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Found 132 results

  1. My doctor prescribed me 0.5 mg of klonopin to take when needed, how should i take it so it reduces visuals.
  2. This is mainly to the newcomers like myself. For those of you just entering your days of hppd, take it from someone who also hasnt had it for very long, ive only had it for 3 months. The first month to months could very well be a hellish ride straight to satans throne. But one thing id tell you is to not lose hope, insert yourself into discussions with friends and on forums(not just about hppd but anything) take some recommended vitamins like vitamin d3 and b complex and magnesium, get a therapist you can talk to and stay active, all these things will help you get better. While my visual symptoms have not subsided, my physical symptoms on the other hand have. Ive always had social anxiety tho, so for the most part i would say i definitely feel like myself again. I attempted suicide in my first month and its now my third month and im so glad i never did. If theres three things of most importance i could tell you to do 1. Acceptance(accept this is your life as of right now, you cant dwell on the fact you MIGHT have this for the rest of your life because you also MIGHT NOT. My girlfriend told me i just need to take it one day at a time, we live day by day not month by month or day by month, you dont know if youll have this tomorrow or a month from now or a year, which leads to my second) 2. Never give up hope (Accepting that you have it in my opinion is a great step to recovery. But also being hopeful in the possibility of recovery is very important) Acceptance and being positive/hopeful are two great things to feel towards hppd. Its at that point imo you can feel true improvement and recovery. 3. CEASE ALL DRUGS. I cant stress that one enough, let your brain rest. Those in my opinion are the three best things to do when faced with hppd. Granted i may have it milder than a lot of hppders but i do want you guys to know i havent smoked or dosed since the onset, i drank maybe 3 or 4 times(avoid that too if you can) i also have a foot injury right now but most of my improvement came when i was going to the gym and running and sweating like a dog. Hppd isnt the end, but in a lot of ways its an eye opener.
  3. Here is the article that appeared as a book chapter. I am sharing it for the purpose of academic and general research for the benefit of the human condition. I do not want to give away the details that I will present, but I will be giving a critical analysis of it, which can have good and bad points. My video review will be part of the series of videos I will provide that will cost a nominal fee per viewing (for the first 6 months or so, and then it can be open to everyone.) However, it takes a lot of work to create, read, pay for the articles, student loans and put together the content so I have to stop feeling guilty for asking for money. This one is free, but as I discussed on the Facebook HPPD and DP/DR group, I will be returning to research and providing research reviews on my youtube channel, opportunities for individuals to learn research methods as a lay person or for work to design and receive funding for their own or co-designed research. If you have issues with the article, good, bad, in between you are encouraged to try and work through reading a research article and make notes either publicly or for yourself. I will go through it from a unique perspective. Even the general emotion it gives you. You get to be the judges. - David Kozin THE LINK IS BELOW: A copy will also be placed in the section for documents also. Current Topics in Behavioral Neurosciences pp 1-28 (2).pdf
  4. I hope people take the time to read this and believe what I am saying because everyone I talk to about this problem does not believe me. I am writing this now because I have had suicidal thoughts recently and need to make a change in my life. My suicidal thoughts are pretty bad. I plan on seeing a therapist this week. When I first started high school in 2008 (9 years ago) I smoked weed once. Just one time. My friends who smoked the same weed were stoners and they recovered the next day like 99% of people do. But I smoked a lot and I had HPPD for about 4 months. I had tingly feeling in my feet and panic attacks everyday. This is when I just started high school where I knew no one and I am a shy introvert. It was absolute hell. I felt alone and scared everyday. But I got through it!!!! And all the symptoms went away like I said in about 4 months. I felt 100% fine. So over a year later I am working out one day and I sit down and my HPPD symptoms came back. ALL of them !!!! But they quickly went away in a few hours. And since then every time I work out (lift weights especially) my HPPD symptoms come back. Please believe me when I say this!!! My mom does not believe me and no one else does. What the fuck is wrong with me. I smoked weed once and now every time I work out I feel HPPD all over again. I have not heard anyone else have this experience before and I have obviously done a lot of research into this. Okay so I lived with the fact that I cant work out for years. I just quit working out-whatever I felt 100% fine just kinda pissed that I could not do it. But this past December I was very upset over things in my life.(Could not get a good job, girl I like a lot has a boyfriend, feel like I have zero friends, lonely) I was so mad that I just started working out. I would wake up and work out and work out some more. I knew that HPPD could come back but I was so sad and wanted my depressed feelings to go away. So now My life is terrible. It is June now and I have not worked out like that for 6 months. But Since that time I have extremly bad visual symptoms of HPPD. They include: -afterimages (These are the worst, get them after looking at something for a second.) -trails, I can see trail when things are moving. For example, if I move my hand across my face. -anixiety, can feel my heart beating at times, feel like I have no personality, feel alone and depressed -tingily feeling in my feet (This feeling gets worse if I work out at all) I love to run but I cant now, makes it worse -floaters all the time, especially outside. -vision makes a huge adjustment from going to light to dark places I seriously can not even go on a 15 minute run right now? If I do , my feet become tingily. What the fuck is wrong with me? No one else with hppd from what I have read has this? I smoked weed once and now I can not work out for the rest of life? What the fuck? This has caused me to have a terrible relationship with GOD. Why would he put this on this earth for me to use? Why would he make me this way? I love working out and want to have a great body but I cant because I smoked weed one. I want a six pack. I am a motivated and focused person. How does this happen when I smoke weed once. I can understand if you take LSD a ton of times, maybe this would happen. One thing that i keep thinking about is the time before I smoked weed once (in 2008) I want to go back to that time and not smoke obviously. I think about that sometimes, makes me feel very regretful. How do i deserve this? I literally smoked weed one time and this is my life. These visual problems are ruining my life. I accepted a job that begins in January and I am considering turning it down now because the job will require me to work 60 hours a week staring at a computer. This a dream job at one of the best companies in the USA to work for. I worked my ass off in college (Magna Cum Laude, graduated in top 15% of my class, made dean or presidents list every semester) And now I get this dream offer and I am afraid to take it because of anxiety I have from HPPD? From smoking weed one fucking time? God What do you want from me? I feel so sad and upset all the time because I have this disorder. I feel so alone. I wish I had cancer instead of this, that would be a piece of cake to deal with compared to this. No one I know can fucking relate to how I feel. That is why I am thinking about suicide. I know that neither of my parents had this disorder or my sister. They have all done drugs and been fine. I must say though that depression runs in my family. My dad has tried to commit suicide multiple times and so have my cousin and uncle. I just found out this information recently. I have seen that fasting can have some affect on the disorder. I have been considering fasting for a couple weeks to see what it does but I have a full time job now, no way I can function without eating food for days on end. I dont know what to do?? Can someone please help me, Make me feel better? I DONT DESERVE THIS. I literally smoked weed one time. God I feel so alone. Will appreciate any feedback. I hope you guys can believe me. Want to make this absolutely clear: I have not done any other drugs besides smoking weed once. I dont even drink alcohol now, (not that it makes my hppd worse but it is just not my thing) I have not done acid or shrooms or anything like that. Nothing.
  5. hppd

    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 out with people in fear that I will start freaking out of no where and have to be alone. Usually when I am inside of an attack everything is so colorful and it looks like I'm on mixtures of drugs and it can last anywhere from a couple of seconds to an hour or 2. The only thing I like so far about this whole situation is that I've been able to find myself through art. I've found that if I'm feeling anxious I can just draw something and it will really help me forget. Everyone always tells me that they like the things I do and how they love that I found a unique style that belongs to me. I'm very happy that those people are supporting me even though I still wish I hadn't done the things I did to get this way. It all started when I did 3 psychedelics in over the corse of 8 days including: LSD, LSA and DXM. It took a while for my symptoms to come through but I can tell that all 3 of these drugs made a huge difference in my life because I feel the things I felt to this day when I was in all of those trips. I have been on a few medications so far to help the visuals and depersonalization. Including Prozac, Busbar, Abilify and Gabapentin. All of these drugs made things worse for me and I wish I never took any of them. Except for Gabapentin because I have a feeling it might work in a higher dosage. I have talked to my psychiatrist about HPPD and she had no clue what it was and didn't seem interested. She just jumped the gun on antipsychotics and labeled me as "psychotic" (because she's an asshole) I've done enough research to know that only in very small cases do antipsychotics help HPPD because it isn't the same thing as Psychosis at all. In my research ive found that Primarily benzos including Klonopin, Valium and Xanax work the best for depersonalization and visuals. And levetiracetam has been able to just help visuals. I really want to find a psychiatrist who understands instead of one who asks me if Acid and LSA are both LSD. I need someone who actually knows about drugs but my mother won't let me switch. Is there anyway that I can get her to understand or believe me and get me the medications I need without seeming like I'm pharma-shopping?
  6. Hello everyone, my name is Matt. I'm a student and I also work alot alongside school. I have experimented with a lot of drugs in the past and have developed considerably difficult anxiety and what I think could be HPPD. This has an effect on my life, work and school. I never had any problems with my drug usage until after I saw one of my best friend leap over a balcony during a mushroom trip. My visual symptoms are tracers, after-images, halos, also got tinnitus (although that was caused by a fireworks accident) but has been excacerbated by what I think is HPPD. My eyes are very sensitive to bright lights and I see bright flashes when staring at something bright, like the sky or my computer screen. I really want some answers because this is pretty frightening for me. I'm pretty much always anxious from day to day, and I was wondering if anxiety could make HPPD symptoms worse. I have researched a lot about these disorders but there isnt alot about HPPD anywhere. So I ask you, anxiety and HPPD = worse symptoms? Thanks in advance, any help is immensely appreciated!
  7. Hello All! My name is Victoria. For the last, about 2 years now, I have been experiencing persisting visual disturbances daily. These vision issues include staticy vision, trails, depth perception issues, light sensitivity, inability to focus. They used to calm down when I rested (I take almost daily naps because of this), but now it doesn't really seem to go away much. I have experimented with a lot of drugs. To be honest, in the past few years though, it has only really been MDMA. Lots of MDMA. I haven't really done much in a while though. One pill in February, and not really anything since last year. I hardly even smoke weed anymore. I feel like somehow the symptoms are getting worse and I am not doing anything anymore. I have been to an optometrist, optamologist, I am getting an MRI of my brain done to see if there is any scarring on my brain. I also now experience migraines. I had a substance abuse issue about 7 years ago and when I ended those days I recovered almost fully. A couple years after that, I would randomly dabble in stuff, but not that often and I never had these issues unless I was super anxious. Now this is a part of my life now. No one can tell me what's going on as everything about me shows perfectly healthy everywhere. I have tinted glasses that really help with the light sensitivity at work, but will this ever go away? Just to clarify, this didn't begin after a particular trip. I recognized these visual disturbances as something I would experience during high points of anxiety as a result of my previous drug use. About 2 years ago, is when it became a daily almost consistent thing throughout the day. Now it's basically present at all points in time. Just would love to hear from people that may be going through something similar.
  8. Hi everyone, i really dont know how to start and i hope you can excuse any mistakes in language as im from europe and i even have problems using my mother language at the moment due to my mental situation (If you want to skip the detailed story you can scroll down to my current symptoms, which basically began after one weekend of smoking too much weed where i had something like a panic attack while smoking alone.) Maybe i just start with a review of my past two months where my current state began and a little about me and my drug usage. Im 22 years old and started with drinking alcohol with 14 like all my other friends, sure i often drunk too much in the future but only at parties and never drunk alone or had the feeling that i need alcohol, pretty normal i guess. Last year (2016) i started smoking weed (just smoked one time before i was 21 and felt nothing so i had no demand doing it again). Due to new friends and an interest in weed because i found out my father smokes pretty often i started to smoke with friends occasionally and somehow i liked that feeling now. I would even say that after a few times i started to love that feeling. Alcohol was no more fun and i said to myself that its better to smoke sometimes and dont drink anymore except a beer or two sometimes (even my father said that to me). In fall last year i moved from my families house to my own place with a friend. That change in life was awesome i was so motivated, happy and loved the new freedom. Someday i bought my first own weed (maybe because it was possible now to do anything without the parents near) and i couldnt resist trying it out alone. It got more often and between november 2016 and march 2017 i smoked almost everyday i got time but i was still going to work everyday and university (sober). I think it still was a „normal“ amount and sometimes i didnt smoked for 2 weeks or so without a problem. In March a friend of mine died i didnt knew him very good because he lived in another town but somehow it bothered me a lot (dont know if this has something to do with my problem). Smoking weed after this incident was almost the same except that i felt a little tension in my chest and when i tried to sleep it took a while. Then there was the weekend whereupon everything started. On saturday march 25th two friends came over to have a nice evening and smoke some weed. I already worked the whole day and was awake since 5am but i didnt smoked for a week or two so i was excited. It was a great evening but after a while i was really tired and fell asleep for a few minutes when my friends were still there. I got some new weed and they left early like 11pm. I dont know why but instead of going back to bed i smoked another one alone. I felt again an odd tension in my chest and was a bit nervous but after a few hours i fell asleep. The following sunday my girlfriend had no time and i had new weed so the first thing in the morning was smoking again. I smoked three joints over the day i think and felt pretty normal (just normally stoned the whole day). Only in the evening the tension came again but harder this time and there were some „stitches“ in my chest. I was getting nervous but was able to calm down myself. Again it was harder to fall asleep this evening. It was like starting to dream while still awake and realizing it and wake up due to this feeling. The next morning i felt normal again i think and at midday i smoked another one with my flatmate because our internet was broken and we didnt know what to do. Suddenly i felt like being between stoned and sober and i just wanted to be fully sober. Everything felt a bit unreal like a dream somehow and the fact that our internet was not working was strange in my eyes and made me ask myself „is this really happening?“. But i managed to keep calm and said too myself that everything is normal that im just stoned and that i will be sober after a few hours. At the evening the internet suddenly worked again and i felt good again as far as i can remember. But instead of asking myself why i felt so strange and why i had this chest tension and stitches the last days i smoked another joint at this evening. Afterwards i was with a friend on skype playing a videogame when i suddenly had the feeling of getting a heart attack or something i had to lay down and was very anxious (i think this was my first little panic attack). The feeling came like in waves but i was able to calm down myself. It was a strange feeling i felt like not getting enough oxygen in my lungs, couldnt sit still and i just wanted to go outside. I took a walk but back home i didnt felt better. The „getting a heart attack“ feeling came multiple times again. Later it got better somehow and i was able too sleep (its hard to remember details since my memory is one of the main problems now). After this evening everything began and before you ask i never smoked or drank again after this evening (2 months now). The next day i said to my girlfriend that i feel strange somehow but not bad it was a strange feeling in my stomach like being a little sick and nervous. But the day was okay i even was in the city buying some led strips for decoration but when turning them on i realized that it make me feel very sick when the lights were flashing fast. I also got that same sick feeling in my stomach when i tried to focus small text. I thought that this weekend was just too much and its like a small withdrawal. The next they i went to university and in the train i was getting a bit nervous and was glad when i got off but otherwise everything seemed good i could concentrate just like normal. The only thing i noticed was that at midday a had to yawn like every 5 seconds for about an hour and felt a bit light sensitive (but it was one of the first sunny days so i thought my eyes just have to adapt to the new light condition). Back at home i started to feel strange and very nervous again, my heart started to beat very hard and fast and i thought again that i dont get enough oxygen. I went to the hospital because i couldnt calm down. I was so nervous that i was a bit confused, they checked my heart and blood values but everything was fine. After a while i got calm and was glad about the results. I left the hospital and felt pretty okay but was scared to stay alone. The days after i started to feel dizzy and extremely anxious and thought that something really is wrong with me i cried the next days very often for no real reason i felt hopeless and empty (hard to describe that emptiness). I went to my father because i couldnt be alone. At this time i knew something is different and everything felt strange and unreal like a nightmare but i couldnt really describe it and had no idea what was going on. After one week since all started i couldnt focus my eyes on anything for longer than a second and felt like seeing everything with 10 fps also every flickering light made me nervous and feel sick. This got better after a few days but i realized a lot new symptoms which stayed since then. So here is a list of what i noticed after the first strong fear was gone: Visual problems trails but by now only in dawn light condition every light and reflection blinds me and glares, even car, bike or traffic lights at daytime long afterimages of everything, positive and negative lots of grey and normal floaters in every light condition starbursting if the environment is dark around the light sources, gets worse if the light is far away ghosting, especially if its dark and there is white text on dark background everything seems a bit oversaturated at daytime very little static my eyes seem flickering and unsettled the whole time looking at a display is hard feels like looking through a slot or that something semi transparent is diagonal about half the display difficulty to focus my eyes on something for a time longer than a few seconds the feeling that my eyes are to slow if scrolling a website or something sometimes one of my pupils is almost double the size of the other one Other problems tinnitus (had tinnitus on one ear before but now worse and on both ears) constant tension in my whole body sometimes my muscles hurt even without doing sports at the beginning it was very hard to eat constant dizziness not strong but its there everything and everyone seems foreign, especially when looking in someones eyes i feel anxious and sick (maybe dp/dr dont know) cant really sleep, it feels like i instantly start to dream when i close my eyes but never get deep sleep, i wake up every 2 hours and sometimes i cant fall asleep again i feel dumb and cant concentrate at all (brain fog?) it feels like i cant think at all if i want or have to my brain just "does nothing" im really depressed i could cry every second but only because of the thought "you ruined your life, you had everything" no feelings except the one above, i feel like a robot and act the right way only because i know how to but i dont feel it (is this dp?) everything feels like a nightmare sometimes i think im still in my bed and its still march and i hope to wake up, i know this is stupid but im somehow not sure if its not true no sense of time at all, if something happend a second ago and i think about it it feels like it happend years before, i dont have feelings connected to the memories, and they all seem to be far away (anyone know this feeling?) my own thoughts "scare me" and feel also kind of far away, even if i plan to take a shower it feels strange in my head somehow old memories are suddenly in my head even if they happened 15 years ago, they are as clear as things which happened minutes ago, also if i look at something i instantly get a memory in my head which my brain seems to associate with what im seeing (i think this is one of the reasons why i feel like im in a dream and im not in here and now) i see faces and eyes everywhere even without looking for them like my brain searches for them without my control, i see them in trees, walls etc. i can say "its just a tree" and i dont see real faces or eyes but i cant see objects just like they are without my brain starting its rollercoaster drive of thoughts and associations (pareidolia i think but its extreme) i feel like the most important filter in my brain is messed up, in the city i see every reflection, movement etc. also sounds seem louder than before and i cant ignore them (i even hear sounds i didnt heard before, they are real but i think they were filtered out before, maybe hyperacusis) sometimes i think about suicide or behaving strangely and because everything feels unreal and like a dream im scared i will do it, i feel disinhibited somehow i feel like i have forgotten how to think, all i do is associate old memories and compare all the time how things were before 2 months Last week (i think) i found out about HPPD and found many of my symptoms which werent explainable with other disorders, especially those visual problems. I would love to hear some opinions about my symptoms and if they are typically for the HPPD related things like dr/dp, anxiety etc. friends say that i behave just normal only a bit sad and not as happy as before. This is what gives me a little hope because sometimes i thought i become insane. Tanks for reading.
  9. Hello Everyone. In an attempt to get a rough unofficial census as to how many of us there are, I have created a link on the NNRF website that will take the user to a map that serves as a census for HPPD. As stated it is not official but the map servers a variety of functions. 1. It allows us to communicate with one another. 2. It displays our general locations and that of specialists who deal with HPPD. 3. It performs a census (however unofficial) of how many people suffer from this condition 4. The census might serve as a means to get more researchers interested in HPPD To view the map and please do, you may click here: http://www.neurogroup.org/map/hallucinogen-persisting-perception-disorder-worldwide-map/ The more of us that appear, the greater the odds that we may get some much needed attention paid to this disorder. All the best Hope1 *Admin Please Pin and if possible send a mass email blast to all registered users on this site.
  10. I didn't see this anywhere though I may have missed it. Are there any conferences or seminars related to HPPD?
  11. Hi all, 19th of march this year i microdosed 3 tabs of acid(my second time doing lsd) after my trip i had a really bad time(felt like tv shows were attacking my insecurities, felt like something watching me, hallucinating a white demonic looking face in the centre of my eye) that has all subsided now, and i am now left with ghosting, visual snow, afterimages and very minor palinopsia. As far as dp/dr goes i no longer feel like a zombie when im in crowds but as long as ive been alive ive felt numb so i cant say i really "feel" things. Anyways, as far as progress goes im feeling pretty good about it. My paranoia is gone and i dont have a whole lot of anxiety. I do tend to have mood shifts an awful lot(between angry-neutral) ill get jolts of happiness but they never really last. My hppd i fine also comes with a weird type of pareidolia where if i look in my jeans i can see little tiny people with weird faces. I also have the ability to see reptiles and demons if i stare at floor with pattern long enough(which makes my visual snow worse, i think its kinda like colour shifts??) Im definitely open to the idea of being schizophrenic or bipolar(i do believe im bipolar tbh) i saw shadow people on my lsd trip. Anyways recently ive started taking the supplements: NAC OMEGA 3 LIONS MANE L TYROSINE GINKO BILOBA. I am very interested in taking piracetam with choline as ive heard some good things but also some bad. My doctor prescribed me lexapro and seroquel but im not interested in taking those until at least up to or over a year. I will be trying to take keppra or lamotrigine after the 6th month mark. Anyways thats my story for the most part. I look forward to hearing your responses.
  12. So im 17 and summer is coming up in one week. I've had pretty minor hppd for about 8 months, and I just want this to go away. All my friends smoke weed and I feel so left out not smoking with them. This leaves me pondering a crucial question: should I just say fuck it and start blazing again or should I dedicate this summer to recovery and mental growth to see if I can still recover? I just miss smoking so much but if I knew for a fact that I would fully recover in a year I would be willing to not drink or do drugs until months after I am fully recovered. What should I do it's killing me? My symptoms are: visual snow floaters slight trails in some lighting walls breathing if I pay attention color enhancement brain fog
  13. 19 year old male. Have had mild visual snow and other slight visual defects as long as can remember. Since approximately 15 have suffered with short, intense migraines around once every three months (I believe caused by sleep pattern inconsistencies) accompanied with classic visual auras (loss of vision spreading across one eye). Around three months ago I tried mdma for the first time (I trust the source and purity) and have done it twice since. Noticed no significant change after first try (small dose). However, second time (very large dose, between 400 and half a g) I noticed difficulty reading, more visual snow, light flashes etc which peaked about four days after and, for the most part, subsided after three weeks. Third time, medium dose, hppd symptoms have returned, particularly visual snow and small amounts of light flashing. Three weeks on and I fear this may be more long term; however, it is currently not something that is an impediment to my day to day life. Naturally, I am fascinated by what substances have to offer, particularly mdma, but also psychedelics. Questions: 1. have others found that all doses of mdma worsen symptoms; or, can low doses that don't fully overload 5htp receptors be used without damage? 2. I feel that those who have visual auras and migraines are far more likely to develop hppd. Would others say that this is particularly true of mdma? Would I also be more at risk of negative effects from more classic psychedelics such as lsd or shrooms? Obviously I am aware that taking any psychoactive substance is a risk and should not be advised however, I would value some objective input. Essentially, I am asking whether my experiences with hppd from mdma would mean my likelihood of hppd from other drugs is higher? Or are there ways to control dosages to reduce the risks (for example, trying half a tab of acid in isolation and observing symptoms over a couple of months). I am prepared to abstain from serotonergic drugs, however, this would not be a comfortable decision. I am grateful to be in a position where I have the option of avoiding serious long-term damage; however, if anyone thinks there is any chance of me being able to manage usage conservatively I am interested to hear. Thanks P.S I have used DMT twice with no observable hppd
  14. So I got very minor hppd from an acid trip around 8 months ago. After the trip I smoked weed and drank a couple times, then I started noticing static and such in my vision... so I have been clean from all substances for 5 months. The anxiety/ depression is much better, and the visuals are pretty ignorable unless in bad lighting and not very bad. If I continue to be healthy and abstain from drug use, having recently quit nicotine as well, do I still have the possibility of recovering? I've heard plenty of cases of ppl recovering and having visuals go away within 1-2 years and that's what I'm hoping for! Is this a possibility? Hppd is minor and I plan on staying healthy as I am 17 and workout on daily basis
  15. Help! I have a very extreme case of HPPD! It all started when I took LSD for about 3 months ago, I was planning on taking 120ug which is a medium dose, but the tab I bought must have been around 800-1200ug. Some say that's good because, "Hey! More acid for less the price!" but in this case, fuck no. I had the worst experience of my life while never tripped so hard before. It was absolutely terrifying and insane. After that trip I decided, being the stupid 19 year old that I am with bad habits, I dropped acid again after about 1 week. I thought hey, this time it is around 100ug (Some friends did it the night before) and I should have a tolerance against it so the same thing can't happen again, guess what? It happend again! I tripped mega balls on 100ug of LSD, I got an level 4 psychedelic experience out of it, also a badtrip. I've been laying off all substances excluding nicotine and caffeine, but my HPPD just gets worse by the day. It started off pretty extreme, but now it's much worse. MY SYMPTOMS FOR ABOUT 2 MONTHS AGO Visual snow, morphing of objects, anxiety, seeing demonic like figures, advanced patterns in walls and shrinking and growing of objects MY SYMPTOMS NOW Visual snow, more extreme and advanced morphing of objects, seeing more demonic like figures, auditory hallucinations, floaters, light beams falling from the sky, more anxiety, seeing objects rotate and morph into advanced structures, I feel like I'm falling into an endless pit when i try to sleep and much more. Have anyone here had symptoms on the same level? If so, please tell me how you got over it, or how you're coping with it. Because right now, I just want to die. And I think it would be sad if I actually go all the way with that thought, I want to live longer than 19-20 years. Wish you all the best of luck!
  16. About 7 months ago I had an acid trip, it was a very small one. Since then I've had these symptoms: visual snow, after images, slight tracers, and light sensitivity. I've also been very spaced out, everything seems kind of Dream like, and stuff like that. Since my visual symptoms aren't really hallucinogenic and mainly just visual distortions, could these be visual symptoms of derealization, or is this just mild hppd? How long should this last
  17. Hi there, I haven't been active here for almost 1,5 year. I had to focus on recovering and there's some negativity in this forum which wasn't good for my mental health. I was so glad that I got help from you guys and girls when I was in the darkest time of my life. I'm better now. Still got it (2,5 years in) but I don't really care about it anymore, even though it's quite loaded. I haven't smoke weed for 3 years. No psychadelics. I've done coke and drinking alcohol without any problems what so ever. Anyways, I've had sleep paralysis since I was 15 and roughly 3 months ago I was having them 5 days a week, several times every night. You can read more about this what is medically referred to as hypnagogic hallucinations. I don't think that there is a correlation between HPPD and the increased rate of sleep paralysis. Since I had it since I was a kid and I'm 25 now. These sleep paralysis session were unbarely to me so I did some research and found about a great study at NCBI which said a man was cured after trying SSRI (Prozac). I was desperate to get rid of it as it was effecting my studies and work. So I went to the doc and as simple as snapping my fingers I got a receipt. It worked straight away. The first night actually. Which is interesting because usually you have to eat those pills for months to achieve an effect. I've never tried it before though. After a month or two with increased anxiety, that side-effect left and I feel just like before right now, except that the sleep paralysis is gone. My main point with this thread is that I would like to cancel all rumours about how SSRI:s has a negativt effect on HPPD. It is simply not true and there's no studies that proves it either. When you start taking SSRI:s your body must adapt to the medicin as it effects serotonin (which is a transmittor that affects a lot of processes, for example, your movement, thinking and your vision). This is why some report that SSRI:s would worsen the symptoms. It is simply not true. Due to this false information on the forum, I didn't use those pills when my HPPD was at its worse and I wanted to kill myself. I stayed sober for 4 months and got out. But it was a really hard time and I had so much support from family, friends and this forum. If that wouldn't been the case, SSRI:s would probably been a good idea for a person in that kind of state. I eat 75mg a day, and I've seen no whatsoever side-effects on my vision. Not even when starting the meds. But if you do, it will pass within the first 2-3 months. And maybe afterwards you will be able to focus more on your life then your vision. Another thing about depersonalization/derealisation is that I had it for roughly 6 months. I couldn't recognize my own face in the mirror. Neither my family or my body. It's gone now. It's not permanent, but a psychological side-effect to HPPD.
  18. So I took lsd around 6 months ago. I realized I had hppd a couple weeks after, with some anxiety tied in there. I kept smoking weed and my visual snow and stuff got worse so I've quit all drugs except for nicotine and have been this way for 3 months. But ever since I took the acid, everything looks kind of different. Like everything looks kind of surreal, and colors are kinda brighter, and I'm always spaced out. I don't feel as if I'm completely in a dream or anything, but it's just the feeling that everything looks kinda "off" and something is slightly different. And when I'm in crowds, sometimes the collection of peoples voices will sound different than it used to. Is this de realization that is just a part of my hppd and slight anxiety, or what? And also, should I quit the nicotine to see if my visuals get better?
  19. Hey guys, in the past I have used a lot of benzos (oxazepam) for what I thought was an anxiety disorder. Well that cleared up very well over the past few months and I don't consider it as a disorder, just natural anxiety. I did some research on benzo withdrawal the other day, and came across something very interesting. https://en.m.wikipedia.org/wiki/Post-acute-withdrawal_syndrome this is a popular term on the forum: Benzo Buddies. PAWS: Post Acute Withdrawal syndrome. This may have nothing to do with a lot of people on this forum, but some can take this in consideration. PAWS is a syndrome that can occur after using benzos for a period around 1-3 months or longer. I read about some people who were suffering from this on the Benzo Buddies forum, and they were suffering from very similar symptoms as HPPD. Suddently my mind became rather clear and i thought: 'why didn't i think of this before.' They reported similar symptoms like afterimages, trails, static, seeing shadows, stuff in the corners of their eyes that arent there, light flashes and tracers. Could this be related? And maybe for some people this was the answer all along? I'm not quite sure if this is the case for me, i used oxazepam for about 3 months but not always everyday. I stopped semi-cold turkey, i stopped in a week so i'd consider that sort of cold turkey. So what do you guys think? Is it PAWS in my case or HPPD. The only symptoms i have now are afterimages and floaters. Just think about it, have you used benzos for a long time and stopped? Or still use them and got weird symptoms. I think this might be the case for some people on this forum, and maybe myself. I'm not a specialist or anything, just curious what you guys think about this. I never experienced mine as 'trippy' but just visual distortions. Ugh i hate the label 'trippy'. http://www.benzobuddies.org/forum/index.php?topic=131814.0 this is the thread I was talking about. Take a look if you want! I read that these symptoms usually fully diminish, but this could also take months and for heavy users even years. So a little bit the same as HPPD. But there are people in that thread who actually fully recovered. Some of them also considered it as a little bit 'trippy'. I think there is DEFINITELY a connection between these two, and for some of you who still use benzos, try to not use them (if you're mentally able to, believe me i know how hard it is) for a few weeks/months and wait for some improvement. houdoe, adios, ciao! Hope this was useful for some of you!
  20. Greetings, I stumbled across this forum/site while researching some mental issues I was/am having and basically I'm just looking for some answers and guidance. First and foremost, the already present mental illnesses. Severe anxiety and depression have been a fairly constant presence for me ever since my early high school days. I've managed and dealt with them for the most part, but within the last year they've taken a turn for the worse with almost weekly panic attacks and frequent suicidal ideation. Also, within the last 2 months or so it feels like I've been gradually losing touch with reality in the sense of continually questioning what is real and what is not. Because of this I finally got in to see a psychiatrist. After the visit I was diagnosed with major depressive disorder, panic disorder and probable schizophreniform disorder (probable pending further diagnostic imaging and meetings, though he feels fairly confident that I have some sort of mild psychotic disorder). As a result, he prescribed me escitoprolam and risperidone for my symptoms, both of which I am supposed to start next week with low doses and tapering up to the effective dose over a few weeks (he emphasized that I may not need the full therapeutic doses of either medication if a lower dose is effective). While I did mention my vision problems and illusory hallucinations, he attributed these to the anxiety and psychosis stating that they were my brain trying to make sense of a weird situation. However, I think these visual problems are HPPD and not related to any of the diagnosed illnesses. I say this because a lot of my visual symptoms are similar to those of HPPD. Furthermore, I have experimented with drugs in the past, namely MDMA (100mg one time over this past summer) and THC (45mg orally once this past summer. Not enjoyable at all since I was just launched straight into the worst panic attack I have ever had). I also used to take 50-100mg diphenhydramine 3-5 times a week to help with sleep, something I haven't done since I started having these symptoms of mild psychosis and potential HPPD. These were all mentioned to my psychiatrist. A summary of my potential HPPD symptoms is below: Lights appear to streak/downward beams come from lights, especially at night. Gets better when holding eyes wide open and when in bright areas. Monocular double vision in both eyes (i.e. double vision still occurs when one eye is closed or covered) especially with brightly lit objects and where there is high contrast. Glare, halos and star bursts, especially at night. Blurriness/cloudiness in vision Very mild trailing when moving something across visual field Some distortion of peripheral vision and perception of movement in peripheral vision Walls and other objects sometimes breathe usually after staring at them for awhile So, are those symptoms consistent with HPPD, or are they just a relatively normal eye problems that I'm getting too paranoid about? If it was HPPD, would the medications I'm supposed to take worsen it? I've been reading stories, articles and studies about how these two drugs interact with HPPD and how they almost universally worsen symptoms. I can deal with where I am right now in terms of VS, but if those get worse, the combination with the other 3 issues may be too overwhelming. Anyways guys, thanks for reading and I would greatly appreciate any help/advice you can give.
  21. I am new to this forum so it would only be polite to say hello to everyone and if anyone could help I would be very grateful. In 2011 I had a very bad acid trip after my 1st time taking the drug, like other people that have had bad trips I will keep it short by saying I saw some pretty crazy things and it took me three days to come back to normal, which I thought never would happen. I haven't taken acid since 2011 and I never will again as it was the worst experience of my life, however from 2011 to October 2016 I was a regular consumer of cocaine, weed and at some point mdma every weekend for 6 months. Anther drug I have tried only a few times is Ketamine which again sent me into a crazy trip, it knocked me out (k hole) but went when I woke up. I feel I should add from 2014 to 2016 I smoked a lot of weed, like a half OZ every couple of days, and not just any weed, this was some strong stuff. Anyway getting to the point in October 2016 I was taking cocaine and smoking weed with my cousin, I didn't sleep and went to work the next day but went home early as I felt really bad, laying in my bed thinking I was going to have a heart attack. From that day I developed what seemed to be exhausting health anxiety, I got head pains, chest pains, pains in my arms couldn't breath, went to A&E and they said I had anxiety. I eventually moved back home as I couldn't be by myself. I went to my local doctors who said I had anxiety and depression and prescribed me propranolol and citalopram. The propranolol helped calm me down but the Citalopram really messed my head up and to this day I am convinced I have some sort of HPPD, and am looking for someone to agree with me or convince me otherwise. Since taking citalopram my vision changed, I see noses and ears slightly more pointed, and still persists to this day, my ears are constantly ringing, floaters which are noticeable all day, Visual snow ,eye strain, I'm sensitive to light, headaches and light trails aswell for example if I look at the TV and look away I can still see the TV light. I know from reading other stories on this forum that my symptoms are very mild compared, but I am not convinced that it is just anxiety. I have stopped smoking weed I still smoke cigarettes, and very stupidly I have taken cocaine twice in the last 5 months which left my body on edge for over a month a time. I also cant consume sugar drinks because it makes my body really on edge, caffeine, I cant even drink tea without feeling like Ive just drunk 10 espressos. Seen a private psychiatrist who diagnosed me with anxiety disorder, but I have never mentioned HPPD to him as I didn't feel confident enough to. Last thing I will add I suppose the thing that makes me think I have some form of mild HPPD is the Vision changes in peoples ears and noses that convinces me the most, especially after trying an SSRI, its a very strange side effect which my doctor cant really explain. I'm trying CBT next week to see how I get on but if anyone could relate, or at least give me some idea on if I have HPPD or similar to what they have read before it would be a great help. I have accepted that something is wrong with me, but the way I see it is if you want to get high then there will be consequences, and I am feeling them now. Thank you for your consideration G.C
  22. Hi. I'm 57 years old and I've carried a deep secret most of my life. I see visual patterns everywhere. They are most prominent in anything with a fine grain. Tar, sand, carpets, curtains, textured ceilings ... you get the idea. I see patterns, shapes, designs, animals, faces, Aztec glyphs, etc. as if intentionally created by an artist. They're not static either. The slowly move, shift, and transform. If I'm looking at a wall I "know" it's a wall. I don't believe the hallucinations are actually visible to anyone else so I guess I'm sane. How did this happen? Just before my 14th birthday I entered High School. An older friend of mine asked me if I would like to try "acid". I had smoked cannabis with him before and he assured me it was similar. Well, acid in the early 70s was quite strong and it was a long day. From that day forward I had this issue with seeing visuals I described earlier. My earliest memory of this was after smoking some cannabis I saw the outline of a flower appear on the fabric covering a speaker. I kept taking hallucinogens until I was about 20 years old and then stopped taking drugs all together. However, the visuals never went away. I can look at a sidewalk and it looks like all the little sand grains were laid out in complex designs. It's as if "random" doesn't exist in my visual experience. I've learned to deal with it in my own way. I look at it as my ability to not just see the mundane. This disorder hasn't stifled my ability to solve complex problems, get a degree, raise a family, and work in a professional career. In a funny way it's like an old friend. I think I might miss it if it "cleared up". I was stunned to find out that there was a term for what I have. For years I figured I was borderline schizophrenic because I was seeing things. Hiding this disorder has caused great anxiety in my life because I knew it wasn't "normal" and I never knew if it would get worse. I'm hoping to find other people with symptoms like mine. I'd also like to give people hope because I've lived with this for over four decades and life is great.
  23. Hey guys, I haven't been on this site in quite some time, but I was reflecting on the past 6 years of perceptual disturbances and thought that I would write a post that may shed a different light on HPPD. I am very thankful that HPPD has become a part of my life(yes, even when I start melting or the room keeps changing sizes). I'm sure by this point many of you are thinking "wow, this guy is fucked in the head" , but let me elaborate a bit more. At this point in my life I am happy, I love who I am, and I am in a great place despite my visual and tactile disturbances not wavering in the slightest. Pre-HPPD, however, I could say none of the good things I listed above. I lived my life constantly brushing my anxiety, depression, and insomnia under the rug like it didn't exist. HPPD amplified these problems to a point where I could no longer just pass them off. It forced me to change. I had to open up to people about myself and my problems like I never had to before. I had to focus on the things that I could control (anxiety, depression) rather than the things that were out of my hands(perceptual disturbances). This was not an easy process at all. I struggled immensely for a year before I developed the coping skills I needed to allow myself to be happy. One of the biggest turning points for me was when I was finally able to forgive myself for the long series of decisions I made to get myself caught up in in everything. I fortunately haven't had any other trauma in my life, but that almost made it harder to forgive myself for creating such a traumatic event for myself all because I wanted to get high. I also thin that it was important that I accepted the fact that HPPD was a part of me; this is the way I see things now and that ok. In fact its more than ok! I have a hugely different perspective on life than I did before and I think that is one of my biggest assets in life. I couldn't imagine where I would be if HPPD didn't come into my life (probably still getting high off of stupid shit all of the time with no future plans). HPPD helped me figure out what I wanted to do with my life (though I almost dropped out because of it) HPPD is the reason I became a social worker and have a great job that I love HPPD helped me learn the communication skills I needed to open up to someone and have an actual meaningful relationship with someone HPPD stopped me from doing drugs allowing me to eventually become an all-american in cross country. HPPD taught me how to enjoy life while coping with insomnia, depression, and anxiety HPPD made me the man I am today I used to blame HPPD for making my life miserable, but now I see it as an integral part of my life. Wish you guys all the best. - Josh
  24. Well, hello there everyone! My name is Amanda, I'm 23 and I'm coming to terms with the fact that I have HPPD. At first, I didn't really know what I was going through. When I was 15 I had taken LSD for the first time and had a wonderful time. Then when I was 18 I experimented with some RC's. I started to notice that from time to time I'd start to see visuals on the floor and walls but I thought it was pretty cool at the time..hah. Then finally at age 19 was when I took some LSD that was from the Grateful dead family and that's just when things took a turn for the worst..I took 2 tabs of it and let's just say it was the strongest freaking acid I've ever had. I also smoked a really fat bowl and shortly after I seriously thought that I was going to die. My tracers weren't as colorful and making me happy as they usually would and the room felt like it was enclosing on me. I actually started to lose my mind and my grip on reality..which wasn't even that tight to begin with. Scared me enough to never touch acid again. So here I am today, 4 years later and that trip still comes back to haunt me. When I roll on MDMA and even smoke weed the visuals come back and my heart starts pounding extremely hard and the room feels like it's enclosing on me. Sometimes, when I'm in my room in the dark I still feel like I'm tripping. It keeps me up at night and I just can't help but think to myself...is this really gonna happen to me for the rest of my life? How can I do anything for myself if this is all I can ever think about? I honestly thought that I was the only one going through this because a lot of my friends are acid heads and when I try to explain to them what's going on in my head..they just think I'm crazy. But then I found this wonderful website thanks to Reddit! It makes me feel so much better that I'm not the only one going through this. I really hope to find different ways to help me either let this fade away or learn how to cope. For whomever took the time to read this, thank you so much. I really hope I get to hear back from some of you it would help me a lot.
  25. I've had what i believe to be HPPD for about 3 years now, after a slew of mushroom trips around age 15. I cant pinpoint exactly when i started showing symptoms because i feel they came on very subtly and gradually, and after 3 long years, seem to still be worsening. I remember the first thing i noticed was a light visual snow or static fuzziness that i could only see at night or in dark places, then slowly it started becoming more noticeable with time. I would start then seeing the visual snow or static fuzziness during the day time, most noticeably when looking at something solid and with minimal detail, like a wall or a cloudless sky. The trend of it getting worse continued, i would start getting progressively stronger tracer vision, beginning with things like car and street lights at night. As before, over a few months these symptoms began to translate over to during the day time. Now its to the point where i get tracers as simply as slowly running my hand past my eyes, and the visual snow is strong like what you see on a television that isn't getting any signal. The visual snow even forms into psychedelic shapes sometimes, spirals and things that look like your phone screen when there is grease on it. This is most often at night and in the morning when i am tired, but is not limited to that. When i close my eyes all i can see are these weird colorful randomly moving shapes and images. If i do something like read a book or read something on my computer, when i close my eyes i just see randomly occurring letters and numbers, and this lasts for 15 minutes or so. Florescent lights make all the symptoms particularly strong, so you can imagine school was quite difficult.There are halos around almost everything i look at, especially letters and numbers. My memory and ability to think straight and clearly feels like its degenerating. I cant focus on anything, and having ADHD doesn't help aha. I've also dealt with things anxiety and depression and depersonalization and severe migraines so that cant be helping. Ive completely stopped all substances except alcohol, the occasional cigarette and the occasional joint to help deal with the stress. But i used all 3 of these things and more up until about a year ago. none of it was hallucinogenic though My point of posting this was not to for attention or plead my case on how hard it is to live with. I know there are people on here that have it worse than i do, but i rather just posted this to see if anybody can relate to my experience so far and has dealt with a similar situation. I haven't read many stories of people with HPPD that seems to be progressively getting worse, so i'm just seeing if someone can confirm its HPPD and not something else. I've been to countless doctors across Toronto and most of them have even heard of HPPD, let alone how to treat it haha, so i kind of gave up on the medical route. Ive had brain scans that all came back negative for anything so HPPD seems to be the only thing i have found that matches my symptoms. Its a scary thought thinking about what it might amount to if the symptoms keep exaggerating like they are doing now. Its only been three years so its pretty debilitating thinking about what it might be like after 10...20...years etc if it doesnt stop, as i only just turned 18 aha. This is my first post so any replies or support really helps, thanks. -Cal