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Found 3 results

  1. Hi guys, I only recently found out about HPPD after googling these symptoms ive had for a while after my first acid trip: Up until this point I had only ever smoked weed, did mdma regularly and tried a very low dose of psilocibin mushrooms, I decided to try acid next so I bought and tested a couple of 100μg tabs and planned to take one after work one day. So the trip went fine, i was a little overwhelmed but overall it was a good experience and i planned to do it again soon with my girlfriend until I noticed slight visual hallucinations when I was sober. I thought nothing of it and that it would go away in a few days, well here I am 3 months later lol. I experience most of the general visual effects people describe e.g. visual snow, trails behind moving objects and objects changing color/shape, but mostly breathing/undulating walls/objects. If I stop concentrating on something for 1 second the room surrounding me begins to close in, and wont stop until I look at something else. This makes it very difficult to watch tv or relax in general and im kinda freaking out haha. Also, Ive just completed my exams at school but im afraid i will have failed them the symptoms became much more serious in the exam room and it was hard to concentrate. Also, the effects become much more prevolent when using weed, and the visuals are almost indistinguishable from LSD when using mdma. Thanks for reading guys hope you can provide some insight
  2. 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 now agitated and overwhelmed by all sorts of visual stimuli, most notably unnatural lighting that I encounter in the evening (i.e. all forms of indoor lighting, car headlights, porchlights etc). Also, as crazy as it may sound, my brain is often extremely agitated and distracted by shadows that are created by such lights...things that my brain would have formerly subconsciously filtered out. For instance, an overhead fan with a light behind it will drive me absolutely crazy. I also have issues during daytime hours, though not as intensely, as I am also now more sensitive to brightness from the sun (as well as daytime shadows). When I am in the throes of my "symptoms", my experience ranges from mild agitation to literally feeling like my brain is on fire and in desperate need of someone popping my skull open to dump ice water onto it. This latter feeling generally arises from prolonged exposure, for instance a situation where I cannot just go take a shower to calm my brain down or lie down in a dark room for a while. I don't know if the condition I have is precisely HPPD, as I do not experience visual snow, halos, trailers, or any of the other "common symptoms" I have seen listed under diagnosis criteria for HPPD. However, I keep coming back to this forum and other websites related to HPPD because I have had a persisting sensory condition that was (however predisposed I may have been) either caused or multiplied a hundred times by taking a psychedelic drug. To wrap up with a few other details: I have suffered from Depersonalization Disorder since my senior year of high school (that I am certain was triggered or at least exacerbated by marijuana use). I have not taken any psychedelic drugs since my LSD experience, and have not smoked pot in about 7 years as it makes all of my symptoms much worse. I mostly try to sleep and exercise consistently to help me battle my problems. I have been to several people for help. A neurologist told me frankly that he understood in theory what I was saying, but had no idea what to do. I was later prescribed Xanax by a psychiatrist. It has helped me quite a bit and I generally take it at night time when my symptoms hit at their worst. I do hope to get off of it someday soon because of the zombie-ish feeling it can create. But for now, I much prefer it to the suffering I endure without it. I have been disciplined and have not upped my Xanax dosage during the 2 1/2 years I have been taking it. I believe that the condition I deal with might line up more closely with some of the sensory overload issues faced by MS or Autistic patients. It might very well be that certain receptors were overstimulated during my LSD experience and now my GABA production has been permanently affected. This would explain why taking a Benzo, like Xanax, temporarily makes me feel better. Drinking alcohol, though I don't often engage in it, has a slightly similar calming effect. If anyone has any thoughts, I would greatly appreciate hearing them. I am quite desperate, to be frank, and am open to all suggestions. N-Met is a product I have seen marketed for sensory overload sufferers, as well as GABA Calm. Keppra intrigues me as well because of it's work on GABA receptors, though I am a bit nervous about trying an anti-convulsant. I have also considered meeting with an Occupational Therapist, or a hypnotist. Thanks everyone! DJ
  3. I understand the relief Benzo's allow when it comes to HPPD symptoms, including obviously the reduction in anxiety and its related symptoms. I am also aware that these drugs can help you to not care or notice the visual disturbances that can sometimes deeply agonise a HPPD sufferer. But has anyone experienced an actual full or even part recovery from any Visual symptoms?