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] 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]>
To: cmlhope  <[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_/)  
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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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