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BMT Update

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Hey Group: my 2 cents. . .

As always, I posted to the Group; and as each of us is an 'individual in our

survival'. . .we are all statistics in the research and development of a CURE

for our CML.

Tracey (gf), I can remember the names of those you have given; and as I have

said many time before. . . " I personally don't wanna lose another brother or

sister survivor to a BMT. . . who would otherwise be surviving on our gold " . As

Angie says 'CML Alive & Kicking'. We could begin a Group and it could function

independently addressing the 'Pros & Cons of a BMT'.

Those of us surviving on our Gleevec, AMS, BMS, Vaccine, BMT, etc., should

email each other privately and become a source of support for each other in our

survival regardless of chosen method of treatment.

Thanx Barb, Tom's Mom and others for posting in response; any and all

information is valuable to us and the Newbies in our survival; as many have left

after their BMT.

" K "

" I AIN'T FINISHED YET " !!!

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