[TMIC] Change of e-mail address

2009-08-31 Thread JHarper33
I'm changing the e-mail address I use on the list from _jharpe...@aol.com_ 
(mailto:jharpe...@aol.com)  to _barbara...@gmail.com_ 
(mailto:barbara...@gmail.com) . I hope it doesn't cause any  confusion -- I've 
used the same 
e-mail address for the 11 or so years I've been  on the list. But there are a 
couple of reasons for doing so. First of all, for  years people have been 
getting Jan H. and I confused, so this should help there.  Secondly, the gmail 
one is one I use for Internet sites and that's the one I  have on Facebook. 
With so many TMers now on Facebook, I keep getting invites to  join when I'm 
already there. By having the same e-mail here and there it should  cut down 
on confusion and make it easier for people to find me.
 
I'll still have the aol address, so you can reach me at either  one.
 
Barbara H.
_http://barbarah.wordpress.com_ (http://barbarah.wordpress.com) 
**A Good Credit Score is 700 or Above. See yours in just 2 easy 
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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] able to move slightly

2009-08-24 Thread JHarper33
Oh Jim -- that brought tears to my eyes as well. How  exciting!
 
Barbara H.
_http://barbarah.wordpress.com_ (http://barbarah.wordpress.com) 
 
 
In a message dated 8/24/2009 4:40:59 P.M. Eastern Daylight Time,  
jlu...@eskimo.com writes:

The past two weeks I started feeling a tingling in my right lower back.  
When I feel this I am able to move my left thumb! It's been 20 yrs, 4 mos  
since I was paralyzed from the neck down due to TM. When I recline the  
tingling stops and I can not move my thumb no matter how much I try  to.

To show that I was actually moving and not just having involuntary  
twitching, I had my nurse tell me when to move and I moved it. Here is the  
video 
_http://www.youtube.com/watch?v=Tw__9ZDv_hU

_ (http://www.youtube.com/watch?v=Tw__9ZDv_hU) 
Jim  Lubin
jlu...@eskimo.com
_http://makoa.org/jim_ (http://makoa.org/jim)   
disAbility Resources: _http://www.makoa.org



_ (http://www.makoa.org/) 



Re: [TMIC] OT:My Pattern published!

2009-08-22 Thread JHarper33
Very cool! Congratulations on being published!!
 
Barbara H.
_http://barbarah.wordpress.com_ (http://barbarah.wordpress.com) 
 
 
In a message dated 8/22/2009 7:35:34 P.M. Eastern Daylight Time,  
a...@artfarm.com writes:


This  is off  Topic, but I am so full of complaints and 
disappointments---  that i share and work on here-- that i wanted to 
share a ray of  hope.

I got a box the other day from Simon and Schuster... i had not  clue 
what it was til i opened it...

My 2010 Crochet A Day Calendar  arrived and my Flower Link scarf 
patternis in it!

This particularly  sweet, not only because the pattern was rejected by 
Interweave ( so if at  first you don't succeed try, try again)

but because my model was my  visually challenged neighbor from the 
complex I stayed in, in Rochester  while learning to live my life anew 
as a paraplegic and awaiting my home's  rehab.

It was a hellishly hard and horrible time and I missed the art i  used 
to make and crochet
was both a salvation and communication. I  offered weekly crochet 
lessons in that building.

The picture was  taken on a sunny but chilly day in the courtyard I 
used to love to roll  to...
the pattern was about turning poison into medicine.
by  hand
from heart


--  





Re: [TMIC] Need some help please

2009-08-12 Thread JHarper33
I have a friend who had a very successful double knee  replacement, but 
before they ever got to that point, they did cortisone  injections and I think 
maybe physical therapy, so I think those would give some  relief at least 
for a while. I would think losing weight could only help, and I  would guess 
water therapy would be good. 
 
I would seek another opinion and ask straight up, If I can't  do surgery, 
what are my other options; what can I do?
 
Barbara H.
http:barbarah.wordpress.com
 
 
In a message dated 8/11/2009 11:41:20 P.M. Eastern Daylight Time,  
cherp...@msn.com writes:

Hi everybody,
 
I'm hoping you guys can help point me in the right direction.  There  are 
so many of us on the TM site there's just got to be someone who knows  
somebody with the same or similar dilemma. 
 
Most of you know that I've had Sjogrens for 20+ years (unfortunately,  
progressive and aggressive) and 7 yrs ago TM came into my life.  I am on  heavy 
chemo meds (Imuran and Rituxan infusions) to suppress my immune system  to 
keep it from attacking my body.  Last Sept I had a minor surgery to  repair 
a torn meniscus in my knee, and my body went into the longest, hardest  
relapse I've ever had.  I'm just now getting my arms and hands back - I  
think this is as much as I'll get this time.  Almost everything else has  
gradually come back.  My one huge problem is that my KNEES took the  biggest 
hit - 
my doctors said it was because they were the weakest part of my  body at 
the time.  I have infected knees (right one to the bone) and am  walking 
(trying) on bone on bone knees.  They both need to be  replaced.  And, I have 
TM, 
so already my walking is not that  pretty.
 
I was sent out of state to a surgeon who does a special knee replacement  
surgery that is less invasive.  Long trip, big disappointment.  He  will NOT 
do surgery on me either because of the aftermath  - said it  would be like 
doing brain surgery due to my autoimmune diseases.   Well that's fine - I 
have always wanted to do anything but the surgery, but  was given no OTHER 
choices.
 
And, I am still being given NO options.  So I've done some of my own  
research.  What about physical therapy to get my thigh and quad muscles  built 
up 
so they can take some of the load off my knee  joints? (I'm a fairly small 
person so we're not talking about losing  50 lbs and that would make things 
all better)  Water therapy?  I'm  not quite sure how to get these muscles 
built up when my knees hurt so bad I  can hardly bend them, but there has to 
be a way.  My doctors have kind of  given up on me, which at first shocked 
me, now I'm just really mad.
 
Any ideas would be much appreciated.
 
Thanks guys,
 
Linda
 
 




Re: [TMIC] Re: [QUAD-L] 35 year anniversary

2009-08-01 Thread JHarper33
Jude, looking back at the posts preceding your  comments, none of them were 
on the TMIC. The address listed on them is _quad-l...@eskimo.com_ 
(mailto:quad-l...@eskimo.com) , not the TMIC address. Did  you inadvertently 
subscribe to the Quad list and get it confused with the TMIC? 
 
And don't you even think about going anywhere. You are a vital  part of the 
TMIC. You made a mistake, apologized, and asked forgiveness -- now  just 
receive it, let's put all this behind us, and move on.
 
There will likely be more comments as too often  people will read the first 
note in a thread and respond before seeing that  the issue has been 
resolved, but if they keep reading they'll see that it  has. 
 
Barbara H.
_http://barbarah.wordpress.com_ (http://barbarah.wordpress.com) 
 
 
In a message dated 8/1/2009 1:06:37 A.M. Eastern Daylight Time,  
heyjude48...@aol.com writes:
 
 
 
Will you people whom do not have  TM along with being  quads  please 
create a site of your own  and use it.  You are breaking into a site for people 
who have a  disease called Transverse Myelitis, and unless you have it, I 
feel you  ought not be here because you will never understand the things we 
talk  about.  Some of the topics you will be able to relate to, simply  
because you are paralyzed or have a similar disability, but you ought to  
create a 
site for Quads all of your own.
 
I am sorry for saying these  things.  I wish I didn't feel the way I do.  
Those of you with  Transverse Myelitis, stay...the rest of you, please begin 
your own web  site and do not clutter up the TM Site.  It very well may 
confuse a  person with new TM who needs a place to go to find solace, to vent 
their  anger, to find the exact same people who have the same problems as they 
 do.  
 
This a TRANSVERSE MYELITIS  site...not simply for paraplegics, 
quadriplegics, or people with  diseases similar to ours.  Unless you have 
Transverse 
Myelitis, you  do not belong here.
 
I am sorry that I feel this  way.  I don't even know why I feel so strongly 
about this.  It  seems that I am the only person on our site who feels this 
way since no  once has written in to back me up.
 
Regardless, I feel that you  ought to have your own site and that means 
that it is time for you to  create your own site, and move on.;  Please respect 
our  site.
 
Thank you  quads,
I love  you,
Jude...Wait a minute.  I just went back to see where you had  
addressed your email and it is addressed to a site that is not this  one.  I 
wonder why all of your mail is being sent to out  site.?  
 
Please accept my apology for all  of the things I have said.  I am so 
sorry.  Why didn't one of  you come on board to correct me? 
 
With my deepest  regrets,
Jude, (big  mouth)
 
In a message dated 7/28/2009 3:53:14 P.M. Eastern Daylight Time,  
lilroamin...@verizon.net writes:


Hey Dana  quadriplegics on 35 yrs. I'm only at 10yrs July 31. I, too, have  
been pretty healthy.( I'm a c6-7 quad. I can't stay still  for long plus I 
do get in a manual as often as possible mainly  for excercise and to keep my 
weight down. I went from 205 to 125  now holding at 130. I've broken my 
right leg 3 times ( shoot  almost can't keep count) LOL Mainly from trying 
things, but if  you don't try, how will you know if you can, right.) For those  
of you who don't know me.
By the way I'm about to be a  grandma, my daughter is 7 mos and its a girl 
(woohoo) I'm so  excited.
 
Oh Dana by the way What I'm  worried the most about the medicare/medicaid 
is they  (government)want to stop in-home care.
One thing I have heard is The  Governor of Texas is really looking into the 
healthcare, like he  did the stimulus thing. He didn't take all the money 
only enough  to help the unemployment and welfare n few other things. What I  
don't understand with the Healthcare is with its hard enough  with getting 
things with medicare/ medicaid I hope and pray  they don't screw it up worse.
 
Regina

Life's greatest  accomplishments are those that at first seem impossible  
and
No one can know what they can do until they  try.

--- On Mon, 7/27/09, dav...@aol.com  dav...@aol.com wrote:



From:  dav...@aol.com dav...@aol.com
Subject: Re: [QUAD-L]  35 year anniversary
To: quad-l...@eskimo.com
Date:  Monday, July 27, 2009, 10:25 AM


congrats on being a tuff ol' goat  DAANO.  I've  had only one close call 
with a uti -  I've been unusually  healthy since 5-24-1967.  yupper 42 years.  
(I had  to think for a minute of the exact date - that's gotta tell  you 
something )  looks like this sci stuff isn't nearly  as deadly as one might 
think.
azdave
 
Young people  talk of the future because they have no past, 
while old  people talk of the past because they have no future. 
_Dave  Patty's Grandkids_ (http://ocgrands.com/)   

 
In a message dated 7/27/2009 7:28:02 A.M. US Mountain  Standard Time, 
daa...@aol.com writes:

I can't believe I made it to my 35 th year  anniversary.  My parents were 
told after each  

[TMIC] August Birthdays

2009-07-31 Thread JHarper33
Happy Birthday to the August birthday kids -- August has one  of the
longest lists!

Please send any additions or corrections to _tmic-l...@eskimo.com_
(mailto:tmic-list@eskimo.com)

8/1 Peachi (_pkeene2...@aol.com_ (mailto:pkeene2...@aol.com) )

8/1 Cindy McLeroy (_cindymcle...@socal.rr.com_
(mailto:cindymcle...@socal.rr.com) )

8-1 Stacy Firth (_safi...@dow.com_ (mailto:safi...@dow.com)  )

8-3 Larry Throne (_lbthr...@hotmail.com_ (mailto:lbthr...@hotmail.com)  )

8-10 Sean Indiveri (_sindiv...@hotmail.com_ (mailto:sindiv...@hotmail.com) )

8-11 Raylene Gökeri (_mrs_gok...@yahoo.com_ (mailto:mrs_gok...@yahoo.com)  )

8-11 Michelle Maricic (_mmari...@aol.com_ (mailto:mmari...@aol.com) )

8-11 Dalida S. Ortiz de Garcia (_py...@yahoo.com_ (mailto:py...@yahoo.com)
)

8-16 _phyllisj...@webtv.net_ (mailto:phyllisj...@webtv.net)

08/17 Sandra (Harth) Brassil (_sbras...@aol.com_ (mailto:sbras...@aol.com) )

8-17 Kim (_jnks...@huntel.net_ (mailto:jnks...@huntel.net) )

08/18 Corinne Cookie Knox (_horsecookies...@wmconnect.com_
(mailto:horsecookies...@wmconnect.com) )

8-19 Saroj (_sarojkumar...@gmail.com_ (mailto:sarojkumar...@gmail.com) )

8-21 Barbara H. (_jharpe...@aol.com_ (mailto:jharpe...@aol.com) )

8/22 - Debi (_debdo...@aol.com_ (mailto:debdo...@aol.com) )

8-23 Cole (_neilandwe...@rogers.com_ (mailto:neilandwe...@rogers.com) )

8-29 Lisa Baker (Judy's daughter) (_judybak...@juno.com_
(mailto:judybak...@juno.com)

8-29 Kathleen (_kkar...@dacor.net_ (mailto:kkar...@dacor.net)  )

8/30 Lynn Pouliot (_lpoul...@cox.net_ (mailto:lpoul...@cox.net) )

8-31 Robin in Ontario(Brampton)(_rjohnson1...@rogers.com_
(mailto:rjohnson1...@rogers.com)  )

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[TMIC] Quote re Victory Over Limitations (OT: Spiritual Content)

2009-07-21 Thread JHarper33
Many of us struggle against the limitations of TM and grieve  over not 
being able to do what we used to or what we'd like to. This year I have  been 
reading through a devotional book called Our Daily Walk by F. B.  Meyer, and 
the reading for today was titled Victory Over Limitations. It  blessed me 
and I thought it might be a blessing to others as well.
 
The full text can be found at 
_http://www.preceptaustin.org/our_daily_walk_by_f_b_meyer_-_july.htm_ 
(http://www.preceptaustin.org/our_daily_walk_by_f_b_meyer_-_july.htm)  under 
July 21, but the first part talks of the apostle 
Paul's  limitations, first of being imprisoned, and then of failing eyesight, 
and then  limitations we struggle with. Then Meyer writes:


Let us accept our limitations as from the Will  of God. There is no way to 
peace or power, save in accepting the Will of God,  making no distinction 
between what He appoints or permits, but believing that  in either we are in 
contact with the Eternal purpose for us. Paul never forgot  that he was the 
prisoner of Jesus Christ. He believed that for every  limitation on the 
earthward side there would be enlargement on the other and  spiritual side. 
Weakness here, added strength there; the being hourly  delivered unto the 
cross, 
and from the ground the blossoming of endless  life.
 
Let us do all the good we can in spite of fetters. St. Paul could  not 
continue his travels over the world, but there were many avenues of  service 
open to him. He could pray, and he did (_Col 1:3_ 
(http://bible.logos.com/passage/nasb/Col%201.3) ; _Col  2:1_ 
(http://bible.logos.com/passage/nasb/Col%202.1) ; _Col 4:12_ 
(http://bible.logos.com/passage/nasb/Col%204.12) ). He 
could  influence others (Phi 1:11-14). He  employed his leisure in writing the 
epistles that have been the perennial  solace of sorrowful hearts. There is a 
door, nearer to you than you think,  opening out of your prison, through 
which God will enable you to render  helpful service for Him. 
PRAYER 
Our Father, we thank Thee Thou canst make no mistakes. We  believe that all 
things are working together for our good, and we trust Thy  guiding hand. 
AMEN.

Barbara H.
_http://barbarah.wordpress.com_ (http://barbarah.wordpress.com) 
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JulystepsfooterNO62)


[TMIC] Veins -- cause or effect of MS

2009-07-20 Thread JHarper33
My son sent me a link to this article about finding linking  vein problems 
to MS. Too early yet to say if it is cause or effect or what it  might all 
mean, but I am just passing it along for your  interest.
 
_http://www.metafilter.com/83205/The-wane-in-veins-draining-the-brain_ 
(http://www.metafilter.com/83205/The-wane-in-veins-draining-the-brain) 
 
Barbara H.
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Re: [TMIC] Please keep praying for Jim

2009-07-14 Thread JHarper33
I'm so sorry, Carol. I just prayed for you both and will  continue to.
 
Barbara H.
_http://barbarah.wordpress.com_ (http://barbarah.wordpress.com) 
 
 
In a message dated 7/14/2009 6:52:34 P.M. Eastern Daylight Time,  
cjb...@aol.com writes:

Today is Tuesday July 14th. It has been 10  days since I posted. 
Unfortunately things are not as good today. They had to  put him back on the 
vent 
because he was running a temp of 104, Sunday morning.  They have switched 
antibiotics and are hopeful that it will start to work. The  doctor said his 
bed 
sores are getting worse instead of better.He tried to pull  out his trach 
last nite and they had to restrain his hand. He is still  fighting hard to stay 
with us, but when he is extra tired and in pain he looks  at me with an I 
don't know how much more I can take look. I am trying so hard  to convince 
him that he has to get well.  GOD BLESS,  Carol It is hard to get the 
internet where we are but  I will try 

 

What's for dinner tonight? Find _quick and  easy dinner ideas_ 
(http://food.aol.com/dinner-tonight?ncid=emlcntusfood0007)  for any 
occasion. 


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Re: [TMIC] Class Reunions

2009-07-02 Thread JHarper33
I agree with what several others have said: I'd do ahead and  RSVP so they
can make adequate preparations and then see how you feel when the  time
comes. Sometimes I am fine answering questions and want to spread awareness
about TM that way: sometimes I can kind of close in on myself and not really
want to get into it. I'd prepare a short response for anyone who asks (I
think I  used to say something like I had an auto-immune attack on my spine)
and then  go further if they want to talk about it more and you feel like it,
or change  the subject if you don't.

But would I let the fact of having TM keep me from such a  gathering? No.
As others have said, a lot of people in your class will have gone  through
any number of situations, too, in the mean time.

Barbara H.
_http://barbarah.wordpress.com_ (http://barbarah.wordpress.com)


In a message dated 7/1/2009 11:47:46 P.M. Eastern Daylight Time,
jan...@centurytel.net writes:

I have another question for you all that want to answer:

I will be having another class reunion shortly and graduating from the
hometown high school, I was usually one of about 15 that
helped to plan it.We had around 500 in our  graduating class.
Anyway, I am debating whether or not to be  a part of the
planning or even attending the reunion.This is the  first reunion since
I got clobbered with TM.  I still have to use a  cane and
would maybe need my wheelchair.I was fairly well  known and I am afraid
I would be answering questions all nite about TM.   My question is:
 Would you let TM keep you from attending a  reunion?Be honest. 
If you were faced with  this decision this weekend,
what would you do?

 Janice


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[TMIC] July birthdays

2009-06-30 Thread JHarper33
Happy birthday to the July kids!!

Please send any additions or corrections to _tmic-l...@eskimo.com_
(mailto:tmic-list@eskimo.com) .

7-5 Sumer (_fjs181...@aol.com_ (mailto:fjs181...@aol.com) )

7/5 Rick in TN (_ashfordrich...@bellsouth.net_
(mailto:ashfordrich...@bellsouth.net) )

7-9 Vicki Frohna (_to...@bright.net_ (mailto:to...@bright.net)  )

7-14 Julie (_chi...@cox.net_ (mailto:chi...@cox.net) )

7-15 Sandi Siegel (_ssie...@myelitis.org_ (mailto:ssie...@myelitis.org) )

7-25 (_jennapa...@aol.com_ (mailto:jennapa...@aol.com) )

7-25 Michelle Balliet (_chelley...@aol.com_ (mailto:chelley...@aol.com) )

7-27 Linda (_lp...@aol.com_ (mailto:lp...@aol.com) )

7/29 Hildred (_missprissgran...@aol.com_ (mailto:missprissgran...@aol.com) )

7/30 Dex Packard (_d...@centurytel.net_ (mailto:d...@centurytel.net) )
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Re: [TMIC] Transverse Myelitis Network

2009-06-28 Thread JHarper33
Good grief, Rick. Todd was not at all griping or insinuating  anything. He 
wrote a very gracious response to the previous e-mails in this  thread.
 
Barbara H.
 
 
In a message dated 6/28/2009 9:19:53 P.M. Eastern Daylight Time,  
ashfo...@att.net writes:

 
Todd' one of the reasons I reclused from this web site is because I had  
three members of my immediately family die and I needed to deal with funeral  
homes and I actually had to ask this list for donations and the people that 
I  thought would help, did just did and I don't remember seeing Todd Tarno's 
name  even as much as a salutation. I'm not picking on you but I know this, 
If you  send a e-mail to Jim or anyone else on this list your email will 
eventually be  answered. This is an amazing web site and if you are not 
satisfied with your  business here, you can always go some where else and I 
guarentee you'll not  find as many people who for you, I'm sorry your a quad, 
and 
is every one  else is too. So please stop gripping because you feel your 2 
cents are not  heard, because it is heard. and we all love you and your 
e-mail gets heard.  This was Jim dream and he could not be able to manage it 
on 
his on. We all  keep it working.  So be carefull when you insinuate. Your 
friend Rick  Ashford.


 

 From: Todd Tarno  toddtm2...@sbcglobal.net
To: ladyno...@aol.com
Cc: TMIC  tmic-list@eskimo.com
Sent: Sunday, June 28, 2009 5:25:50  PM
Subject: Re: [TMIC]  Transverse Myelitis Network

That won't happen again.
 
We do enjoy reading  ALL of your e-mails.
I'm sadden that I'm  unable to answer a few of your e-mails because of how 
TM has hit  you.  But, you are right that this site doesn't have many quads, 
 like you  Jim.  I'm amazed at ALL of your's e-mails.   What it must take 
just to write an e-mails.  Both of you DO write  wonderful long e-mails.  I 
do treasure each  everyone of your  e-mails. 
I have trouble  keeping up with this site, 
more power to you  to do more than one sit.
Just know ya'll do  have a FAN,
Todd in Corpus  Christi, TX


--- On Wed, 6/17/09, ladyno...@aol.com  ladyno...@aol.com wrote:



From:  ladyno...@aol.com ladyno...@aol.com
Subject: Re:  [TMIC] Transverse Myelitis Network
To:  heyjude48...@aol.com, tmic-list@eskimo.com
Date: Wednesday, June  17, 2009, 12:03 PM


Jude,
First of all, I never said I PREFER the paraplegic/quadriplegic  site. I 
said I IDENTIFY more. I feel as though I offended you by  saying this. There 
are issues and concerns of being a quad they are  not addressed in the TM 
site and I would imagine it's because most  people on this site are not 
quadriplegics. I go where I can find the  information that helps me. If I did 
not 
want to be on this site, I  could simply delete it from my contacts. There is 
nothing holding me  back. I have asked questions on here regarding 
autonomic dysflexia,  only to have no one respond. Because I later found out 
that 
it's a  medical condition for quadriplegics, so I went to the  
paraplegic/quadriplegic site to get the answers I needed. I'm sure Jim  uses 
these sites, 
HE CREATED THEM! Where is his hostility?? He knew  that there would be a need 
for additional information, and that's all  it is, is additional 
information.
I have been a member of this site, since I came home from the  hospital in 
2006, but I am always looking for any and all information  that could be of 
help to me (as I'm sure all of us would be). There  are people that use this 
site that are also members on the Yahoo  Transverse Myelitis site. Should 
they just pick one or the  other.
I have met many people through this site, one who has become my  best 
friend who has TM. I would not trade that for anything, but your  e-mail makes 
me 
feel as though I am unwelcomed or a traitor of sorts.  This brings me to 
tears. As I have poured my heart out on this site  (reluctant to make my 
personal problems public), but felt comfortable  enough to share with others 
who 
are, also suffering with relationship  problems, pain and depression. That 
won't happen  again.



-Original Message-
From:  heyjude48...@aol.com
To: ladyno...@aol.com
Sent: Wed, Jun 17,  2009 4:26 am
Subject: Re: [TMIC] Transverse Myelitis  Network


 
 
Then what is holding you back?   Why don't you simply quit this site and 
use the other one that  you say you prefer?  What's the big  deal?
 
Jude
 
 
In a message dated 6/15/2009 2:11:29 P.M. Eastern Daylight  Time, 
_ladyno...@aol.com_ 
(http://us.mc822.mail.yahoo.com/mc/compose?to=ladyno...@aol.com)  
writes:

I am also a member of the  paraplegic/quadriplegic website that Jim has 
started. Although  I have TM, which left me a quadriplegic, I identify more 
with  the members of the paraplegic quadriplegic site then with the  members of 
the TM site.
 
Naomi
C-4 Quadriplegic, since  July 2, 2005
Due to Transverse Myelitis

 

An Excellent Credit Score is 750. _See Yours in Just 2 Easy  

Re: [TMIC] I'm on you tube

2009-06-28 Thread JHarper33
I just watched the first bit, but very cool! We could have  used this years 
ago -- we had a Bentwood rocker with a cane seat that kept  needing to be 
replaced every few years, so we finally got rid of it. But I  rocked all of 
my babies in it -- pleasant memories!
 
It was neat to see you. It's great that you put this online  for others 
to benefit from.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 6/27/2009 12:41:44 A.M. Eastern Daylight Time,  
we4king...@verizon.net writes:

My  husband and I made a you tube video, Mainly for chair caners and it's 
long (10  min) but if any of you know anyone who wants to restore one of 
those oak and  cane WW1 wheelchairs send them to my video site as they are done 
the same way  as the chair I'm working on.


Mindy the Artist 
_http://www.youtube.com/watch?v=dr75Po5pinM_ 
(http://www.youtube.com/watch?v=dr75Po5pinM) 



=

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Re: [TMIC] Facebook Page

2009-06-26 Thread JHarper33
I looked up Tracey Black but there were over four pages of  them!! Which 
one are you?
 
I'm on FB but not Farm Town.
 
Barbara Harper
 
 
 
In a message dated 6/26/2009 9:18:39 A.M. Eastern Daylight Time,  
tracey.bl...@hnoins.com writes:

 
I am  addicted to Farm Town. So is Ashlee and her brother and sister. I am 
up to  level 26 and have over $435,000.  
Great  way to talk to people from all over the world!! 
If you  have a facebook, can you give me your info so that I can add you to 
 mine??? 
Tracey L.  Black 
Certified  Insurance Service Representative 
Hockley   O'Donnell Insurance Agency 
Phone-  717-334-6741, x 29 
Fax-717-334-3414 
My hours:   9:00 a.m. - 5:00 p.m. 
Thank you for  providing information to us. Please be aware that no 
coverage is bound and no  change to your insurance program is confirmed until 
verified by a licensed  agent during regular business hours. If you do not hear 
from us within 1  business day, please re-contact us in case your information 
has not been  retained 
 
From: Grace M.  [mailto:grace...@gmail.com] 
Sent: Thursday, June 25, 2009 10:54  PM
To: Jim Lubin
Cc: Akua;  tmic-list@eskimo.com
Subject: Re: [TMIC] Facebook  Page
 
 
Hi  Jim,  

 


 
I'm  afraid to even start Farm Town---I KNOW I'll get addicted...as it 
is, I  already need to start attending Mahjong Addicts Anonymous 
meetings   ;-)   Gracie

 





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Re: [TMIC] Sex

2009-06-25 Thread JHarper33
Just to hopefully offer encouragement to some, for me  sensation did come 
back -- better than ever. I was really surprised the first  time we tried 
after TM, and I can't remember how long that was, that my  sensation then was 
not normal. It wasn't that I had no sensation, but it was a  little off. 
For instance, at first when I used the bathroom I had to make sure  the seat 
was up because it felt like I was sitting on the closed lid  even though I 
wasn't. I hadn't even thought about that in relation to sex  until  that first 
time we tried, and I was surprised and dismayed. But my  husband encouraged 
me to just keep trying and called it our therapy.  :-)
 
In addition to TM, though, age and being out of shape are  other factors. 
Some of you may remember a long time ago an Ann Landers poll that  showed 
many women enjoyed the cuddling and closeness as much or more than the  act. 
There are times that we just enjoy that, too. I would encourage anyone not  
to give up on that part even if you can't go all the way. There are times 
I've  avoided that physicality because I really didn't feel like sex, but I 
think that  is a mistake.
 
Sandy Siegel wrote a great article on this in one of the TMA  newsletters 
-- let me see if I can find it...here it is:
_http://www.myelitis.org/newsletters/v3n2/newsletter3-2-01.htm_ 
(http://www.myelitis.org/newsletters/v3n2/newsletter3-2-01.htm) 
 
BTW, past newsletters are all available at
_http://www.myelitis.org/newsletters/index.html_ 
(http://www.myelitis.org/newsletters/index.html) 
 
I saw some about caregivers while searching for this one -- I  know we 
discussed that recently, too.
 
Barbara H.
_http://barbarah.wordpress.com_ (http://barbarah.wordpress.com) 
**Shop Popular Dell Laptops now starting at $349! 
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Re: [TMIC] Need your prayers

2009-06-22 Thread JHarper33
Is it possible to talk to the daughter privately about how  much this means 
to her father -- or would that not go over well? I can see how  it might 
make things worse with the mother.
 
Barbara H.
 
 
In a message dated 6/22/2009 8:05:47 P.M. Eastern Daylight Time,  
camoa...@yahoo.com writes:



   
Family reasons.  Blended family.  Mother did  her best to poison both 
children. The mother divorced my  husband, she wanted her cake and eat it too.  
My  husband was very good to both her and his children.  He  even asked her 
to remarry him  ...  answer was a  distinct no!   She promised him on our 
wedding  day she would poison his children against him.  She  told them over 
and over that Daddy chose a new little boy to  live with and be his Daddy.  
My husband had many talks  with his children, took them out alone.  But no 
matter  how much ,  we gave, their mother made more than  both of us 
together.  Money speaks louder than  words.  I hope this does not send my 
husband into a TM  event.  He has looked forward to walking his only  daughter 
down the aisle always.  

Thank you for  your kindness.






From:  kimr1...@bellsouth.net  kimr1...@bellsouth.net
To: Catherine  camoa...@yahoo.com
Sent: Monday, June 22, 2009  7:27:27 PM
Subject: Re: [TMIC] Need your  prayers


Catherne, is it because of his TM or  family reasons?
-- Original message from  Catherine camoa...@yahoo.com: 
--  



 
 
To My TM  Family,

I need your support today.   Right now I am trying to help my husband deal 
with his  daughter not wanting him to walk her down the aisle.   He is 
devastated!  My heart bleeds for  him.

I will have to continue to pray for the  situation.   Please pray for our 
family ...   it is on the verge of never being the same  again.

Catherine
  

  
  






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Re: [TMIC] Checking In

2009-06-21 Thread JHarper33
Always good to hear from you, Larry! Hope you're doing  well.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 6/21/2009 8:19:23 P.M. Eastern Daylight Time,  
okielar...@yahoo.com writes:

This is Larry from Oklahoma checking in for the first time in a  while. 
First off, happy fathers day all of you dads out there, bio dads,  step dads, 
foster dads or just stand in dads. There is not  enough dads in this world so 
keep up the good work!
 
Second, I've been checking the archives almost daily since my last  post 
(which was another email address) and I'm never surprised at  the love, 
support and concern this group has for each other. It's so  good to see how 
this 
has group concerns for those going through so much  like when Jude was having 
so much trouble with her health or helping  another go through the grief of 
losing a family member, or losing one of  our own such as Pam or Doc or 
Dennis. That's why I  love you so much.
 
Last but not least Thanks for being here, each and everyone of you!  Talk 
with you soon.
 
P.S. Happy Summer Solstice  Phanque!



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Re: [TMIC] Transverse Myelitis Network

2009-06-15 Thread JHarper33
I was wondering this, too. I got an invite but no information  and anything
I clicked on just took me back to the same invitation.

The TMIC is plenty for me and the forum (_http://www.myelitis.org/forum/_
(http://www.myelitis.org/forum/) ) is there for  people who want more. The
forum is kind of overwhelming to me.

If some want another network, that's fine, but please don't be  offended if
some of us have enough on our plates and don't join in.

Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/)


In a message dated 6/15/2009 9:14:50 A.M. Eastern Daylight Time,
rp...@neillsupply.com writes:

Jim:
Do you  have any feedback on the new Transverse Myelitis Network many of us
have been  invited to join. What is the difference between our present
network :the  Transverse Myelitis Internet Club and this one…and why was it
needed….the  only explanation is it can do things our present network cannot!
I  presently get enough info. On our site and was wondering if this is
simply  overkill.
Thx
Rob in New  Jersey

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Re: [TMIC] Transverse Myelitis Network

2009-06-15 Thread JHarper33
I agree, Debbie, the more support groups that help more  people, the more 
the word gets out, the better. No quibbling here at all. 
 
I just didn't want the people who start new support groups to  get offended 
if they invite people from the TMIC and we decline. It's nothing  personal, 
it's just that, for me,  between TMIC, blogging, and Facebook I  have more 
than I can keep up with already. But for those who want/need another  
support group, more power to ya. :-)
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 6/15/2009 12:23:38 P.M. Eastern Daylight Time,  
dca...@earthlink.net writes:

I have to respectfully add to  Grace's comment below.  She is absolutely 
correct when she states that  the groups are formed to spread awareness of TM, 
ADEM, NMO and the other  neuroimmunologic disorders.  The TMA was not 
formed to hold a monopoly on  support groups.  It was formed as a non-profit 
organization to enable us  to raise funding for research into causes and cures, 
form a Medical Advisory  Board of excellent physicians who support our 
cause, raise awareness around  the world, and help facilitate emotional support 
for those who have these  disorders.  Without the ability to raise money 
which is tax deductible  for our contributors, none of this would have 
happened. 
 Without the  non-profit status, we can not request grants or funding from 
the NIH, NINDS or  other groups for research support.
 
We applaud all those individuals  who start the support groups both online 
and in their geographic areas, as  without their help, transverse myelitis 
does not have a face.  Pretty  much all of these groups have been started 
by TMA members.  Jim Lubin was  our pioneer into this medium.  He started the 
first Internet support  group when he became a vent-dependent quadriplegic 
from TM.  He also  started many other support groups, such as the 
vent-dependent quad  list. 
 
We will never have enough support  groups.  I myself have joined several of 
these groups just to see the  sharing and emotional support that goes on.  
It is very heart-warming to  see this happening.
 
I think that having all of the  support groups makes us more noticeable to 
the news media and the talk  shows.  I don't think that any of these shows 
ever mentioned TM prior to  1997.  This awareness has happened because those 
of us with TM are not  just sitting quietly and let it consume our lives.  
We are doing  something about it!
 
Also, in my opinion, I don't  think that there is any bickering going on 
about this topic; I think it  is just productive conversation and helps to 
make all the newer subscribers  aware that these lists are all out there for 
their information, and let's not  forget our caregivers.  They need support 
groups too!
Take care,
Debbie Capen
Secretary
The Transverse Myelitis  Association
 

- Original Message - 
From:  _Grace  M._ (mailto:grace...@gmail.com)  
To: _jharpe...@aol.com_ (mailto:jharpe...@aol.com)  
Cc: _rp...@neillsupply.com_ (mailto:rp...@neillsupply.com)  ; 
_jlu...@makoa.org_ (mailto:jlu...@makoa.org)  ; _tmic-l...@eskimo.com_ 
(mailto:tmic-list@eskimo.com)  
Sent: Monday, June 15, 2009 9:00  AM
Subject: Re: [TMIC] Transverse Myelitis  Network



The Transverse Myelitis  Network is another great way for patients to 
communicate and compare  notes.  Many of the TMIC members participate there.  
Our 
 own Marieke is one of the administrators.  I advocate for NMO,  and work 
with Sandy Siegel and the TMA crew, and I also have my own site,  of which 
Mr. Siegel is extremely supportive.  It's all about  spreading awareness of 
issues like TM, and other causes of non traumatic  SCI.  There is enough room 
for everyone an no need to quibble.   



Respectfully,  



Grace

 




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Re: [TMIC] read receipts?

2009-06-15 Thread JHarper33
I've never noticed that, Kathy. Maybe it's just one of those  automatic
things from some e-mail servers? I think if anything it's just a way  of making
sure you got and saw it and that it didn't get lost in  cyberspace.

Does it appear along the bottom of e-mails? That's where ads  usually are
from the e-mail provider, and I don't usually pay attention to that  area,
but I'll have to keep an eye out to see if it's there.

Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/)


In a message dated 6/15/2009 1:11:29 P.M. Eastern Daylight Time,
k...@frontiernet.net writes:


I have a question  for you all and I would really appreciate an answer. I
would like to know why  people send an email into the list with a “Read
Receipt”  attached.  For some reason I cannot explain, this  really bothers me
and makes me feel Violated. I would really like to know what  they do with
this receipt or why they need it. To me sending the receipt makes  me feel as
if I am being monitored for how much I read the emails on the list.  I
thought this list was supposed to be there to be another support and we can  
read
and write as we please to the list. I am not trying to center one person
out here as I get it from quite a few on the list. Are the people asking for
the read receipt monitors of this list or not?  I don’t mean to offend
anyone just  checking.
Kathy
(whom has now checked off “Never send a read receipt” in tools,  options,
and receipts  )


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[TMIC] Depends and Poise

2009-06-14 Thread JHarper33
My mother-in-law in an assisted living facility nearby uses  Depends briefs 
and Poise pads. They do add up even at the discount store. Does  anyone buy 
them in bulk somewhere or know of a place to get a good price on  them?
 
Thanks,
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
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[TMIC] Managing in winter

2009-06-14 Thread JHarper33
This may seem like an odd question here at the beginning of  the summer, 
but my husband and I were talking about job situations and long-term  
possibilities and the like, and he made the comment that he never considered  
moving 
up North where there was a lot of snow because of my  situation.
 
It's true that when we do have snow and ice, which isn't too  often here in 
SC, I pretty much am confined inside. I walk without a cane or  walker, but 
my balance and footing aren't sure enough that I could walk where it  is 
slippery.
 
Though I love him for taking that into account, I hate that he  is limited 
in that way.
 
How DO some of you manage in wintry weather? Does just  sprinkling rock 
salt on your driveway or front step help, or are there other  things you do to 
cope, or do you just stay inside when it's slippery  out?
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
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Re: [TMIC] I am not receiving mail

2009-06-10 Thread JHarper33
It's not unusual for a really busy time on the list such as we  have just 
had to be followed by a quieter time.
 
Whenever I haven't heard anything from the list in a while I  always check 
the archives 
(_http://www.mail-archive.com/tmic-list%40eskimo.com/maillist.html_ 
(http://www.mail-archive.com/tmic-list@eskimo.com/maillist.html) ) to 
see if anything came through but for whatever reason I haven't  received it 
-- occasionally I have been inadvertently kicked off, as have  others. But 
this is just a quiet time.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 6/10/2009 11:13:18 P.M. Eastern Daylight Time,  
camoa...@yahoo.com writes:



   
 
Can anyone tell me what might be going  on?

Catherine






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Re: [TMIC] Honoring Pam

2009-06-09 Thread JHarper33
Oh, I didn't set up anything -- Jim did all that. I was  just sharing my 
agreement. :-)
 
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 

 
 
In a message dated 6/9/2009 11:17:29 A.M. Eastern Daylight Time,  
jmh1...@sbcglobal.net writes:

Thanks Barbara, I should have known that you  and 
Jim would set this up for us!!   jan


--- On Mon, 6/8/09, jharpe...@aol.com  jharpe...@aol.com wrote:



From:  jharpe...@aol.com jharpe...@aol.com
Subject: Re: [TMIC]  Honoring Pam
To: jlu...@eskimo.com, jmh1...@sbcglobal.net,  tmic-list@eskimo.com
Date: Monday, June 8, 2009, 9:09 PM


I think that's a great idea.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
In a message dated 6/8/2009 8:43:42 P.M. Eastern Daylight Time,  
jlu...@eskimo.com writes:


I setup this link you can use that goes  through PayPal.

TMA Donation In Memory of Pam Montz
_http://www.myelitis.org/PamMontz
_ (http://www.myelitis.org/PamMontz) 

Jim  Lubin
jlu...@eskimo.com





_http://makoa.org/jim_ (http://makoa.org/jim) _  
disAbility Resources: _ (http://www.myelitis.org/PamMontz) 
_http://www.makoa.org
_ (http://www.makoa.org/)  (http://www.myelitis.org/PamMontz) 

In a message dated 6/8/2009 5:21:55 P.M. Eastern Daylight Time,  
jmh1...@sbcglobal.net writes:

 

Dear group,
 
I'm sorry that my thinking is off right now, but this  morning someone 
suggested
we send money for reseatch in honor of Pam.my  thought was that some
yars ago we lost a very active helpful member named  Roger.sorry I 
can't bring
his last name up, but he was the one who did the info  for our membership 
who
needed Social Security Disability on the TMA  site.anyway, I get 
off track,
what I was going to suggest that any honoraium could be  sent to the TMA in
memory of Pam.  That is our homebase for things  tm and they know where
the needs areit's self supporting  organization headed by Sandy 
Siegel
and would be a great place to honor Pam's  memory!!
Donations can be sent to:Paula  Lazzeri,  Treasurer






At  02:29 PM 6/8/2009, jmh1...@sbcglobal.net wrote:


Well, I hit the  wrong button and sent what I hadn't finished, but knowing 
me  
helps you understand!!

Paula Lazzeri,  Treasurer
10105 167th Place NE
Redmond, WA  98054-3125

I just read what I sent earlier and it  sounds like I'd been imbibing for 
hours

Point  about Roger, was the TMA accepted my check in his memory, so  I'm
certain that they would gladly accept money in Pam's  memory...

I'd better quit while I seem to be making  sense!!

!!TIAD!!  janh  Stillwater, OK




 (http://www.makoa.org/) 

 

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Re: [TMIC] I looked up Pam's obit for us

2009-06-09 Thread JHarper33
Thanks so much for finding it for us. I tried to find it a day  or two ago 
but wasn't sure exactly where she was. 
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
 
In a message dated 6/9/2009 7:43:18 P.M. Eastern Daylight Time,  
alle...@aol.com writes:

 
 
_E-mail_ 
(http://obits.nola.com/obituaries/nola/obituary-email.aspx?n=pamela-montzpid=128218443)
 
_Pamela Montz_ 
(http://obits.nola.com/obituaries/nola/obituary.aspx?n=pamela-montzpid=128218443)
  

MONTZ Pamela Montz at New Orleans, LA on Saturday, June 6, 2009.  Beloved 
wife of Daniel P. Montz, Jr. Mother of Sean P. Montz.  Mother-in-law of 
Bonnie Meyers Montz. Daughter of Richard W. Rholdon,  Sr. and the late Janis 
Rholdon. Also survived by seven brothers and  sisters, 4 grandchildren, 5 
nieces 
and nephews and 1 great niece.  Relatives and friends of the family are 
invited to attend the Funeral  Service at Tharp-Sontheimer-Tharp, 1600 N. 
Causeway Blvd. at 43rd St.,  on Wednesday, June 10, 2009 at 12:00 noon. 
Interment 
in Greenwood  Cemetery. Visitation on Wednesday, June 10, 2009 from 9:00 
a.m. until  12:00 noon. For information, call 835-2341. 

Published in The Times-Picayune on  6/9/2009_Continue to death notice_ 
(http://obits.nola.com/obituaries/nola/obituary.aspx?n=pamela-montzpid=128218443
)  
 
Ways to help
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Re: [TMIC] PAM MY VERY LOVING WIFE

2009-06-08 Thread JHarper33
Dan, thanks so much for writing. As others have said so much  more 
eloquently, as much as we feel the loss to the TMIC, we know your loss is  even 
greater. Pam was a genuinely caring person and the TMIC was one of her  
passions. She will be greatly missed.
 
Jude, I wouldn't wear the earrings either all the time or none  of the time 
-- just as often as you feel like it, in special memory of Pam and  her 
friendship.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 6/8/2009 7:56:37 A.M. Eastern Daylight Time,  
montzma...@aol.com writes:

 Thank you all so very, very, very much for writing back to 
_montzma...@aol.com_ (mailto:montzma...@aol.com) .  I am sitting  down reading 
all the 
wonderful mail about my wife Pam. I  can,t stop  crying!!! This has met so much 
to me. I do not think the friends of Pam Montz  will ever know how much. I 
am a very simple man who never asked for much. My  whole life has been Pam. I 
 waited on her as much as i could and now  this is gone,taken  from me. Pam 
do you need a bottle water or some  crushed ice and coke. You want me to 
brink you your pill box. What lean cuzine  do you want for me to warn for you. 
I want to walmart and found this great buy  on a nightgown . The dollar 
store guess what i found for you. Some nice coke  glasses to enjoy your 
beverage of the day.It's Saturday Pam you want your  shrimp and lobster sauce 
from 
the local Chinese restaurant? PAM YOU MUST READ  YOUR FORTUNE COOKIE. .i 
feel so bad i let her down. She did not get the help  she needed at the 
hospital as usual.We all thought Pam going into the hospital  was a routine, 
she 
lose the strength in her legs and within 2 weeks be back up  walking ok and 
doing home therapy.Yes she always lived in pain some days  better than others. 
She was smart and knew her meds well. The wrong doctors  were on call not 
her usual. I think, HELL I do not know what to think  anymore I hashed it out 
over and over. Thank all of you!!
Pam said if things get real bad on the bank account and we have tough  
times, One thing you will never take away from me is my computer   She 
loved her TM friends writing.to her and writing back to them. I would come  
home from work sometimes and the door was locked having a arm full of stuff 
to  bring in. The lights were off in the front room which i hated. I yell are 
you  on the puter again? That was Pam.
 
I do not know anyone on here but I PRAISE GOD YOU WERE THERE FOR  HER!!!
GOD BLESS ALL OF YOU!
I KNOW PAM WOULD WANT ME TO SAY
TIAD
I LOVE YOU  PAM , I LOVE YOU BABY WILL ALL MY HEART
IT WILL BE IMPOSSIBLE WITHOUT YOU--DAN

 

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Re: [TMIC] Honoring Pam

2009-06-08 Thread JHarper33
I think that's a great idea.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
In a message dated 6/8/2009 8:43:42 P.M. Eastern Daylight Time,  
jlu...@eskimo.com writes:


I setup this link you can use that goes through PayPal.

TMA  Donation In Memory of Pam Montz
_http://www.myelitis.org/PamMontz
_ (http://www.myelitis.org/PamMontz) 

Jim  Lubin
jlu...@eskimo.com

_http://makoa.org/jim_ (http://makoa.org/jim) _ 
disAbility Resources: _ (http://www.myelitis.org/PamMontz) 
_http://www.makoa.org
_ (http://www.makoa.org/)  (http://www.myelitis.org/PamMontz) 

In a message dated 6/8/2009 5:21:55 P.M. Eastern Daylight Time,  
jmh1...@sbcglobal.net writes:

 

Dear group,
 
I'm sorry that my thinking is off right now, but this morning  someone 
suggested
we send money for reseatch in honor of Pam.my thought was  that some
yars ago we lost a very active helpful member named  Roger.sorry I 
can't bring
his last name up, but he was the one who did the info for our  membership 
who
needed Social Security Disability on the TMA site.anyway,  I get 
off track,
what I was going to suggest that any honoraium could be sent to  the TMA in
memory of Pam.  That is our homebase for things tm and  they know where
the needs areit's self supporting organization headed  by Sandy 
Siegel
and would be a great place to honor Pam's memory!!
Donations can be sent to:Paula Lazzeri,  Treasurer






At  02:29 PM 6/8/2009, jmh1...@sbcglobal.net wrote:


Well, I hit the wrong button  and sent what I hadn't finished, but knowing 
me 
helps you  understand!!

Paula Lazzeri, Treasurer
10105 167th Place  NE
Redmond, WA 98054-3125

I just read what I sent earlier  and it sounds like I'd been imbibing for 
hours

Point about  Roger, was the TMA accepted my check in his memory, so I'm
certain that  they would gladly accept money in Pam's memory...

I'd better  quit while I seem to be making  sense!!

!!TIAD!!  janh Stillwater,  OK




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Re: [TMIC] Pam

2009-06-08 Thread JHarper33
There is one on the TMA Member Photo Gallery  here:
 
_http://www.myelitis.org/gallery/displayimage.php?album=searchcat=0pos=0_ 
(http://www.myelitis.org/gallery/displayimage.php?album=searchcat=0pos=0) 
 
Another here:
 
_http://www.myelitis.org/gallery/displayimage.php?pos=-609_ 
(http://www.myelitis.org/gallery/displayimage.php?pos=-609) 
 
This would be a good time to remind or tell new folks that  there is such 
an album to look through and see fellow members' pictures and  encourage 
people to submit theirs.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 6/8/2009 10:25:30 P.M. Eastern Daylight Time,  
jan...@centurytel.net writes:

I received a picture of Pam on May 27.   For those of you who  are 
interested,  you can go into the sent files.   I do
not know how to do that, but I bet most of you do.   If someone  does know 
how, how about putting her picture out
so everyone can see her.   She was lovely.
 
Janice


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Re: [TMIC] Wii Fit

2009-06-02 Thread JHarper33
Hi Jan,

I'm glad I inspired you! :-)

I was afraid at first maybe it would be a waste of money  because there are
many of the exercises I can't do -- like anything involving  standing on
one foot.But there are plenty of things I can do with it that  challenge me,
and there are plenty of things my kids can do that challenge them  even
though they're younger and more fit and able than I am.

The first time I used it I could barely do ten minutes. Then  one day last
week I had worked up to almost half an hour.

The more you do with it, the more it unlocks new  exercises, so it
doesn't become old hat and boring.

I'm enjoying it! I hope you are, too.

Barbara H.
_http://barbarah.wordpress.com_ (http://barbarah.wordpress.com)


In a message dated 5/27/2009 5:38:19 P.M. Eastern Daylight Time,
jmh1...@sbcglobal.net writes:

Barbara,

You were my inspiration, or maybe you just  'pushed' me to get the Fit for
our Wii...
Thank you, though my first time on it wasn't  pretty!!  We'd talked about,
but after
they were out the first time Frank went to get  one we just forgot and
then your
message.I'll need practice alot to get  the balance test to say I'm
doing OK!!
jan


--- On Tue, 5/26/09, jharpe...@aol.com  jharpe...@aol.com wrote:






I'm wondering if any other of the walking wounded  have tried a Wii Fit?
I just got one for Mother's Day (it's something  I asked for).They place a
lot of emphasis on balance, which I have  trouble with. Hopefully there will
be some improvement on that  front!

It has one exercise where you step on and off the  board. Some years back I
had tried low-impact step aerobics, but my  knees couldn't handle the step.
But the Wii board is low enough that  it is no problem.

So far it's pretty fun, though I am not placing well  as far as scores go.
But at this point I'm just trying to get some  kind of movement and activity
in, whether I make big scores or not.  But even my younger and more active
sons enjoy it. I didn't think it  would be challenging enough for them, but
it is.

Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/)



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[TMIC] Wii Fit

2009-05-26 Thread JHarper33
I'm wondering if any other of the walking wounded have tried  a Wii Fit?
I just got one for Mother's Day (it's something I asked for).They  place a
lot of emphasis on balance, which I have trouble with. Hopefully there  will
be some improvement on that front!

It has one exercise where you step on and off the board. Some  years back I
had tried low-impact step aerobics, but my knees couldn't handle  the step.
But the Wii board is low enough that it is no problem.

So far it's pretty fun, though I am not placing well as far as  scores go.
But at this point I'm just trying to get some kind of movement and  activity
in, whether I make big scores or not. But even my younger and more  active
sons enjoy it. I didn't think it would be challenging enough for them,  but
it is.

Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/)
**We found the real ‘Hotel California’ and the ‘Seinfeld’
diner. What will you find? Explore WhereItsAt.com.
(http://www.whereitsat.com/?ncid=emlwenew0004)


Re: [TMIC] test

2009-05-16 Thread JHarper33
Whenever I think I imght have missed some messages, I check  out the 
archives at
_http://www.mail-archive.com/tmic-list%40eskimo.com/maillist.html_ 
(http://www.mail-archive.com/tmic-list@eskimo.com/maillist.html) 
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 5/16/2009 11:10:26 P.M. Eastern Daylight Time,  
jan...@centurytel.net writes:

How do we know if we miss several of  them?I would just think people 
were not being very active  on
the web.Silly  me. Janice


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[TMIC] May Birthdays

2009-05-02 Thread JHarper33
Happy birthday to all the May kids, and may you have a great  day!
 
Please send any additions or corrections to _tmic-l...@eskimo.com_ 
(mailto:tmic-list@eskimo.com) .

5/5/47 Linda Garrett  (_limoga43...@yahoo.com_ 
(mailto:limoga43...@yahoo.com) )
 
5-9-53 Lynn - Rhode Island (_lrm...@cox.net_ (mailto:lrm...@cox.net) )
 
5-11-46 Lynn (_roseofr...@aol.com_ (mailto:roseofr...@aol.com) ) 
 
May 11,1939 Jim Belz (_cjb...@aol.com_ (mailto:cjb...@aol.com) )
 
5-12-46 _mother...@msn.com_ (mailto:mother...@msn.com)  
 
5-12-43 Mary Woods (_misssy...@webtv.net_ (mailto:misssy...@webtv.net) )
 
5- 19 Maureen Wroblewski Hallagan (_walterhalla...@msn.com_ 
(mailto:walterhalla...@msn.com) )
 
5- 26-62 Maria in Tonawanda (_mtripim...@aol.com_ 
(mailto:mtripim...@aol.com) )
 
5/27/51 Jim (_wv...@aol.com_ (mailto:wv...@aol.com) )
 
5/31/66 Wendy Wood (_ww...@optonline.net_ (mailto:ww...@optonline.net) )
 
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[TMIC] Spironolactone -- diuretics

2009-05-01 Thread JHarper33
My doctor put me on Spironolactone as a diuretic -- I'd had  some swelling 
in my lower legs and other diuretics contain sulfa, which I am  allergic to. 
At first I thought, Oh, great...I go to the bathroom so often as it  is, 
I'll just live in there now. But it actually seemed to help. I still go  
pretty often but I go more when I do. I think I must have been retaining urine  
without realizing it. I knew I was right after TM, but it seemed like it had  
gotten significantly better over the years -- but I think I still must have 
been  retaining a little.
 
So I was surprised that the Spironolactone helped. Has anyone  else had 
that experience with diuretics?
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
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Re: [TMIC] Spironolactone -- diuretics

2009-05-01 Thread JHarper33
No, I don't cath. I haven't really needed to since the first  few days of 
TM.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 5/1/2009 11:42:41 P.M. Eastern Daylight Time,  
jan...@centurytel.net writes:

Barbara,
Haven't tried a diuretic, but I still  cath twice a day so I know I am not 
retaining any urine.Do  you cath? 
Janice

- Original Message - 
From:  _jharpe...@aol.com_ (mailto:jharpe...@aol.com)  
To: _tmic-l...@eskimo.com_ (mailto:tmic-list@eskimo.com)  
Sent: Friday, May 01, 2009 7:48  PM
Subject: [TMIC] Spironolactone --  diuretics


My doctor put me on Spironolactone as a diuretic -- I'd  had some swelling 
in my lower legs and other diuretics contain sulfa, which  I am allergic to. 
At first I thought, Oh, great...I go to the bathroom so  often as it is, 
I'll just live in there now. But it actually seemed to help.  I still go 
pretty often but I go more when I do. I think I must have been  retaining urine 
without realizing it. I knew I was right after TM, but it  seemed like it had 
gotten significantly better over the years -- but I think  I still must 
have been retaining a little.
 
So I was surprised that the Spironolactone helped. Has  anyone else had 
that experience with diuretics?
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 

 

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Re: [TMIC] transverse myelitis

2009-04-19 Thread JHarper33
Ouch, Heather!! I'm glad it wasn't any worse, but I imagine  you'll feel 
pretty sore. It's strange how parts of our bodies don't turn or move  how 
we're expecting them to sometimes.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 4/19/2009 11:21:18 P.M. Eastern Daylight Time,  
pieterheat...@shaw.ca writes:

Well,  talking about feet.
I guess I should say that I don't always watch my  feet.

Tonight would have been a good time to watch my feet but don't  think it 
would have helped my situation.

We drove into our driveway  after being at the grandsons first birthday 
party.
Husband lets me out  on the driveway as we park two cars in the garage.

I got out.
My  right foot (which is my weak foot) goes out first, followed by me 
turning  
my body,
putting my left foot out and hoisting myself with my cane  etc.

I stood up (or tried to,  like I usually  do).
Howevermy right foot remained firmly (and I mean firmly)  
planted.

I moved.
My right foot didn't.
I was enough out of  the car that I shut the car door.

Then BAM...down I  went.
Onto my right hip, side etc.

Hubby (thank goodness) couldn't  figure out where I moved to so fast. (do 
any 
TMer's move  fast?)

Fortunately he realized that I 'moved too fast'.
He got out  of the car and there I was.

Flat on my side.

On the driveway.  with my cane and purse with me.

Glad he didn't try and drive into the  garage.
Not sure how much of me was near the car.

So..not  too sure if looking at my feet would have helped.
Haven't had that happen  for a while, that my right foot doesn't want to go 
when I want  to.

It used to happen quite often.
So Pieter had to help me stand  up.

That is my story and I'm sticking to it.
Now I just have to wait  and see if I end up with a big bruise on my right 
hip and see if  my
right foot will be swollen tomorrow.

Hope everyone else had a  good weekend.
The wee grandson had a good birthday and ate his first taste  of chocolate 
cake.  Too cute.

Heather in Calgary

-  Original Message - 
From: pjv1...@chartermi.net
To:  tmic-list@eskimo.com; Betty Shaffer  vasso...@gmail.com
Sent: Sunday, April 19, 2009 6:33 PM
Subject:  Re: [TMIC] transverse myelitis


 Hi Betty
 Welcome to our  on-line TM family.  I was diagnosed in 2003 at age 53 at 
  C4-C6.  I also have balance problems and just gave in to using a walker  
 during a short vacation.  I was surprised that I was able to  walk and 
 enjoy looking at something besides my feet.  I hadn't  thought about the 
 seat problem, however, your right - I look and  touch before I sit.  I 
 think we TMers have trust issues.   We just don't trust much of anything 
 that has to do with where we are  or where we're going to be in the next 
 few seconds!

  Patti - Michigan
  Betty Shaffer vasso...@gmail.com  wrote:
 I'm a new subscriber to the TM internet club and find the  messages
 interesting.
 I was diagnosed with T.M. ( Cl  and C 2 level) in 2004 at the age of 77.
 Numb from my toes up to  and inclucing my neck, I rar3ly feel pain but 
 have
  much discomfort from the banding, especially in my torso and neck.  I  
 walk
 well with a walker, but need my eyes to tell me  where my feet ( and 
seat)
 are.  Without the walker , balance  is a problem.

 Anybody have problems similiar to those  ?  I live in a retirement home 
 where
 I'm able to  walk and to exercise 5 days a week, and I know this helps.
 There  is no support group in the area

 Betty in  Oregon

  




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Re: [TMIC] Balance

2009-04-14 Thread JHarper33
Yes, that's one of my continuing problems. My balance is worse  when 
standing still (even with eyes open) than walking, though I sometimes lose  
balance while walking, too.
 
When I was taking physical therapy, my PT had a name for that,  but I don't 
remember what it was. She had me stand on a pillow with my eyes  closed and 
lean as far as I could in one direction and then another while she  stood 
by to catch me if I fell (don't try this at home alone!!!)
 
It's improved, but it is still a factor. Sometimes at church a  larger 
group will be singing across on stage just holding their music, and I  think, I 
could never do that! I ended up leaving choir because I felt like I  
couldn't keep my balance. Having some reference point helps -- the back of my  
legs 
touching a chair or just touching a table or the wall. I don't need to hold 
 on to or lean on something, usually -- just have something to  touch.
 
Barbara H.
_http://barbarah.wordpress.com_ (http://barbarah.wordpress.com) 
 
 
In a message dated 4/14/2009 9:25:04 A.M. Eastern Daylight Time,  
mother...@gmail.com writes:

P. S. I cannot close my eyes and balance myself. I get dizzy..  anyone  
else??? 

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[TMIC] April Birthdays

2009-03-31 Thread JHarper33
There is a short list for April! But that just means more cake  for all of 
you!
 
Happy Birthday!
 
Please send any additions or corrections to _tmic-l...@eskimo.com_ 
(mailto:tmic-list@eskimo.com) .
 
4-1 Ken (_kenoliver...@hotmail.com_ (mailto:kenoliver...@hotmail.com) )
 
4-14  Kris  (_rizahdo...@aol.com_ (mailto:rizahdo...@aol.com) )
 
4/18 Bernard Butcher (_bernie.butc...@honeywell.com_ 
(mailto:bernie.butc...@honeywell.com) )
 
4/20 Dianna (_carg...@cs.com_ (mailto:carg...@cs.com) )
 
04/20 Todd Tarno (_toddtm2...@sbcglobal.net_ 
(mailto:toddtm2...@sbcglobal.net) )
 
4/21 Robert Diehl (_sawmil...@verizon.net_ (mailto:sawmil...@verizon.net) )
 
4-25 Shelia (_sc...@aol.com_ (mailto:sc...@aol.com) )
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Re: [TMIC] Embrionic Stem Cell Discussion

2009-03-27 Thread JHarper33
Jim, I am with you completely in this and the other posts you  have written 
on this issue, and I believe your words carry much weight precisely  because of 
the position you are in physically. Terri Schiavo's case horrified  me, that 
people could not discern the difference between turning off the life  support 
of someone who is brain dead vs. actively starving someone who had a  loving 
family who wanted to care for her.
 
And, by the way, you're one of the most productive members of  society that I 
know. :-)
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 3/26/2009 8:08:24 P.M. Eastern Daylight Time,  
jlu...@eskimo.com writes:

They are just going to throw those unused blastocysts away only because  
someone is making the choice to do so. After they are created they remain  
frozen 
indefinitely until a decision is made by someone to remove them from  their 
frozen state.

I've seen the argument be made that they are going  to die anyway so why not 
use them to help others, such as organ donation. I  started thing about that 
reasoning a few years ago. As someone who is only  being kept alive by a 
ventilator breathing for me I began thinking that  someone could decide that 
if I 
was taken off the ventilator I would die  anyway so why not use my organs to 
better someone else's life. Someone might  decide that my heart, my liver, my 
lungs would be better used by someone else  who might be more important or more 
productive, less of a burden cost wise, to  society. I am not an organ donor.

Remember the Terri Schiavo case in  2005? It was a big topic on the 
vent-users list. Her husband claimed she was  in a Persistent vegetative state, 
her 
family said she was not. The media kept  saying they want to remove her from 
life support. She was not on life  support, she had a feeding tube. Big 
difference. A ventilator is life support.  Her feeding tube was removed and she 
was 
starved to death because nutrition  was withheld. It was very scary to everyone 
who is on life support they way  people were fighting to get her feeding tube 
removed. If people felt so  strongly about her being removed what about us?

I believe that human  life begins at conception and that those blastocytes 
should be protected until  natural death. Use them what they were created for 
or 
keep them frozen (i.e.  on life support). I don't think these blastocytes 
should have been created in  the first place, if a couple can't have a baby 
without intervention then it's  not meant to be. That's just what I believe. 
Obviously it's legal so the world  doesn't operate the way I believe. 

Jim

At 10:24 AM 3/26/2009,  Westgold wrote:

They just throw  those unused blastocytes in the garbage, they end up in some 
medical waste  dump somewhere.  Would you rather than that, than see those 
cells being  used to help cure a lot of horrible diseases?  You say that you 
support  organ donation -- isn't giving these blastocytes a chance to help save 
 
somoene's life similar to organ donation?  Don't you think they would  rather 
do some good with whatever life they have, rather than just be thrown  in a 
dump? 

Jim  Lubin
jlu...@eskimo.com
_http://makoa.org/jim_ (http://makoa.org/jim)   
disAbility Resources: _http://www.makoa.org



_ (http://www.makoa.org/) 

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Re: [TMIC] stem cell (OT?)

2009-03-27 Thread JHarper33
Mindy, by that logic, a baby who needed life support at birth  would not be 
entitled to it. I've known many families of children born  prematurely who 
needed a great deal of help at first, but who grew and thrived  with help, 
including ventilators.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
In a message dated 3/25/2009 8:27:24 P.M. Eastern Daylight Time,  
we4king...@verizon.net writes:

My experience also led me to the conclusion that a life that cannot survive  
outside the mother is not entitled to citizenship rights equal to that of  the 
mother until it is mature enough to survive once the umbilical cord is cut  
(or has turned 18, which ever comes first).
Mindy the  Artist
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Re: [TMIC] stem cell (OT?)

2009-03-27 Thread JHarper33
Thanks for the clarification. Just taking the statement at  face value it 
sounded different.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 3/27/2009 12:58:11 P.M. Eastern Daylight Time,  
we4king...@verizon.net writes:

I'm not  implying that at all.  I just didn't go into that definition for the 
sake  of brevity.  The light hearted comment about turning 18 meant that  
every child takes a tremendous amount of life support to raise.  but if  you 
insist on a definition:  I believe that any infant who is alive at  the time of 
onset of labor (whether natural or surgical) is entitled to what  ever life 
support we have to offer.  In some cases like ancephaly there  are hard choices 
for parents to make.  But I am sharing my views and not  writing a policy that 
will be used to make life and death decisions beyond my  own family.  


Mindy the  Artist


On Mar 27, 2009, at 9:03 AM, _jharpe...@aol.com_ (mailto:jharpe...@aol.com)  
wrote:






Mindy, by that logic, a baby who needed life support at  birth would not be 
entitled to it. I've known many families of children  born prematurely who 
needed a great deal of help at first, but who grew and  thrived with help, 
including ventilators.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
In a message dated 3/25/2009 8:27:24 P.M. Eastern Daylight Time, 
_we4king...@verizon.net_ (mailto:we4king...@verizon.net)   writes:

My experience also led me to the conclusion that a life that  cannot survive 
outside the mother is not entitled to citizenship  rights equal to that of the 
mother until it is mature enough to survive  once the umbilical cord is cut 
(or has turned 18, which ever comes  first).
Mindy the  Artist

 

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Re: [TMIC] stem cell (OT?)

2009-03-25 Thread JHarper33
 
Gary, thanks so much for this. I cringed, too, when I saw the  former 
president characterized this way. I don't mind civil discussions of  
differences of 
opinions, but name-calling of anyone should not be a part of  the process. 
There are many things I disagree with the current president about,  but I would 
never call him names out of respect for his position.
 
I appreciated Deb's clarifications.
 
Nevertheless, there has been great, promising  research using adult stem 
cells. One article is here:
_http://www.sciencedaily.com/releases/2008/06/080606102603.htm_ 
(http://www.sciencedaily.com/releases/2008/06/080606102603.htm) 
 
And another article about the man who began stem cell research  (and who did 
use an embryo then) is here:
_http://www.nytimes.com/2007/11/22/science/22stem.html?_r=1_ 
(http://www.nytimes.com/2007/11/22/science/22stem.html?_r=1) 
 
Even he says in the article, 'If human embryonic stem cell  research does 
not make you at least a little bit uncomfortable, you have not  thought about 
it 
enough,” he said, and he has found ways to do it now without  embryos.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 

 
 
In a message dated 3/25/2009 12:12:01 P.M. Eastern Daylight Time,  
dca...@earthlink.net writes:

I will make just a short statement  regarding this, as I do not wish to 
become involved in a debate.  Dr.  Kerr has stated in all of his talks that the 
BIGGEST mistake in the very  beginning was to even give it the name embryonic 
stem cells.  They are  NOT embryos.  They are NOT aborted fetuses.  They are 
blastocysts  - only two cells that could not ever survive outside of a petri 
dish on their  own.  Because the scientists made this mistake in the beginning 
of giving  it the name embryonic stem cell, all of the right-to-life people 
came out  and attacked this research from the git-go.
 
If you view the talks from all of  our symposia at 
_http://www.myelitis.org/events.htm_ (http://www.myelitis.org/events.htm)
and listen carefully to Dr. 
Kerr's talks on stem cell research, you will have  better knowledge of this.
 
Regarding the idea of going out of  the country to receive treatments, Dr. 
Kerr has also discussed this.  The  research is there, but the follow-up on the 
patients is lacking, so they have  no record of how the patients did AFTER 
they left the country to go back  home. 
 
Take care,
Debbie

- Original Message - 
From:  _gbthomas8...@sbcglobal.net_ (mailto:gbthomas8...@sbcglobal.net)   
To: _Westgold_ (mailto:westg...@interlog.com)  ; _Amanda  Diskey_ 
(mailto:adis...@yahoo.com)  ; _tmic-l...@eskimo.com_ 
(mailto:tmic-list@eskimo.com)  
Sent: Wednesday, March 25, 2009 8:05  AM
Subject: Re: [TMIC] stem cell  (OT?)


Our former president, George W. Bush, so  disrespectfully referred to on this 
list as dumdum, was simply against the  use of our tax money for embryonic 
stem cell research in  consideration for those opposed, on moral grounds, to 
the use of  aborted fetuses. Stem cell research  was not  stopped.  It has 
widely been proclaimed  (even on this  list) that adult stem cell research 
has 
actually been more  successful than embryonic cell research.
 
_http://www.stemcellresearchfacts.com/_ 
(http://www.stemcellresearchfacts.com/) 
 
What should be of concern is the attitude, manifest in  the new presidential 
administration,  of disregard for sanctity of  life.  Surely such thinking in 
our governmental  leadership would tend to provoke questioning as to 
compassion for  TM'ers, especially those in adult years.  Rather an irony-- a 
claim to  
compassion to help the suffering yet being quick to reinstate tax money for  
research which gives a boost to the abortion industry!
 
 I am not, by far, as learned as I would like to  be on this subject, but 
just wish to include the opposite side to those who  seem to hear that fetal 
embryonic research is the only answer to  finding relief for those suffering 
from 
conditions such as ours (and, of  course, worse).
 
Gary in Michigan
 

- Original Message - 
From:  _Westgold_ (mailto:westg...@interlog.com)  
To: _Amanda Diskey_ (mailto:adis...@yahoo.com)  ; _tmic-l...@eskimo.com_ 
(mailto:tmic-list@eskimo.com)  
Sent: Tuesday, March 24, 2009 2:25  PM
Subject: Re: [TMIC] stem cell


Hi -- there have been many success stories all over the  world with stem 
cells, I am so glad our new president decided to let the  researchers get back 
to 
it in a big way.  You can google stem calls +  various diseases, or stem cells 
+ success, etc, and you'll get a lot of  stuff.  There were twin girls who 
went to China for stem cells a  couple years ago, and they were helped 
tremendously.  You used to be  able to find their stories by googling stem 
cells + 
twins + Toronto -- try  that.  I personally believe that now that the research 
is 
back under  way full steam, we will be seeing amazing things happening in just 
a year  or two.  Too bad those 8 years of 

Re: [TMIC] Testing

2009-03-23 Thread JHarper33
That has happened to me a number of times. I don't know why it  happens.
 
Welcome back!
 
Barbara H.
 
 
In a message dated 3/23/2009 11:42:53 A.M. Eastern Daylight Time,  
ladyno...@aol.com writes:

I was kicked off the list up and had to re subscribe.  

Naomi
C-4 Quadriplegic, since July 2, 2005
Due to Transverse  Myelitis

 

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Re: [TMIC]

2009-03-21 Thread JHarper33
Jeanne is right. There is so much going on when someone has  surgery, and I'm 
sure Jude is in no condition to write just now and needs her  husband there 
with her. I'm sure someone will let us know something as soon as  possible.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 3/21/2009 12:46:47 P.M. Eastern Daylight Time,  
jrush...@columbiaenergyllc.com writes:

I think someone will let  us know as soon as they find out themselves, 
Janice.  We're all  anxiously awaiting!  Hugs..Jeanne
 
 
---Original  Message---
 
 
From: _Janice_ (mailto:jan...@centurytel.net) 
Date: 3/21/2009  11:30:23 AM
To: _transverse myelitis_ (mailto:tmic-list@eskimo.com) 
Subject:  [TMIC]

 
Why haven't I heard about Jude? How did she  do with the surgery? 
JANICE
 



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Re: [TMIC] Levothyroxine Sodium 50mg

2009-03-16 Thread JHarper33
I would get a second opinion on the Levothyroxine Sodium. I take it (125  
mcg), but that's because I had half my thyroid removed about 19 years ago due 
to  
a benign nodule on it. Incidentally, I had a horrible digestive reaction to 
the  generic, which I think this is, vs. the name brand Synthroid. One astute 
doctor  asked me if I had any changes in prescriptions when I was having these 
symptoms,  and I almost said no, when I realized I had started this new 
generic. I had been  taking Synthroid for years with no problems, even the 
generic 
kind, but when I  compared the dates, my digestive symptoms started when I 
started this version,  We switched to the name brand, and then I was fine. Lots 
of 
people use it with  no problems, but my body chemistry just didn't mesh with 
it.
 
I think what he prescribed is a low dosage (Frank, correct me if I am  wrong 
on that), so you could try it and see what happens.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
 
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[TMIC] Mottos

2009-03-13 Thread JHarper33
Trudy said in the How to Dance in the Rain thread, 
 
When I was first injured someone I had  never met sent me a book called You 
Gotta Keep Dancin by Tim  Hansel That's my motto!  I fall down, I get up 
and  I keep on  dancing!!!   
 
For some reason that brought to mind something that's often  said at our 
house. I still have balance issues, so sometimes I'll be swaying  almost too 
far 
over, and my oldest son will say, Stay upright! And I'll say,  That's one of 
my goals in life!
 
I thought it would be fun to share -- anyone else have any  mottos or regular 
sayings around your house?
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
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[TMIC] Missing

2009-03-10 Thread JHarper33
Evidently I was somehow inadvertently unsubscribedagain. I  know 
sometimes the list is quiet, but it hit me it had been several days since  
anything 
had come through from TMIC. I can't get in the archives to see what  I've 
missed 
-- I keep getting a Problem loading page message. I'll try it  again later. 
If anyone has sent me an update for the birthday list since Friday,  please 
send it again.
 
Thanks!
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
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Re: [TMIC] For you MSr's

2009-03-01 Thread JHarper33
I think that's excellent. The only word I have a little  trouble with is 
imposing -- Individuals who insist on imposing their own  beliefs on 
discussions risk alienating others whose beliefs differ. I agree  completely 
with that 
statement, but I have experienced sometimes people thinking  I am imposing my 
beliefs when I am just sharing them. But I don't know if there  is a better 
way to word it. I think readers just have to take things in that  vein-- that 
anything shared is the individual's own perspective and what each  individual 
believes is his or her own choice.
 
Barbara H. in SC where we have 5 inches of snow (a big deal  for us :-) )
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 3/1/2009 11:24:26 P.M. Eastern Standard Time,  
we4king...@verizon.net writes:

Hi all,  
if it were up to me (and I know that it's not!) this is  how I would  write 
such a policy:
 
Transverse Myelitis is a  disease, which strikes without mercy or regard to 
sex, race, nationality,  religious belief and political affiliation.   It’s 
impact reaches  into every area of our lives, from our relationships with 
family 
and friends,  to our physical, mental, and emotional well being, and to our 
spiritual lives  in ways few of us could have ever imagined.  
For some of us Tm brings about  a renewal of faith and for others a crisis, 
still others find no connection  between this disease and spiritual matters.  A 
great many of us discover  that a re-examination of our beliefs is part of 
our journey.   For  those of us who do have faith, its aspects: readings, 
meditations, prayers,  rituals and communities are as fundamental to our 
recovery 
and survival as our  medications and therapies. 
If we are to fully help each  other in coping with this disease and it’s 
aftermath, spiritual discussions  are at times unavoidable. But for our group’s 
purpose, there is no affiliation  with any one religion or doctrine.  
Individuals who insist on imposing  their own beliefs on discussions risk 
alienating 
others whose beliefs differ  and this diminishes our service to each other.  In 
the same way that each  one of us takes away suggestions of products, 
medications and therapies that  we think may be helpful and disregards the 
rest, so 
should it be with  spiritual discussions.   
As for politics: there is no  place for such discussions here as our members 
come from many nations.  However, notices of pending legislation(s), which 
directly impacts this  disease and its sufferers, may be posted.  Our sole 
purpose is to help  each other and there is no support when tempers flare and 
condemnations rather  than sympathies are expressed. 
copywrite  2009 Mindy  King 

 
Mindy the Artist


On Mar 1, 2009, at 9:09 AM, _heyjude48...@aol.com_ 
(mailto:heyjude48...@aol.com)  wrote:



 
 
 

Trudy and Mindy,
 
I believe that what you are suggesting regarding a way to share  religious 
discussions in a manner that would respect each of us and our  individual and 
shared beliefs is just a wonderful idea.
 
I have long wanted to express the way I feel about Prayer and the  Father, 
Son and Holy Ghost.  Prayer works, regardless of who or what we  Pray to as 
long 
as it is done in a pleasing manner to Our Father.
 
There would probably have to be some ground rules.  Maybe a small  committee 
could be formed to address the issues that may come up, as they do  in any 
large group.  We always need organization, blah, blah,  blah.  It is a good 
thing.
 
It's time for me to get off of the computer.  I love and Pray for  you all.
 
Jude
 
In a message dated 2/28/2009 3:48:14 P.M. Eastern Standard Time, 
_mother...@msn.com_ (mailto:mother...@msn.com)  writes:
Mindy
So much of what you shared is exactly where I am at. I cannot organize  my 
thoughts. It's awful, and my memory is totally gone! I take a drug called  
sanctura for incontinence and I'm not sure it's worth it. Also I hear that  
copaxone is another drug that causes memory loss. It's been 7 yrs now and my  
friends 
and family have finally begun to understand how fatigue is such an  
incredible factor in this disease. My husband is awesome but it all takes  
awhile. I 
also agree with you on the religion. I wonder if we just make  sure we put 
OT-Religious Content in our Subject area, those of us who wish  to share our 
spiritual
side can do so. I think that would be great. I wouldn't mind asking Jim  
Lubin if that's acceptable to him??? I agree, I think we are missing out on  a 
very crucial part of who we are! Our spiritual side And we would  be 
adamant 
that all religions are welcome as long as we respect each other  and no 
evangelizing. 
Just my thoughts, meanwhile know you are in my prayers. Hang  tough!! 
Trudy



Worrying does not empty tomorrow of its troubles; 


It empties today of its strengths.



Date: Sat, 28 Feb  2009 11:42:01 -0800
From: _jmh1...@sbcglobal.net_ (mailto:jmh1...@sbcglobal.net) 
Subject:  Re: [TMIC] 

[TMIC] February birthdays

2009-01-31 Thread JHarper33
Happy Birthday to the February kids! Hope it's a great one!
 
Please send any additions or corrections to _tmic-l...@eskimo.com_ 
(mailto:tmic-list@eskimo.com) .
 
2-1 Jeanne Rushton (_jrush...@columbiaenergyllc.com_ 
(mailto:jrush...@columbiaenergyllc.com) )
 
2/2 Ursula (_uma...@t-online.de_ (mailto:uma...@t-online.de) )
 
2/2 Lisa in TN (_lsim...@aol.com_ (mailto:lsim...@aol.com) )
 
2-5 Tita in Delaware (_te...@flash.net_ (mailto:te...@flash.net)   ) 
 
2-6 Barbara Alma (_balmat...@aol.com_ (mailto:balmat...@aol.com) ) 
 
2-7 Barbara in Texas (_babbsie1...@yahoo.com_ (mailto:babbsie1...@yahoo.com) )
 
2-9  Frank (_ftrascr...@aol.com_ (mailto:ftrascr...@aol.com) )
 
2/11 Mary (_mster...@yahoo.com_ (mailto:mster...@yahoo.com)   )
 
2-11 Deb Casey (_casey...@myway.com_ (mailto:casey...@myway.com) )
 
2/15 Jill (_jillybean60...@yahoo.com_ (mailto:jillybean60...@yahoo.com) )
 
02/16 David T. Gibson (_david-gib...@uiowa.edu_ 
(mailto:david-gib...@uiowa.edu)  )
 
2/16 Diane Aja  (_diane...@comcast.net)(returned_ 
(mailto:diane...@comcast.net)(returned) )
 
2-17 JOAN FINK (_mafi...@yahoo.com_ (mailto:mafi...@yahoo.com) )
 
2-20 Norma (_dgti...@aol.com_ (mailto:dgti...@aol.com) )
 
21/02 Phyllis Pollock (_pjpoll...@rogers.com_ (mailto:pjpoll...@rogers.com) )
 
2/26 Patti - Michigan (_pjv1...@chartermi.net_ (mailto:pjv1...@chartermi.net) 
)
 
2/27 Cindy (_rdavi...@san.rr.com_ (mailto:rdavi...@san.rr.com) )
 
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Re: [TMIC] Bladder control

2009-01-29 Thread JHarper33
Bladder problems are very much a part of TM, but that sounds  like symptoms 
of prostrate problems as well. Definitely should get it checked  out.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 1/29/2009 9:40:39 A.M. Eastern Standard Time,  
sally.wilkin...@genesisdesign.uk.com writes:

 
Hi  Guys 
Am I right in thinking  that bladder control can be an issue with TM? My TM 
husband thinks its not,  and that his visits to the loo 7-10 times a night and 
needing to suddenly pee  urgently at any time have nothing to do with his TM! 
Kind  regards 
Sally in the  UK 
Sally  Wilkinson 
Business Development  Manager 
Genesis  Design 
The Barn Ipsden  Oxfordshire OX10 6AS 
+44(0)1491  682277 
_sally.wilkin...@genesisdesign.uk.com_ 
(mailto:sally.wilkin...@genesisdesign.uk.com)  



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Re: [TMIC] Surgery Update on Kim

2009-01-26 Thread JHarper33
Thanks so much for the update, Jenna!!
 
Barbara H.
 
 
In a message dated 1/26/2009 4:45:12 P.M. Eastern Standard Time,  
jkste...@yahoo.com writes:

Kim  is out of surgery.  Everything went really well.  Her strength is  
really good in her arms again.  Since she is in a wheel chair and uses a  
walker 
that is very important.

Depending on how she is feeling she  might be able to go home tomorrow 
afternoon, or the day after for sure.   

Thanks for all the wonderful thoughts and prayers.  

If  you have any questions let me know I don't she will be online tonight.

Jenna  






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Re: [TMIC] Re: Jude in hospital

2009-01-22 Thread JHarper33
I am so sorry to hear about this. I have been and will be  praying for her.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 1/20/2009 11:24:54 P.M. Eastern Standard Time,  
cherp...@msn.com writes:

Hello everyone, it's Linda.  I received a call tonight from  Pam.  Jude's 
husband called Pam to let her know that Jude's blood  pressure went very low, 
she 
is very weak and with her infection she was  admitted to the hospital.  Her 
husband was very tired and on his way to  bed so this is all the information 
that was given. He did want to make  sure that this was posted to the list.  He 
is going back to the  hospital early in the morning.
 
You are in our thoughts and prayers, dear  Jude.


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Re: [TMIC] Re: tmic-digest Digest V2009 #3

2009-01-04 Thread JHarper33
I am so very sorry to hear about Rick's son, Patti's nephew,  and Mindy's 
father-in-law. This is a rough time of year to lose anyone -- though  it is 
never 
a good time to lose someone. My thoughts and prayers are with  you.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
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[TMIC] January birthdays

2009-01-01 Thread JHarper33
Happy Birthday to the January kids! Happy Birthday and Happy  New Year!
 
Please send any additions or corrections to _tmic-l...@eskimo.com_ 
(mailto:tmic-list@eskimo.com) .
 
1- 7 Lauren (_sugal...@adelphia.net_ (mailto:sugal...@adelphia.net) )
 
1/8 Nancy Williams   (_willj...@aol.com_ (mailto:willj...@aol.com) )
 
1-8 Sandi (_sam...@fidmail.com_ (mailto:sam...@fidmail.com) )
 
1/9 Julienne (_julesin...@aol.com_ (mailto:julesin...@aol.com) )
 
1/13 Debi (_brade...@hotmail.com_ (mailto:brade...@hotmail.com) )
 
1-17 Jenna Stentz (_jkste...@yahoo.com_ (mailto:jkste...@yahoo.com)  )
 
1/20 Kay Cole (_...@cole.gen.nz_ (mailto:k...@cole.gen.nz) )
 
1-21 Blaine Frye (_xring...@mwt.net_ (mailto:xring...@mwt.net) )
 
1/21 Carol Easterday _snow121...@hotmail.com_ (mailto:snow121...@hotmail.com) 
 
1/23 Patti Dotson (_ll...@aol.com_ (mailto:ll...@aol.com) )
 
1-27 Pat S. (_w2sm...@aol.com_ (mailto:w2sm...@aol.com) )
 
1-28 Holly (_r...@aol.com_ (mailto:r...@aol.com) )
 
1-28 Sally (_thenavigato...@aol.com_ (mailto:thenavigato...@aol.com) )
 
1/30 Cora (_ceckenb...@wildblue.net_ (mailto:ceckenb...@wildblue.net) )
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Re: [TMIC] NEW YEAR!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!

2008-12-31 Thread JHarper33
Happy New Year to you all, too!
 
Someone sent me this a few years ago I thought I'd share with  you -- the 
author is unknown:

New Year’s  Greetings!
 
May you get a clean bill of health from your  dentist, our cardiologist, your 
gastro-endocrinologist, your urologist, your  proctologist, your podiatrist, 
your psychiatrist, your gynecologist, your  plumber and the IRS. 
May your hair, your teeth, your face-lift, your  abs and your stocks not 
fall; and may your blood pressure, your triglycerides,  your cholesterol, your 
white blood count and your mortgage interest not  rise. 
May you find a way to travel from anywhere to  anywhere in the rush hour in 
less than an hour, and when you get there may you  find a parking space. 
May Sunday evening, December 31, find you seated  around the dinner table, 
together with your beloved family and cherished  friends, ushering in the new 
year ahead. You will find the food better, the  environment quieter, the cost 
much cheaper, and the pleasure much
more  fulfilling than anything else you might ordinarily do that night. 
May you wake up on January 1st, finding that the  world has not come to an 
end, the lights work, the water faucets flow, and the  sky has not fallen. 
May you ponder how did this ultramodern  civilization of ours manage to get 
itself traumatized by a possible slip of a  blip on a chip made out of sand. 
May what you see in the mirror delight you, and  what others see in you 
delight them. 
May someone love you enough to forgive your  faults, be blind to your 
blemishes, and tell the world about your  virtues. 
May the telemarketers wait to make their sales  calls until you finish 
dinner, and may your check book and your budget balance  and may they include 
generous amounts for charity. 
May you remember to say “I love you” at least once  a day to your spouse, 
your child, your parents, your friends; but not to your  secretary, your nurse, 
your masseuse, your hairdresser or your tennis  instructor. 
May we live as God intended, in a world at peace  and the awareness of His 
love in every sunset, every flower’s unfolding petals,  every baby’s smile, 
every lover’s kiss, and every wonderful, astonishing,  miraculous beat of our 
heart. 
A Very Happy New Year to All! 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 12/31/2008 8:42:13 A.M. Eastern Standard Time,  
montzma...@aol.com writes:

   ANOTHER  YEAR IS HERE
MY OH MY!
2008 JUST FLEW BYE
 
   WE  ALL HAVE HAD PROBLEMS
 IT DOES NOT SEEM FAIR
   WHO  EVER SAID LIFE WAS FAIR!

ITS HARDER ON MANY OF US
OTHERS NOT SO MUCH
I TAKE IT DAY BY DAY
 THATS  WHAT I HAVE LEARNED!!!
 
WE CANNOT LIVE IN THE PAST
BUT  THE FUTURE IS IN OUR CONTROL
WE  HAVE OUR FAMILY AND FRIENDS
 SOME JUST HAVE THE LIST!!!
 
THIS  LIST IS PRECIOUS
 REALLY ITS A GOD GIVEN GIFT
 HELPED BY MR. LUBIN
 THERE WOULD NOT BE ANY LIST!!
 
I  THANK GOD EVERYDAY
 FOR HAVING THIS WONDERFUL LIST
ITS  SO INFORMATIVE TO EVERYONE ON IT
I DO NOT KNOW WHAT I WOULD DO
IF THERE WAS NO 
LIST!!!
 
OUR  TM FAMILY IS SUCH A HELP
WE KNOW WHAT WE GO THRU
   WE SHARE THINGS PERSONAL 
OUTSIDE THE LIST WE CANNOT DO
   EVERYONE DOES NOT UNDERSTAND BUT WE 
DO!!
 
   SO LETS BE GREATFUL!
   WE HAVE THIS SPECIAL BOND
  2009  IS TOMORROW
   LIFE WILL GO ON!!
 
I  WISH YOU ALL THE BEST!
I THINK OF YOU ALL
   WE  ALL WILL BE BLESSED
   LETS  NOT FORGET
GOD IS WATCHING OVER  US ALL!
 
   HAPPY NEW YEAR EVERYONE 
TIAD  
PAM!  

 




 
 

 HAPPY NEW YEAR  EVERYONE!!!  
 TIAD 
PAM!
   
 


















 

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[TMIC] Merry Christmas!!

2008-12-25 Thread JHarper33

I hope you all have a wonderful Christmas with those you love  remembering 
the birth of our Savior and Lord, who came from everything familiar,  
comfortable, right, and glorious to live among sinful people who would  
misunderstand 
and reject Him, in order to provide salvation for us.
 
Barbara H.
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inline: Untitled.jpg

Re: [TMIC] Re: tmic-digest Digest V2008 #478

2008-12-05 Thread JHarper33
Doc's info. about SS is here:
 
_http://www.myelitis.org/tmic/resources/ssd-tm.htm_ 
(http://www.myelitis.org/tmic/resources/ssd-tm.htm) 
 
Barbara H.
 
 
In a message dated 12/5/2008 7:04:48 P.M. Eastern Standard Time,  
[EMAIL PROTECTED] writes:

In response to:
 
 
Jeanne,
 
When I went on SS Disability, I got my full benefits and then the  next year 
Medicare 
kicked in...The month before I was hit wih tm...,my disability was  for 
another health 
problem.so when I reached 65, nothing changed.  I would  assume that's 
true for
all.if it isn't, someone will speak up and tell it like  they see it! 
 As to whether 
you would get your hubby's SS, I would assume that would follow  same rules 
for 
all folks, you get whichever is higher.  There again, I'm no  authority!!   I 
think you 
can work and still receive SS, but there are limits.
 
This question would have been answered correctly and quickly had we  not lost 
our
SS genius a few tears back!  Doc could talk SS backwards and  forwards, and 
helped 
many of our members get their SS Disability.
 
He is missed!!!
 
janh
 
I'm sorry I missed Doc.  Some people have such a  hard time getting the 
disability even started, don't they??
 
I really tried to find and understand what it says  on-line but couldn't find 
anything close to what I needed.  I know  you can do into their office and 
talk to someone but that's not always a  good idea, I'm thinking, because 
sometimes that puts a hick-up by your  name!   j



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Re: [TMIC] Happy Thanksgiving to all my TM'rs

2008-11-27 Thread JHarper33
Amen! Happy Thanksgiving, Everyone!
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 


 
 
 
 







 
In a message dated 11/27/2008 9:24:34 A.M. Eastern Standard Time,  
[EMAIL PROTECTED] writes:




My heart is filled with love and great joy as I reflect and  give thanks for 
each and every one of you whom the Lord has given me to share  a part of my 
life with. You have all had such an impact on my life and are a  part of the 
love that I express today. 
Have a wonderful day.
Kim  dg 10/04   T-10



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Re: [TMIC] Re: BONE-ROTTING DRUGS....

2008-11-24 Thread JHarper33
I get SVTs -- supraventricular tachycardia -- and my dr. has  talked about an 
ablation as well, but I haven't done it yet. I am warming up to  the idea, 
though. But I have never been on Fasomax. I thought for sure this was  related 
to TM -- the stray nerve signals sure seemed related to others in the  rest of 
my body. But my drs. say it is not, and I've known several people now  who 
have them without having TM, so I guess it's just one of those  things.
 
If I remember correctly I think Bob Cook (RCookHook) had them  as well (are 
you still here on the list, Bob?)
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
 
In a message dated 11/24/2008 6:16:37 A.M. Eastern Standard Time,  
[EMAIL PROTECTED] writes:

 
This question from Regina was meant for the list and only came to me so I  am 
sending it on in case anyone can help her.
   ~ Lynn
 
I took Fasomax for years, and about 3 years ago, began complaining of  
irregular heart action, tachycardia.
At first the doctor dismissed it, but after a year or so, she advised me  to 
go the the ER as soon as my heart started jumping again.  Which it  did.  To 
make a story short, after many tests, the cardiologist advised  me to has a 
procedure called ablation, which I did.  
 
I'm wondering whether the risk of atrial fibrillation the following  
article refers to is similar to tachycardia.  I am also wondering whether  I 
would 
not have had the problem had I not been prescribed Fasomax.
 
Any comments anyone?
Thanks.
R


 

 From: [EMAIL PROTECTED]  [EMAIL PROTECTED]
To: tmic-list@eskimo.com
Sent: Friday, November 21, 2008 12:59:51  PM
Subject: [TMIC] BONE-  ROTTING DRUGS


 
Bone-rotting  drugs are targeting your ticker  
Add another brick to the wall you should keep between  you and 
bisphosphonates, the popular (and dangerous) class of  bone-building drugs. 
You've heard me 
say before that bisphosphonates,  often used to treat osteoporosis and people 
who have suffered hip  fractures, can actually result in bone destruction — 
often rotting away  your jaw – and unusual fractures that hit out of the blue. 

Turns  out these dangerous drugs are targeting your ticker, too. Researchers  
have discovered that bisphosphonates, such as Fosamax, Boniva, Actonel,  and 
Reclast, increase the odds that you will develop atrial fibrillation  — an 
erratic heart rhythm that sometimes results in blood clots. A year  ago, the 
FDA 
announced it was looking into the risk of atrial  fibrillation from those 
taking bisphosphonates, and the agency set up a  mechanism for gathering 
complaints from patients and doctors about side  effects of these drugs. But 
the 
faint-of-heart FDA stopped short of  advising docs to change their prescribing 
practices for bisphosphonates.  

One thing to keep in mind is to not overestimate the risks of  bone loss. 
Bone density only predicts a small fraction (15 percent) of  your risk of 
fracture. A little bit of bone loss is natural as you move  past 40 years of 
age. 
Osteoporosis results mainly from lower estrogen  levels after menopause in 
women 
and from reduced absorption of calcium  with aging in both sexes. An 
underutilized key to preserving your bones  is vitamin D. It helps your body 
absorb 
calcium. Over 50% of the  population is deficient which means you need to know 
your vitamin D  status. Ask your doctor about a blood test that measures your 
25 
hydroxy  vitamin D level. Other vitamins and minerals found in fresh 
vegetables  –especially magnesium -- also can keep your bones strong.  
Dr. Alan  Inglis










 

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Re: [TMIC] Re: tmic-digest Digest V2008 #431

2008-11-24 Thread JHarper33
Yes, that's right, but some people have no lesions at all show  up on the MRI 
on spine or brain. I was one. Perhaps they are too small to show  up? I don't 
know
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 11/24/2008 2:07:13 P.M. Eastern Standard Time,  
[EMAIL PROTECTED] writes:

Hello All,
 
It has been my understanding that with TM one must  have lesions on the spine 
but not on the brain.  If one has lesions on  the brain it is indicative of 
MS.
 
Am I misinformed regarding this information?   

God Bless You,
Jude
 
 
In a message dated 11/24/2008 8:34:00 A.M. Eastern Standard Time,  
[EMAIL PROTECTED] writes:

Frank,
They were never able to locate a lesion on my spine and  from what I have 
read on the message forums this is true for alot of  people.  

I had mutiple MRIs done both with and without  contrast.
Lynne


--- On Sun, 11/23/08, [EMAIL PROTECTED]  [EMAIL PROTECTED] wrote:

 From:  [EMAIL PROTECTED] [EMAIL PROTECTED]
 Subject: Re:  [TMIC] Re: tmic-digest Digest V2008 #431
 To: jrushton  [EMAIL PROTECTED], [EMAIL PROTECTED], TMIC 
 tmic-list@eskimo.com
 Date: Sunday, November 23, 2008, 4:30  PM
i have a question, has anyone else  been told that
 they don't have  lesions on their spine? my  neuro
 says mine is just swelling from c6-t3  and t9-t10.,  so
 what does that mean? 
 
 What does  swelling  from c6-t3  and t9-t10 mean??
 
 Did you have an MRI with  and with out gadolium
 (enhansement)?
 
  F




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Re: [TMIC] Caregivers

2008-11-21 Thread JHarper33
Oh Gunny --- I am so very sorry. I just can't  imagine.
 
Barbara H.
_http://www.barbarah.wordpress.com_ (http://www.barbarah.wordpress.com) 
 
 
In a message dated 11/21/2008 10:38:06 A.M. Eastern Standard Time,  
[EMAIL PROTECTED] writes:

 I've been keeping quiet about this  situation, but, I've been reading a 
lot on the list about caregivers so I  thought I would spout off. August 8th, 
my caregiver apparently decided she had  enough. I came home from a meeting 
around 10:30 PM, this was on a Friday, and  no one was home. I valled my wife's 
cell phone as she is usually home by this  time, and it went directly to voice 
mail. I looked in her room, and saw that  her Computer was gone, so, I 
immediately thought someone had broken in. I  called the Police to file a 
report, 
but then I noticed her pet bird was gone.  After reading all the signs that 
were 
right in front of me, I came to the  conclusion that she had left. I called 
my Granddaughter to see what she knew,  and she confirmed, the wife was gone. 
So, I walk into an empty house, no  warning, no note, just gone. Now, a month 
after this, she sends $500 to my  Granddaughter for bus fare, so her and my 
Grandson can come to California.  Well, they left about a week later with the 
intention of coming back in a  months time. Needless to say, they're still 
there 
after three  months.
 
My birthday is the 25th of this month, and it'll be the  first time in three 
years that my Grandson wont be with me. It's not so much  that the wife 
deserted me, but she enticed my Grandkids to go to California  with her, so, 
here I 
am, back where I started. That little boy and I had a  bond, no one could 
break, so I thought. Little did I know. Those of you that  have caregivers 
staying 
at your side through good and bad times, relish them.  Let them know every 
day how you appreciate what sacrifice thay're  making.  Oh yeah, the wifw 
calles 
a couple weeks ago wanting me to send  her $100 to get her air conditioner 
fixed in her car. After I threw up, I told  her what I thought about the way 
she 
left, and thanked her for being so  considerate. I guess i'll never see any 
of them again. I don't want to be  vindictive, but, what goes around, comes 
around. As for her, I couldn't care  less, but I'm sure gonna miss that little 
boy. Enough sad stories, let's get  back to normal.



 

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Re: [TMIC] Re: tmic-digest Digest V2008 #431

2008-11-20 Thread JHarper33
Amanda,
 
I also don't have lesions on my spine but was told I had  swelling. You'd 
think that when the swelling went down. everything would go back  to normal, 
but, 
though I did gain back a great deal, I didn't have full  recovery. In an 
informal survey several years ago that the TMA did, about a  third of the 
respondents had no lesions.
 
Don't believe in deadlines!! Many have experienced improvement  even years 
after TM. For me the most improvement came within the first several  months, 
but 
more did come.
 
And it does come verrry slowly. I can remember each week  thinking not much 
was happening, but then when I would look back over several  weeks or months I 
could see significant gains.
 
Are you having physical therapy? That (next to prayer) was the  biggest help 
to me. It is hard to balance pushing yourself yet not overdoing it. 
 
Is Calhoun anywhere near Douglasville? I lived in Douglasville  when I first 
encountered TM, diagnosed By Dr. Richard Bashuk at what was then  Cobb 
Hospital. There is a support group that meets regularly in  Douglasville now -- 
unfortunately I didn't know anyone else there with TM when I  was there, but 
they 
send notices here when they meet.
 
Best wishes for as much recover as possible,
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 11/20/2008 2:19:47 P.M. Eastern Standard Time,  
[EMAIL PROTECTED] writes:

i have a question, has anyone else been told that they don't have  lesions on 
their spine? my neuro says mine is just swelling from c6-t3  and t9-t10., so 
what does that mean? will the swelling go down? will i  be able to recover? i 
am a single mother of two and i really want to be  able to take care of myself 
and my babies. i keep thinking i am not  trying hard enough. i am wheelchair 
bound, and it seems recovery is  happening but very slow. got diagnosed aug. 
11th of this year and was  told i would see most of recovery from 3-6 months. i 
feel like i am on  some deadline and my time to get better will be up soon. i 
am scared and  i am not sure what to do. any advice?
 
thanks
amanda in calhoun,  ga



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Re: [TMIC] Anybody else been there?

2008-11-20 Thread JHarper33
Oh, Gilly, I don't think you upset anyone -- I think we've all  been having a 
great conversation seeing things from both sides.
 
We have a relative like that, too -- it IS always about  her (in her mind), 
no matter what else is going on with anyone else. When  someone in her family 
had a serious illness, all she could say was maybe now he  understood how she 
felt -- seemingly no sympathy or concern for him, just her  wanting more 
sympathy for herself.
 
I think that is all we've all been saying, that sometimes  people don't 
understand what we deal with (and I think you're right, it's  because we look 
healthy -- or else as Todd said, they don't understand the  long-term nature of 
it 
and think we should be well again -- but that their aches  and pains are 
valid, too.
 
As Jan said, no apologies needed. That's one thing this list  is for, venting 
with people who understand.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 11/20/2008 5:21:47 P.M. Eastern Standard Time,  
[EMAIL PROTECTED] writes:

Dear  Jude,
 
As usual, beautifully  said and of course so right.
 
I'm afraid I had a  bit of a rant which was not aimed at our list and 
certainly not of the  many wonderful caregivers, who I acknowledge suffer as 
much as 
we do in a  different way.  I also acknowledge that we certainly don't suffer 
from  the worst afflictions. 
 
My rant was very  personal and comes from recent events which affected me 
fairly deeply and Rob  was the catalyst for me to have a bit of a lash about 
them.
 
One of my children's  in laws has health problems and she seems to think I'm 
her personal support  group and when we are all together as a family, it's 
always all about her and  I'm expected to be very sympathetic and when I'm not 
I'm the wicked witch of  the west!  Happened again on Wednesday.  I do try to 
be 
supportive  but there are days when it's just too hard for me and I know you 
all  understand that.
 
I do think it's  because mostly we look so damned healthy that it's hard for 
others to  comprehend the pain and difficulties we endure.
 
Sorry to ramble so  much but I've been feeling very badly about upsetting 
people.  Especially  our truly wonderful caregivers without whom we could not 
exist I'm  sure.
 
much love to you  all
Gilly


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Re: [TMIC] GOOD NEWS!

2008-11-17 Thread JHarper33
Wow, what great news, Sandy!! How exciting!
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 11/17/2008 1:40:47 P.M. Eastern Standard Time,  
[EMAIL PROTECTED] writes:

8 1/2 years + with TM for Terry and he just spontaneously walked at our  
friends house the other last night. (Our friend being follow TM-er Rick  
Steele).  
He stands up from his wheelchair all the time and cooks,  gardens, etc.  He 
sometimes walks up stairs with the support of the  banisters and has taken a 
few steps unassisted before.  But, last night  he just got up and walked 
without 
any support or assistance for a total of  perhaps 40 steps!   He was quite 
well balanced, all things  considered.   
 
My suggestion to him was to get out the walker and the arm crutches and  
clean off the cobwebs and start practicing more at home.   It's just  amazing 
how 
much progress Terry has made.  He's so determined and has  such a good 
attitude through all his pain.
 
For those of you that went from a wheelchair to walking or walking with  
assistance, what helped you?   Any advise is greatly  appreciated!
 
Sandy Parker



 

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[TMIC] California Fires

2008-11-16 Thread JHarper33
I don't remember who all is in CA besides Barbara Alma and Deb  Capen, but 
how is everyone doing out there? Anyone in danger of the fires  there?
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
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Re: [TMIC] OT - Facebook

2008-11-12 Thread JHarper33
I have gotten a few notices about people adding me as a  friend on Facebook, 
but when I try to confirm them, it is not working. According  to Facebook that 
may happen if a different e-mail is used other than what I am  registered 
with. Over there and for a lot in Internet things I use [EMAIL PROTECTED] 
(mailto:[EMAIL PROTECTED]) . If you've tried adding me  as a friend and 
haven't received confirmation yet, would you try again using  that e-mail? 
Thanks!
 
BTW there are a few TM groups  there.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 

- Original Message - 
From:  _CANDIS KALLEY_ (mailto:[EMAIL PROTECTED])  
To: _tmic-list_ (mailto:tmic-list@eskimo.com)  
Sent: Tuesday, November 11, 2008 3:15  PM
Subject: [TMIC] OT - Facebook


I would like any and all of you to join facebook. 
I said  I wouldn't use this site for political notes but I do listen to alot 
of TV,  especially CNN and MSNBC (occasionally FOXNEWS).
Please join facebook and  see my note on TORT.



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


Prayers and thoughts  for you and yours,

Candy  K.





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Re: [TMIC] Normal

2008-11-06 Thread JHarper33
I agree with Jeanne. Rob -- this would make a great article  (Reader's 
Digest, maybe?) 
 
I do remember having to adjust my thinking from getting back  to normal to 
getting used to a new 'normal.'
 
I would encourage any TMer here to try to get their spouses  here also. My 
husband told me that he understood a lot more of what I was going  through both 
from what other people said but also from what I said here. I  wasn't trying 
to keep anything from him -- we talked a lot and he was very open  to trying to 
understand. But I guess maybe I expressed myself differently or  asked 
questions here because of the possibility of finding others with like  symptoms 
that 
revealed to him more of what I was feeling than I thought to say  to him.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 11/6/2008 12:41:52 P.M. Eastern Standard Time,  
[EMAIL PROTECTED] writes:

I tried sending this as an attachment ..but I just  found out you can not do 
attachment on the list…anyway I am going to try and  cut and paste a small 
essay I tried to write about TM  me…as always I am  open to comments.

NORMAL 
Normal….what a simple word! This is a word I took for  granted until one week 
past my 50th birthday. What did normal mean  to me? Normal meant being like 
everyone else….it was being  able to run,  walk, exercise, climb up stairs, 
play sports…basically being able to do  everything that “normal” people do 
without giving it a thought. I guess I  figured as I got older I would slow 
down a 
little…maybe replace basketball  with golf. Perhaps I would have to exercise a 
little longer to stay in  shape…no big deal…this was “normal”. Sure like 
all normal people I would get  sick from time to time and maybe break a bone or 
two….but I always knew that I  would get better…and until one week after my 
50th birthday that was  just how life was…normal. 
Now let us go back 11 or so years where in a period of  several hours I went 
from “normal” to cripple. In a few hours I had zero  feeling from my waist 
down….that can’t be possible…I had played  ball  all  weekend…there had to be 
a simple answer. Maybe a pinched nerve or  something like that…..the idea that 
I would never be normal again never  crossed my mind…I was sure it would be 
just a matter of time until I was all  better…and “normal again “. Even after 
3 MRI’s and 2 Lumbar Punctures I was  certain that Dr. House would figure out 
the problem, give me some medicine and  I would be all better…I would be 
normal again…just like everybody else I knew.   
Three weeks after being crippled from the waist down I  was told what I have…
..Transverse Myelitis….what the heck is that…I never  heard the words before 
and had no idea of their meaning. The Neurologist at  the top New York City 
hospital explained it to me…he said he was sure I would  eventually walk again…
but he could not say for sure what assistance I would  need. Perhaps a walker 
(how embarrassing), maybe a quad cane (better but not  great) and if I was 
lucky perhaps I could graduate to a straight cane (better  but not normal) 
After spending 3 weeks in the hospital I was  transferred to the Kessler 
Rehabilitation facility in West Orange, New Jersey  (same place Christopher 
Reeves 
rehabbed in). Slowly over a period of 3 months  I started getting a little 
better…I went from a walker to a quad cane to upon  leaving the rehab center a 
straight cane….I was surely getting better. I would  prove all of the doctors 
wrong…..oh just one little side note…while it was  true that I was learning to 
walk better there also came some small side  effects. When I first came down 
with TM I had no feeling and therefore I had  no pain or discomfort….but…as 
some feeling came back these feelings were so so  bad. Where previously I felt 
nothing…now one of my legs was pins and needles  and numb (how is that 
possible?)…whereas my other leg was numb with excessive  banding (tightness) 
which 
caused me to walk with a “stiff leg”. But at least I  was walking and it seemed 
that I was getting better everyday…soon I would be  all better…I would be 
normal. The improvement was constant for the first 6  months…then it continued 
to a lesser extent over the next 6 months….then I  just stopped improving. How 
can this be? I know…I just have to work harder at  getting better…just keep 
exercising harder and longer…I was so determined to  prove the medical 
profession wrong! But it turned out that they were right and  I was wrong…I hit 
a 
plateau where all I could accomplish was abnormal  fatigue…I was not getting 
better and worse yet I probably never would! However  I would keep all of the 
pain 
and discomforts probably for the rest of my life!   
Now for most people walking with a limp, and being in  weird discomfort 24/7 
would be bad enough…but not for me, for me not being  “normal” was the worst 
part of the condition. I did not want people to see me  as crippled and feel 

[TMIC] November Birthdays

2008-11-01 Thread JHarper33
Happy Birthday to the November kids!
 
Please send any additions or corrections to [EMAIL PROTECTED] 
(mailto:tmic-list@eskimo.com) 
 
11-01 Ella ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
11-2 Jeff ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
11-03 Gina ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) ) 
 
11-6 Margaret Monson ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
11-8 Diane ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
11-12 Marie ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
11/13  Kevin ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
11-13 Lauren Bresse ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
11-17 Becky [EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) 
 
11/18 Drema ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
11/20 Cossy ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
11-21 Pearl Bernocchi ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
11/22 Judy Hoops ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED])  
(mailto:[EMAIL PROTECTED]) )
 
11-25 Gunny ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
11-27 Jack McMillan at [EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) 
 
11-30 Louise Flagg ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
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Re: [TMIC] Re: humble pie

2008-10-27 Thread JHarper33
I heard from him back in June when I sent him a birthday  greeting. His 
oldest son had had a heart attack but had a stent put in and was  due to go 
back to 
work soon. His little grandson, Dane, whom some of you will  remember praying 
for when he had heart surgery at five weeks of age, is now two,  was 
scheduled for a second aortic heart valve operation in July (it just  occurred 
to me 
that I never followed up to see how that went.) Errol seemed to  be doing well. 
His address is [EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) .
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 10/27/2008 7:50:46 A.M. Eastern Daylight Time,  
[EMAIL PROTECTED] writes:

It is great to hear  from both of you.  Has anyone had  any word from Errol 
in Australia??? 
Sue

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Re: [TMIC] Re: humble pie

2008-10-26 Thread JHarper33
Gilly and Saroj, it is so good to hear from both of you!! 
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 10/26/2008 7:15:55 P.M. Eastern Daylight Time,  
[EMAIL PROTECTED] writes:

SAROJ!!
 
It's so very very  good to hear from you.  I've been so terribly worried 
about you as have  many of your old friends on the list.  The last time we 
heard 
from you,  you were going to New Zealand and you were stopping by to see me on 
the  way.
 
You were also having  a lot of difficulties with your property and many legal 
matters.  I do  hope those are all behind you.
 
I'm so sorry about  your depression but it's also very understandable, having 
TM makes you  depressed without all of the other issues you had to deal  with.
 
Please write to me  and tell me in detail what's been happening to you.  My 
email address is  [EMAIL PROTECTED] 
(mailto:[EMAIL PROTECTED]) 
 
Gilly
 
Whose is confirming  she is Gillian from Australia and who survives only by 
having a sense of  humour and tolerance.

- Original Message - 
From:  _Saroj Kumari_ (mailto:[EMAIL PROTECTED])  
To: _Gillian Clark_ (mailto:[EMAIL PROTECTED])  
Sent: Monday, October 27, 2008 8:39  AM
Subject: Re: [TMIC] Re: humble  pie


Hello Gilly,
 I am as if waking up from a long sleep after four 
years . I  was very  depressed
but have started making slow recovery . So resubscribed to the list.  There 
seem to be lots of changes in the membership list. Pam and Heyjude  seem to be 
passing through some difficult times. believe , I am  writing to Gillian in 
Australia with a sense of  humour. Please confirm.
 
Saroj


On 10/27/08, Gillian  Clark [EMAIL PROTECTED] 
(mailto:[EMAIL PROTECTED])   wrote:  
 
Having TM (or any disability)  definitely changes values.  I'm sure that you 
were always capable of  being humble though Phran3quee, you probably just 
didn't need to  be.
 
Gilly
 
Who always approves of  Phran3ques posts.









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Re: [TMIC] Fwd: New Company Policy

2008-10-24 Thread JHarper33
Just a reminder of the TMIC Guidelines on the TMIC site at 
_http://www.myelitis.org/tmic/#guidelines_ 
(http://www.myelitis.org/tmic/#guidelines) :
 
 Please keep messages plain text.  Do not post personal information that you 
don't want the world  knowing. The message archive is searchable by anyone 
with Internet access.  Please do not use excessive quoting when replying to a 
message.  Please do not use graphics in messages.  Please do not forward or 
post 
long jokes or fictional  stories.  Please do not forward virus warning unless 
you have verified  it to be true and not a hoax. Check these sites:
 
 
In a message dated 10/24/2008 7:59:38 A.M. Eastern Daylight Time,  
[EMAIL PROTECTED] writes:

  

 
 
 
 
Subject: Fw:  New Company Policy
 


 
 
 
 
 
Notice  to All Employees

As of November 5, 2008, when President Obama  is officially elected into 
office, our company will instill a few  new policies which are in keeping with 
his 
new, inspiring issues of  change and fairness:

1. All  salespeople will be pooling their sales and bonuses into a common 
 pool that will be divided equally between all of you.  This  will serve to 
give those of you who are underachieving a fair  shake.  

2. All low level  workers will be pooling their wages, including 
overtime, into a  common pool, dividing it equally amongst yourselves.  This 
will  
help those who are too busy for overtime to reap the rewards from  those who 
have more spare time and can work extra  hours.

3. All top management will now  be referred to as the government.  We 
will not participate in  this pool ing experience because the law doesn't 
apply to  us.

4. The government will give  eloquent speeches to all employees every 
week, encouraging it's  workers to continue to work hard for the good of 
all.=E  2

5. The employees will be thrilled  with these new policies because it's 
good to spread the  wealth.  Those of you who have underachieved will finally 
get  an opportunity; those of you who have worked hard and had success  will 
feel more patriotic.

6.  The last few people who  were hired should clean out their desks.  Don't 
feel bad,  though, because President Obama will give you free healthcare, free 
 handouts, free oil for heating your home, free food stamps, and  he'll let 
you stay in your home for as long as you want even if you  can't pay your 
mortgage.  If you appeal directly to our  democratic congress, you might even 
get a 
free flat screen TV and a  coupon for free haircuts (shouldn't all Americans 
be entitled to  nice looking hair?) !!!

If  for any reason you are not happy with the new policies, you may  want to 
rethink your vote on  November  4th.



 











 

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Re: [TMIC] Guidelines

2008-10-24 Thread JHarper33
Amen to that!!
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 10/24/2008 11:16:29 A.M. Eastern Daylight Time,  
[EMAIL PROTECTED] writes:

The  guidelines need to include political messages  We are one group united 
 by our common factor TM.  but when a  member spouts political  rhetoric we 
are divided into the right and the left.  There are tons of  groups devoted to 
this type of political banter but only  one for TM  sufferers!  I happen to be 
very politically active (even volunteering for  my party) but I respect the 
rights of my fellow TM family members to have  their Own Opinion politically,  
I respect that they were not born  yesterday,  have a lifetime of experiences 
shaping their views and have  a sovereign right to their opinions!   keep 
politics out of  this one please!  


Mindy the Artist

 
On Oct 24, 2008, at 8:51 AM, [EMAIL PROTECTED] (mailto:[EMAIL PROTECTED])  
wrote:


Just a reminder of the TMIC Guidelines on the TMIC site at 
_http://www.myelitis.org/tmic/#guidelines_ 
(http://www.myelitis.org/tmic/#guidelines) :
 
 Please keep messages plain text.  Do not post personal information that you 
don't want the world  knowing. The message archive is searchable by anyone 
with Internet access.  Please do not use excessive quoting when replying to a 
message.  Please do not use graphics in messages.  Please do not forward or 
post 
long jokes or fictional  stories.  Please do not forward virus warning unless 
you have  verified it to be true and not a hoax. Check these  sites:






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Re: [TMIC] re:guidelines

2008-10-24 Thread JHarper33
It's been generally agreed on in the past that speaking  naturally of 
religion in terms of what helps you in dealing with TM is ok, but  
inspirational 
forwards or Bible-thumping is over the line. For many of us we  could not 
make 
it without spiritual undergirding. To me a request for prayer is  a far 
different thing than slamming someone's political views. 
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 10/24/2008 2:37:27 P.M. Eastern Daylight Time,  
[EMAIL PROTECTED] writes:

I am going to agree with the addition of  religion.  I have been silent on 
the chronic requests for prayers and  thanks to god and such...but if we are 
going to eliminate politics lets get  rid of religion as well.  I delete more 
messages now than I read so I can  just continue to do that. But if we are 
going 
to respect each others politics  then lets respect each others religion as 
well and stop with all those  messages too.  
Sandy


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Re: [TMIC] The Web

2008-10-19 Thread JHarper33
When mine does that it usually means I need to either reset  the router or 
clean out my cache or empty my recycle bin.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 10/19/2008 6:00:32 P.M. Eastern Daylight Time,  
[EMAIL PROTECTED] writes:

Is anyone else having difficulty getting on the  Web?  I have tried five 
sites and keep getting the same message, Sorry,  cannot find server.
 
Am I doing something wrong?  I need to do some  research on blood diseases 
and cannot get access...Help!
 
Peace,
Jude


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Re: [TMIC] Pam called about Jude

2008-08-21 Thread JHarper33
 
Thanks, Ella. Poor Jude! 
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
In a message dated 8/21/2008 11:57:22 AM Eastern Daylight Time,  
[EMAIL PROTECTED] writes:

I received a call from Pam about 15 mins ago and she asked that I write  as 
her computer line is messing up. Last night, Jude took a turn for the worse  
and has been rushed back to Hurley. She has yet another UTI and is now in  
C.C.U. If she calls back I will let you  knowElla







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Re: [TMIC] Re: tmic-digest Digest V2008 #228

2008-06-03 Thread JHarper33
 
Thanks, Patti!
 
In a message dated 6/3/2008 11:16:44 PM Eastern Daylight Time,  
[EMAIL PROTECTED] writes:

I'm not sure if you have mine
Patti 9/30



 



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Re: [TMIC] birthdays

2008-06-01 Thread JHarper33
 
I didn't omit it -- I never received it, but I have now, so I  will add it 
in. :-)
 
To any others, if you would like your birthday included for  any month, not 
just this one, just let me know and I will add it on the master  list. If you 
are not sure if you ever sent it in but you'd like to be included  on the 
monthly birthday list, go ahead and send it. The only way I have it is if  you 
send 
it in. The only ones I omit are those whose birthday greetings I send  are 
returned to me with user unknown.
 
Barbara H.
 
In a message dated 6/1/2008 6:13:09 AM Eastern Daylight Time,  
[EMAIL PROTECTED] writes:

mine was  omitted gerry 06 22 [EMAIL PROTECTED]


 



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[TMIC] June Birthdays

2008-05-31 Thread JHarper33
Is it June already? Where did May go?
 
Hope all of you first-of-summer kids have a great  birthday!
 
As always, please send any additions or corrections to [EMAIL PROTECTED] 
(mailto:tmic-list@eskimo.com) 
 
6-1 Akua ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
6-2 Crystal ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) 
) 
 
6-5 Tobe Kanon ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
6-11-42  Irene ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
6/11/50 Marabeth ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
6-11-51  Sharon Marsden ([EMAIL PROTECTED] 
(mailto:[EMAIL PROTECTED]) )
 
6-17-46  Cheryl ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
6-19 Tom in Delaware ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED])  ) 
 
6-19   Debbie Capen ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
6-22 Ann Moran ([EMAIL PROTECTED] 
(mailto:[EMAIL PROTECTED]) )
 
6-25 1943 Errol White ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) 
 )
 
6-29-59  Pauline ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
6/30/40 Bobby Jim ([EMAIL PROTECTED] 
(mailto:[EMAIL PROTECTED]) )
 
For those who remember them, there are two birthdays this  month of fellow 
TMers who have passed on. Tom Carr's is June 2 and Dennis  Galvin's is June 25. 
I don't know their family members or how to reach them, but  if you do, it 
might be nice to send them a little note that we're remembering  them and 
thinking of them.



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Re: [TMIC] [How to] unsubscribe!!!!!!!!!!!!!!!!!!!!!!!!!

2008-05-26 Thread JHarper33
 
According to _http://www.myelitis.org/tmic/_ (http://www.myelitis.org/tmic/) :
 
 To unsubscribe from the list, send email to [EMAIL PROTECTED] 
(mailto:[EMAIL PROTECTED]body=unsubscribe) ,  
with the Subject unsubscribe. That's all that's needed.  
To unsubscribe from the digest, send email to 
[EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]body=unsubscribe) 
,  with the Subject unsubscribe. That's all that's needed. 
Note: AOL users  some other mailer may require something written in  the 
message body before it will send. 
What you sent before was to the regular tmic address at 
[EMAIL PROTECTED] (mailto:tmic-list@eskimo.com) . To unsubscribe you  have to 
send the request 
to [EMAIL PROTECTED] 
(mailto:[EMAIL PROTECTED]body=unsubscribe)  and  for the digest 
[EMAIL PROTECTED] (mailto:[EMAIL PROTECTED],When) ,When  you sent the 
unsubscribe request before, you those addresses in the e-mail  itself but not 
in 
the To: section, so the e-mail didn't go to those automated  addresses to 
unsubscribe you. 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
In a message dated 5/26/2008 9:59:43 PM Eastern Daylight Time,  
[EMAIL PROTECTED] writes:

I WAS TOLD I UNSUBSCRIBED WRONG. I DID WHAT THE HOME PAGE. SAID ALSO A  
FRIEND TOLD ME DIFFERENT. I TRIED BOTH WAYS AND NEITHER WORKS.
IF SOMEONE KNOWS ANOTHER WAY LET ME  KNOW
TIAD PAM



 



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Re: [TMIC] relapse?

2008-05-22 Thread JHarper33
 
I have had episodes of numbness getting worse to wear I  thought I was about 
to have a relapse, but it never got as bad as the  original onset.It just 
flared up from time to time. Often being tired or not  getting enough sleep had 
a 
lot to do with it, but sometimes it just happened for  a while and then went 
back down after a few hours or days.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
In a message dated 5/22/2008 11:17:47 AM Eastern Daylight Time,  
[EMAIL PROTECTED] writes:

I swear it feels like I am getting worse..my right  leg the past 2 or 3 
days has been numb and feeling *asleep* , just like the  very first day 3 years 
ago. My *anniversary* of getting this autoimmune  disorder was 
yesterday.3 years nowmy leg started to feel *numb* at the  foot and has 
progressed 
to right below my knee. My other foot also feels a  little numb, but not too 
bad. I am scared. I know if I call the neuro, he will  order mri's. (of which I 
cannot afford right nowour insurance has a huge  deductible and we would 
almost end up paying the whole thingwhich would be  $3000-$4000! )...I know 
sometimes you can have recurrences with TM...I guess I  just didnt expert it.
I'm afraid to call neuro.  I'm afraid of  results. I HOPE its just the 
weather...but I somehow I dont think  so.
It's  not affecting my walking it just feels asleep and sorta  numb.


 



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Re: [TMIC] 19 year TM Anniversary

2008-05-21 Thread JHarper33
 
I just wanted to add my thank yous. When I first encountered  TM 12 1/2 years 
ago, I had never heard of it and thought perhaps the doctors  might be 
mistaken. At my first opportunity I went to the library to find out  what I 
could, 
but there was nothing about TM except for a two page spread in a  medical book. 
So I began to read about some of the other diseases I had been  tested for. 
When we got our computer over a year later, the very first thing I  searched 
for was TM, and found one of the original posts. I found the place to  register 
and shared a condensed version of my story and my many questions, and I  was 
amazed at the warmth, generosity, and knowledge of the folks who responded.  
Though I have a loving family who tries their best to understand, it helps to  
communicate with someone who has experienced some of the same weird symptoms,  
who knows what I am talking about -- I guess it reassured me that it was real  
and I wasn't crazy after all. :-)
 
So thanks so much, Jim, for creating this place for us and  amassing all the 
links and other information. My first several months here I  read a lot of the 
resources on the TMIC and TMA pages. Thank you for using your  time and 
energy to help others, and for your positive outlook.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
In a message dated 5/17/2008 5:21:08 PM Eastern Daylight Time,  
[EMAIL PROTECTED] writes:

On May  17, 1989, I became paralyzed from the neck down and dependent on a 
ventilator  to breathe due to Transverse Myelitis. I was 21.

I woke up with a pain  in my shoulder. Went to work and about 30 mins later 
the pain got very  intense. I suddenly could not stand then stopped breathing. 
I later found out  that my heart stopped and it took awhile for them to 
stabilize me to even  transport me to the hospital a few blocks away. The 
doctors 
had no idea what  had happened to me. initial thought were possibly a stroke, 
lyme disease, or  Guillain-Barre Syndrome. I was in and out during that time, 
could not talk,  only remember bits. After about 2 weeks I had a MRI and was 
given the  diagnoses of Acute Transverse Myelitis.

I was in ICU until July 31 then  transfered to rehab. In rehab I was treated 
as a person with a spinal cord  injury. I had physical therapy which consisted 
of giving me range of motion  and practice driving my sip and puff operated 
wheelchair. In speech therapy  and occupational therapy I learned morse code to 
access the computer. I  practiced typing and played tetris and chess. In 
October, I was able to leave  the hospital for the first time and went to see 
the 
Batman movie. I started  going to movies about once a week. The nurses always 
tried to get the other  patients to go out when I went because I was the only 
vent dependent high  level quadriplegic and enjoyed going out. Others were 
paraplegics, having  problems dealing with their condition. I was in rehab 
until 
January  31st.

I've been paralyzed most of my life. Wow how time  flies.



Jim  Lubin
[EMAIL PROTECTED]
_http://makoa.org/jim_ (http://makoa.org/jim)   
disAbility Resources: _http://www.makoa.org
_ (http://www.makoa.org/) 






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[TMIC] May Birthdays

2008-05-01 Thread JHarper33
Happy Birthday to the May babies!
 
Please send any additions or corrections to [EMAIL PROTECTED] 
(mailto:tmic-list@eskimo.com) .
 
5/5/ Linda Garrett  ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
5-9- Lynn - Rhode Island ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
5-11- Lynn ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) ) 
 
5-12- [EMAIL PROTECTED] (mailto:[EMAIL PROTECTED])  
 
5-12- Mary Woods ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
5- 19 Maureen Wroblewski Hallagan ([EMAIL PROTECTED] 
(mailto:[EMAIL PROTECTED]) )
 
5- 26- Maria in Tonawanda ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
5/27/ Jim ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
5/31/ Wendy Wood ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )




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Re: [TMIC] Misunderstood

2008-04-24 Thread JHarper33
In a message dated 4/24/2008 4:16:22 PM Eastern Daylight Time,  
[EMAIL PROTECTED] writes:


DOES  ANYONE ELSE HAVE TROUBLE RECEIVING JRUSHTON'S EMAIL 
 
Nope, I receive it fine
 
Barbara H.
http://barbarah.wordpress.com/








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Re: [TMIC] WalkAid - Foot drop

2008-04-23 Thread JHarper33
 
In a message dated 4/23/2008 4:51:00 PM Eastern Daylight Time,  
[EMAIL PROTECTED] writes:

Thanks, Rob...prayer is the only reason I am upright!!!
 
Jeanne 
 
 
 



 
That just reminded me.. often when I lose my balance and begin  to tip one 
way or another, my oldest son will say, Stay upright! and I'll say,  That's 
one of my goals in life!
 
Doesn't have anything to do with the topic at hand, but  thought I'd share 
it. :-)
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 



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Re: [TMIC] again Lyrica

2008-04-22 Thread JHarper33
 
The archives are just previous messages that have come through  the TMIC. If 
it is in the archives that just means it has been discussed before,  but that 
doesn't mean it can't be discussed again for those who weren't here  then. 
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
In a message dated 4/22/2008 8:56:34 PM Eastern Daylight Time,  
[EMAIL PROTECTED] writes:

Wim,  (and all of you who have been with TMIC longer) please  forgive my 
ignorance but why do we have both this site plus the  archives?  I just went 
into 
the archives (thank you!) and  notice the same 'type' of conversations but 
they are divided into  'subject' and it is helpful to see that some are pretty 
current. I tried  to find the answer before even sending this message.  Thank 
you ALL  for all of your input.  I do so appreciate it!
 
Jeanne in Dayton
   



 



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Re: [TMIC] Questions

2008-04-19 Thread JHarper33
 
1. Yes, as a child.
2. No
3. No
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
In a message dated 4/19/2008 3:31:52 PM Eastern Daylight Time,  
[EMAIL PROTECTED] writes:

Hi, everyone (again!)
 
I have three questions for those who would be willing to  respond:
 
1)  Did you ever have chicken pox?
 
2)  Did you ever suffer from shingles?
 
3)  Did you have a flare-up of shingles prior to your being  stricken with TM?
 
These are a few of the theories with TM and I'm just curious to see  if any 
of 'us' have experienced any or all of these.
 
Jeanne in Dayton
 



 



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Re: [TMIC] Prayer Request

2008-04-10 Thread JHarper33
 
Oh, I am sorry Candy. I'll be praying.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
In a message dated 4/10/2008 1:57:53 PM Eastern Daylight Time,  
[EMAIL PROTECTED] writes:

 
I just learned that my baby sister, Deb St. John, was taken to the  
hospital yesterday.  She has a brain tumor, doesn't reconize anyone, is  having 
seizures.  Trying to find out more info but at this time it  doesn't look good. 
Please pray for her. 
Prayers and thoughts for you and yours, 
Candy K.



 



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Re: [TMIC] When do you know if it is time to quit!

2008-04-03 Thread JHarper33
 
That's a hard one, Rob. Do you have any other job  options?
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
In a message dated 4/3/2008 9:32:45 AM Eastern Daylight Time,  
[EMAIL PROTECTED] writes:

I am obviously  on a letter writing campaign…this is due to what I perceive 
as a worsening of  my condition…ok here is my question….I have been working 
full time for the  past 10 years after contacting TM (obviously this was after 
the hospital and  rehab)…I drive more than 2 hours a day (welcome to New York 
City) and for the  first time I am really wondering how much longer I will be 
able to keep this  up…it just keeps getting harder. On the one hand if I stop 
working I will have  all the time in the world to think of my condition (bad!), 
on the other hand  work just keeps getting harder and harder both physically 
and mentally(bad  too!). Please don't tell me to just cut down..that cannot 
work…..therefore  what I have done mentally is say to myself that if I can just 
work 2 more  years then I can retire…only problem is that 2 years seems like a 
very very  long time!  
I am  going for a spinal MRI next week and Dr Kerr hooked me up with an 
excellent  Dr. in New Jersey whom I will be seeing in a couple of weeks…so I am 
trying to  be proactive…just not sure how much longer my positive attitude 
will 
be  enough to get me by! 
Sorry  about this I truly hate complaining when I know so many of you are so 
much  worse than I am!  
Thanks for everything!  
Rob in New Jersey 


 



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Re: [TMIC] queston

2008-03-31 Thread JHarper33
 
In a message dated 3/31/2008 9:13:03 AM Eastern Daylight Time,  
[EMAIL PROTECTED] writes:

I know all of us do not have one day that is exactly the  same as the 
previous one…but have any of you experienced new feelings (good or  bad) that 
was not 
a result of a relapse?


Yes, Rob, I have experienced strange sensations and feelings  and feared a 
relapse or second episode, but it ended up just being some weird  thing. 
Sometimes it would just be for a day, sometimes it would last for months  and 
then 
fade away. You're doing well to get it checked out, and I hope that's  all it 
will be for you, just some strange nerve signal that will resolve in  time.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 



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Re: [TMIC] This Is a Test

2008-03-31 Thread JHarper33
 
That has happened to me and others a few times -- just a  technical glitch, I 
think. You're coming through fine now.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
In a message dated 3/31/2008 10:12:38 PM Eastern Daylight Time,  
[EMAIL PROTECTED] writes:

I have been kicked off the list, and I judging from the archives, it  has 
been a great while.  I hope this message makes it through.  

Naomi



C4-incomplete, quadriplegic since July 2005
due to Transverse  Myelitis 





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[TMIC] April Birthdays

2008-03-31 Thread JHarper33
The list for April is short!! Hope you al have very special  days to 
celebrate your lives!
 
As always, send any additions or corrections to [EMAIL PROTECTED] 
(mailto:tmic-list@eskimo.com) .
 
4-1-25 Ken ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
4-14  Kris  ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
4/18 Bernard Butcher ([EMAIL PROTECTED] 
(mailto:[EMAIL PROTECTED]) )
 
4/20 Dianna ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
04/20 Todd Tarno ([EMAIL PROTECTED] 
(mailto:[EMAIL PROTECTED]) )
 
4-25 Shelia ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )

For those who rememeber Doc, a former active list member who  passed away a 
few years ago, his birthday was  4/24.



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Re: [TMIC] A month before TM -

2008-03-27 Thread JHarper33
I am one of those weird ones who doesn't really seem to have a  cause for my 
TM. I wasn't under any undue stress. We had moved out of state the  year 
before but were well-settled by then. We were in the first week of our  second 
year 
of home schooling, and though there is some pressure getting ready  for the 
school year and switching over from a summer schedule, it wasn't what  I'd call 
major stress. No colds, flu, viruses, or  immunizations.
 
I had had a biopsy of my cervix in the weeks before, so there  is some 
possibility that something got into my system then. The night before, I  had 
opened 
a jar of nacho cheese sauce that was covered in mold -- it was new  from the 
store and I had noticed that the little indention on the top of the lid  that's 
supposed to pop up when it is opened was already popped up, and I took  the 
lid off and sniffed to see if it smelled spoiled before realizing there was  
mold. We mentioned that to the doctors and they thought it laughable that mold  
caused it, but we held on to that theory for a long time. There was a former  
TMIC member whose every post had to do with mold in her building causing TM -- 
I  don't know if that's the same type of mold as in food, but I think it 
certainly  might be a contributing factor.
 
I was sent for a second opinion to Emery University, and the  doctor there 
said that even if they could have analyzed everything I had been in  contact 
with the day I contracted TM, they wouldn't be able to pin down which  thing 
set 
it off.
 
To me what's more interesting and perplexing than the specific  factor that 
causes TM is wondering what makes exposure to one thing set off  another 
reaction for some people but not for others or at one time but not  another. 
For 
example, people get flu and viruses every day, but it doesn't  always go into a 
more serious illness. Some who got TM after having the flu  probably had the 
flu before with no further problems -- what triggered the  switch this time? 
Thousands of people get vaccines every day, but only a few go  on to develop TM 
and other problems: what made the difference? I do believe  stress and 
general health are two contributing factors, but I don't think  they're the 
only 
ones and the whole story. I hope someone somewhere is  doing a study on this 
kind 
of thing
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 



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Re: [TMIC] Fluid retention

2008-03-27 Thread JHarper33
 
Hi Jan,
 
I am allergic to sulfa and many diuretics apparently contain  sulfa 
(Thankfully I caught that while reading the prescription information that  came 
with 
the prescription before I took any!!) I am supposed to be on something  now 
called something like spironolactone. I took it one day and had some  bowel 
trouble, but I don't know if it was related to that or not. I need to try  it 
again 
before I go back to see the doctor.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
In a message dated 3/26/2008 10:10:09 AM Eastern Daylight Time,  
[EMAIL PROTECTED] writes:

Do you take Lasix or any other diuretic? I take generic Lasix, and have  
since I
was diagnosed.That keeps the retention problem in check with exceptions  like 
having to stand a long time.as to your cellulitis, I'm not  much 
help except
to say that you should be sure to take the total bottle of pills, i.e.,  
don't stop when
you feel betterand I think your dr.'s suggestion to put your  
feet up is im-
portant...it'll also help with retention problemNow, you  
have an excuse
to let the housework go and get a good book! what a stroke of  luck!!!
Hope this clears up quickly!  hugs,  janh



 



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[TMIC] Fluid retention

2008-03-26 Thread JHarper33
Does anyone else tend to retain fluid in their lower limbs? I  seem to -- but 
it may be due to age/excess weight/lack of exercise. No doctor  has been 
concerned about it til the one I just started seeing this past year (my  
previous 
doc left his practice). She wanted me to wear an ace bandage or support  
stockings, but my lower legs get so hot as it is I can't stand it. When I walk  
around the mall or Wal-Mart in the summer they get insufferably hot. Many 
people  
on the list have said they don't sweat below the area that was affected by 
TM,  so I always attributed the legs getting overheated to that.
 
I had a bout of cellulitis on one shin in Jan. after  accidentally banging it 
on a shelf. I was put on Clindamycin and told to keep my  leg elevated. I was 
also told to use the ace bandage, but after trying it the  first time it 
seemed to make the redness worse. I thought it had mostly cleared  up, but it 
came 
back at the end of last week. I am on Clindamycin again as well  as 
Doxycyclin (sp?) and supposed to keep my leg up at least 20 minutes out of  
every hour. 
I am concerned because it seemed to cover more area and take a  little longer 
to fade out than last time, but it is fading.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 



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Re: [TMIC] Fluid retention

2008-03-26 Thread JHarper33
 
Hi Linda,
 
Cellulitis is a skin infection. The swollen ankles aren't a  symptom of it 
but from what I understand it makes the skin there more  susceptible to it.
 
The Mayo Clinic site says:

Introduction:
 
Cellulitis (sel-u-LI-tis) is a common,  potentially serious bacterial skin 
infection. Cellulitis appears as a swollen,  red area of skin that feels hot 
and 
tender, and it may spread rapidly.  
Skin on lower legs is most commonly  affected, though cellulitis can occur 
anywhere on your body or face. Infections  on the face are more common in 
children and older adults. Cellulitis may affect  only your skin's surface — 
or, 
cellulitis may also affect tissues underlying  your skin and can spread to your 
lymph nodes and bloodstream.  
Left untreated, the spreading  infection may rapidly turn life-threatening. 
That's why it's important to seek  immediate medical attention if cellulitis 
symptoms occur.  
More information can be found  here: 
_http://www.mayoclinic.com/health/cellulitis/DS00450_ 
(http://www.mayoclinic.com/health/cellulitis/DS00450)  
Barbara H. from TMIC
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
In a message dated 3/26/2008 6:40:00 PM Eastern Daylight Time,  
[EMAIL PROTECTED] writes:

Hi, 
 
 What is cellulitis?  I also start the day  out with thin ankles and end 
up with fat ones.  I find not eating any  salty junk food and cutting way back 
on sodium helps.  I also find if I  can lay down for about an hour a day, 
seems to help.
 
Linda 
in Pa



 



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Re: [TMIC] Hello from Germany

2008-03-11 Thread JHarper33
 
So good to see you pop up here again! I am so glad you were  able to start a 
TM support group in Germany.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
In a message dated 3/10/2008 7:00:33 PM Eastern Daylight Time,  
[EMAIL PROTECTED] writes:

Dear  TMIC-members,

some of you may remember me, I´m Ursula from Germany.  This list has 
been a big help for me at my onset of TM in 2001. I got to  know many 
wonderful people here from all over the world and with some of  them I´m 
connected in a deep friendship.
And as I see the list still is  helpful and busy and I was especially 
touched about all the support Jude  got from you. I hope things will 
develop well for her, she´s in my  thoughts.

The list (Thank you, Jim!) and getting in contact with Sandy  Siegel 
motivated me to build up a TM-support group in Germany, which  meanwhile 
is a formal society with a great bunch of people.

A few  weeks ago I subscribed again, actually with the hope being able 
to  participate active. But I had to realize that my time and strength 
is too  limited and I even get overwhelmed with the many emails to read.

So  I´ll unsubscribe again soon, but before I want to greet especially 
these  people who I know from the past, for example Janh, Wim, Tobe, 
Kevin, Sam,  Gunny, Barbara and many more - you know who is meant!
You all have a good  time, be well and take good care about you!
Love
Ursula

Ursula  Mauro
Transverse Myelitis Association
1. Vorsitzende Myelitis  e.V.
Neugasse 32
77743 Neuried
Telefon:  07807-3154
mailto:[EMAIL PROTECTED]
http://www.myelitis.de


 



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[TMIC] Listening, attention, and solitude

2008-03-06 Thread JHarper33
I think we have talked before here about having shortened  attention spans 
that what we used to.
 
I am wondering if anyone else has trouble listening to  anything for very 
long? Conversations, speeches, sermons? I get lost after a  while and have to 
struggle to maintain attention. And along with listening,  sometimes I get 
impatient when someone takes way too long to say something  simple or continues 
explaining a point they have already made and I already  understood. I just 
want 
to take them by the shoulders and say, I got it  already!! LOL!
 
I guess I am wondering if I van blame it on TM or if I am  becoming grouchy 
and impatient in my old age!
 
Even if it is somehow an aftereffect of TM, of course, it's  not an excuse -- 
I still need to strive to be attentive as much as possible. I  can't impose a 
time limit on everyone's conversations.
 
I also find that I really need a certain amount of solitude to  stay sane. I 
think that's my personality in some respects -- I've always been  better with 
one or two friends than a crowd and I have always enjoyed time  alone. But 
sometimes now I just have to slip off by myself where it is quiet and  nothing 
is 
demanding my attention. I don't want to be a hermit or live alone --  but I 
do need some solitude.
 
Anyone else?
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 



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[TMIC] March Birthdays

2008-02-29 Thread JHarper33
Happy Birthday to the March babies! I love that spring comes  this month! And 
an early Easter this year, too. Hope you all have  a great  birthday.
 
As always, send any corrections or additions to [EMAIL PROTECTED] 
(mailto:tmic-list@eskimo.com) .
 
3-3 Marsha Scholes  ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
03.05 Bettie Imus ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
3-6 Robert Lovette [EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) 
 
3-7 Sue Mattis ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
3-15  Sandra Melville ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
3-17  Joy S. ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )
 
3/24 Rachel ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) 
) 
 
3/24 john h (JOHNLOVESKARAOKE)
 
3/30 Gary ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) ) 
 
3-31 Jan H ([EMAIL PROTECTED] (mailto:[EMAIL PROTECTED]) )




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Re: [TMIC] Hello from Jude

2008-02-22 Thread JHarper33
 
Hi, Jude, 
 
It's so good to hear from you!
 
I think everything here as settled down, as it usually does  within a few 
days.
 
Praying for your continued healing,
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
 
In a message dated 2/22/2008 4:58:15 PM Eastern Standard Time,  
[EMAIL PROTECTED] writes:

It seems as though my faculties have been stretched to the limit and what  I 
want to say doesn't come out the way I intend it to.  Life has become a  
lonely place away from my home, Dave and Sadie  Dee-Dee.  And, of  course, 
each 
and every one of you.
 
Thank you so much for the cards and flowers.  They are colorful and  lovely 
and go a long way to get me through the days and nights.
 
It hurts my soul to read about all of the strife and disrespectful  attitude 
between my good friends.  This support group has always been a  place of 
refuge for me.  And, it has been a place to share information  regarding TM and 
the 
other disorders that tag along with this dread  disease.  It is a place for 
me to exchange ideas, a few laughs, talents,  and even a place to vent.  This 
group has been always tolerant of my way  out emails and tangled thoughts.
 
I beg of you all...we are so fortunate to live in a free society.   Look up 
freedom in the dictionary and then say Thanks and Praise to whomever  it is 
that you pray to.
 
I love you all,
Jude


Practice Random Acts of  Kindness



 



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Re: [TMIC] OT Politics

2008-02-21 Thread JHarper33
 
I do agree, Tracey, with freedom of speech as a country. But  there are some 
instances of agreeing to disagree in certain places on certain  topics and 
going on.
 
I don't mind a discussion of politics or what's going on in  the media when 
people stick to the issues: it's when people make snarky,  condescending, 
cutting comments about the other side that it bothers  me.
 
Years ago the consensus on the TMIC in regard to religion was  that it was ok 
to write in the sense of what I had felt God had done for me, how  I relied 
in Him personally to cope, etc., but that getting preachy, writing to  try to 
convert others, and sending loads of religious forwards was crossing the  line 
here though it was fine on other contexts.
 
I don't personally have a problem with discussing religion or  politics, even 
when there is disagreement: I think it can be enlightening --  if it can be 
done in a civil manner.
 
My plea to cut the politics was based on other people's  frequent pleas along 
the same lines. But if it is ok with Jim, the creator and  maintainer of our 
list, and ok with the group in general, I am fine with it. I'd  just ask for 
civility and respect and grace. We can discuss the issues without  putting down 
anyone's choice for president disrespecting another's viewpoint  opposite our 
own. Attack the problem, not the person is a good general  maxim.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
In a message dated 2/21/2008 10:17:14 AM Eastern Standard Time,  
[EMAIL PROTECTED] writes:

I agree  completely with how the subject line should read. As much as
this world  should be made up of freedom of speech, it does tend to hit
a nerve when  certain subjects are discussed and not agreed upon by
everyone. It does  seem strange to me that we can praise God on here
for the miracles that  he has given and thank God for the prayers that
have been answered and  everyone seems ok with that(regardless of their
religious background) but  the minute that politics are discussed (even
though it is all a repeat of  something being told in the media) feelings
get hurt and people get  offended. I am not saying that it is right or
wrong, I am just stating a  fact. Our world is a melting pot of so many
different religious and  political backgrounds and we should all be able
to value the opinion of  someone else, even if we don't agree with it.
Everyone should have their  right to their own opinion. No one should
have to apologize for making a  statement on what they believe. Everyone
should stand up for what they  believe in. Isn't that what we all try to
teach our children and their  children?  


Tracey L. Black
Certified Insurance Service  Representative
Hockley  O'Donnell Insurance Agency
Phone -  717-334-6741, x 29
Fax - 717-334-3414


 



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