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Hallucinogen Persisting Perception Disorder (HPPD) Support Forum


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About Tyler

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  1. I have tried a sleep formula with valerian root but didn’t have any success. But thank you for the suggestion. I’ll keep that in mind if I do get my hands on some. Might need to see a different psychiatrist to get it but I think for the short term it would be beneficial.
  2. Thank you for your reply Nick. Again it is nice to hear that there are others who can relate. I am definitely working hard on meditation and hope to get better at it. Practice makes perfect and as I’m only 4 weeks into this I am putting faith into time healing things. A lack of sleep definitely makes things worse for me and often feeds the cycle of anxiety. In your experience has there been anything you have done to help with sleep? That is true that my drug history isn’t excessive but that’s the thing about this odd condition is that it could happen with first time use! I appreciate your advice on abstinence, I’m sure that would have been a difficult setback but I’m glad to hear that things are better now. we do all make mistakes but I understand it’s important to not dwell on the past and work towards a happier and healthier you, leaving the past in the past where it belongs. This SUCKS right now but I believe if others can overcome it than so can I.
  3. Thank you very much for your reply. It’s relieving to hear that I’m not the only one going through this. I decided to stop taking it after 4 nights as it made me feel twitchy and too out of it. My goal is to take the most natural approach for the time being. It is great to hear your psychiatrists experience with hppd, gives me hope. My psychiatrist said there’s nothing we can do but here’s some antidepressants to get rid of your anxiety. Sleep has been my biggest issue here. The first few weeks I basically didn’t but the mirtazapam helped me sleep a great deal. My psychiatrist dismissed my request for any benzos for short term relief so I think I’ll try and find one who might be willing to try this for me. Other than that is there ANYTHING at all that you or others here have had success with for sleep? Mindfulness meditation has been really good for me too and I’ve been eliminating as much stress as possible. I even had to give up my part time job at KFC as this was the biggest stressor with shift work. Thank you and I hope you are able to work through this yourself.
  4. Hi there my name is Tyler. I’m 19 from Australia and have recently developed HPPD. I have done some deep reading on here and on other webpages and have been overwhelmed by the feeing of uncertainty and just how different people’s experience with this condition vary. So with that I am seeking advice on how to deal with and adjust to living with symptoms. I will start with saying I have used marijuana on and off for the last year, have had LSD once in January and once in February this year and tried what I believed was MDMA three times spread between May and June. The last time I had MDMA I smoked marijuana at the end of the night and had a traumatic experience having to care for a friend who had a panic attack while on the same intake. Two nights after I smoked again by myself and this is where the visuals first presented themselves (very intense acid like) which I dismissed as just a bad trip and got too high. I didn’t touch any drugs what so ever since, 4 weeks later I woke up with the trails in my vision and panic set in not knowing what was wrong. Two weeks in things got a lot worse including VS, floaters, depersonalisation, depression, anxiety, and continued to get worse under stress including halos, flickering in my vision feeing like things were moving around me, brain fog. And I’m constantly worried that I am going to lose my mind as my symptoms have been worsening. I am seeing a psychologist and have seen a psychiatrist who has prescribed me mirtazapine to target anxiety and depression. What I would like to know from you guys: is it normal that my visuals began 4 weeks after I touched any psychoactive substances, is there any rhyme or reason as to why my symptoms have been getting worse? Is mirtazapine an appropriate medication or can it make my visuals worse? I have been on it for three nights now and adjusting has made me feel like things seem to shake in my vision a little and things seem to flash across my vision and longer tracers. Finally I would like to say that I have been Keeping active going to the gym and runs, eating healthy, vitamin B supplements and teas, no caffeine and no alcohol while I adjust to this. I am now three weeks into having HPPD and would love to receive some support to know that I’m not alone and to hear that things will get better (whether that’s recovery or just getting use to things). - Tyler
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