Ink

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?