Hello Jody:
Sorry about your son having CML, I have been around a long 
time with it.  I never had been lucky enough to get into 
remission, about twice a year for 35 years I have taken 
drugs to get WBC under control.  My doc would allow 
my WBC to run up to 100,000 before he started Myleran,
I would take it until my counts went down to around 20,000
the residual effect would then come into play. I would then
go about my life until I reached 100,000 or there about again.
Then we would start all over, all along I felt good never a
sick.The reason for the drug Myleran, was that there was no
other drug available, mind you this was a long time ago
and CML was not around as much.  So no one had 
the experience they have the last 15 or 20 years.   About 
5 years ago I started in the Nibs (imatnib, dasatinib, nilotinib)
one after the other failed.  I feel great tho so I would do not
worry , there are so many drugs coming down the pike
 for CML maybe even a cure.Here is an article from the QE2 foundation
raising funds maybe it will help to ease your fears. I hope it does?
http://www.qe2foundation.com/en/home/stories/patientsuccess/stewartduffie.aspx

  


________________________________
 From: Jody <[email protected]>
To: [email protected] 
Sent:Saturday, June 16, 2012 8:07:28 AM
Subject:[CMLHope] For Kelly
 

Hi Kelly
 
My son was diagnosed with CML 3 years ago He goes to Dana Farber in Boston and 
still is not in remission. He is on Sprycel. I am wondering how long was it  
before you went into remission? I am concerned that after 3 years he should be! 
 
Does anyone out there go to Dana Farber??
 
Thanks
Jody 
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