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Hello, I found this site searching for neurosarcoidosis. I was

diagnosed 5 years ago and felt very alone. No one seems to know much

about it. I'm glad to see there are people that can relate. I have

tried most of the normal drugs -prednisone, imuran, methotrexate, and

still have growth. My doc wants me to try humira (he did mention

remicade) but my insurance won't pay because its experimental for

sarcoidosis. I'm starting to have symptoms such as loss of balance

and weaknes on my right side. It just isn't fair that insurance

denies you something you need. Well, thanks for letting me complain.

Angie

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