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Rha and Lupus

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I've been a member for awile but never really was . I would look here

but never did participate. I found out that I need to stay connected to

others with the same medical and life situations. so, here I am . I

live in sw ny state where my Rhumey is at least 50 miles away and in

the winter, I never can get there so, basically for the last month or

two I'm w/o meds. I've been on so many and the only two that work is

celebrex and I did start Remicade treatments which worked , up till I

couldn't get there . I'm on a mission to get a rhumatologist in my town

one way or another. It's not a small place and hard for me to believe

that there aren't alot of others around here who need one , too. Anyone

have any ideas where to start ? or any ideas on what I can do for pain

and my hands are terrible with swollen knuckles and feet . I'm just so

tired all the time and it's affecting everything I try to do.

Thanks

Debbie in NY

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