Shannon,
Thanks for posting.  Glad to see that Gleevec has done well for you.  
It is always uplifting to hear from you veterens too.  Please keep us 
posted on how your feeling, it is always in the back of my head what 
the long term side effects will be with Gleevec, sharing your 
experience can prepare us for what to possibly expect down the road.  
I understand what your saying about family and friends not really 
wanting to have a lot of conversation about the disease, I have the 
same situation, that's why these groups are so important, you guys 
understand were I'm coming from and visa versa.  Take care!
Brenda (43)
dx 5/04
pcru 5/05

--- In [email protected], "Shannon" <[EMAIL PROTECTED]> wrote:
> Dear Members
> My name is Shannon in Sydney Australia
> Its been along time since i last posted
> I was dx 3/98
> Was on interferon & ara c still 100% +
> started Glevic Apri; 2001, reached remission within 6 months, still 
in
> remission (over 4yrs) I am due for my annual bone marrow at the end 
of
> June.
> I keep up with the posts & felt sad at some of which I replied, The
> positive & helpful post are uplifting.
> I am starting to find that Glevic is getting harder to cope with i.e
> nausea increasing ( mind you not as bad as older drugs) bone & 
muscle
> pain.
> They recently found a lump in my breast which didin't show up on
> mammagram or ultrasound am seeing a surgeon on friday will let you
> know.
> I am very busy with my son who is 8 now & have started oil painting
> classes & help out at school
> I suppose the hardest thing presently is the stress & the emotional
> worries of what if, most family & friends don't want to hear about 
my
> cml it gets a bit lonely but I try my best.
> Well I have finally posted thanks for listening




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