Guest guest Posted January 20, 2002 Report Share Posted January 20, 2002 I deal with the RP by taking my meds regularly, seeing my doctors regularly and trying not to push myself when I'm exhausted. With the exception of getting more rest, I am carrying on with my life (or trying to) as I did before I was diagnosed. I read everything I can find that relates to RP, although I must confess that I find most information on autoimmune diseases terribly complex and confusing. Some of the best information I've received has been right here with this group. The worst part for me is the lack of energy and complete exhaustion I feel from time to time. Quote Link to comment Share on other sites More sharing options...
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