Ink Posted January 11, 2011 Report Share Posted January 11, 2011 I've had HPPD for over three years now. During the winters it seems to flare up. Since day one I've wanted a support group for people to talk and share about their experiances with hppd. I read on the forums about the whole skype session idea, I think its a great one if a bunch of people would like to get together for it! Quick question for you guys too...Have you ever met someone else with HPPD? Link to comment Share on other sites More sharing options...
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