I wish I had the good news that all is well and in hand after almost a year 
at taking TKI - Gleevec and Dasatinib for my CML. But, my genetics results 
today -.63 meant no cytogenic recovery of -2.00 or the molecular at -4.00. 
My doctor informed me I was 'unique'... not quite the time you want to be 
unique as I continue to fail on the treatments and she does not think other 
medications will work. I do not have any mutations based on the test 
results. So, I was screened today for a BMT and have contacted my bothers 
and sisters for a donor.. I need to send their contact information to the 
BMT Coordinator tomorrow.  I had to phone both my sisters and both brothers 
(I was very nervous asking them) if they would be willing. I am so 
fortunate to have such a wonderful family as they all consented to be 
tested. It will take the next 5-6 weeks to find a donor and move towards 
the next step. In the meantime I am at 20 mg of Diasanib every second day 
and to only stop the medication if my blood levels become severely rather 
than mildly or moderately low. So, I will be working at home if possible 
during these periods of low counts (especially the neutraphils) periods. 

 I know this can be great news as a BMT may be a cure. But, I also am very 
anxious as I know this is quite the process and can be high risk. I don't 
know of anyone who has had a Bone Marrow Transplant and any responses to 
others experiences and thoughts are appreciated.

Hope all of you are doing well.

Mar

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