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My name is and I live in Elk Grove, CA. I just came upon this

site when I was searching for support groups. I was diagnosed with

Lupus/RA almost one year ago, and still have not fully accepted

what's happened!! For me, my problems began following a car accident

in 2002. Since then there has been many doctors appointments going

back and forth over symptoms, aches and pains, tests, and xrays.

Once diagnosed, I was put on plaquenil, bextra, and elavil. It seemed

to be working pretty well for me until about 3 months ago, when I

started working. Then the pain came back with a vengence. Last

week, I was put on methotrexate, which I took for the first time a

week ago. I take my next dose tomorrow night. I don't know if it'll

help or not, and it sure makes me feel awful. I have a very

supportive husband and two young sons (7 & 5). I feel like I am

letting them down. My mom, who suffers from fibromyalgia, was pretty

helpful for awhile, but recently has not been too supportive. She is

not happy that my doctor and I decided to try methotrexate and is now

telling me that I'm behaving like a victim and that I don't care

about my family. It's putting more stress on an already stressful

situation, and I'm running out of places to turn. I was so excited to

find a website devoted to lupus and support, it may just be exactly

what I need!!

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