Hello CML Friends, I have been battling CML for 9 years now. And I still gett 
very ill from gleevec. Nausea daily, bone pain, chills and my vision has 
changed drastically. I am on 600mg. I am thankful to be here, but am wondering 
if any 8 year veterans experience the same side effects like I do?
Hoping you all are having a great week-end! Love & Good Health, Marcia in MN


________________________________
From: Suzieq <[email protected]>
To: CMLHope <[email protected]>
Sent: Sat, February 27, 2010 12:59:57 PM
Subject: [CMLHope] Re: Paying the donor of Bone Marrow

Marty:
I was diagnosed in late January of 2004.  Put on Gleevec about three
weeks afterwards as the lab where I went then kept losing tests & I
would have to go through all the testing again.  The first BMB was
done in doc's office with nothing but local and he was unable to
retrieve any bone marrow,  but did get the sliver of bone.  I left him
about a week later and transferred to Siteman Cancer Center in St.
Louis & have been much happier with there and how they do things.  I
feel more confident in their set up of lab and treatment centers as
well as their doctors that I've seen.
My last visit a month ago,  she told me that since I show a very low
level of the CML still after six years,  I most likely will have to
stay on the Gleevec for life as it would just come right back in full
force if I went off of it as some are now who've been PCRU negative
for some time.

Thank you, Marty for all your answers and help for those of us who
survive this disease......you have a great story as some others who've
paved the way before us.  May God continue to bless your life.  Will
keep you in my prayers leading up to the possible kidney transplant.
Keep us posted.

Keep Looking Up,
Suzieq











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