Michelle,
It always breaks my heart when I hear of the little ones.  I'm glad 
she has done so well on Gleevec, I hope she has continued success.  I 
can imagine how hard it is for you to try to make a decision between 
current treatment or a BMT, but MD Anderson is a 'great' center and I 
trust they have her best interest at heart.  There have been so many 
break throughs in treatment for this disease I just think that 
something great is on the horizon that would eliminate taking the 
risks involved with a transplant.  Wishes of happy holidays and lots 
of cheer to your whole family and a special Merry Christmas to Morgan.
Brenda
dx 5/04
Gleevec 6/04
6mth bmb, pending results


--- In [email protected], michael blackford <[EMAIL PROTECTED]> 
wrote:
> happy holidays to everyone.  i don't post very often
> but i read everyday.  my daughter Morgan is 6 and was
> diagnosed 2 and a half years ago.  She has been on
> gleevec since her diagnosis and is doing great.  She
> is treated at MD Anderson.  Although her doctor
> recommended she stay on gleevec (no sibling match) 
> there is always that what if in the back of our heads.
>  Would transplant be better for a child?  There are
> days i can't even breath thinking of everything
> happening to her and yet i am also very thankful for
> the advances in treatment.  You all encourage us so
> much with your positive outlooks and positive
> comments.  I thought I should let you all know how
> grateful we are for this group.  
> Michelle
> 
> 
>               
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