I was wondering if anyone has had any problems with pins and needle feeling 
 in there hands.
I thought i have read in the past about hand cramping  with   Gleevec is 
that true.
This is mostly pins and needle feeling in hands...once or twice hand  
cramping..
Could  any of you on the list tell me anything you know about  this....
                                                                          
Thank You 
                                                                           
Teepee
 
 
In a message dated 10/25/2011 3:08:16 P.M. Eastern Standard Time,  
[email protected] writes:

The first brain bleed, my face and arm on the  right side went numb.  I 
happened to be in a doc's office with someone I  was watching over.  They 
insisted on shipping me via ambulance to the  E.R. across the street.  They saw 
it on an MRI.  A cat scan showed  it also.  Then 2 yrs later I had a 
full-blown stroke when I was NOT on  gleevec.  Had an eye bleed again this 
week, so 
am becoming a little  concerned.  Last week my cbc showed normal.  


18's,
Susan










Hi and how did you know you had a brain bleed?
Jeanie<3
 
 
In a message dated 10/1/2011 4:41:07 P.M. Pacific Daylight Time, 
[email protected]_ (mailto:[email protected])  writes:

Teepee,  


I have been off gleevec for 4 1/2 years now since the first brain  bleed.  
I'm still in cellular remission and am so glad.  I am on  no medication for 
CML at all, but very very slowly my numbers are climbing  up there.  I had 
been in total remission for 2 years before going off.  I'm sure that helps.  
More doctors are giving vacations from the  drugs as they
see people are holding their numbers if they've been in total remission  
for a long time.  My doc wants me on something, but I am waiting until  I come 
out of cellular remission.
Blessings,  
 
Susan F. Zimmerman



-----Original  Message-----
From: Teepee710 <[email protected]_ (mailto:[email protected]) >
To: cmlhope  <[email protected]_ (mailto:[email protected]) >
Sent:  Sat, Oct 1, 2011 12:59 pm
Subject: Re: [CMLHope] Re: Problems with Food  and Gleevec


MaggyMay
Thanks... i had mentioned that to him about the saline solution,  as our 
weather is changing.
                                                                  TEEPEE
 
 
 
In a message dated 10/1/2011 8:36:18 A.M. Eastern Daylight Time, 
[email protected]_ (mailto:[email protected])  writes:

Gleevec dries out the sinuses which then creates nose bleeds.   Use a 
saline nasal mist and a neti pot.  It helps a lot.  Be  sure if u live in the 
snow country your furnace has a working  humidifier.
On Sep 30, 2011 9:46 PM, <[email protected]_ (mailto:[email protected]) > 
wrote:
> Could anyone tell me if thee is any connection  between nose bleeds and 
> gleevec.
> 
> teepee
>  
> In a message dated 9/30/2011 3:38:41 P.M. Eastern Daylight Time,  
> [email protected]_ (mailto:[email protected])   writes:
> 
> 
> Was on Sprycel and experienced shortness  of air. Hematologist stopped 
the 
> Sprycel. Before that was on  400mg Gleevac and it was stopped due to Eye 
> bleeds, bilateral.  Now am reinitiated on Gleevac 100mg every day and all 
> is well.  Barely detectable Philadelphia Chromosomes per the BCR ABL.
>  
> 
> 
> 
> 
> 
> From: kellyelise  <[email protected]_ (mailto:[email protected]) >
> To:  CMLHope <[email protected]_ 
(mailto:[email protected]) >
>  Sent: Friday, September 30, 2011 1:05 PM
> Subject: [CMLHope] Re:  Problems with Food and Gleevec
> 
> Thank you for the info on  Dr. Talpaz - I had sent him an email a while
> back but received no  reply. My onc NP recommended Dr. Jorge Cortes at
> MD Anderson in  Houston - and that's where I'm going!! They called
> yesterday and I  have an appt. on Oct. 10. Thank God for my mother, I
> could not  afford to go without her. Wishing you all the best!! Those
> on  Sprycel, please watch for symptoms of SOB, weakness, inability to
>  climb stairs, weight loss (initially I had a lot of weight gain -
>  Aldactone and Demadex took most of the fluid off), loss of  appetite,
> etc. You can find the symptoms of PAH through any search  engine
> (Google). It is a disease that is VERY difficult to  diagnose!!
> 
> Bless you all!!
> 
> Kelly
>  
> On Sep 27, 9:30 am, kellyelise <[email protected]_ 
>  (mailto:[email protected]_ (mailto:[email protected]) ) >  wrote:
>> Suzieq,
>>
>> You are not whining or  complaining!! We all have to vent sometime!
>> Quite frankly, I  am grateful to be off all TKIs as of now. The Sprycel
>> about  did me in. I don't know if you remember, but, I now have PAH
>>  (pulmonary arterial hypertension) as a result of the Sprycel.  I
>> underwent a heart cath in 1/11 and am now sporting a  continuous
>> infusion pump carrying Remodulin through a central  venous catheter.
>> Not pretty, but I feel better than I have in  YEARS. I can actually
>> walk around town now whereas I could  barely climb 3 steps without
>> help.
>>
>> My  onc wants to put me on Tasigna, but I am highly resistant. I'd
>>  rather wait until the other 2 new drugs come out and see if I  could
>> try one of those. I have tried getting an appointment at  MD Anderson
>> with Dr. Jorge Cortes, but, so far have been  unsuccessful. I REALLY
>> need a CML specialist....I live in  Ohio....any ideas anyone??? I am
>> willing to travel, hopefully,  before the snow flies.
>>
>> I stopped complaining,  Susieq, and the PAH ramped up to the point I
>> was taken by  ambulance to CCF (50+ miles away from where I live). My
>> onc  always made me feel like I was a whiner...so, I stopped  whining.
>> "No one else on Sprycel has had these symptoms....."  Well, I bet NOW
>> they DO!! He still denies that the Sprycel was  the culprit even
>> though my cardiologist and pulmonologist BOTH  dictated in my discharge
>> summaries that it WAS the cause....it  progressed too rapidly to be
>> anything else. Also, I am on a  minimal dose of the Remodulin and my
>> health has dramatically  improved. I just wish I could get put on a
>> subcutaneous  pump....bleh! Nothing like waking up in the heart
>> failure unit  with no clue.... so, now I'm complaining, ha ha!!
>>
>>  Keep fighting, the side effects suck!! We will all just muddle
>>  through and praise the fact we are still alive even though we  feel
>> like shit. Truthfully, I am grateful to still be alive  and I wouldn't
>> be if hadn't been for the Gleevec putting me in  remission in the first
>> place - now I am waffling between  undetectable and "weakly positive"
>> and I have been off the  Sprycel since December 2010. I'll take the
>> chemo and whine  like a baby but still, in fact, be grateful for every
>> day with  my family. :)
>>
>> Kelly
>>
>> On Sep  26, 3:38 pm, [email protected]_ (mailto:[email protected]_ 
(mailto:[email protected]) )  wrote:
>>
>>
>>
>> > Hi Suzieq, We  all here have had our good days and our bad days. 
>  That's
>> > what's so great about this CML group. We are all  good listeners. 
> greenie
>>
>> > In a message  dated 9/26/2011 12:12:45 P.M. Pacific Daylight Time,  
>>
>> > [email protected]_ (mailto:[email protected]) _ 
(mailto:[email protected]_ (mailto:[email protected]) )  
writes:
>>
>> > Susan:
>>
>> >  Good to hear from you again......& a great big "THANK YOU"!  I
>> > remember your struggles.....& I just want you to  know, I wasn't
>> > "complaining" about mine, cause I, too, am  very grateful for Gleevec
>> > & the wonderful doctors  that I've had since my journey with CML began
>> > in Jan.  2004. I am very thankful to still be alive and kicking! If
>>  > my recent post sounded like I might be "whining" or "complaining",  I
>> > didn't mean it that way. Was just going through a bit  of a rough
>> > spot. I never thought of it before, but I  think that week was also
>> > the time of some very emotional  family drama going on as well a close
>> > friend's son &  his family in a serious car accident. A lot to digest
>> > in  one week, so could have set off some of this side effect of
>>  > Gleevec. Thanks again, Susan, for your uplifting post  here.
>>
>> > God Bless you,
>> >  Suzieq
>>
>> > -- 
>> >  [CMLHope]
>> > A support group of __http://cmlhope.com__ (http://cmlhope.com_/)  
(_http://cmlhope.com/_ (http://cmlhope.com/) )  
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> Pacific  Daylight Time, 
>>
>> > [email protected]_ (mailto:[email protected]) _ 
(mailto:[email protected]_ (mailto:[email protected]) )  
writes:
>>
>> > Susan:
>>
>> >  Good to hear from you again......& a great big "THANK YOU"!  I
>> > remember your struggles.....& I just want you to  know, I wasn't
>> > "complaining" about mine, cause I, too, am  very grateful for Gleevec
>> > & the wonderful doctors  that I've had since my journey with CML began
>> > in Jan.  2004. I am very thankful to still be alive and kicking! If
>>  > my recent post sounded like I might be "whining" or "complaining",  I
>> > didn't mean it that way. Was just going through a bit  of a rough
>> > spot. I never thought of it before, but I  think that week was also
>> > the time of some very emotional  family drama going on as well a close
>> > friend's son &  his family in a serious car accident. A lot to digest
>> > in  one week, so could have set off some of this side effect of
>>  > Gleevec. Thanks again, Susan, for your uplifting post  here.
>>
>> > God Bless you,
>> >  Suzieq
>>
>> > -- 
>> >  [CMLHope]
>> > A support group of _http://cmlhope.com_ (http://cmlhope.com/) 
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