Greetings,
I have not been active on the list for the last several months, and
reading again, I notice lots of new names. I hope the "old folks"
like me are still around and doing well...
I just had to post to tell you today is the 10th anniversary of my
diagnosis with CML, and the 5th anniversary of my first dose of
Gleevec. Needless to say I am a much happier camper the last five
years than the four years before that when I was taking large doses
of Interferon. My PCR alternates between negative and barely
positive, so I'm doing well. For those of you newly diagnosed, take
heart!
To celebrate, I have formed a team ("Team Ten Years') to do the LLS'
Light the Night Walk here in Seattle on September 17. I'm the VP of
the Board of Trustees for the Washington/Alaska Chapter. The LLS was
and is a major funder of Dr. Druker's research, so I believe in what
they do whole heartedly. I welcome any and all contributions to the
effort. My fundraising page is
http://www.active.com/donate/ltnWA-AK/ltnGraham5
Blessings and good health to you all
Jane Graham
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