Hi Marty,
 
I'm not sure why my name is showing up QTK98....that's my screen name, but  
my name is Karen and that's what you can call me.  In any event, I wanted  
to answer a few questions that you put out there with regards to my response 
on  transplants.  My doctor and I did talk about doing a DLI, which is a 
donor  lymphocytes infusion, however my donor cells depleted so quickly that 
by the  time we actually realized it, another transplant was the better 
chance for a  successful graft.  However, that did not happen.  We had enough  
frozen stem cells to do another transplant, so that is what we chose to  do.  
That answers your question...i.e., bone marrow or stem cells.   Both my 
transplants were non-myloablative stem cell transplants.
 
One of the conditioning drugs used in my second  transplant was Campath, 
which did depleat my T-cells and that was the  reason for all the problems 
with the virus and pneumonia post second  transplant.  I had no GVHD after my 
first transplant, which probably was  another sign that things were not going 
to work, since all the doctors I talk  with say that a little GVHD is 
good.....it's the key to a successful  graft.
 
I did not have a kidney transplant, in fact when I responded to Susan's  
post on transplants, I thought she was looking for people with CML who had  
transplants, however she wanted to see if anyone with CML had a kidney  
transplant.  In any event I am happy to say I have not had any other  problems 
"organ" wise with this CML nightmare I've been dealing with over the  last 
year, however the drug I'm on right now for the virus can cause significant  
problems with the kidneys, so I really pray that I don't encounter more 
problems  thru this all.
 
It sounds like you have been thru alot, but I'm very happy to hear that  
your transplant has worked for 22+ years....and I'm sure you will see many  
more years to come.  I will check out the CML2 group and I wish for  you 18's 
also.
 
Karen

-- 
[CMLHope]
A support group of http://cmlhope.com
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