Re: [CMLHope] New member

2010-07-06 Thread Martin Gartenberg
Hi Severinsen,

Welcome to this group. Although I am not on any medications for CML I had to
have a bone marrow transplant more then 21+ years ago.

I make sure to keep up on the latest things that can help with the
management of CML or any other types of Leukemia.

Believe me Severinsen you can consider yourself lucky to have this disease
rather then many types of other cancers. What I wouldn't have given if these
current drugs, and others to follow weren't around when I was ill.

This is a time that people such as yourself can really benefit from this
technology. I have no doubt that you will do well having CML, in fact most
of the people on this site are alive because of drugs such as these, and
there is a great expectation of newer and better ones to follow.

Please keep everyone apprised of what is happening with you. There are a lot
of very caring people here that will be of great comfort to you with any
questions you may have. I wish you the best of luck

GOD bless you.

Marty
.



On Mon, Jul 5, 2010 at 5:31 PM, Severinsen styrkecoac...@gmail.com wrote:

 Hi all.

 I am a newly diagnosed CML patient. I am 30 years old, and live in
 Denmark.

 I will start my medication monday the 12th of july, it will be
 Tasigna. I will be participating in a test group, aiming at getting
 Tasigna approved as standard treatment i Denmark. Gleevec is the
 present standard treatment.

 What can I expect my future as a CML patient to be? I´m still in chock
 from the diagnosis, but has found comfort in all of the positive
 articles on the web, about CML.

 I am looking forward to participating in this group.

 Regards,
 Severinsen

 --
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Re: [CMLHope] New member

2010-07-06 Thread Mustardny
Hi Severinsen,  
Sorry you have CML but I found that it is a disease that  is very 
treatable  that this is a very  good Group to be a part  off.  I was diagnosed 
with CML in June '05, started taking Gleevec right  away  have been doing ok 
to this day. I found this group a little  while after being diagnosed  
found CML Hope to be most kind   considerate group around  found it to be an 
information highway to all my  questions concerning this disease. 
 We think of ourselves as CML Warriors who don't  have to fight this 
battle  on our own, God Bless  keep coming back  here  share your fears, 
strengths   most of all your Hope with  us.
   Regards, Frank
 
 
In a message dated 7/6/2010 10:27:14 A.M. Eastern Daylight Time,  
styrkecoac...@gmail.com writes:

Hi  all.

I am a newly diagnosed CML patient. I am 30 years old, and live  in
Denmark.

I will start my medication monday the 12th of july, it  will be
Tasigna. I will be participating in a test group, aiming at  getting
Tasigna approved as standard treatment i Denmark. Gleevec is  the
present standard treatment.

What can I expect my future as a CML  patient to be? I´m still in chock
from the diagnosis, but has found comfort  in all of the positive
articles on the web, about CML.

I am looking  forward to participating in this  group.

Regards,
Severinsen

-- 
[CMLHope]
A support  group of  http://cmlhope.com
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Re: [CMLHope] Re: Hi Greenie

2010-07-06 Thread Mustardny
Welcome Nadia, I think that your english  is just fine.
Frank
 
 
In a message dated 7/5/2010 9:45:13 P.M. Eastern Daylight Time,  
nadia...@earthlink.net writes:

 
Thank  you so much to all of you. I read all yours mail every days, but 
never post  because my poor English. You make me feel good and proud to be part 
of the CML  Warriors. Merci. Nadia 
 
 
From:  cmlhope@googlegroups.com [mailto:cmlh...@googlegroups.com] On Behalf 
Of  C.M. Houtz
Sent: Monday, July 05, 2010 7:46 PM
To:  cmlhope@googlegroups.com
Subject: Re: [CMLHope] Re: Hi  Greenie

 
Hello  Nadiia
 
Welcome  to our group.  We do have a great bunch here, and everyone tries 
to help  everyone else when we can.  Glad you're joining  usMillie

 
-  Original Message - 
 
From:  _Nadiia Noles_ (mailto:nadia...@earthlink.net)   
 
To:  _cmlh...@googlegroups.com_ (mailto:cmlhope@googlegroups.com)   
 
Sent:  Monday, July 05, 2010 7:32 PM
 
Subject:  RE: [CMLHope] Re: Hi Greenie
 

Hi  Jeanie:  My name is Nadia and I  just moved to Florida in Winter Haven. 
  I’d like to go to Moffit , 
but  I don’t know the right Hematologist. Can you recommend yours?   And if 
you can would  you 
give  me his name please?  I’ve been  diagnosed with CML since 8/2006, and 
am on Gleevac ,  300/mg 
a day and feeling good. Thank you and  thanks to all of you. Your mail has 
been a big help.  
Thanks 
 
 
From:  cmlhope@googlegroups.com [mailto:cmlh...@googlegroups.com] On Behalf 
Of  icandoall...@aol.com
Sent: Monday, July 05, 2010 6:25  PM
To: cmlhope@googlegroups.com
Subject: Re: [CMLHope]  Re: Hi Greenie

 
Good  luck on your move to Florida.  I'm a Florida Cracker so I love  it.
 
What  doctor will you go to in Florida.
 
I  go to Moffitt Cancer Center.
 
Blessings,
 
Jeanie3
 

 
 
In  a message dated 7/2/2010 11:43:19 A.M. Pacific Daylight Time,  
myvet...@aol.com writes:

 
Hi  Suzieq,  Port Richey is nice, we checked it out put my brother wants  
us to move his way. Sorry, we are not looking for a house.  We are  looking 
to rent, condo, etc. No more up keep, would like to find some  folks in our 
age group. Not much into golf, but we do like to go  fishing.  Grace likes 
just to be near water and I like to check out  the babes (smile). I'll be 71 
on July 22nd, my body no's it's 71 but my  mind thinks it's 21.  We are 
selling all our belongings and just  taking our cloths, and of course my 
fishing 
gear.  
 

 
This  part is for the guys,  one thing that did happen to me yesterday is 
my wife gives me a shot of  testosterone every Wednesday.  I've been back on 
the shots for almost  two months.  About 30 min. after my shot I started to 
get fatigue and  I do mean fatigue, it lasted all day into the night.  Then 
it went  away almost as fast as it started.  This is the third time in the  
last 2 months.  I know this is not a women thing but maybe one of the  guys 
out their may have had this same thing happen to them.  I use  to take a gel 
each day but that didn't do much for me, always had a  lack of energy, etc. 
 When I first started STI-571 in 2000 my study  at Northwestern I was on 
the shots and never had a problem, now 9 years  later something new.  I still 
think that their are things out their  that they don't know what side 
effects and others drugs will not mix with  Gleevec. I called my nurse this 
morning and told her what happened and her  reply was take the shot before bed 
time and sleep through the  fatigue.  WOMEN, they just don't understand us men. 
 (smile)  Greenie
 

 
 
In  a message dated 7/1/2010 4:11:15 P.M. Central Daylight Time,  
sheila.a.wat...@gmail.com writes:

Greenie:

If  you want to live a little further up the coast line,  my mom  still
has her house in
Port Richey, Fl.   It's north of  Tampa off Hwy. 19.  It's not far from
Hudson Beach, so  that's
a plus.   She still wants to sell it, if  you're interested.
It's not on the market right now.
she plans  to go back down in a few months and get it ready to list
once  again.  Her house
sits on a corner lot..has nice full size  treesan extremely
nice retired elderly couple
across the  street from her that always helps with anything she needs.
Course,  you'll might looking more for a condo or something.and be
closer  to your
brother.  This is a wee bit back up the other way.   Anyway, just
wanted to let you
know.  Are you'll gonna be  going to do this just through the winter
time and then
go back up  North in the summer months?

Suzieq

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Re: [CMLHope] New member

2010-07-06 Thread sylwia
Hi, Severinsen

I'm so sorry you belong to this group because of you have CML :( But the
bright side is you can find really nice and helpful people in here. I know
it because from time to time I'm a lurking member of this group.
I joined this group last year because I have wanted to know much more about
people diagnosed CML living in the whole world.
Otherwise, one of my present goals is to become a bone marrow donor, so we
may say I stay at the opposite side of that disease 
Anyway, I wish U and all of you reading my words, strength and patience
fighting the disease.
Btw I live in Poland and as I've noticed, we're probably the only Europeans
in this group :)

I believe that your medication will work. I keep my fingers crossed!

best wishes,



2010/7/5 Severinsen styrkecoac...@gmail.com

 Hi all.

 I am a newly diagnosed CML patient. I am 30 years old, and live in
 Denmark.

 I will start my medication monday the 12th of july, it will be
 Tasigna. I will be participating in a test group, aiming at getting
 Tasigna approved as standard treatment i Denmark. Gleevec is the
 present standard treatment.

 What can I expect my future as a CML patient to be? I´m still in chock
 from the diagnosis, but has found comfort in all of the positive
 articles on the web, about CML.

 I am looking forward to participating in this group.

 Regards,
 Severinsen

 --
 [CMLHope]
 A support group of http://cmlhope.com
 -

 You received this message because you are subscribed to the Google Groups
 CMLHope group.
 To post to this group, send email to CMLHope@googlegroups.com
 To unsubscribe from this group, send email to
 cmlhope-unsubscr...@googlegroups.com
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 http://groups.google.com/group/CMLHope

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