I appreciate everyone's thoughts and opinions on the subject of gleevec vs. transplant. I was diagnosed with CML about three weeks ago. Luckily, I caught it in the very early stages, so I have time to figure out my treatment plan. Yesterday I met with a bmt specialist at Fred Hutch, and next week I have an appointment with Dr. Druker. I am very torn on the subject of gleevec vs. transplant because I am young (26), otherwise healthy, and in the early stages of the disease. I want to rid my body of this completely, but at the same time I don't want to destroy my chances of having children down the road due to a transplant, along with the other complications related to the transplant.
I am new to this group, and would appreciate hearing how others have dealt with this same conflict. I have been feeling really positive since my diagnosis because I have received such a huge amount of support from friends and family. But I think the reality of the decision I am faced with about treatment finally caught up with me yesterday and it is really tough.
Thank you,
Meghann
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