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    • By jacob
      i can either tell my parents my brother has hppd or i can tell the me had a flashback whats better?
    • By Psycho
      Hey guys, i'm 18years, HPPD since 16y later drug abuses. My life completely changed with this. I never stopped with the drugs, i Smoke weed Every day... Yes, My life is a madness, but if isn't easy with drugs, imagine without drugs... The most important is = ever try to be happy...
    • By jacob
      The story starts a month ago when my brother visited tulum for the weekend he took 1/4 of a 1200micrograms rick and morty lsd, since then he was different, one weak ago were hitting the bong and suddenly he had a psychedelic trip and it seemed like the one he had 3 weeks before when we dropped acid so any way he got on a bad trip and told me that it felt like an lsd bad trip just by smoking weed, the trip that lasted 2 days then he came down. now he's always paranoid i cant talk to him for longer than 5 min. my question is should i be worried? and how could i help him? how should i treat him?
    • By HDDeer
      Do you think we will or maybe some of us will get answers to this one day? I feel like not enough people know of it to consider trying to help us, especially now that Dr. Abraham is retired. I just want answers. I know the terminology drug induced psychosis is something that gets tossed around a lot which, maybe we have it all mixed up.
      Some claim damage to gaba receptors, which also doesn't make much sense to me considering there have been the odd case where people have cured their hppd with psychedelics.
      Why do some get rid of theirs using meds like lamotrigine and keppra, and others dont find success in meds at all.
      Im sure when RC's become more common, thats when more people will end up with it. Anyways, 11 months tomorrow with no end in sight, good times ahead. 
    • By SeekingLife
      Hey all, been a bit since I've posted here. I've been holding up well, and even though I get the occasional DP/DR, I'm managing. I'm heading back to school real soon, and was wondering if anyone had any experience with non-stim ADD meds. Used to take Adderall, but had some really bad DP/DR the day after, and have read that in general stims are not great for HPPD. Doc just prescribed me some Intuniv ER (Guanfacine HCL ER) and said it should kick in after a couple weeks. I'm worried if I should even start taking it though, and pretty much no one has any input on non-stim ADD meds with HPPD online. If anyone's had some firsthand experience, or even some scientific as to why it should/shouldn't make my HPPD worse, I'd greatly appreciate it