I thought I was alone in my strange neurological symptoms until I discovered APS Foundation of America, Inc. website. Visit forum at www.apsforum.com.
The Faces of APS:
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Posted on YouTube by Scott Whitney
APS Awareness Month is in June
Lupus and Cellcept: Slowly Tapering My Way Down
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Gosh - I've been delinquent in celebrating my medication victories over
here!
Every step you make toward living well with lupus is worth rejoicing over -...
4 weeks ago



