydration.  This is accomplished by a large syringe to a port in
my stomach just below the rib cage.  Jill and I were able to pick this up
very quickly.  By the way, for the first time in many moons, today I was
able to get into a size 34 waist, yahoo. God Bless ..

 

We had one major bad evening last week in the effort to find a pain killer
that agreed with me.  I certainly qualified as a zombie for about 16 hours,
and Jill thought she was seeing one.  The medication now seems to be working
much better.  

 

Under the heading on miscellaneous, I have certainly been given the
opportunity to practice; humility, gratitude, patience, and numerous others
on a daily basis.  I could not do this without my family and all the friends
who send notes and stop by. 

 

Here is my schedule for the next round of chemo.   The first treatment will
be October 6th, 9:30 am until about 2:00 pm.  Second treatment is the 7th
from 1:30 pm until about 4:30 pm.  Third treatment is October 8th, 1:30 pm
to about 4:30 pm.  All are at the cancer center, 3rd floor on 13th  street,
just east of Colby in Everett

 

If none of the above times are convenient, here is the radiation schedule.
Treatment is on the 2nd floor.  28th September to October 2nd - 4:20 pm.
Week of October 5th - 4:20 pm.  October 12th until 29 - 4:20 pm.

 

You do not have to visit just there... our home phone is 360 658 5878, and
our home address is 4924 66th Ave NE, Marysville, WA  98270.  Either Google
for directions or I can give them to you. 

 

Take care until next time, Mike, Jill and the rest of the team

 



[TMIC] Update on Mike

2009-09-27 Thread Jill Hammond
 

Hi, everyone! 

 

First a little update on what has happened since the last update a couple
weeks ago, and then the schedule for the next round..  

 

Radiation has really started to take a toll on me. Last Friday, Jill took me
in for my 12th rad treatment.  The Tomotherapy machine that they are using
is state of the art.

 

 Even thought our son took me in to have the old bowling ball shaved, now,
my eyebrows are falling out.  We think we may have the perfect Halloween
costume, Dr. really not-so-evil. All I need now is to find the hairless
cat to complete the costume. 

 

Had a feeding tube put in last Thursday   I have completely lost the sense
of smell, and most of taste.  The salivary glands are so far gone that it is
painful to swallow.   Now, I eat 8 cans a day of a liquid nutrient, and
some of my hydration.  This is accomplished by a large syringe to a port in
my stomach just below the rib cage.  Jill and I were able to pick this up
very quickly.  By the way, for the first time in many moons, today I was
able to get into a size 34 waist, yahoo. God Bless ..

 

We had one major bad evening last week in the effort to find a pain killer
that agreed with me.  I certainly qualified as a zombie for about 16 hours,
and Jill thought she was seeing one.  The medication now seems to be working
much better.  

 

Under the heading on miscellaneous, I have certainly been given the
opportunity to practice; humility, gratitude, patience, and numerous others
on a daily basis.  I could not do this without my family and all the friends
who send notes and stop by. 

 

Here is my schedule for the next round of chemo.   The first treatment will
be October 6th, 9:30 am until about 2:00 pm.  Second treatment is the 7th
from 1:30 pm until about 4:30 pm.  Third treatment is October 8th, 1:30 pm
to about 4:30 pm.  All are at the cancer center, 3rd floor on 13th  street,
just east of Colby in Everett

 

If none of the above times are convenient, here is the radiation schedule.
Treatment is on the 2nd floor.  28th September to October 2nd - 4:20 pm.
Week of October 5th - 4:20 pm.  October 12th until 29 - 4:20 pm.

 

You do not have to visit just there... our home phone is 360 658 5878, and
our home address is 4924 66th Ave NE, Marysville, WA  98270.  Either Google
for directions or I can give them to you. 

 

Take care until next time, Mike, Jill and the rest of the team

 



Re: [TMIC] Update on Mike

2009-09-27 Thread Janice
Mike,
You don't know me from Adam, but I am a TM'er and following these emails.
You have my prayers, but also
my complete respect for your courage and outlook/attitude that endears you to 
all of us.I guess you realize
you have the dubious honor of being the one that I can look at and say he is 
worse off than I am.You have a
lot to fight and it sounds as if you have a lot of fight in you.Don't think 
that because we are not there with you
that you are not in our thoughts and prayers.   Please keep us posted - we 
care - and God bless.
Janice, Missouri
  - Original Message - 
  From: Jill Hammond 
  To: Anna  Jim ; Annie ; Becky  Steve ; Beth  Greg ; Bob  Beverly ; Carole 
Matteson ; Char Brower ; Cheryl Hammond ; Cindy Dunn ; Craig  Candi ; David 
Brooks ; Denise  Pam ; Elaine Boos ; Eric  Eri ; Fred  Susan ; Gil  Mari ; 
'James Fulmer' ; Jan Hlavaty-LaPosa ; Jim and Bobbi ; Johanna ; Judy  Karl ; 
Keenan ; Kendra ; Lenny Lisa ; Lisa ; Lynn  Jade ; Mari  Gary ; marie swanson 
; Mike  Nancy ; Nancy ; Noah ; Pat Allegretti ; Pat and Corky ; Pat Doebele ; 
Pat Massey ; Paula ; PJ ; Ron ; Sally ; Sarah Bell-Schell ; Sharon  Steve ; 
'Sheri Meyer' ; Steve  Gail ; Steve and Jo ; Susan  Ted Roth ; Tmic ; Tom  
Deb ; Wayne ; Zsolt  Patty 
  Sent: Sunday, September 27, 2009 11:25 AM
  Subject: [TMIC] Update on Mike


   

  Hi, everyone! 

   

  First a little update on what has happened since the last update a couple 
weeks ago, and then the schedule for the next round..  

   

  Radiation has really started to take a toll on me. Last Friday, Jill took me 
in for my 12th rad treatment.  The Tomotherapy machine that they are using is 
state of the art.

   

   Even thought our son took me in to have the old bowling ball shaved, now, my 
eyebrows are falling out.  We think we may have the perfect Halloween costume, 
Dr. really not-so-evil. All I need now is to find the hairless cat to 
complete the costume. 

   

  Had a feeding tube put in last Thursday   I have completely lost the sense of 
smell, and most of taste.  The salivary glands are so far gone that it is 
painful to swallow.   Now, I eat 8 cans a day of a liquid nutrient, and some 
of my hydration.  This is accomplished by a large syringe to a port in my 
stomach just below the rib cage.  Jill and I were able to pick this up very 
quickly.  By the way, for the first time in many moons, today I was able to get 
into a size 34 waist, yahoo. God Bless ..

   

  We had one major bad evening last week in the effort to find a pain killer 
that agreed with me.  I certainly qualified as a zombie for about 16 hours, and 
Jill thought she was seeing one.  The medication now seems to be working much 
better.  

   

  Under the heading on miscellaneous, I have certainly been given the 
opportunity to practice; humility, gratitude, patience, and numerous others on 
a daily basis.  I could not do this without my family and all the friends who 
send notes and stop by. 

   

  Here is my schedule for the next round of chemo.   The first treatment will 
be October 6th, 9:30 am until about 2:00 pm.  Second treatment is the 7th from 
1:30 pm until about 4:30 pm.  Third treatment is October 8th, 1:30 pm to about 
4:30 pm.  All are at the cancer center, 3rd floor on 13th  street, just east of 
Colby in Everett

   

  If none of the above times are convenient, here is the radiation schedule.  
Treatment is on the 2nd floor.  28th September to October 2nd - 4:20 pm.   Week 
of October 5th - 4:20 pm.  October 12th until 29 - 4:20 pm.

   

  You do not have to visit just there... our home phone is 360 658 5878, and 
our home address is 4924 66th Ave NE, Marysville, WA  98270.  Either Google for 
directions or I can give them to you. 

   

  Take care until next time, Mike, Jill and the rest of the team

   


[TMIC] Update on Mike

2009-09-14 Thread Jan Hargrove



Jill,

So glad that Mike's treatment has begun!! Also super that it went 
smoothly...so now you know what's going on and next week you'll get the 
second part under your belt.  I'm not making light of what Mike has to face, 
but in my opinion the unknown is most often more frightning than the reality!! 
Please know that our thoughts and prayers continue!!
Hugs, janh

 






Hi Everyone,
 
We finally got Mike’s schedule for radiation and chemo.  Mike had his fist 
radiation treatment Thursday.  The anticipation of the unknown was the most 
stressful part of the treatment, but the 20 minute session went relatively 
smooth.  Eight consecutive weeks have been scheduled thus far and will overlap 
with chemo.  Next Tuesday the 15th starts his first chemo treatment.  The first 
appointment is going to last six hours starting at 9am….the next two 
consecutive days are scheduled at 2pm and last 2 to 3 hours.  The crib board 
will be on hand for anyone that wants to take him on….he would love the 
company!!!.
 
Both Mike and I are very please with the Oncology facility on 13th street .  
The doctors and support staff have been very accommodating and helpful in every 
possible way.  We both know that the next few weeks are going to be very rough, 
but with the support of family, friends and a whole lot of prayers, Mike is 
going to gain strength through YOU……Keep the prayers going.  I’ll keep you 
posted, HUGS, Jill and Mike  

[TMIC] Update on Mike

2009-09-13 Thread Jill Hammond
Hi Everyone,

 

We finally got Mike's schedule for radiation and chemo.  Mike had his fist
radiation treatment Thursday.  The anticipation of the unknown was the most
stressful part of the treatment, but the 20 minute session went relatively
smooth.  Eight consecutive weeks have been scheduled thus far and will
overlap with chemo.  Next Tuesday the 15th starts his first chemo treatment.
The first appointment is going to last six hours starting at 9am..the next
two consecutive days are scheduled at 2pm and last 2 to 3 hours.  The crib
board will be on hand for anyone that wants to take him on..he would love
the company!!!.

 

Both Mike and I are very please with the Oncology facility on 13th street.
The doctors and support staff have been very accommodating and helpful in
every possible way.  We both know that the next few weeks are going to be
very rough, but with the support of family, friends and a whole lot of
prayers, Mike is going to gain strength through YOU..Keep the prayers going.
I'll keep you posted, HUGS, Jill and Mike  



Re: [TMIC] Update on Mike

2009-09-06 Thread Janice
 Jill and Mike,
 You both will need so much strength for this whole ordeal.   You know you have 
all of our prayers.   We will be
 thinking of you and praying for you during this entire fight.
Janice
  - Original Message - 
  From: Jill Hammond 
  To: tmic-list@eskimo.com 
  Sent: Thursday, September 03, 2009 6:40 PM
  Subject: [TMIC] Update on Mike


  Well, everyone, here is your first update.  Before I begin, however, I would 
like to thank all of you who have kept me and my family in your prayers, it 
means a lot.  Don't stop, though, as the  next 7 weeks or so are going to be a 
little rough.  I especially want to thank my family, without their help and 
support; I cannot imagine where I would be.

   

  For those that like to be very specific, I found out I do not have what I 
told you last time.  What I have is a tumor in the Maxillary Sinus.  This tumor 
is a Neuro-endocrine type (small cell) of cancer.   There, that should make it 
clear as mud.  

   

  Went in yesterday to the Chemo doc, and when he heard that we had to wait 
until next Thursday for our radiation Doc appointment, left the room, came back 
and told us as soon as we were through with him, we could go downstairs and 
talk to the radiation doctor.  The right people and a little help from above 
just cut off another 8 days of waiting.  I can start fighting back.  

   

  Today I went in to the doctor's office and got fitted for my Hannibal 
Lector mask.  This mask ensures that you do not move your head at all while 
receiving radiation. Radiation for this is received from a Tomography machine 
which produces the rays electronically.  I will tell you that I could not even 
open my eyes while wearing the mask.. Very claustrophobic, so a little Xanac 
helped.  Now, I go back in for my very first radiation treatment next Thursday. 
 During this 7 week, five day a week treatment, I will receive at least 6,000 
RAD (Radiation Absorbed Dose) to the cancer.  For those who are not aware, just 
let me say that 6,000 RAD is a LOT.  Unfortunately, my right optic nerve may 
receive much of this.  The optic nerve begins to show damage at 4,500 RAD, So, 
I may loose some, or all, vision in my right eye.  There are a lot of other 
little complications like loss of salivary glands, loss of taste (Have that 
already), possible teeth problems,  and hair loss (time for a Kojack shave).  

   

  The Chemotherapy introduction session is tomorrow and I learn what I get, 
when it will start, if I will need a port and lots of other questions I am 
sure.  

   

  So another update in a week or so.  Take care and be talking with you soon.   

  God bless us, everyone,

   Mike and Coach Jill.  

   


[TMIC] Update on Mike

2009-09-04 Thread Jan Hargrove
Mike ( JILL),
 
Thanks for the update, your explanation was very clear
and now all of us will know what's happening as your
treatments continue. Your attitude is positive and even
humerous (Kojak)*...both of those things and prayer
from your family and your TM family should serve you 
well!!
 
We're here for you and want to be kept up to date!!
 
janh
 
*as for the new hairstyle, my hubby started to shave 
his head when I offered to cut his hair...looks good!
and I don't get to do it!!


--- On Thu, 9/3/09, Jill Hammond 3jmhamm...@clearwire.net wrote:









Well, everyone, here is your first update.  Before I begin, however, I would 
like to thank all of you who have kept me and my family in your prayers, it 
means a lot.  Don’t stop, though, as the  next 7 weeks or so are going to be a 
little rough.  I especially want to thank my family, without their help and 
support; I cannot imagine where I would be.
 
For those that like to be very specific, I found out I do not have what I told 
you last time.  What I have is a tumor in the Maxillary Sinus.  This tumor is a 
Neuro-endocrine type (small cell) of cancer.   There, that should make it clear 
as mud.  
 
Went in yesterday to the Chemo doc, and when he heard that we had to wait until 
next Thursday for our radiation Doc appointment, left the room, came back and 
told us as soon as we were through with him, we could go downstairs and talk to 
the radiation doctor.  The right people and a little help from above just cut 
off another 8 days of waiting.  I can start fighting back.  
 
Today I went in to the doctor’s office and got fitted for my “Hannibal Lector” 
mask.  This mask ensures that you do not move your head at all while receiving 
radiation. Radiation for this is received from a Tomography machine which 
produces the rays electronically.  I will tell you that I could not even open 
my eyes while wearing the mask.. Very claustrophobic, so a little Xanac 
helped.  Now, I go back in for my very first radiation treatment next 
Thursday.  During this 7 week, five day a week treatment, I will receive at 
least 6,000 RAD (Radiation Absorbed Dose) to the cancer.  For those who are not 
aware, just let me say that 6,000 RAD is a LOT.  Unfortunately, my right optic 
nerve may receive much of this.  The optic nerve begins to show damage at 4,500 
RAD, So, I may loose some, or all, vision in my right eye.  There are a lot of 
other little complications like loss of salivary glands, loss of taste (Have 
that already), possible teeth
 problems,  and hair loss (time for a Kojack shave).  
 
The Chemotherapy introduction session is tomorrow and I learn what I get, when 
it will start, if I will need a port and lots of other questions I am sure.  
 
So another update in a week or so.  Take care and be talking with you soon.   
God bless us, everyone,
 Mike and Coach Jill.  
 

RE: [TMIC] Update on Mike

2009-09-04 Thread Patricia Cooley
MIKE AND JILL:

 

I HAVE PUT YOU IN MY PRAYER BASKET AND WILL INCLUDE YOU IN MY PRAYERS.  IT
IS THE LOVE OF OUR FAMILY AND FRIENDS THAT GIVES US THE STRENGTH TO GO ON.
PLEASE KEEP US INFORMED.

 

PATTI - WISCONSIN

 

From: Jill Hammond [mailto:3jmhamm...@clearwire.net] 
Sent: Thursday, September 03, 2009 6:40 PM
To: tmic-list@eskimo.com
Subject: [TMIC] Update on Mike

 

Well, everyone, here is your first update.  Before I begin, however, I would
like to thank all of you who have kept me and my family in your prayers, it
means a lot.  Don't stop, though, as the  next 7 weeks or so are going to be
a little rough.  I especially want to thank my family, without their help
and support; I cannot imagine where I would be.

 

For those that like to be very specific, I found out I do not have what I
told you last time.  What I have is a tumor in the Maxillary Sinus.  This
tumor is a Neuro-endocrine type (small cell) of cancer.   There, that should
make it clear as mud.  

 

Went in yesterday to the Chemo doc, and when he heard that we had to wait
until next Thursday for our radiation Doc appointment, left the room, came
back and told us as soon as we were through with him, we could go downstairs
and talk to the radiation doctor.  The right people and a little help from
above just cut off another 8 days of waiting.  I can start fighting back.  

 

Today I went in to the doctor's office and got fitted for my Hannibal
Lector mask.  This mask ensures that you do not move your head at all while
receiving radiation. Radiation for this is received from a Tomography
machine which produces the rays electronically.  I will tell you that I
could not even open my eyes while wearing the mask.. Very claustrophobic, so
a little Xanac helped.  Now, I go back in for my very first radiation
treatment next Thursday.  During this 7 week, five day a week treatment, I
will receive at least 6,000 RAD (Radiation Absorbed Dose) to the cancer.
For those who are not aware, just let me say that 6,000 RAD is a LOT.
Unfortunately, my right optic nerve may receive much of this.  The optic
nerve begins to show damage at 4,500 RAD, So, I may loose some, or all,
vision in my right eye.  There are a lot of other little complications like
loss of salivary glands, loss of taste (Have that already), possible teeth
problems,  and hair loss (time for a Kojack shave).  

 

The Chemotherapy introduction session is tomorrow and I learn what I get,
when it will start, if I will need a port and lots of other questions I am
sure.  

 

So another update in a week or so.  Take care and be talking with you soon.


God bless us, everyone,

 Mike and Coach Jill.  

 



Re: [TMIC] Update on Mike

2009-09-04 Thread Catherine
Mike  Jill,

You are both in my thoughts and prayers.  God will hold you in the palm of his 
hand and protect and guide you.

Catherine





From: Jill Hammond 3jmhamm...@clearwire.net
To: tmic-list@eskimo.com
Sent: Thursday, September 3, 2009 7:40:14 PM
Subject: [TMIC] Update on Mike

 
Well, everyone, here is your first update.  Before I begin, however, I
would like to thank all of you who have kept me and my family in your prayers,
it means a lot.  Don’t stop, though, as the  next 7 weeks or so are going
to be a little rough.  I especially want to thank my family, without their help
and support; I cannot imagine where I would be.
 
For those that like to be very specific, I found out I do not have what
I told you last time.  What I have is a tumor in the Maxillary Sinus.  This
tumor is a Neuro-endocrine type (small cell) of cancer.   There, that should
make it clear as mud.  
 
Went in yesterday to the Chemo doc, and when he heard that we had to
wait until next Thursday for our radiation Doc appointment, left the room, came
back and told us as soon as we were through with him, we could go downstairs
and talk to the radiation doctor.  The right people and a little help from
above just cut off another 8 days of waiting.  I can start fighting back.  
 
Today I went in to the doctor’s office and got fitted for my
“Hannibal Lector” mask.  This mask ensures that you do not move
your head at all while receiving radiation. Radiation for this is received from
a Tomography machine which produces the rays electronically.  I will tell you
that I could not even open my eyes while wearing the mask.. Very
claustrophobic, so a little Xanac helped.  Now, I go back in for my very first
radiation treatment next Thursday.  During this 7 week, five day a week
treatment, I will receive at least 6,000 RAD (Radiation Absorbed Dose) to the
cancer.  For those who are not aware, just let me say that 6,000 RAD is a LOT. 
Unfortunately, my right optic nerve may receive much of this.  The optic nerve
begins to show damage at 4,500 RAD, So, I may loose some, or all, vision in my
right eye.  There are a lot of other little complications like loss of salivary
glands, loss of taste (Have that already), possible teeth problems,  and hair
loss (time for a Kojack shave).  
 
The Chemotherapy introduction session is tomorrow and I learn what I
get, when it will start, if I will need a port and lots of other questions I am
sure.  
 
So another update in a week or so.  Take care and be talking with you
soon.   
God bless us, everyone,
 Mike and Coach Jill.  


  

[TMIC] Update on Mike

2009-09-03 Thread Jill Hammond
Well, everyone, here is your first update.  Before I begin, however, I would
like to thank all of you who have kept me and my family in your prayers, it
means a lot.  Don't stop, though, as the  next 7 weeks or so are going to be
a little rough.  I especially want to thank my family, without their help
and support; I cannot imagine where I would be.

 

For those that like to be very specific, I found out I do not have what I
told you last time.  What I have is a tumor in the Maxillary Sinus.  This
tumor is a Neuro-endocrine type (small cell) of cancer.   There, that should
make it clear as mud.  

 

Went in yesterday to the Chemo doc, and when he heard that we had to wait
until next Thursday for our radiation Doc appointment, left the room, came
back and told us as soon as we were through with him, we could go downstairs
and talk to the radiation doctor.  The right people and a little help from
above just cut off another 8 days of waiting.  I can start fighting back.  

 

Today I went in to the doctor's office and got fitted for my Hannibal
Lector mask.  This mask ensures that you do not move your head at all while
receiving radiation. Radiation for this is received from a Tomography
machine which produces the rays electronically.  I will tell you that I
could not even open my eyes while wearing the mask.. Very claustrophobic, so
a little Xanac helped.  Now, I go back in for my very first radiation
treatment next Thursday.  During this 7 week, five day a week treatment, I
will receive at least 6,000 RAD (Radiation Absorbed Dose) to the cancer.
For those who are not aware, just let me say that 6,000 RAD is a LOT.
Unfortunately, my right optic nerve may receive much of this.  The optic
nerve begins to show damage at 4,500 RAD, So, I may loose some, or all,
vision in my right eye.  There are a lot of other little complications like
loss of salivary glands, loss of taste (Have that already), possible teeth
problems,  and hair loss (time for a Kojack shave).  

 

The Chemotherapy introduction session is tomorrow and I learn what I get,
when it will start, if I will need a port and lots of other questions I am
sure.  

 

So another update in a week or so.  Take care and be talking with you soon.


God bless us, everyone,

 Mike and Coach Jill.  

 



Re: [TMIC] Update on Mike

2009-09-03 Thread Barbara H.
Thanks for the update, Mike. I am so very sorry you have to go through all
of this. I will be praying for you and your family.

Barbara H.

On Thu, Sep 3, 2009 at 7:40 PM, Jill Hammond 3jmhamm...@clearwire.netwrote:

  Well, everyone, here is your first update.  Before I begin, however, I
 would like to thank all of you who have kept me and my family in your
 prayers, it means a lot.  Don’t stop, though, as the  next 7 weeks or so are
 going to be a little rough.  I especially want to thank my family, without
 their help and support; I cannot imagine where I would be.



 For those that like to be very specific, I found out I do not have what I
 told you last time.  What I have is a tumor in the Maxillary Sinus.  This
 tumor is a Neuro-endocrine type (small cell) of cancer.   There, that should
 make it clear as mud.



 Went in yesterday to the Chemo doc, and when he heard that we had to wait
 until next Thursday for our radiation Doc appointment, left the room, came
 back and told us as soon as we were through with him, we could go downstairs
 and talk to the radiation doctor.  The right people and a little help from
 above just cut off another 8 days of waiting.  I can start fighting back.



 Today I went in to the doctor’s office and got fitted for my “Hannibal
 Lector” mask.  This mask ensures that you do not move your head at all while
 receiving radiation. Radiation for this is received from a Tomography
 machine which produces the rays electronically.  I will tell you that I
 could not even open my eyes while wearing the mask.. Very claustrophobic, so
 a little Xanac helped.  Now, I go back in for my very first radiation
 treatment next Thursday.  During this 7 week, five day a week treatment, I
 will receive at least 6,000 RAD (Radiation Absorbed Dose) to the cancer.
 For those who are not aware, just let me say that 6,000 RAD is a LOT.
 Unfortunately, my right optic nerve may receive much of this.  The optic
 nerve begins to show damage at 4,500 RAD, So, I may loose some, or all,
 vision in my right eye.  There are a lot of other little complications like
 loss of salivary glands, loss of taste (Have that already), possible teeth
 problems,  and hair loss (time for a Kojack shave).



 The Chemotherapy introduction session is tomorrow and I learn what I get,
 when it will start, if I will need a port and lots of other questions I am
 sure.



 So another update in a week or so.  Take care and be talking with you
 soon.

 God bless us, everyone,

  Mike and Coach Jill.





Re: [TMIC] Update on Mike

2009-09-03 Thread jrushton
 Bless your hearts, Mike and Jill..  We will all be holding you in our
hearts, minds, and prayers.  I wish we could be close to help you with other
things...Jeanne
 
---Original Message---
 
From: Jill Hammond
Date: 9/3/2009 6:47:19 PM
To: tmic-list@eskimo.com
Subject: [TMIC] Update on Mike
 
Well, everyone, here is your first update.  Before I begin, however, I would
like to thank all of you who have kept me and my family in your prayers, it
means a lot.  Don’t stop, though, as the  next 7 weeks or so are going to be
a little rough.  I especially want to thank my family, without their help
and support; I cannot imagine where I would be.
 
For those that like to be very specific, I found out I do not have what I
told you last time.  What I have is a tumor in the Maxillary Sinus.  This
tumor is a Neuro-endocrine type (small cell) of cancer.   There, that should
make it clear as mud.  
 
Went in yesterday to the Chemo doc, and when he heard that we had to wait
until next Thursday for our radiation Doc appointment, left the room, came
back and told us as soon as we were through with him, we could go downstairs
and talk to the radiation doctor.  The right people and a little help from
above just cut off another 8 days of waiting.  I can start fighting back.  
 
Today I went in to the doctor’s office and got fitted for my “Hannibal
Lector” mask.  This mask ensures that you do not move your head at all while
receiving radiation. Radiation for this is received from a Tomography
machine which produces the rays electronically.  I will tell you that I
could not even open my eyes while wearing the mask.. Very claustrophobic, so
a little Xanac helped.  Now, I go back in for my very first radiation
treatment next Thursday.  During this 7 week, five day a week treatment, I
will receive at least 6,000 RAD (Radiation Absorbed Dose) to the cancer. 
For those who are not aware, just let me say that 6,000 RAD is a LOT. 
Unfortunately, my right optic nerve may receive much of this.  The optic
nerve begins to show damage at 4,500 RAD, So, I may loose some, or all,
vision in my right eye.  There are a lot of other little complications like
loss of salivary glands, loss of taste (Have that already), possible teeth
problems,  and hair loss (time for a Kojack shave).  
 
The Chemotherapy introduction session is tomorrow and I learn what I get,
when it will start, if I will need a port and lots of other questions I am
sure.  
 
So another update in a week or so.  Take care and be talking with you soon. 
 
God bless us, everyone,
 Mike and Coach Jill.  
 
 01_tile.jpg01_side.gif

Re: [TMIC] Update on Mike

2009-09-03 Thread kimr1999
Mike and Jill

Through every trial and moment of pain, we stand together to help one another.
Sometimes the hand of a stranger comes along and lifts up our hearts..
Our responsibility is to continue that selfless act of love and pass on the 
comfort.
Blessed are those who mourn for they shall be comforted.
~ Mathew 5:4





From: jrushton jrush...@columbiaenergyllc.com
To: Jill Hammond 3jmhamm...@clearwire.net; tmic tmic-list@eskimo.com
Sent: Thursday, September 3, 2009 7:21:20 PM
Subject: Re: [TMIC] Update on Mike


 Bless your hearts, Mike and Jill..  We will all be holding you in our hearts, 
minds, and prayers.  I wish we could be close to help you with other 
things...Jeanne
 
---Original Message---

From: Jill Hammond
Date: 9/3/2009 6:47:19 PM
To: tmic-list@eskimo.com
Subject: [TMIC] Update on Mike

Well, everyone, here is your first update.  Before I begin, however, I would 
like to thank all of you who have kept me and my family in your prayers, it 
means a lot.  Don’t stop, though, as the  next 7 weeks or so are going to be a 
little rough.  I especially want to thank my family, without their help and 
support; I cannot imagine where I would be.
 
For those that like to be very specific, I found out I do not have what I told 
you last time.  What I have is a tumor in the Maxillary Sinus.  This tumor is a 
Neuro-endocrine type (small cell) of cancer.   There, that should make it clear 
as mud.  
 
Went in yesterday to the Chemo doc, and when he heard that we had to wait until 
next Thursday for our radiation Doc appointment, left the room, came back and 
told us as soon as we were through with him, we could go downstairs and talk to 
the radiation doctor.  The right people and a little help from above just cut 
off another 8 days of waiting.  I can start fighting back.  
 
Today I went in to the doctor’s office and got fitted for my “Hannibal Lector” 
mask.  This mask ensures that you do not move your head at all while receiving 
radiation. Radiation for this is received from a Tomography machine which 
produces the rays electronically.  I will tell you that I could not even open 
my eyes while wearing the mask.. Very claustrophobic, so a little Xanac 
helped.  Now, I go back in for my very first radiation treatment next 
Thursday.  During this 7 week, five day a week treatment, I will receive at 
least 6,000 RAD (Radiation Absorbed Dose) to the cancer.  For those who are not 
aware, just let me say that 6,000 RAD is a LOT.  Unfortunately, my right optic 
nerve may receive much of this.  The optic nerve begins to show damage at 4,500 
RAD, So, I may loose some, or all, vision in my right eye.  There are a lot of 
other little complications like loss of salivary glands, loss of taste (Have 
that already), possible teeth
 problems,  and hair loss (time for a Kojack shave).  
 
The Chemotherapy introduction session is tomorrow and I learn what I get, when 
it will start, if I will need a port and lots of other questions I am sure.  
 
So another update in a week or so.  Take care and be talking with you soon.   
God bless us, everyone,
 Mike and Coach Jill.  

Re: [TMIC] Update on Mike

2009-09-03 Thread Akua

Heal Fast!
Know Peace!
Heal and be Well!

Wishing you strength and perseverance,
Akua
--

Re: [TMIC] Update on Jim

2009-08-25 Thread JHarper33
Will be praying. I love what you said about there is still  time for more.
 
Barbara H.
_http://barbarah.wordpress.com_ (http://barbarah.wordpress.com) 
 
 
In a message dated 8/24/2009 8:09:17 A.M. Eastern Daylight Time,  
cjb...@aol.com writes:

We are still in a holding pattern and has been getting harder for me to  
keep up my hopes. But have decided today I will BELIEVE. I will be heading  
down to Pontiac soon and will present my case, again, to both hospitals(  the 
one he is in and the one I am hoping he will be in. He is getting very  
discouraged. I must find something in myself to encourage him. I want to grow  
old with him. I know some of my friends would say I already have, but there 
is  still time for more. Please enjoy every minute you have. Keep the prayers 
 coming.  carol and jim  

 




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Re: [TMIC] Update on Jim

2009-08-25 Thread Catherine






Carol and Jim,

I have you in my prayer box and continue to pray for you often.  Don't give up, 
because you are right there is still time for more!

Catherine




 
In a message dated 8/24/2009 8:09:17 A.M. Eastern Daylight Time, 
cjb...@aol.com writes:
We are still in a holding pattern and has been getting harder for me to 
  keep up my hopes. But have decided today I will BELIEVE. I will be heading 
  down to Pontiac soon and will present my case, again, to both hospitals( 
  the one he is in and the one I am hoping he will be in. He is getting very 
  discouraged. I must find something in myself to encourage him. I want to 
 grow 
  old with him. I know some of my friends would say I already have, but there 
 is 
  still time for more. Please enjoy every minute you have. Keep the prayers 
  coming.  carol and jim   



 






  

Re: [TMIC] Update on Jim

2009-08-25 Thread Alle111
Carol you keep your hopes and prayers upward and we are behind  you and Jim 
with our prayers that it will be alright. Sending my prayers and  positive 
thoughts your way.Ella


[TMIC] Update on Jim

2009-08-24 Thread CJBJWB
We are still in a holding pattern and has been getting harder for me to  
keep up my hopes. But have decided today I will BELIEVE. I will be heading 
down  to Pontiac soon and will present my case, again, to both hospitals( the 
one  he is in and the one I am hoping he will be in. He is getting very 
discouraged.  I must find something in myself to encourage him. I want to grow 
old with him. I  know some of my friends would say I already have, but there 
is still time for  more. Please enjoy every minute you have. Keep the prayers 
coming.  carol  and jim  


[TMIC] update on Jim

2009-08-19 Thread CJBJWB
I will be on my way to Pontiac soon, yes Jim is still there, and yes he is  
not a happy patient, He wants to get this show on the road. It is hard to 
keep  telling to be patient. We both need your prayers and we thank you for 
them. til  next time.Praying for each of you.


[TMIC] Update on Jim

2009-08-11 Thread CJBJWB
Wish I had something more definite to tell but this is what I know for  
sure. Jim is still in the Select Speciality hospital in Pontiac,Mi. They are  
telling me he is almost definitely going to be transferred to Marlette 
Hospital  which is only 22 miles from home instead of about 65. He has an 
infection which  they are monitoring. I am pulling for this as I have very good 
feelings about  this place. Please say a few more prayers for him as we will 
continue to for  each of you. Our love, carol and jim TIAD


Re: [TMIC] Update on Jim

2009-08-11 Thread L T CHERPESKI
Hi Carol,

Late last night when I was reading the posts I was just about to ask if anybody 
had heard from Carol regarding Jim's current condition.  You must have known we 
were thinking of you.  Carol, is this infection the same one he has had for a 
while, or is this one new?  You and Jim are in my prayers each day.  I hope 
that Jim is transferred to Marlette Hospital - you seem to feel good about this 
hospital, and it is definitely closer to home which will be a positive thing 
for you.  Carol, please remember how very important it is to take care of 
yourself too.  My love and prayers to both you and Jim.
Linda  ***TIAD***
  - Original Message - 
  From: cjb...@aol.commailto:cjb...@aol.com 
  To: tmic-list@eskimo.commailto:tmic-list@eskimo.com 
  Sent: Tuesday, August 11, 2009 6:42 PM
  Subject: [TMIC] Update on Jim


  Wish I had something more definite to tell but this is what I know for sure. 
Jim is still in the Select Speciality hospital in Pontiac,Mi. They are telling 
me he is almost definitely going to be transferred to Marlette Hospital which 
is only 22 miles from home instead of about 65. He has an infection which they 
are monitoring. I am pulling for this as I have very good feelings about this 
place. Please say a few more prayers for him as we will continue to for each of 
you. Our love, carol and jim TIAD


--


Re: [TMIC] Update on Jim

2009-08-11 Thread Janice
   Our thoughts and prayers are with both of you.You two have been through 
so much - please take care of
yourself.Jim will need you to be strong when you get him home.
Janice
  - Original Message - 
  From: cjb...@aol.com 
  To: tmic-list@eskimo.com 
  Sent: Tuesday, August 11, 2009 7:42 PM
  Subject: [TMIC] Update on Jim


  Wish I had something more definite to tell but this is what I know for sure. 
Jim is still in the Select Speciality hospital in Pontiac,Mi. They are telling 
me he is almost definitely going to be transferred to Marlette Hospital which 
is only 22 miles from home instead of about 65. He has an infection which they 
are monitoring. I am pulling for this as I have very good feelings about this 
place. Please say a few more prayers for him as we will continue to for each of 
you. Our love, carol and jim TIAD


--


Re: [TMIC] Update on Jim

2009-07-06 Thread Jill Z
Carol, 
That is great news!  Glad to hear he's on the road to a speedy recovery.  
Continue to Keep us posted!
Jill

--- On Sat, 7/4/09, cjb...@aol.com cjb...@aol.com wrote:


From: cjb...@aol.com cjb...@aol.com
Subject: [TMIC] Update on Jim
To: tmic-list@eskimo.com
Date: Saturday, July 4, 2009, 10:30 PM



What a difference a week can make. I am so thankful to have my honey on the 
road to recovery. The doctor said today that he will be at the hospital a 
couple more weeks and then to an in patient rehab. I am voting for Marlette 
which is where he had the rehab in 2005. I know many of the therapists he had 
have moved on to bigger and better things but the new ones will be good too and 
it is much closer than the over an hour ea way I have been driving each day. He 
is off the vent and ready to start building his muscles back up.Thank you all 
for your prayers and concern.GOD is so good. love ya carol and jim



Make your summer sizzle with fast and easy recipes for the grill.

Re: [TMIC] Update on Jim

2009-07-05 Thread Catherine
   I SECOND THAT! THE BEST TO BOTH OF YOU!CatherineFrom: Akua a...@artfarm.comTo: tmic-list@eskimo.comSent: Sunday, July 5, 2009 12:35:19 AMSubject: Re: [TMIC] Update on JimRe: [TMIC] Update on Jim HOORAAY!What adifference a week can make. I am so thankful to have my honey on theroad to recovery. The doctor said today that he will be at thehospital a couple more weeks and then to an in patient rehab. I amvoting for Marlette which is where he had the rehab in 2005. I knowmany of the therapists he had have
 moved on to bigger and betterthings but the new ones will be good too and it is much closer thanthe over an hour ea way I have been driving each day. He is off thevent and ready to start building his muscles back up.Thank you all foryour prayers and concern.GOD is so good. love ya carol andjim--

  

Re: [TMIC] Update on Jim

2009-07-05 Thread Trudy Ogilvie
Carol,What fantastic news! You must be absolutely exhausted and
exhilarated  Please remember to take care of yourself. I am so blessed
to have a
caregiver just like you. Always there!
 Blessings !
Trudy
Everything is possible for one who believes,still more for one who hopes,
even more for one who loves




On Sat, Jul 4, 2009 at 11:30 PM, cjb...@aol.com wrote:

  What a difference a week can make. I am so thankful to have my honey on
 the road to recovery. The doctor said today that he will be at the hospital
 a couple more weeks and then to an in patient rehab. I am voting for
 Marlette which is where he had the rehab in 2005. I know many of the
 therapists he had have moved on to bigger and better things but the new ones
 will be good too and it is much closer than the over an hour ea way I have
 been driving each day. He is off the vent and ready to start building his
 muscles back up.Thank you all for your prayers and concern.GOD is so good.
 love ya carol and jim

 --
 Make your summer sizzle with fast and easy 
 recipeshttp://food.aol.com/grilling?ncid=emlcntusfood0005for the grill.



Re: [TMIC] Update on Jim

2009-07-05 Thread Celrods
I AM SO GLAD TO HEAR THAT HE IS GETTIN BETTER. MY THOUGHTS ARE WITH BOTH OF 
 YOU.
 
JANE
**Make your summer sizzle with fast and easy recipes for the 
grill. (http://food.aol.com/grilling?ncid=emlcntusfood0005)


Re: [TMIC] Update on Jim

2009-07-05 Thread Alle111
Very good news Carol! May Jim's health continue going  forward. I can feel 
you elation in your letter, bless you both. I'll be  waiting for the next 
update and I hope he will be able to go to  Marlette.Ella
**It's raining cats and dogs -- Come to PawNation, a place 
where pets rule! (http://www.pawnation.com/?ncid=emlcntnew0008)


Re: [TMIC] Update on Jim

2009-07-04 Thread Akua

HOORAAY!


What a difference a week can make. I am so thankful to have my honey 
on the road to recovery. The doctor said today that he will be at 
the hospital a couple more weeks and then to an in patient rehab. I 
am voting for Marlette which is where he had the rehab in 2005. I 
know many of the therapists he had have moved on to bigger and 
better things but the new ones will be good too and it is much 
closer than the over an hour ea way I have been driving each day. He 
is off the vent and ready to start building his muscles back 
up.Thank you all for your prayers and concern.GOD is so good. love 
ya carol and jim


--

Re: [TMIC] Update on my honey

2009-06-18 Thread jrushton
What wonderful news, Carol...  Aren't prayers just so darned wonderful and
exciting???  Jeanne

---Original Message---
 
From: Trudy Ogilvie
Date: 6/16/2009 10:08:30 PM
To: cjb...@aol.com
Cc: transverse myelitis
Subject: Re: [TMIC] Update on my honey
 
YES! YES! YES! Enjoy every single second of this red letter day! dance in
the moment
for Dance is the hidden language of the soul.
Blessings and continued prayers!
Trudy



On Tue, Jun 16, 2009 at 10:39 PM, cjb...@aol.com wrote:

This is a red letter day. Today is the first day that I can say I really
believe the words I've been professing each day. I believe he is going to
make it. They put a trach in today and he was breathing good and looking
sexy again. I even got a couple kisses and a mouthed I love you before I
left. I just about floated home. Now I know we have a long ways to go but he
has overcome so many challenges with his TM that I am sure he will beat this
too! God Bless all of you for your prayers. We love you. carol and jim.  Our
family is the glue that has kept me together, we are so blessed.



An Excellent Credit Score is 750. See Yours in Just 2 Easy Steps!


 02.jpg

[TMIC] Update on my honey

2009-06-16 Thread CJBJWB
This is a red  letter day. Today is the first day that I can say I really 
believe the words  I've been professing each day. I believe he is going to 
make it. They put a  trach in today and he was breathing good and looking sexy 
again. I even got a  couple kisses and a mouthed I love you before I left. 
I just about floated home.  Now I know we have a long ways to go but he has 
overcome so many challenges with  his TM that I am sure he will beat this 
too! God Bless all of you for your  prayers. We love you. carol and jim.  Our 
family is the glue that has  kept me together, we are so  blessed.
**An Excellent Credit Score is 750. See Yours in Just 2 Easy 
Steps! 
(http://pr.atwola.com/promoclk/100126575x1221823265x1201398681/aol?redir=http://www.freecreditreport.com/pm/default.aspx?sc=668072hmpgID=62bcd=Jun
eExcfooterNO62)


[TMIC] Update on my honey-Jim,

2009-06-16 Thread kimr1999






From Carol


This is a red letter day. Today is the first day that I can say I really believe the words I've been professing each day. I believe he is going to make it. They put a trach in today and he was breathing good and looking sexy again. I even got a couple kisses and a mouthed I love you before I left. I just about floated home. Now I know we have a long ways to go but he has overcome so many challenges with his TM that I am sure he will beat this too! God Bless all of you for your prayers.We love you. carol and jim. Our family is the glue that has kept me together, we are so blessed.


An Excellent Credit Score is 750. See Yours in Just 2 Easy Steps!






Re: [TMIC] Update on my honey

2009-06-16 Thread Trudy Ogilvie
YES! YES! YES! Enjoy every single second of this red letter day! dance in
the momentfor Dance is the hidden language of the soul.Blessings and
continued prayers!
Trudy

On Tue, Jun 16, 2009 at 10:39 PM, cjb...@aol.com wrote:

  *This is a red letter day. Today is the first day that I can say I really
 believe the words I've been professing each day. I believe he is going to
 make it. They put a trach in today and he was breathing good and looking
 sexy again. I even got a couple kisses and a mouthed I love you before I
 left. I just about floated home. Now I know we have a long ways to go but he
 has overcome so many challenges with his TM that I am sure he will beat this
 too! God Bless all of you for your prayers. We love you. carol and jim.  Our
 family is the glue that has kept me together, we are so blessed.*

 --
 *An Excellent Credit Score is 750. See Yours in Just 2 Easy 
 Steps!http://pr.atwola.com/promoclk/100126575x1221823265x1201398681/aol?redir=http://www.freecreditreport.com/pm/default.aspx?sc=668072%26hmpgID=62%26bcd=JuneExcfooterNO62
 *



Re: [TMIC] Update on my honey

2009-06-16 Thread Akua

Hooray!

Many Blessings,
Akua
--

Re: [TMIC] Update on Jim

2009-06-11 Thread Grace M.
*Still praying for Jim, Carol.  Keep us posted.*
**
*Hugs,*
*Grace*


Re: [TMIC] Update on Jim

2009-06-11 Thread Jan Hargrove
Carol,
 
Know that we're holding your hand thru thisbe sure you take care of 
Carol, too!!
 
Hugs, jan

--- On Thu, 6/11/09, cjb...@aol.com cjb...@aol.com wrote:





It is morn June 11th and I will be leaving soon for the hospital. Jim had a 
very bad day yesterday. They will be inserting a feeding tube tomorrow as he 
can't swallow and the temporary system they tried yesterday is not working and 
he has to have nourishment.His mind did not seem to be affected at first and we 
are hoping that the what he is going thru now is causing the confusion and 
agitation he is having now. Please continue to pray for him as he has for any 
and all of you our friends. I will try to keep the updates coming. Love carol 
and jim  



Dell Deals: Don't miss huge summer savings on popular laptops starting at $449.

Re: [TMIC] Update on Jim

2009-06-11 Thread Trudy Ogilvie
Please know Jim is in my prayers and my thoughts ..  May the Holy Spirit
fill you with peace today!
Blessings
Trudy


On Thu, Jun 11, 2009 at 6:59 AM, cjb...@aol.com wrote:

  It is morn June 11th and I will be leaving soon for the hospital. Jim had
 a very bad day yesterday. They will be inserting a feeding tube tomorrow as
 he can't swallow and the temporary system they tried yesterday is not
 working and he has to have nourishment.His mind did not seem to be affected
 at first and we are hoping that the what he is going thru now is causing the
 confusion and agitation he is having now. Please continue to pray for him as
 he has for any and all of you our friends. I will try to keep the updates
 coming. Love carol and jim

 --
 Dell Deals: Don't miss huge summer savings on popular laptops starting at
 $449.http://pr.atwola.com/promoclk/100126575x1221770187x1201425153/aol?redir=http:%2F%2Fad.doubleclick.net%2Fclk%3B215566131%3B37864407%3Bi



Re: [TMIC] Update on Jim

2009-06-11 Thread Catherine
Carol and Jim,

Know that you are in my thoughts and prayers.  Take care God Bless.  

Catherine





From: cjb...@aol.com cjb...@aol.com
To: tmic-list@eskimo.com
Sent: Thursday, June 11, 2009 6:59:43 AM
Subject: [TMIC] Update on Jim

It is morn June 11th and I will be leaving soon for the hospital. Jim had a
very bad day yesterday. They will be inserting a feeding tube tomorrow as
he can't swallow and the temporary system they tried yesterday is not working
and he has to have nourishment.His mind did not seem to be affected at
first and we are hoping that the what he is going thru now is causing the
confusion and agitation he is having now. Please continue to pray for him
as he has for any and all of you our friends. I will try to keep the updates
coming. Love carol and jim  



Dell Deals: Don't miss huge summer savings on popular laptops starting at $449.


  

Re: [TMIC] Update on Jim

2009-06-11 Thread Alle111
I'm sending my best to you and Jim that all goes  well...Ella


In a message dated 6/11/2009 7:00:21 A.M. Eastern Daylight Time,
cjb...@aol.com writes:

It is morn June 11th and I will be leaving soon for the hospital. Jim had
a very bad day yesterday. They will be inserting a feeding tube tomorrow  as
he can't swallow and the temporary system they tried yesterday is not
working and he has to have nourishment.His mind did not seem to be  affected at
first and we are hoping that the what he is going thru now is  causing the
confusion and agitation he is having now. Please continue to  pray for him as
he has for any and all of you our friends. I will try to keep  the updates
coming. Love carol and jim



_Dell  Deals: Don't miss huge summer savings on popular laptops starting at
 $449._
(http://pr.atwola.com/promoclk/100126575x1221770187x1201425153/aol?redir=http://ad.doubleclick.net/clk;215566131;37864407;i)


**Dell Deals: Don’t miss huge summer savings on popular laptops
starting at $449.
(http://pr.atwola.com/promoclk/100126575x1221770187x1201425153/aol?redir=http:%2F%2Fad.doubleclick.net%2Fclk%3B215566131%3B37864407%3B
i)


Re: [TMIC] Update on JIM and so sad about Pam,

2009-06-08 Thread jrushton
 As I will, also, Carol.  He is in my little Prayer Pot.  Hugs for you and
Jim and all of your family...j
 
---Original Message---
 
From: L T CHERPESKI
Date: 6/7/2009 11:20:17 PM
To: tmic-list@eskimo.com;  cjb...@aol.com
Subject: Re: [TMIC] Update on JIM and so sad about Pam,
 
Carol,
 
I'm sorry to hear that Jim has been moved into ICU.  Will definitely keep
him in my prayers.  How wonderful that grandpa was able to spend time with
those sweet granddaughters.  I'll be watching for the update.  Hope and pray
all goes well.
 
Linda
- Original Message - 
From: cjb...@aol.com 
To: tmic-list@eskimo.com 
Sent: Sunday, June 07, 2009 8:44 PM
Subject: [TMIC] Update on JIM and so sad about Pam,


Got home from the hospital this evening and as I usually do,sat down in
front of the computer to see what had been written today. How sad but also
happy to know that Pam has been called home into the loving arms of the GOD
that she loves so much. I also will miss her writings to the list and the
TIAD that I didn't figure out for some time.This morning the hospital called
and said they were moving Jim into ICU as they think he has Pneumonia. My
son and and 2 of our precious grandaughters drove about 3 hours to see Jim.
It was wonderful to see them and put sunshine in Jim's room. The ones that
came are the almost 8 yr old twins and mommy and the 11 yr old and 2 yr old
stayed home. They stayed overnight and we went to church this morning and
then went to the hospital after lunch to see granpa for a little while
before they had to head back home.There is still 5 days of school for all of
them. Daddy is a teacher. Anyway tomorrow morning early they are doing a
bronchialscopy test. I will kepp you posted and we thank you for your
prayers. carol



An Excellent Credit Score is 750. See Yours in Just 2 Easy Steps!
 tile12.jpg

Re: [TMIC] Update on JIM and so sad about Pam,

2009-06-08 Thread jrushton
 How very beautifully said..TIAD...J
 
---Original Message---
 
From: heyjude48...@aol.com
Date: 6/8/2009 12:30:02 PM
To: jrush...@columbiaenergyllc.com
Subject: Re: [TMIC] Update on JIM and so sad about Pam,
 
Please Carol,
 
Accept my Prayers for Jim's continued improvement of this persistent illness
  I remember when I was in ICU with pneumonia, and it was very surreal.  I
only made it through by the Prayers from my friends and my TMIC family.
 
I Pray that Jesus Christ hold Jim in His Comforting Arms until this crisis
is over with.  And I Pray that you find solace in Our Savior as well.  May
He cure all of your woes and replace your cares with Pam's angel wings to
lift you up.
 
TIAD,
Jude 
 
In a message dated 6/8/2009 12:48:02 P.M. Eastern Daylight Time,
jrush...@columbiaenergyllc.com writes:
 As I will, also, Carol.  He is in my little Prayer Pot.  Hugs for you and
Jim and all of your family...j
 
---Original Message---
 
From: L T CHERPESKI
Date: 6/7/2009 11:20:17 PM
To: tmic-list@eskimo.com;  cjb...@aol.com
Subject: Re: [TMIC] Update on JIM and so sad about Pam,
 
Carol,
 
I'm sorry to hear that Jim has been moved into ICU.  Will definitely keep
him in my prayers.  How wonderful that grandpa was able to spend time with
those sweet granddaughters.  I'll be watching for the update.  Hope and pray
all goes well.
 
Linda
- Original Message - 
From: cjb...@aol.com 
To: tmic-list@eskimo.com 
Sent: Sunday, June 07, 2009 8:44 PM
Subject: [TMIC] Update on JIM and so sad about Pam,


Got home from the hospital this evening and as I usually do,sat down in
front of the computer to see what had been written today. How sad but also
happy to know that Pam has been called home into the loving arms of the GOD
that she loves so much. I also will miss her writings to the list and the
TIAD that I didn't figure out for some time.This morning the hospital called
and said they were moving Jim into ICU as they think he has Pneumonia. My
son and and 2 of our precious grandaughters drove about 3 hours to see Jim.
It was wonderful to see them and put sunshine in Jim's room. The ones that
came are the almost 8 yr old twins and mommy and the 11 yr old and 2 yr old
stayed home. They stayed overnight and we went to church this morning and
then went to the hospital after lunch to see granpa for a little while
before they had to head back home.There is still 5 days of school for all of
them. Daddy is a teacher. Anyway tomorrow morning early they are doing a
bronchialscopy test. I will kepp you posted and we thank you for your
prayers. carol



An Excellent Credit Score is 750. See Yours in Just 2 Easy Steps!
 







Download the AOL Classifieds Toolbar for local deals at your fingertips.
 tile12.jpg

[TMIC] Update on JIM and so sad about Pam,

2009-06-07 Thread CJBJWB
Got home from the hospital this evening and as I usually do,sat down in  
front of the computer to see what had been written today. How sad but also 
happy  to know that Pam has been called home into the loving arms of the GOD 
that she  loves so much. I also will miss her writings to the list and the 
TIAD that I  didn't figure out for some time.This morning the hospital called 
and said they  were moving Jim into ICU as they think he has Pneumonia. My 
son and and 2 of our  precious grandaughters drove about 3 hours to see Jim. 
It was wonderful to  see them and put sunshine in Jim's room. The ones that 
came are the almost 8 yr  old twins and mommy and the 11 yr old and 2 yr old 
stayed home. They stayed  overnight and we went to church this morning and 
then went to the hospital after  lunch to see granpa for a little while 
before they had to head back home.There  is still 5 days of school for all of 
them. Daddy is a teacher. Anyway tomorrow  morning early they are doing a 
bronchialscopy test. I will kepp you posted and  we thank you for your prayers. 
carol
**An Excellent Credit Score is 750. See Yours in Just 2 Easy 
Steps! 
(http://pr.atwola.com/promoclk/100126575x1222377042x1201454362/aol?redir=http://www.freecreditreport.com/pm/default.aspx?sc=668072hmpgID=62bcd=Jun
eExcfooterNO62)


Re: [TMIC] Update on JIM and so sad about Pam,

2009-06-07 Thread L T CHERPESKI
Carol,

I'm sorry to hear that Jim has been moved into ICU.  Will definitely keep him 
in my prayers.  How wonderful that grandpa was able to spend time with those 
sweet granddaughters.  I'll be watching for the update.  Hope and pray all goes 
well.

Linda
  - Original Message - 
  From: cjb...@aol.commailto:cjb...@aol.com 
  To: tmic-list@eskimo.commailto:tmic-list@eskimo.com 
  Sent: Sunday, June 07, 2009 8:44 PM
  Subject: [TMIC] Update on JIM and so sad about Pam,


  Got home from the hospital this evening and as I usually do,sat down in front 
of the computer to see what had been written today. How sad but also happy to 
know that Pam has been called home into the loving arms of the GOD that she 
loves so much. I also will miss her writings to the list and the TIAD that I 
didn't figure out for some time.This morning the hospital called and said they 
were moving Jim into ICU as they think he has Pneumonia. My son and and 2 of 
our precious grandaughters drove about 3 hours to see Jim. It was wonderful to 
see them and put sunshine in Jim's room. The ones that came are the almost 8 yr 
old twins and mommy and the 11 yr old and 2 yr old stayed home. They stayed 
overnight and we went to church this morning and then went to the hospital 
after lunch to see granpa for a little while before they had to head back 
home.There is still 5 days of school for all of them. Daddy is a teacher. 
Anyway tomorrow morning early they are doing a bronchialscopy test. I will kepp 
you posted and we thank you for your prayers. carol


--
  An Excellent Credit Score is 750. See Yours in Just 2 Easy 
Steps!http://pr.atwola.com/promoclk/100126575x1222377042x1201454362/aol?redir=http://www.freecreditreport.com/pm/default.aspx?sc=668072%26hmpgID=62%26bcd=JuneExcfooterNO62

RE: [TMIC] update granddad

2009-03-10 Thread Tami Streeter
What a precious little blessing!  And I love her name.

 

Tami

 

  _  

From: wim from holland [mailto:wim_from_holl...@hotmail.com] 
Sent: Tuesday, March 10, 2009 5:59 AM
To: TMIC
Subject: [TMIC] update granddad
Importance: High

 

I'll try again.
 
On this photo she had the same pose as we saw her on a photo in the womb.
Vingers in het mouth and a hand besides her head.
 
The first time I sended more but they did not came trough.
 
Wim from Holland

  _  

Plan je feest, nodig mensen uit en deel je foto's met Windows
http://windowslive.microsoft.nl/WL/Explore/Events  Live Events



Re: [TMIC] update granddad

2009-03-10 Thread Pieter and Heather
She is beautiful Wim,

Lucky parents and grandparents. 
Hugs from 
Heather in Calgary 
  - Original Message - 
  From: wim from holland 
  To: TMIC 
  Sent: Tuesday, March 10, 2009 4:58 AM
  Subject: [TMIC] update granddad


  I'll try again.
   
  On this photo she had the same pose as we saw her on a photo in the womb. 
Vingers in het mouth and a hand besides her head.
   
  The first time I sended more but they did not came trough.
   
  Wim from Holland


--
  Plan je feest, nodig mensen uit en deel je foto's met Windows Live Events 

RE: [TMIC] update granddad

2009-03-10 Thread Patricia Cooley
WIM:

 

SHE IS ABSOLUTELY BEAUTIFUL.  YOUR FAMILY IS SO BLESSED TO HAVE A HEALTHY
GRANDCHILD.  THERE IS NOTHING MORE WONDERFUL THAN BEING A GRANDPARENT.
ENJOY HER AND DON'T FORGET IT IS A GRANDMOTHER'S JOB TO SPOIL YOUR
GRANDCHILDREN.  I HAVE 2 GRANDDAUGHTERS WHICH IS LOVE TO PIECES AND DO MY
BEST TO SPOIL.

 

PATTI IN WISCONSIN

 

From: wim from holland [mailto:wim_from_holl...@hotmail.com] 
Sent: Tuesday, March 10, 2009 5:59 AM
To: TMIC
Subject: [TMIC] update granddad
Importance: High

 

I'll try again.
 
On this photo she had the same pose as we saw her on a photo in the womb.
Vingers in het mouth and a hand besides her head.
 
The first time I sended more but they did not came trough.
 
Wim from Holland

  _  

Plan je feest, nodig mensen uit en deel je foto's met Windows
http://windowslive.microsoft.nl/WL/Explore/Events  Live Events



Re: [TMIC] update granddad

2009-03-10 Thread Grace M.
*Oh Wim!  She's an angel!  You are the luckiest soul alive.  :-)  Enjoy her,
and yes spoil her just a bit.*
**
*Love,*
*Grace*


Re: [TMIC] Update on Kim

2009-01-24 Thread LadyNotes
Kim, I am so happy to hear that your paralysis is not due to your TM.   And 
that it can be repaired.  I have had the steroid injections and the  disc of my 
C4, C5 and C6 vertebrae.  It did help me for a good while.   I'm hoping that 
if that's the option you choose, that it will help you  also.  I know what you 
mean about sleep deprivation from steroids.   They affect me the same way.  
Good luck with whatever option you  choose.  I will pray for your recovery
 
Naomi
C4 quadriplegicdue to Transverse Myelitis
since July 2,  2005  

 
In a message dated 1/23/2009 10:37:02 P.M. Eastern Standard Time,  
kimr1...@bellsouth.net writes:




First I would like to thank Jenna  for coming to the hospital to help me 
today (and the visit was great)   
Nero  left and good news the paralysis and  stinging in my arms and hands has 
nothing to do with my TM. The MRI’s they did  last night found 3 herniated 
discs on my neck that is causing spinal cord  depression causing my arms and 
hands to go numb. He called neurosurgeon to  come see me tomorrow and let me 
know 
what my options will be. So far a friend  that had the same this said the 
least evasive is to inject steroids directly  into the disc to stop the bone on 
bone rub and release the compression on the  spinal cord this is good news!!! 
So this explains why after receiving the  first dose of IV steroids my arms and 
hand improved 90% within 5 hours.   
If it were TM related the damage  can not be reversed!  But the  herniated 
disc can be repaired! So YIPPIE!!! 
Down side right now is with all  the steroids I have not slept at ALL since I 
go up Wed at 6:30 am, serious  best I have done is a 20 minute nap today! 
They gave me morphine and Ambian  sleep pills tonight so hoping I get some 
sleep 
tonight! I am starting to feel  like a zombie going thru the motions, getting 
harder to focus with sleep  deprivation. 
Will post what Nero-surgeon says  once I hear from them tomorrow 
Again thanks for the one on one  email I have gotten the concern and advice 
mean a lot to  me 
What a great second family we all  have in each other! Note   J 
Note: to the Atlanta TM suport group if I get out of the hospital  by Sunday 
in time for our meeting I will be there!! 




**From Wall Street to Main Street and everywhere in between, stay 
up-to-date with the latest news. (http://aol.com?ncid=emlcntaolcom0023)


[TMIC] Update on Kim

2009-01-23 Thread kimr1999







First I would like to thank Jenna for coming to the hospital to help me today (and the visit was great) 
Nero left and good news the paralysis and stinging in my arms and hands has nothing to do with my TM. The MRI’s they did last night found 3 herniated discs on my neck that is causing spinal cord depression causing my arms and hands to go numb. He called neurosurgeon to come see me tomorrow and let me know what my options will be. So far a friend that had the same this said the least evasive is to inject steroids directly into the disc to stop the bone on bone rub and release the compression on the spinal cord this is good news!!! So this explains why after receiving the first dose of IV steroids my arms and hand improved 90% within 5 hours. 
If it were TM related the damage can not be reversed! But the herniated disc can be repaired! So YIPPIE!!!

Down side right now is with all the steroids I have not slept at ALL since I go up Wed at 6:30 am, serious best I have done is a 20 minute nap today! They gave me morphine and Ambian sleep pills tonight so hoping I get some sleep tonight! I am starting to feel like a zombie going thru the motions, getting harder to focus with sleep deprivation.

Will post what Nero-surgeon says once I hear from them tomorrow

Again thanks for the one on one email I have gotten the concern and advice mean a lot to me
What a great second family we all have in each other! Note J

Note: to the Atlanta TM suport group if I get out of the hospital by Sunday in time for our meeting I will be there!!







Re: [TMIC] Update on Kim

2009-01-23 Thread Grace M.

  *Hi Kim,  *



  *Like Barbara, I feel odd telling you congratulations on the
 herniated discs, but I'm so relieved that it isn't a recurrent TM attack.
 Good luck sleeping tonight.  I'm always a mess while on IV SoluMedrol but
 the sleeping pills do knock me out.  *



  *Feel better soon!  *



  *Gracie*



[TMIC] Update on Kim

2009-01-22 Thread Jenna
Hi gang!

I just wanted to give you an update on Kim.  She did go to the ER last night, 
because she got much worse as the night went on.  They stared the IV steroids 
and Morphine.  She was admitted and will be there for at least a few days.  
They are going to do an MRI and some other test today.

She will have her laptop later on today and will update everyone.

Make it a great day!
 Jenna 


  

Re: [TMIC] Update on Kim

2009-01-22 Thread Pieter and Heather
Thanks Jenna, 

Please do keep us posted if Kim doesn't get on her laptop.  I do hope she is 
not having a relapse of some sort.  Unusual to do that with TM unless it is the 
'recurring' type or MS. 

Heather in Calgary 
  - Original Message - 
  From: Jenna 
  To: TMIC 
  Sent: Thursday, January 22, 2009 7:57 AM
  Subject: [TMIC] Update on Kim


  Hi gang!

  I just wanted to give you an update on Kim.  She did go to the ER last night, 
because she got much worse as the night went on.  They stared the IV steroids 
and Morphine.  She was admitted and will be there for at least a few days.  
They are going to do an MRI and some other test today.

  She will have her laptop later on today and will update everyone.

  Make it a great day!
   
  Jenna 



[TMIC] Update

2009-01-22 Thread kimr1999






First I would like to express my heartfelt prayes and good thoughts to Jude, from the email contacts I have had with her she is truly an inspirational woman and has help support so many others in there time of need without thinking about her self

So to All My TM family Thank Youall for the broadcast and personal responses last night. I as at a total loss on what to do as never had issue with my arms or hands. I did go to the ER and I am back in Piedmont hospital in Bukhead (Downtown Atlanta GA) Got up Wed am neck and back was stiff and I thought I slept wrong and went on in to work, by 2 my hands started to sting and get stiff (like when you have been raking leaves all day and last there stiff and sore) I could not make a fist or straighten them out… to painful to even pick up my office pen left work on time and went home… progressively got worse and pain was almost unbearable 
Talked to Jenna for awhile kicking around what to do, she gave me the number to our on call Nero. He said to go back and rest and only go to ER if my mobility is effected… well after and hour of “rest” I could not get comfortable, and when I went to stand up my good left leg it gave out like my right would and I hit the floor, we had already packed an ER bag so headed to Piedmont. From time in door to ER bed was less than 15 minutes… Nero on call was the one I talked to at home, he told ER doc to start running the usual test too see if there was any infections, if not start the steroids ASAP, then comes my friend Morphine! 
I was admitted to a room by 3 and by 5 I could make a fist and straightened my hands out, was still painful but I could do it... by 9 am most the pain is gone now still a little sore, There going to give me triple the steroids required to keep the left leg from getting worse ! (Oh and let me tell you Morphine at 9am for breakfast ROCKS)!!
I had my MRI’s today Brain (yep was confirmed I have a Brain) Neck, upper and lower spine), they did contrast and Non contrast, Let me tell you 3 hours in a MRI, not fun! Will know results tomorrow and will post ya all

They are talking about sending me home tomorrow with the IV pump and bags and I can changed myself or see how I feel and if I am still week I will be here until Sunday (I vote for stay here and let them do the work, will have plenty on my plate once I get home)

So good new is the left leg did not spread and the pain level is back to what it was Tuesday before the newest relapse

So all and all this flair up /relapse is turning out good new and I get all the free “Sugar Free Pudding” I want!, Bad new is if I see "House" walk in I will just cash my chips in LOL
(Note with the Morphine I have not had any sleep since I got up at6:00amWed to go to wokdso going on 45 hours and no sleep, from here on you will have to “sound out a lot of my emails) Per Jenna last year when I was sending out email on Morphine they were funny to read (they made sense to me and I even spell checked but guess Morphine plays tricks with my spell check ability) The words look fine to me but she said there not. Sso will keep ya posted if you can’t understand the email pass it to a small child and they will translate for you!
Hugs and prayers to all of you!
(Oh and looks like I wont be making the Atlanta support group this weekend
Kim






[TMIC] Update on Health Status

2009-01-11 Thread Heyjude48458
 
 
This is only for those of you that give a damn.  
In an effort to write of things regarding the  
topic of Transverse Myelitis I thought some of  
you might find what I am going through to  be
somewhat interesting.  If not, delete this  email 
now, because that's what this is  about.
 
You are aware of the two pressure wounds  that
 go deeply...all the way to the bones, on  each 
side of my behind on the ischeal area, where  
we sit.
 
Well,  I have been up all night in  pain...yes, 
I have a true pain in the ass!  with a  wound 
vac attached by lots and lots of tape to  attach 
a suction device to each wound site.   Both sites
are infected, including the bone.  That is  the 
bad news, except for the fact that the machine  
that sucks the infection out of the wounds  really and actually, sucks!   

It has an alarm system built in and every  
couple of minutes it goes off with one warning  
after another.  And it keeps alarming  until I 
press the reset button.  That is why I am  awake 
at three in the morning.  As of yet, there  has 
not been a real problem except for the darn  
machine.
 
Anyway,  for a few months I have been  hooked 
up at home with IV antibiotics, Vancomycin,  
which I found out yesterday is not working so  
today I started out on something else I hope  
will have the desired effect on the  infection.  
This too is an IV medication but I take it in  
conjunction with Reglan because the IV meds  
makes me sick to my stomach which is one of  
the side affects of the IV  stuff.
 
Well, my apologies for being a bit testy  
regarding recent topics on the TM site.  As  far 
as those persons go who keep threatening to  
leave the site because they are unhappy with  
the topics and /or some person's  opinions...
simply quietly go to a different site.  One  day 
someone will write, where is so and so?   
Haven't heard from them in a while and we  
will come to the conclusion  that you needed  
something we were unable to  give and   you
went elsewhere.
 
The World will not end and we will go about  
the business at hand, trying to help the new  
members and ourselves deal with the  
physical and psychological effects left after  an
attack of TM.  
 
The psychological effects are sometimes as bad,  
or worse than the physical.  Being bed  ridden is no fun.  Missing out  on 
family events at holiday and other  times sucks a big one.  Having family 
believe that we don't take part in dinners, etc  because we are too lazy or 
simply  
don't care any more hurts almost as  much or more than the Transverse  
Myelitis.
 
Thank the Lord that we have this  wonderful
 family to come to when the realities of  life 
with a debilitating disease gets us down.   It is
great to have friends who truly understand how  we feel.  
 
Having to travel by ambulance may sound  like
fun to some, but believe me, it isn't any  picnic.  Besides, if one is not  
being transported to a TM related  appointment, it can get quite expensive at 
$180.00 round trip.  And that is providing  the destination is fairly close to  
home. Then when one arrives to  wherever it is that they are going,  if the 
wounds are like mine, one has to spend the whole time on the stretcher which  
is not like laying on a feather  filled sofa.
 
The persons on this site understand how much  
a visit like that takes out of us.  I know  how
worn out I am after a round trip visit to the  
hospital ER or to my Dr.'s office.  Spend a  few
weeks in bed, not moving your legs at all and  
see how much energy it takes out of you  simply
transferring out of bed and into your  
wheelchair.  I haven't had the luxury of  sitting 
in my wheelchair for almost two years now,  
and it is getting me down.
 
So, life with TM is just like any other  chronic
illness;  It is the pits.  Just like  getting older 
and finding things more  difficult to  do. 
 
I am finding myself falling asleep in  
mid-sentence and waking up hours later, so I  
guess it's time t0  get some shut  eye.
 
Love and Hugs,
Jude
 
 
 
 
 
 


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[TMIC] Update from Randy

2008-11-12 Thread Jenna


 
The ENT came by and is sure that this Rhyemes (look up the spell sorry) - 
caused by herpes zoster - other words shingles. Being that I had tm and the 
pain associated with TM in O5 it makes sense. He agreed and sees a correlation. 
Also since there are no lessions then it mkes since. They r starting me on 
virals immediately-which I have been asking for since day one. And I have 
saying all this time that I believed it was shingles. 
Sent from my Verizon Wireless BlackBerry

From:  Jenna [EMAIL PROTECTED]
Date: Wed, 12 Nov 2008 10:19:18 -0800 (PST)
To: TMICtmic-list@eskimo.com; Kim[EMAIL PROTECTED]; Martha Fleming[EMAIL 
PROTECTED]; Betty[EMAIL PROTECTED]
Subject: [TMIC] Question from Randy

Randy  asked me to forward this.  Anyone what to tell him their experience with 
Solu-Medrol? 

 Jenna

[EMAIL PROTECTED]



Ok u might forward this to group. I have no forward ability on blackberry. They 
are treating me with IV methyprnisolone (solu-medrol) and added tergetal for 
the facial pain. Could someone look up, explain or add personal experiences 
from the methyprnisolone. 
Sent from my Verizon Wireless BlackBerry

From:  Jenna [EMAIL PROTECTED]
Date: Wed, 12 Nov 2008 05:39:18 -0800 (PST)
To: [EMAIL PROTECTED]
Subject: Re: October TM meeting

Very good Randy!  Hopefully the new ENT will have good news too!  Take care and 
keep me updated.

 Jenna





From: [EMAIL PROTECTED] [EMAIL PROTECTED]
To: Jenna [EMAIL PROTECTED]
Sent: Wednesday, November 12, 2008 9:01:11 AM
Subject: Re: October TM meeting

Great news the doc says that it  isn't ms. The facial nerves are inflamed but 
the brain stem is ok. Theyu don't knw the cause but believe it is an ear 
infection that attacked the nervous system. But it isn't a nuro problem per 
say. The steriods seem to be working. They also have a better ENT going to look 
at me. They say that I will probably have to have surgery on inner ear. But 
that is left up to the ENT. 
Sent from my Verizon Wireless BlackBerry

From:  Jenna [EMAIL PROTECTED]
Date: Tue, 11 Nov 2008 15:56:05 -0800 (PST)
To: [EMAIL PROTECTED]
Subject: Re: October TM meeting

Wow what a day.  Well I am praying for you and hoping you will recover quickly.

 Jenna





From: [EMAIL PROTECTED] [EMAIL PROTECTED]
To: Jenna [EMAIL PROTECTED]
Sent: Tuesday, November 11, 2008 7:43:57 PM
Subject: Re: October TM meeting

I had two lumbar punctures. The first got nothing. The second was not much 
better and the guy hit a nerve TWICE that sent a shock to my testees. It was 
horrific. They did some evoke potential tests where they electricute ur hands 
and ankles. I had another mri. They did some visual and auditory tests. 
Sent from my Verizon Wireless BlackBerry

From:  Jenna [EMAIL PROTECTED]
Date: Tue, 11 Nov 2008 15:36:30 -0800 (PST)
To: [EMAIL PROTECTED]
Subject: Re: October TM meeting

How are you feeling?  What are they doing for you??

 Jenna





From: [EMAIL PROTECTED] [EMAIL PROTECTED]
To: Jenna [EMAIL PROTECTED]
Sent: Tuesday, November 11, 2008 7:33:59 PM
Subject: Re: October TM meeting

Sunday is best for me. I should b out. I thnk the girls said sunday. 
Sent from my Verizon Wireless BlackBerry

From:  Jenna [EMAIL PROTECTED]
Date: Tue, 11 Nov 2008 15:28:19 -0800 (PST)
To: [EMAIL PROTECTED]; Susan[EMAIL PROTECTED]; [EMAIL PROTECTED]
CC: Martha  Fleming[EMAIL PROTECTED]; Betty Budnek[EMAIL PROTECTED]; RANDY  
RANKIN[EMAIL PROTECTED]
Subject: Re: October TM meeting

I can meet on Saturday or Sunday just let me know.

 Jenna





From: [EMAIL PROTECTED] [EMAIL PROTECTED]
To: Jenna [EMAIL PROTECTED]; Susan [EMAIL PROTECTED]; [EMAIL PROTECTED]
Cc: Martha Fleming [EMAIL PROTECTED]; Betty Budnek  [EMAIL PROTECTED]; 
RANDY RANKIN [EMAIL PROTECTED]
Sent: Tuesday, November 11, 2008 6:12:21 PM
Subject: Re: October TM meeting


R we going to meet this weekend???
-- Original message from Jenna [EMAIL PROTECTED]: -- 


When and where are we meeting.  Sunday is fine with me so that Randy can be 
there.  Please let me know.  Thanks so much!!  Have a great week all. 

 Jenna





From: [EMAIL PROTECTED] [EMAIL PROTECTED]
To: Susan [EMAIL PROTECTED]; [EMAIL PROTECTED]
Cc: Martha Fleming [EMAIL PROTECTED]; Betty Budnek [EMAIL PROTECTED]; Jenna 
[EMAIL PROTECTED]; RANDY RANKIN  [EMAIL PROTECTED]
Sent: Sunday, November 9, 2008 7:40:53 PM
Subject: Re: October TM meeting


Maybe we can find something between Hiram and D'ville?
-- Original message from Martha Fleming [EMAIL PROTECTED]:  
-- 


Okay. Sounds good to me.

--- On Wed, 11/5/08, [EMAIL PROTECTED] [EMAIL PROTECTED] wrote:

From: [EMAIL PROTECTED] [EMAIL PROTECTED]
Subject: Re: October TM meeting
To: 

[TMIC] UPDATE ON JIM

2008-11-04 Thread CJBJWB
After more than a week of tests, because of a large spike in blood  sugar and 
a couple of episodes of severe gas and heartburn problems. The  tests 
included blood tests of course. He has not had any problem with elevated  sugar 
since 
the beginning , caused by the IV steroids they used to stop his  spinal cord 
from expanding any further. Anyway the doctor did the blood test and  from 
that decided to do an upper GI. After that he did an ultrasound on his  liver( 
didn't like the sound of that) When he got the ultrasound results back he  set 
up a catscan and waited til he had those results before he told us the  
ultrasound results. He didn't want to tell us those because they suggested a  
possible tumor on the pancreas. By the catscan results it is almost certain 
that  it 
is gall stones and we will be meeting with a surgeon tomorrow morning.  
Naturally we are very happy that this is the diagnosis and are hoping they will 
 be 
able to do the scope procedure. I will keep you all posted as we find out  
more. As always we appreciate prayers. Carol and  Jim   PS have any of you 
in 
ourTM family had  any surgical procedures like this and have any stories to  
share?
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[TMIC] Update on Pam

2008-10-26 Thread Jenna
Okay I just talked to Pam and she is recovering from surgery and is hoping to 
go home on Wednesday!!  She has a hugh boot on her foot.  So if you would like 
to call her that would be great!!!

 Jenna



  

Re: [TMIC] Update on Pam

2008-10-26 Thread jrushton
Does she have a laptop, Jenna, so we could e-mail her??  

Jeanne in Dayton

Re: [TMIC] Update on Pam

2008-10-26 Thread Jenna
Thanks for asking, but the hospital she is in does not allow, laptops, or cell 
phones.  So Pam is pretty cut off unless you call her.  She can't even make 
long distant phone calls unless her husband is at home to say that he accepts 
the charges.  

 Jenna





From: jrushton [EMAIL PROTECTED]
To: Jenna [EMAIL PROTECTED]; tmic tmic-list@eskimo.com
Sent: Sunday, October 26, 2008 4:44:54 PM
Subject: Re: [TMIC] Update on Pam


Does she have a laptop, Jenna, so we could e-mail 
her??  
 
Jeanne in Dayton


  

[TMIC] Update on Jude

2008-09-15 Thread pjv1234
I spoke with both Jude and her husband Dave for just a minute today.  She went  
back in the hospital after being home for seven days.  (Being home is a big 
desire of Jude's so any amount of time that she is able to spend there is 
good.) 
She was moved today to a private room, because of the return of MRSA, but I 
will be able to visit and talk with her (tomorrow) as she isn't on a vent.  

Jude said she is weak and tired and asked me to wait until tomorrow to visit -  
I'll
let you know how it goes.

Patti - Michigan

(Hurley Hospital  Room 718)



[TMIC] Update for Jude

2008-09-13 Thread Alle111
Hello all,
I had called the other day but the nurse said she was not in I.C.U.  and to 
call later. Then Pam had said she was moviing to a regular room so I waited and 
when I called a few moments ago, she was resting/asleep BUT had gone home for 
a few days but re-admitted this morning with yet another U.T.I. Her husband 
isn't sure what course of action they will try and asked that I call back 
tomorow..Ella



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[TMIC] Update on Jude

2008-07-24 Thread Jenna
Hi everyone I got this from Pam today and wanted to let everyone know how Jude 
was doing.  
 Jenna



LATEST UPDATE.JUDE IS HAVING A SLIGHT PROBLEM GETTING OFF THE VENTILATOR. THEY 
LOWERED IT MORE SO SHE IS HANDLING IT BETTER. SHE GOT HER HAIR WASHED TODAY AND 
THAT MADE HER FEEL BETTER.
SHE SAYS SHE SEES NO PROBLEM WITH JUDE WEANING OFF THE VENTILATOR.


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Re: [TMIC] Update on Jude

2008-07-24 Thread Grace M.

   Thanks so much for the update on Jude, Jenna.  She's in my thoughts and
 prayers.

 Gracie

  **



Re: [TMIC] Update on Jude

2008-07-24 Thread jrushton
As she is in mine and so are you, Gracie...Jeanne 
 
---Original Message---
 
From: Grace M.
Date: 7/24/2008 8:19:43 PM
To: Jenna
Cc: tmic-list@eskimo.com
Subject: Re: [TMIC] Update on Jude
 
Thanks so much for the update on Jude, Jenna.  She's in my thoughts and
prayers.
 
Gracie
 
 

[TMIC] UPDATE ON JUDE....

2008-02-24 Thread ROSEOFRENO
Hi Everyone ~
   I had a wonderful chat with Jude today.  She wanted me to  tell all of you 
how very much she is appreciating all of the cards, flowers,  books, CD's, 
etc.and to tell all of you that you are keeping her spirits  up...!!  She 
is 
just amazed at the outpouring of love she's receiving from  this TM family.  
 
   I learned she has five new bed sores since going into this  nursing home.  
She described them to me and I about fell off my  chair.one of them is 
the size of a small orange.  I told her she needed  to go back into the 
hospitaland she agreed...and will be calling her PCP  (personal care 
physician) 
tomorrow.
 
   They have done nothing for these bed sores so I got a package  together 
for her with Melaleuca Oil, bandages, triple antibiotic cream,  everything I 
could think of and got it off to her.  She has Dave looking  for it now because 
she is going to try it on the sore on her ankle.  I told  her to just do the 
one sore and see if there is improvement...if so, use it on  the other sores.  
She will need more than just the Melaleuca Oil but it's a  start in the right 
direction.  This is the best tree tea oil on the  marketit soaks in and 
heals from the inside out.another paraplegic  friend of mine used it and 
now 
swears by it he uses it whenever his skin  gets the least bit red because 
he knows a sore is beginning and he nips it in  the bud with this oil.
 
   I even got some advice from Jude today regarding Fentanyl  patches.  My 
neuro just took me off my Oxycontin and has me trying the  Fentanyl patch and 
I've been curled up in a ball of pain for the past three  days.  Jude told me 
he 
needs to up my dosage...what he gave me isn't strong  enough...so I'm calling 
my neuro tomorrow regarding this.  My pain has been  off the charts this 
winterworse winter with TM in ten years of living with  this dang 
syndrome..!
 
   Jude needs us now more than ever so please keep those prayers  going up.
 
   Love to all,
   ~ Lynn



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[TMIC] Update/Woman from the Netherlands/Heather.

2007-11-14 Thread Grace M.
*Hi Heather and all,*
**
*I have just spoken to the young man from the Netherlands who's wife is so
very ill right now.  Her neuro will be requesting a telephone consult with
Dr. Wingerchuk from the Mayo.  I am praying that the Mayo will be able to
help.  In the last four weeks she has had methylprednisolone, plasmapheresis
and is currently doing Rituxan with no improvement as yet.  She is currently
vented.  Of course it is still very early.  I intend to pray with all of my
heart and soul, that a successful chemo/meds protocol can be found for
her.   Again, thank you Heather for sending me a heads up.  Helping those
with this horrid disease is what I'm all about right now---it keeps me
going. *
**
*Hugs,*
*Grace *


Re: [TMIC] Update/Woman from the Netherlands/Heather.

2007-11-14 Thread Balmatmic
Wow, I am so amazed how, in such a short time, this  communication has 
occured.  I forget how powerful and wonderful the  internet is sometimes.  And 
then, 
something like this happens and people  reach out to each other with 
information and support from so far away that they  couldn't get from their 
doctors.
 
It's horrible to be ill, but even more so when information is  so hard to 
come by.
 
Thank you Jim and thanks to the TMA.
 
Many hugs, Barbara A



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[TMIC] Update on hospital stay

2007-04-30 Thread MissPrissGrandma
I haven't written to the list in so long that half of you have  probably 
forgotten me.
 
First let me thank HeyJude for my contest winnings.  They  arrived in perfect 
shape and just made my day.  Thank you so  much.
 
I went back to my doctor two weeks after I got out of the  hospital.  He 
basically asked me why I was there as I had just seen him 6  weeks before.  He 
had 
no discharge summary on me and no results of the  stress test.  I find that 
really strange as he is in a practice owned by  the hospital and he couldn't 
even find anything on the computer.  After all  that searching, he did say 
Let's talk about when you were here six weeks  ago.  I didn't remember 
throwing a 
fit as I tend to do in the hospital  when something doesn't go as I want it 
to, but I have made a promise to his  nurse to behave from now on.  Anyway, 
come to find out that I am insulin  resistant which I guess means pre-diabetic. 
 
That shouldn't surprise  me.  Seems to be a family trait, plus I just lay in 
bed all day so I don't  burn up anything.  He gave me a choice of pills or a 
shot and I chose the  shot as it supposedly helps take your appetite away and 
believe me,  it  does.  The problem I am having is that he wants me to consume 
150-180 grams  of protein a day.  I just can't eat that much and those drink 
things aren't  real good.  I go back in a couple of weeks so maybe he'll know 
something  about my hospital stay by then.  He at least knew I was in the 
hospital and  that his hospitalist was seeing me every day.
 
On another note, hubby has to go to a conference in Myrtle  Beach early in 
June.  The last time I went with him I was able to stand a  little, so we took 
my wheelchair and went, however, sitting still for that ride  and not being 
able to move my feet caused to get blood clots when I got back and  I am still 
on 
Coumadin.  This time we have to find a van to rent that takes  wheelchairs.  
My manual wheelchair that comes apart was too wide to go  through the hotel 
room door.  My electric wheelchair doesn't have that  problem.  I am just 
worried about back pain because just going to the  doctor in it hurts my back 
so 
bad.  I can imagine what a trip to the beach  will do but I am not staying her 
alone.
 
Not leading a very exciting life these days, can't even watch  my soaps cuz 
channel 6 goes off every day when they are on.   MEAN
 
That's about it for now.  Will try to visit more  often.
 
Hildred
in hot North Carolina
TM since '76



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RE: [TMIC] Update on hospital stay

2007-04-30 Thread Candis Kalley
Hildred,

When traveling, I have found that  the Homedic seat cover very helpful.  It has 
heat and vibrationl.  My back pain is severe when sitting so long, but the heat 
seems to help along with the lower back vibration.

I still need to stop every hour or so and get out to move but I don't hurt as 
bad as I did without the Homedic seat cover.

Hope this info helps.

Candy K.

- Original Message - 
From: 
To: [EMAIL PROTECTED];tmic-list@eskimo.com
Sent: 4/30/2007 5:16:52 PM 
Subject: [TMIC] Update on hospital stay


I haven't written to the list in so long that half of you have probably 
forgotten me.

First let me thank HeyJude for my contest winnings.  They arrived in perfect 
shape and just made my day.  Thank you so much.

I went back to my doctor two weeks after I got out of the hospital.  He 
basically asked me why I was there as I had just seen him 6 weeks before.  He 
had no discharge summary on me and no results of the stress test.  I find that 
really strange as he is in a practice owned by the hospital and he couldn't 
even find anything on the computer.  After all that searching, he did say 
Let's talk about when you were here six weeks ago.  I didn't remember 
throwing a fit as I tend to do in the hospital when something doesn't go as I 
want it to, but I have made a promise to his nurse to behave from now on.  
Anyway, come to find out that I am insulin resistant which I guess means 
pre-diabetic.  That shouldn't surprise me.  Seems to be a family trait, plus I 
just lay in bed all day so I don't burn up anything.  He gave me a choice of 
pills or a shot and I chose the shot as it supposedly helps take your appetite 
away and believe me,  it does.  The problem I am having is that he wants me t!
 o consume 150-180 grams of protein a day.  I just can't eat that much and 
those drink things aren't real good.  I go back in a couple of weeks so maybe 
he'll know something about my hospital stay by then.  He at least knew I was in 
the hospital and that his hospitalist was seeing me every day.

On another note, hubby has to go to a conference in Myrtle Beach early in June. 
 The last time I went with him I was able to stand a little, so we took my 
wheelchair and went, however, sitting still for that ride and not being able to 
move my feet caused to get blood clots when I got back and I am still on 
Coumadin.  This time we have to find a van to rent that takes wheelchairs.  My 
manual wheelchair that comes apart was too wide to go through the hotel room 
door.  My electric wheelchair doesn't have that problem.  I am just worried 
about back pain because just going to the doctor in it hurts my back so bad.  I 
can imagine what a trip to the beach will do but I am not staying her alone.

Not leading a very exciting life these days, can't even watch my soaps cuz 
channel 6 goes off every day when they are on.  MEAN

That's about it for now.  Will try to visit more often.

Hildred
in hot North Carolina
TM since '76






See what's free at AOL.com. 

Re: [TMIC] UPDATE on tingling pins/needles spreading in leg

2006-11-15 Thread L T CHERPESKI
Trudy,
I am also appalled about your treatment. How awful. I am very sorry you had to 
go through all of that. And Carol, your son-in-law is right, it does depend on 
the type of needle used that helps prevent the horrible spinal headache. My 
neurologist did my lumbar puncture himself, and he told me he was using a very 
small needle - it takes longer to do the tap, but almost guarantees no 
headache. And I did not have one, thank goodness.  Carol, we don't want you to 
have to tell us any horror stories so good luck with yours this Friday. I'll be 
thinking about you.
Linda in Eagle, ID
  - Original Message - 
  From: Carol Emailto:[EMAIL PROTECTED] 
  To: Trudy mailto:[EMAIL PROTECTED]; 
tmic-list@eskimo.commailto:tmic-list@eskimo.com 
  Sent: Wednesday, November 15, 2006 6:47 AM
  Subject: Re: [TMIC] UPDATE on tingling pins/needles spreading in leg


  Trudy, 
  I am appalled that you would have to lie on the rock hard table for 2 hours!  
I would think they would have a more comfortable bed to move you to for the 2 
hour holding time.  I am guessing that they wanted you to lie still for 2 hours 
to prevent the very pounding headaches that can occur after a spinal tap.  
Although my son-in-law, who is an anesthesiologist, says that it depends on the 
type of needle that is used for the tap on whether or not you will get the 
spinal headache, not the lying still for 2 hours.  I would sure be conveying my 
disconcert with someone at the hospital.  Call and ask to speak to the person 
in charge of complaint resolution.  Tell that person that you were abandoned 
and no one came in to check on you and you were not even given a buzzer to use 
in case of an emergency.  That's just my opinion.  But I am extremely sorry 
that you had to lie on that hard table for 2 hours.  



  Certainly hope my experience is going to be better.  I am having a spinal tap 
this Friday.  Maybe I will have a horror story to share with you!!! :)

  Carol in Culver, IN



- Original Message - 
From: Trudy mailto:[EMAIL PROTECTED]
To: 'Sharon Marsden'mailto:[EMAIL PROTECTED] ; 
tmic-list@eskimo.commailto:tmic-list@eskimo.com 
Sent: Tuesday, November 14, 2006 8:00 PM
Subject: RE: [TMIC] UPDATE on tingling pins/needles spreading in leg


Sharon,

I had almost the exact same reaction to Lyrica. But because I had fallen 
and fractured a bone in my knee I had to go back to a wheelchair for 3 months. 
I had just started taking Lyrica when I fell.. so I thought the awful numbness 
was due to being in a wheelchair for so long and then my right leg would drag 
and buckle on me! So I have stopped taking Lyrica but the numbness has not gone 
away completely but it has improved. I was sure I was having an MS attack. I 
will see my neuro in 3 weeks and we are comparing all tests taken the night I 
experienced my attack and how things look today (4 years later). Is it MS??? Is 
it TM???



Is this normal:  I went for a spinal tap last week. I was given a gown and 
put on an examination table. When it was over I was told I had to stay on the 
table and remain on my side for 2 hours. The exam table was extremely hard and 
the pillow was pathetic.. It had a paper covering.  During that time not once 
did any one come in to check on me to see whether I had fallen asleep and 
fallen off the table or that I just might need to use the restroom.. After two 
hours I worked my way off the table, got dressed and walked out!  Is it me or 
is there something wrong here???

Hang in there Sharon

Trudy in Virginia where it's leaves, leaves, leaves falling all over!!!






From: Sharon Marsden [mailto:[EMAIL PROTECTED] 
Sent: Tuesday, November 14, 2006 5:47 PM
To: tmic-list@eskimo.com
Subject: [TMIC] UPDATE on tingling pins/needles spreading in leg



Thanks to everyone who wrote offering advice and urging me to see/call the 
doc.  I'm stubborn and contrary for sure. :)  

You may remember that I have severe nocturnal nerve pain in my legs.  I 
have been so excited to have the Lyrica because it was helping with that pain. 
Then this past week I started having the problems I wrote about earlier.  The 
numbness/tingling got worse after I wrote before until I couldn't feel anything 
at all, no pin prick... nada, zip, zilch. My leg was dragging and the leg kept 
buckling when I put weight on it.  

Yesterday evening I finally gave up and called my neuro's after hours 
number.  The on-call NP called me back and wanted to put me in the hospital for 
IV Solumedrol.  She felt I was in an MS exacerbation and I did too.  I asked 
her though if  Lyrica could cause something like that but she didn't think so.  
I have wondered about it because the increasing symptoms have gone along with 
the Lyrica use--but I didn't want to think it could be that.  

I did some research before bedtime on Lyrica.  I had to go

[TMIC] UPDATE on tingling pins/needles spreading in leg

2006-11-14 Thread Sharon Marsden
Thanks to everyone who wrote offering advice and urging me to see/call the doc. 
 I'm stubborn and contrary for sure. :)  

You may remember that I have severe nocturnal nerve pain in my legs.  I have 
been so excited to have the Lyrica because it was helping with that pain. Then 
this past week I started having the problems I wrote about earlier.  The 
numbness/tingling got worse after I wrote before until I couldn't feel anything 
at all, no pin prick... nada, zip, zilch. My leg was dragging and the leg kept 
buckling when I put weight on it.  

 Yesterday evening I finally gave up and called my neuro's after hours number.  
The on-call NP called me back and wanted to put me in the hospital for IV 
Solumedrol.  She felt I was in an MS exacerbation and I did too.  I asked her 
though if  Lyrica could cause something like that but she didn't think so.  I 
have wondered about it because the increasing symptoms have gone along with the 
Lyrica use--but I didn't want to think it could be that.  

 I did some research before bedtime on Lyrica.  I had to go to NINDs and then 
to Medline to get the info because the Lyrica site doesn't tell.   According to 
Medline, Lyrica's side effects can be burning, tingling, numbness or pain in 
the hands, arms, feet, or legs.  Those are lists as more common side 
effects.  The less common include burning, crawling, itching, numbness, 
prickling, pins and needles or tingling feelings.  That was all me!

So, I didn't take my bedtime dose and my numbness/symptoms was a little better 
this morning.  I didn't take my morning dose either and I feel I'm still 
improving.  The NP called me this morning at 7:30 to tell me she spoke to the 
doctor and he agreed with hospitalization.  I told her about the Lyrica and 
that I was feeling better.  She had already called the hospital to get me a bed 
today.  Whew!  That was a close one!  

 I've been telling my daughter for the last week that my leg was 
hurting/itching where I had the skin sores from Bextra.  Anyone remember about 
Bextra?  It was taken off the market 2 years ago because it caused necrotizing 
fasciitis.  I was on Bextra and had black sores on my leg.  That's when I was 
living in the backwoods of Alaska and couldn't get out to the doctor.  I heard 
about the Bextra problem on NPR Radio and stopped taking it.  The sores started 
getting better within a week.  Anyway, on the Lyrica that area started hurting. 
 Odd, hey?  Lyrica is made by the same company as Bextra (and Neurontin).  I 
think I may feel like staying away from their products!  lol 

Now this morning my daughter-in-law told some people at work that I had a 
problem with Lyrica and had to stop taking it.  A co-worker walked over to her 
and said let me guess--she went numb and couldn't walk.  The same thing had 
happened to her when she was taking it.  What do you think of that!  

 So that's my story of a close call with Solumedrol and hospitalization.  I 
will do nearly anything to avoid being in the hospital anyway...  lol

 Sharon
 who is feeling better today, but I think I have a long way to go.   
 
  
 Sharon --from Arizona TM 1997 to MS 1998 
  It's not easy taking my problems one at a time when they refuse to get in 
line.  ~Ashleigh Brilliant
  http://health.groups.yahoo.com/group/MSersLife/
 






- Original Message 
From: Sharon Marsden [EMAIL PROTECTED]
To: tmic-list@eskimo.com
Sent: Thursday, November 9, 2006 9:17:50 PM
Subject: [TMIC] tingling pins/needles spreading in leg

Hi everyone:

My left leg is always my weaker leg.  And I always have numbness and strange 
sensations.  But yesterday morning my left foot started tingling in a different 
way with pins/needles.  It was uncomfortable to step down, but not painful.   
Now it's spreading up my leg and is up to my upper thigh.  I was dxed with 
Transverse Myelitis in 1997 (then MS dx came the next year).  I just realized 
today that the left leg is reminding me of the beginning of my experience with 
Transverse Myelitis in 97.  It is kind of like the feeling of a foot going to 
sleep but my leg is feeling draggy.   

Now my right foot is more numb than normal and is feeling stranger than normal. 
 I thought about calling my neuro but he's 45 miles away and I don't want to go 
in to see him.  And I don't want to be on solumedrol.  I'm contrary, you know.

Just wondering. 

hugs)))
Sharon
 
 
Sharon --from Arizona TM 1997 to MS 1998 
  It's not easy taking my problems one at a time when they refuse to get in 
line.  ~Ashleigh Brilliant
  http://health.groups.yahoo.com/group/MSersLife/















RE: [TMIC] UPDATE on tingling pins/needles spreading in leg

2006-11-14 Thread Trudy
Sharon,

I had almost the exact same reaction to Lyrica. But because I had fallen and
fractured a bone in my knee I had to go back to a wheelchair for 3 months. I
had just started taking Lyrica when I fell.. so I thought the awful numbness
was due to being in a wheelchair for so long and then my right leg would
drag and buckle on me! So I have stopped taking Lyrica but the numbness has
not gone away completely but it has improved. I was sure I was having an MS
attack. I will see my neuro in 3 weeks and we are comparing all tests taken
the night I experienced my attack and how things look today (4 years later).
Is it MS??? Is it TM???

 

Is this normal:  I went for a spinal tap last week. I was given a gown and
put on an examination table. When it was over I was told I had to stay on
the table and remain on my side for 2 hours. The exam table was extremely
hard and the pillow was pathetic.. It had a paper covering.  During that
time not once did any one come in to check on me to see whether I had fallen
asleep and fallen off the table or that I just might need to use the
restroom.. After two hours I worked my way off the table, got dressed and
walked out!  Is it me or is there something wrong here???

Hang in there Sharon

Trudy in Virginia where it's leaves, leaves, leaves falling all over!!!

 

  _  

From: Sharon Marsden [mailto:[EMAIL PROTECTED] 
Sent: Tuesday, November 14, 2006 5:47 PM
To: tmic-list@eskimo.com
Subject: [TMIC] UPDATE on tingling pins/needles spreading in leg

 

Thanks to everyone who wrote offering advice and urging me to see/call the
doc.  I'm stubborn and contrary for sure. :)  

You may remember that I have severe nocturnal nerve pain in my legs.  I have
been so excited to have the Lyrica because it was helping with that pain.
Then this past week I started having the problems I wrote about earlier.
The numbness/tingling got worse after I wrote before until I couldn't feel
anything at all, no pin prick... nada, zip, zilch. My leg was dragging and
the leg kept buckling when I put weight on it.  

Yesterday evening I finally gave up and called my neuro's after hours
number.  The on-call NP called me back and wanted to put me in the hospital
for IV Solumedrol.  She felt I was in an MS exacerbation and I did too.  I
asked her though if  Lyrica could cause something like that but she didn't
think so.  I have wondered about it because the increasing symptoms have
gone along with the Lyrica use--but I didn't want to think it could be that.


I did some research before bedtime on Lyrica.  I had to go to NINDs and then
to Medline to get the info because the Lyrica site doesn't tell.   According
to Medline, Lyrica's side effects can be burning, tingling, numbness or
pain in the hands, arms, feet, or legs.  Those are lists as more common
side effects.  The less common include burning, crawling, itching,
numbness, prickling, pins and needles or tingling feelings.  That was all
me!

So, I didn't take my bedtime dose and my numbness/symptoms was a little
better this morning.  I didn't take my morning dose either and I feel I'm
still improving.  The NP called me this morning at 7:30 to tell me she spoke
to the doctor and he agreed with hospitalization.  I told her about the
Lyrica and that I was feeling better.  She had already called the hospital
to get me a bed today.  Whew!  That was a close one!  

I've been telling my daughter for the last week that my leg was
hurting/itching where I had the skin sores from Bextra.  Anyone remember
about Bextra?  It was taken off the market 2 years ago because it caused
necrotizing fasciitis.  I was on Bextra and had black sores on my leg.
That's when I was living in the backwoods of Alaska and couldn't get out to
the doctor.  I heard about the Bextra problem on NPR Radio and stopped
taking it.  The sores started getting better within a week.  Anyway, on the
Lyrica that area started hurting.  Odd, hey?  Lyrica is made by the same
company as Bextra (and Neurontin).  I think I may feel like staying away
from their products!  lol 

Now this morning my daughter-in-law told some people at work that I had a
problem with Lyrica and had to stop taking it.  A co-worker walked over to
her and said let me guess--she went numb and couldn't walk.  The same
thing had happened to her when she was taking it.  What do you think of
that!  

So that's my story of a close call with Solumedrol and hospitalization.  I
will do nearly anything to avoid being in the hospital anyway...  lol

Sharon
who is feeling better today, but I think I have a long way to go. 

 

Sharon --from Arizona TM 1997 to MS 1998 

It's not easy taking my problems one at a time when they refuse to get in
line.  ~Ashleigh Brilliant

 http://health.groups.yahoo.com/group/MSersLife/
http://health.groups.yahoo.com/group/MSersLife/



 

 

- Original Message 
From: Sharon Marsden [EMAIL PROTECTED]
To: tmic-list@eskimo.com
Sent: Thursday, November 9, 2006 9:17:50 PM
Subject: [TMIC

[TMIC] Update Newbie Inquiry

2006-10-11 Thread EnMChavez
Good evening Group,

I'm Newbie Michelle from Bothell, WA who was just diagnosed several weeks ago with MS. 9/10 I awoke to the numbness again in my legs only to be hospitalized two days later. Not walking without assistance the symptoms only increased throughout the week. 2000 I was diagnosed with TM after an attack with all the same symptoms but recovered with little limitations. Now just finishing finally my prednisone/steroids I am improving daily. Now walking again on my own just a little wobbly at times ;-) and muscles are strengthening. My hands are still asleep with pins and needles though due to my lesion being at C5 this time whereas before it was T5-T7. I know that I am fortunate to be recovering again and walking on my own again. I am grateful and blessed. The doctors want to put me on Copaxone (daily injection). I wanted to ask if anyone is on this, their experience with it and if insurance covers this medication. I received a letter from Shared Solutions, which is through PPARX (Partnership for Prescription Assistance) who stated that insurance companys did not cover this. We currently do not unfortunately have medical insurance and this prescription is $1,300 to $1,500 a month. OUCH! Who can afford that! We are applying for PPARX assistance of course. Also has any MSrs out there discovered any successful alternative treatments. Is Copaxone my only option? {sigh} Thanks!!! 

Michelle
Bothell, WA
TM2000 to MS2006


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