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Found 20 results

  1. This is interesting.... Was browsing some medical things today and came across this med that came out recently. It made me think it may be beneficial to this underserved area due to its unique mechanism of action. It's essentially an add on antipsychotic BUT it doesn't work like any other antipsychotic on the market. It targets 5HT2A almost exclusively as an inverse agonist and to a much lower extent at 5HT2C. You guys probably know that LSD, psychedelics, ect, target 5HT2A as an agonist, this is essentially a down regulator at that site in other words calming overexcitab
  2. 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 onlin
  3. I recently developed HPPD and have had a ton of trouble sleeping, so my doctor recommended I try a dosage of one 3.5 mg Zopiclone tablet per night. For the first time in a couple weeks or so I managed to get more than 3-5 hours of sleep (got around 9 hours of sleep) and felt refreshed the next day; the next night went smoothly as well. However I can notice my visual symptoms feel worse than usual. I was wondering if there are others on here that have had similar experiences. Should I stop taking the prescription altogether? Is there any conflicting side effects known with HPPD and Zopiclone th
  4. Im wondering on your experience with oxycodone and hppd specifically your visuals.
  5. Im wondering on your experience with oxycodone and hppd specifically your visuals.
  6. Hello i was recently prescribed soma (carisoprodol) for my back pain, i was wondering how it affected your visuals as i'm contemplating on taking it. A little background is that my hppd is super mild, i've only had it for around a month, i barely get after images and i get slight tracers which are not noticeable too much during the day but get slightly worse at night when bright objects move past my field of view eg. a phone screen. Also i can take benzodiazepines like diazepam and gabaergics like gabapentin without a change in any visuals. thank you for reading and i'm looking forward to
  7. Hello i was recently prescribed soma (carisoprodol) for my back pain, i was wondering how it affected your visuals as i'm contemplating on taking it. A little background is that my hppd is super mild, i've only had it for around a month, i barely get after images and i get slight tracers which are not noticeable too much during the day but get slightly worse at night when bright objects move past my field of view eg. a phone screen. Also i can take benzodiazepines like diazepam and gabaergics like gabapentin without a change in any visuals. thank you for reading and i'm looking forward to you
  8. "BPC-157 is a synthetic peptide that is being investigated for its regenerative effects. It shows high efficacy for rats suffering toxic or surgical trauma, but there is currently no evidence that it provides benefits for people." I stumbled upon this peptide after browsing some websites and then I found reddit posts of users claiming that they cured their anhedonia. This substance does not mask symptoms like traditional drugs, but really has some sort of a healing mechanism that rapidly undoes damage from the dopamine system, with almost no side effects reported. This got my interest and
  9. I have had HPPD for about four months now. I know it's not a very long time for how long it can last but, it's so awful living with this every day. The only way I'm personally able to describe it is that the air around me is suffocating, like a have no space in an empty room filled with breathing walls, visual snow, static or tiny patterns. Another thing I have is very bad depersonalization and it's the whole reason why my anxiety comes out like it does. Before I had HPPD I have only had an anxiety attack 3-4 times but now I get one almost every other day and it's so hard to manage hanging ou
  10. My psych agreed to start me on clonidine, saying that there's at least anecdotal reports of it easing HPPD symptoms. Has anyone had success with it?
  11. For those of you who have tried SSRI's have they increased your visual symptoms or decreased them? Or had no apparent effect? I'm considering changing my medication since it seems like a lot of people are saying SSRI's make HPPD worse. Also if it is making my symptoms worse should they return to a baseline when I go off them? I went on the ssri around the same time my HPPd symtoms began so it's my hope that they might die down a bit if I discontinue the drugs. Currently on 20mg lexapro
  12. Hi everyone, Thanks for your time to anyone who is reading this. I have aways been a "sensory sensitive" person (i.e. only kid on a youth soccer team to have to wear sunglass sports goggles). I took LSD (one time only) during the summer after I graduated from college in 2006. Upon waking up the next morning (after little sleep lol) and getting my day started, it was overwhelmingly evident that something in my brain had changed. I have for the 8 years since then been dealing with a variety of extremely bothersome, what I would describe as, visual sensory overload issues. My brain is n
  13. Hey all! I'm still searching for a medication to treat my anxiety problems that won't simultaneously aggravate my HPPD. As many of you know, that is one tough nut to crack. My immediate thoughts: SSRIs: Seem somewhat effective for my anxiety. Aggravates visuals, had to discontinue. At least HPPD symptoms returned to ''baseline'' upon discontinuation. Benzodiazepines: Greatly attenuates my anxiety (particularly etizolam and clonazepam) and helps HPPD symptoms as well (particularly clonazepam). Very addictive, not a long term solution. I build tolerance to benzodiazepines pretty quickly. Busp
  14. hey guys, im new here, so i have been suffering from this thing for about 2 months now, but i actually don't know what it is ? whether DP/DR ? or HPPD ? or something else. i got all this from smoking weed, out of a printing paper (A4). havent touched LSD, MDMA etc ever. ohh!, and i never had that 'i am going to die feeling, when i was high'. and i believe i have a bit of social anxiety. i'm a 22 year old male, with no history of mental illnesses. here is what i have:- visual snow (mostly in darkness and dim lights) very sensitive to all kinds of light. (even sunlight) very inte
  15. need help asap please! i nearly committed suicide the other day and would really appreciate if anyone could help me in finding a doctor that understands hppd in my area. I live in Tacoma, WA, USA, which is about 30 miles south of Seattle, WA. I just want to be better so i can finally have the confidence to meet a girl and to love as well as my lifelong dream to pursue a career as a piano composer. I am 18 years old now and have had it since i was 16 (September 2, 2012)- yes i remember the exact date because since then it has been a living nightmare. Ever since I developed HPPD I have had Const
  16. I'm sure there has to be a thread for this somewhere but I couldn't seem to find any info so if a thread already exists please let me know. I understand recreational drugs can make HPPD worse, permanently in some circumstances. And as we all know alcohol and caffeine can affect it as well. My question is, are there any prescription meds known to worsen HPPD, particularly, meds that don't have a strong psychoactive component and aren't typically associated with neurological side effects? The reason I ask is because I take a TNF-inhibitor for severe arthritis, which can make me drowsy for
  17. I have a huge problem, my neurologist won't subscribe me keppra. I explained her about HPPD but I'm not good of a talker.. I used to be very social but now i suffer from HPPD I'm not that smooth anymore. She said she could only help me with issues in the form of neurology, like migraine. She also said I probably have to go to a psychiatrist with my hppd What do I have to do to get keppra from a neurologist / doctor / psychiatrist? Please, I need advice!
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