Hi Marie and so good to hear from a CML survivor for so many years.  I  get 
those mouth sores also and I wonder what causes them?
I was on 150 mgs of Sprycel in the beginning as I had a battle with my  
counts all going too high; then I was reduced to 100 but as of late my counts  
started going low.  I cut down to 50 for a few days and then 100 for a  few.
We have our ups and downs but we are still here kicking and fighting.
Blessings,
Jeanie<3
 
 
In a message dated 3/30/2011 8:18:47 A.M. Pacific Daylight Time,  
[email protected] writes:

 
I am so sorry that you are in this spot. I was there 3 yrs ago. I was  
diagnosed with CML 11 yrs ago. At that time gleevec was in the experimental  
stage. My oncol. got me on the exper. program and within 3 mos. I was in  
remission. After 8 yrs. gleevec turned on me. My insides were torn open and I  
had a huge infection. After surgery I went to Boston to Dana-Farber Cancer  
clinic for advice about other meds. My oncol. and the dr. from D-F put me on  
sprycel. I am a petite person and the dosage that I was on pretty near did  
away with my platlets. In the hosp. I went for 3 weeks to get treated . Now 
I  am on a very low dosage of sprycel. The side affects that you had with 
gleevec  are the same that I had. With sprycel, I have bad aches and pains 
with my  whole body, and at times I get mouth sores and can't eat. I found out 
by that  if I take myself off my sprycel for maybe 2 days that the sores go 
away. Also  get leg cramps, but it beats the alternative. Let me tell you , 
I am now 83  yrs old, and expect to get achy bones and body, it may not 
happen to you.  Sprycel is not so bad though. It is easy to take. Between 
gleevec and sprycel,  I have been living all these years and keep active. I 
don't 
baby myself and I  do not whine. I thank God every day that I was born in 
these times when a  disease can be controlled. Years ago , this would be 
fatal. My prayers are  with you. Marie Hillenbrand


 
____________________________________
 From: Ana Burgos  <[email protected]>
To: [email protected]
Sent: Tue, March 29, 2011 1:31:47  PM
Subject: Re: [CMLHope]  Just got the bad news, Gleevec out after 7 years!


 
what does “3 fold” means?, I mean , the same happen to my mun , after 7  
years pcru, her last pcrs have been 0.036; 0.012; 0.,216 ; 0.012
 
 

 
From: _Len Clapp_ (mailto:[email protected])  
Sent: Tuesday, March 29, 2011 2:57 PM
To: [email protected]_ (mailto:[email protected])  
Subject: Re: [CMLHope] Just got the bad news, Gleevec out after 7  years!


 

Thannk  you for the information. 

On Wed, Mar 23, 2011 at 4:38 PM, John Kuptz <[email protected]_ 
(mailto:[email protected]) > wrote:

I was diagnosed in 11-05 and started on Gleevec but within  2 months had 
developed liver function failure.  Was started on Sprycel  70mg bid and that 
just about wiped out my platlets.  Waited for bone  marrow to recover and was 
put on only 20 mg bid.  I have been on that  ever since.  My pcr tests 
comes back UNDECTABLE almost every time they  do it every three months.  Once 
in 
a great while a very smalll amount  is detected.  Onocologist said that is 
the name of the game.  I do  have joint pain and have put on 30 lbs but 
basically that is the only side  effect in 4 years.  Best of luck to you.
Carolyn
----- Original  Message ----- From: "kneesrbad2" <[email protected]_ 
(mailto:[email protected]) >
To:  "CMLHope" <[email protected]_ 
(mailto:[email protected]) >
Sent:  Tuesday, March 22, 2011 10:59 PM  

Subject: [CMLHope] Just got the bad news, Gleevec out  after 7 years!





 
I don't know what went wrong but my abnormal cells  increased 3 fold on
my last BMA.  Now going onto Sprycel!  I  need everyone who is on
Sprycel to give me your quick stories of what  to expect with the new
round of side affects from Sprycel.  On  Gleevec, here is MY list of
side affects, Diarehea, fatique, eye  bleeds, water retention, thin
skin, pale skin (burn easily), cramps,  sinus operation, pumpkin face,
joint pains, insomnia, etc etc  etc.

What am I faced with for side affects on Sprycel?   Suppose to start
it next week.

I am a 55 year old, male,  Michigan resident, DX'd on my  Wedding
anniversary in 2004, in  full blast stage with a spleen they were going
to take out immediately  and when I say immediately, I mean 3:30 am
with a full siren ambulance  to a major hospital but they saved it!! I
was tested for a full Bone  Marrow Transplant with my brothers and I
have a 100% match from my  younger brother if I need it.  I just want
to hear the good, the  bad and the ugly from those on Sprycel,
please.

Also, and almost  as important to our CML family for one reason or
another I have a few  extra bottles of Gleevec 400 mg bottles still
with the seal on it if  anyone is interested in talking with me in
private. I would like to  help someone who may have a huge co pay on
their Gleevec  payments.  This will be handled away from this site and
all  parties will get to know who the other parties are.  I just  don't
want these expensive drugs to go to waste because my body  decides, the
heck with you, drug change.

Please reply and let me  know!  Thanks

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