Pat, thank you for this information, it's going to be very  helpful.  A 
good friend of mine lives in Cave Creek, AZ.
 
Greenie
Ft. Myers, FL.
 
 
In a message dated 3/12/2012 2:08:23 P.M. Eastern Daylight Time,  
[email protected] writes:

There  are several reasons for a loss of response, your physician will
need to  order testing to determine if there is a gene mutation. In the
meantime,  education on current CML options can help ease your mind.
This is also a  topic we all need to think about and a key reason why
the National CML  Society and Patient Power have teamed up to bring
current clinical  information from the country's top experts directly
to patients through  video interviews. Please see what Dr. Michael
Mauro from OHSU has to say,  from ASH 2011, in this interview:
Considering Your Treatment Options to  Better Manage  CML
http://www.patientpower.info/video/considering-your-treatment-options-to-bet
ter-manage-cml

There  are additional interviews on Patient Power  from ASH on the
three FDA  approved drugs and the two additonal drugs now in clinical
trials and  showing very positive results for those dealing with loss
of response. In  short, there are more options than ever before for us
and many reasons to  be optimistic!

Hope this is helpful!

Pat Elliott
Phoenix,  Arizona

On Mar 12, 10:54 am, skink1100 <[email protected]>  wrote:
> I have had cml for nearly 10 years.  For several years I  was at the
> not detectable level in my pcr tests.  Last year the  gleevec seemed to
> no longer be as effective...and my doctor switched  me to
> sprycel...about 4 months ago...my results continue to  decline,
> although my blood looks ok.  Has anyone had a  similar
> experience...could it be a new mutation?  Where does on  go from
> here...getting worried.

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