How ironic, I have issues with what I call "cysts" on my face. The Dr. lowered 
me to 70 mg per day since I had immediately gone into remission on 100 mg per. 
Well that pretty much did the trick. Now the outbreaks are much less frequent 
and much smaller when I do get an eruption.

On Aug 9, 2010, at 4:12 AM, Suzan Collins wrote:

> 
> The doctor did try me on Sprycel but within the first week I broke out with 
> severe skin ulcers on my stomach but we did not connect the two together for 
> weeks because they had also given me so medicine for my bad back. So when my 
> doctor realized it he took me off and started me on Tasigna.
>  
>  
> --- On Sun, 8/8/10, 73hunley <[email protected]> wrote:
> 
> From: 73hunley <[email protected]>
> Subject: [CMLHope] Re: remission
> To: "CMLHope" <[email protected]>
> Date: Sunday, August 8, 2010, 7:03 PM
> 
> Suzan, I'm surprised you weren't placed on Sprycel first. That has
> been the usual progression after gleevec. I was on gleevec for 5.5
> years before I started getting mutations that gleevec couldn't handle.
> Sprycell is like 300 times stronger. I will say the side effects for
> me were totally different than the gleevec. At this point I'm been on
> the Sprycel for a little over a year and I'm still totally negative.
> 
> P.S. I was diagnosed in Dec 2004 with a white count of 360,000.
> 
> 
> On Aug 7, 6:09 am, Suzan Collins <[email protected]> wrote:
> > Hello all I was dxed on June 4, 2004 at 98% positive. I was on Gleevec from 
> > then until Nov 2008 and was switched to Tasigna because of all the bad side 
> > effects I continued to suffer. I continue to have side effects with Tasigna 
> > but not as severe except now I get skin ulcers with the Tasigna. I lost 30 
> > pounds right off the bat when I stopped the Gleevec which was good. HOWEVER 
> > my last fish test in July showed me at ZERO on the molecular level. WHOO. 
> > It has been a long journey as it is for all of us with side effects and all 
> > but what a BLESSING to get the good news.
> > Suzan
> 
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