Hi Carol, I have been on Sprycel since 2009 with no PE.   I reached 
remission on Sprycel. Cutting back on the dose makes sense to  me.
Good luck,
Jeanie<3
 
 
In a message dated 6/6/2013 9:35:44 A.M. Eastern Daylight Time,  
sion...@aol.com writes:

What is your dose and your PCR results? 

On Jun 6, 2013, at  7:46 AM, _Cakrek@aol.com_ (mailto:cak...@aol.com)  
wrote:


 
I haven't posted in a while, but always read everyone else's...now i have  
a question for everyone on Sprycel. I was switched to Sprycel 2 years ago 
due  to kidney issues with the Gleevec. I was diagnosed in July of 2001.Have 
been  undetectable for years...now I am getting pluerral effusions.   I  just 
had the second one drained yesterday....The onc has taken me off Sprycel  
for 2 weeks.....In everyone else's experience does that seem long  enough.   
I took an 8 day break a month ago but the effusion was  back in 5 
days....probably was going to happen anyway....I think he is being  very 
cautious, but 
just wondering what everyone else has done...went into the  archives and 
learned a lot....but need a little more advice to argue my point  of a longer 
break....thanks....Carol Kalat
 
 
In a message dated 6/5/2013 7:43:23 A.M. Eastern Daylight Time, 
_cmlhope@googlegroups.com_ (mailto:cmlhope@googlegroups.com)   writes:

   Today's Topic Summary
Group: http://groups.google.com/group/cmlhope/topics 
    *   _Taking a break from  gleevec after over 12 years_ 
(mip://0faa0d80/default.html#group_thread_0)  [4 Updates] 
 _Taking a break from gleevec after over 12 years_ 
(http://groups.google.com/group/cmlhope/t/495a7def56c96b43) 
Marty Gartenberg <_wa2yyx@gmail.com_ (mailto:wa2...@gmail.com) > Jun 04  
08:59AM -0400  

Hi Sylvia,

First, welcome back to  the group. How well I remember those "good" olden
days of when gleevec  first came out. Unfortunately it wasn't around when I
was diagnoised  with CML in 1989. The only thing at the time was interferon
but for me  it would have a blind study case weather I would get it or just
a  placebo.

Since my WBC was well over 480K (480,000+) at the  time and I wasn't sure if
I would get it or not I opted for a bone  marrow transplant. Not much choice
in the matter.

Anyway,  since you were on gleevec for so many years do you know if you are
PCRU  now? I would imagine that you are but you still need to be tested  to
see if you are just as your doctor suggests.

I actually  don't blame you for wanting to stop the gleevec but you must be
aware  of the mutations that could come about. However since your doctor
wants  to test you for if you are PCRU within four months I think that is  a
wise choice.

Nice to see you on Zavies Zero List. I hold  the number one place on the
list. I sure do miss him and Mommy Lottie  as well. (from the
_CML2@yahoogroups.com_ (mailto:c...@yahoogroups.com) )

Sylvia  you just take one day at a time just as I do. After all, neither of
us  would still be hear if there were nothing in the arsenal to fight  CML

18's (symbol for  life)

Marty



Darlene <_seceshky@yahoo.com_ (mailto:seces...@yahoo.com) > Jun 04  08:09AM 
-0700  

Two years ago I insisted on a break from  gleevec as well although my 
oncologist wasn't keen. My counts immediately  began to creep up after being 
undetectable for almost 10 years. I couldn't  feel the difference in the 
counts--in fact I felt great -but after 2  BCR-abl tests which showed the 
upward 
trend, my doctor ( and my family)  insisted I resume Gleevec. Within 6 months 
I was undetectable again. The  muscle cramps had been pretty bad before the 
break but stopped completely  for awhile. Now they're back but not as bad as 
before. I think your doctor  is wise to monitor you closely but I also 
think a break can do your body  some good if you're careful. I may be wrong but 
I got the idea somewhere  that some people are able to stay off longer. 
Maybe you' will be one of  the lucky ones. Good luck!

ANGELYN ESDERS <_esders@rogers.com_ (mailto:esd...@rogers.com) > Jun 04  
08:13PM -0700  

I started Gleevec at McMaster University  Medical Centre in Hamilton, 
Canada, on Jan. 22, 2001. My tests in June  2001 confirmed that I had reached 
cytogenic remission. I think I was #69  in Zavie's Zero Club.
I am planning to discuss a holiday from Gleevec  next time I see Dr. 
Walker, my hematologist at Juravinski in Hamilton. We  shall see....12 years is 
a 
long time....


What lies  behind us and what lies before us are tiny matters compared to 
what lies  within  us....
Angie


________________________________
From:  Richard H <_richard1huffman@comcast.net_ 
(mailto:richard1huff...@comcast.net) >
To:  _cmlhope@googlegroups.com_ (mailto:cmlhope@googlegroups.com)   
Cc: "_CMLHope@googlegroups.com_ (mailto:CMLHope@googlegroups.com) "  
<_CMLHope@googlegroups.com_ (mailto:CMLHope@googlegroups.com) >  
Sent: Monday, June 3, 2013 11:25:59 PM
Subject: [CMLHope] Re:  Taking a break from gleevec after over 12  years



That's great news.  When I went off  Gleevec 5 years ago. I was tested 
every month for a while then as I  progressed with excellent results to 3 
months 
and then 6 months.  The  body also responded nicely, I gained energy, lost 
30 pounds and my leg  edema went away.  I am glad your ONC is willing to 
work with  you.

Richard H.

On Monday, June 3, 2013 9:35:22  PM UTC-5, Sylvia wrote:
Hello everyone 
>It has been many years  since I have written to this group. I was 
diagnosed with CML in June 1998  at 37 years old and many friends I met through 
this 
group are no longer  with us.  Those were the days of interferon and ara-c, 
procrit etc  (all via injection).  I was one of the first to start Gleevec 
in  Canada in April 2001.  I am number 80 in Zavies Zero club! Gleevec  has 
given me back my life and I am very thankful for it.  That being  said the 
last few months I have had swelling in my legs and stiff knees  and I have 
taken myself off the Gleevec.  In 12 years I have barely  missed any days, but 
now I am feeling my body need a rest.  I am  worried about my liver and 
Millie's email reinforces my feelings that I  need a break from the Gleevec.  I 
told my dr and he wants me to come  in for a PCR in a month and not wait 
until my 4 mos check up in Aug. I am  very interested in what everyone in this 
community thinks and if they can  offer me some advice. 
>My prayers to Millie and all those with  challenges. Thanks to everyone 
for their support all these years.  

>Sylvia 

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Marty Gartenberg <_wa2yyx@gmail.com_ (mailto:wa2...@gmail.com) > Jun 05  
06:12AM -0400  

Hi Angie, I wish you the very best of luck on  your Gleevec "holiday" Yes,
12 years is a long  time.

18's

Marty

Number 1 on Zavies  Zero List. I sure do miss him.
Disgnosed July 1989
Bone Marrow  Transplant May 21St 1990 (23 years ago)




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