I live in Central Oregon and finally after 3 years my Dr. sent me to the Fibromyalgia Rhumatology Dept at OHSU
in Portland, OR as I wanted to see a well known Rhumatologist to diagnosis me for my SS Claim started in
Aug 2007 and now waiting for a hearing.
To my surprise, after my long painful trip to Portland, they assigned me to a MD without me knowing it. She
did diagnosis me but I feel as though her report in my file is either missing information about my condition or
is making light of it. I am mostly bedbound. I Female, Age 53 and I am in bad shape. I cannot drive anymore so a friend took me.
Even the ride there caused me a lot of pain and I was a mess once I got there having to sit in brutal stiff
waiting room chairs for 3 hours.
I'm just wondering - does anyone think I should write to her so she can fill in the missing or wrong info?
Also in a section of her report "Document for primary DX" (I'm assuming doctor)
she wrote under "Question" Inj/III/Acci and "Answer" Illness 
Does anyone know what this means?
about SS Disability. I am freaked out as I haven't worked since 2006 AND I'M RUNNING OUT OF MONEY. No one
can care for me or care for me financially. I have always lived well, had great paying jobs and the fact that
I can no longer care for my self even financially, is frightening. Does anyone have any suggestions for me for
when I run out of money? My medical insurance is $575 a month alone. So I will also have to drop my
insurance coverage. I never knew my life would come down to this.