I was placed on long term disability through my work place in Jan. I also had to apply for SS which was turned down once. I am in the appeal process now. My long term disability required me to apply and they take out so much money each month that they say SS owes me. Once all is said and done if SS turns me down twice then the disability company goes back and pays me all they have taken out. I just could not continue to work. I was tired all the time, pain in joints, pain in legs, muscle spasms so bad i would double up in pain. I was dx in June 2004 and continue to experience most of the yucky side effects. My doc is on top of the side effects and they are mostly managed by other meds'. On the good side my last BMB showed 1 in 20 cells still positive which was better then the 98% at dx. It took me until Sept this year to get to the point I am at now.
Suzan
"[EMAIL PROTECTED]" <[EMAIL PROTECTED]> wrote:
"[EMAIL PROTECTED]" <[EMAIL PROTECTED]> wrote:
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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