I was wondering how many of you are on some sort of disability for the CML. I was diagnosed at the beginning of October. I took a few weeks off of work and started back at 2 days per week, then upped to three days....6 hours per day. I am totally wiped after my work days and have lots of bone pain and exhaustion. My doctor said he'd sign my disability papers from work if I wanted him to (we have long term disability). I was just wondering how many of you are out of work because of this desease and the pills side effects.
Thank you,
Alicia
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