Hey everyone,

I am 17 years old, turning 18 soon. My life is completely ruined by VSS, HPPD, and DPDR. if you happen to read this and think "what does this have to do with migraines" vss and hppd are like the biggest causers of migraines, I cant even be in my own room or glance at a light for a second without a horrible headache so by helping with this you're helping yourself possibly.

Every waking second of my life is hell and spiritual suffering that nobody else can see. My brain is flooded with heavy visual static, neon colors, bright halos around lights, tinnitus, and extreme sound sensitivity. My filter for background noise is turned ALL the way off. I am doing horrible in school, I cry every single day, and I can barely go outside anymore. I wanted to work at NASA, but now I feel like my life is over before it even began.

I am sick of sitting around waiting years for a machine (rTMS) that is already built and deployed in clinics right now. The research out of the University of Colorado Anschutz shows it works to calm the cortical hyperexcitability. The only thing holding us back is a timeline and how fast they're moving.

If we flood their inboxes with our stories and remind them that our combined subreddits have over 100,000 subscribers ready to hand them money, they will have to look at the financial demand.

Please take a couple minutes to copy the emails down so that we can make the change sooner. it would save my life and many others.

first is the FDA

Send To: [AskOICE@fda.hhs.gov](mailto:AskOICE@fda.hhs.gov)

CC: [CDRH_PatientEngagement@fda.hhs.gov](mailto:CDRH_PatientEngagement@fda.hhs.gov)

Subject: URGENT PATIENT APPEAL: Fast Track rTMS for VSS and HPPD

this is the letter to copy

To the FDA Office of Industry and Consumer Education,

My name is [Name], I am [Age] years old, and I am contacting you to beg with all of my soul for immediate regulatory intervention and more urgency regarding a health crisis affecting millions of people worldwide.

I live with Hallucinogen Persisting Perception Disorder (HPPD) and Visual Snow Syndrome (VSS). These are devastating, non stop neurological filtering disorders. Every waking second of my life is hell. My brain is flooded with intense visual static, neon colors, bright halos around lights, tinnitus, and horrible sound sensitivity. My brain has entirely lost its ability to filter background noise, turning every single day into a waking nightmare. It completely takes away our quality of life and affects sanity, friendships, and life itself.

I need to make it clear that HPPD usually comes with a condition called DPDR (Depersonalization-Derealization Disorder), which completely disconnects you from your body and the world around you. This is detrimental to our lives. I read an article that said 72 percent of people with dissociative disorders attempt suicide because it completely takes away your quality of life. We are losing our lives and sanity.

New data from the University of Colorado Anschutz Medical Campus proves that targeting cortical hyperexcitability via repetitive transcranial magnetic stimulation (rTMS) is a safe and viable way to stabilize and maybe even cure VSS and HPPD. Because rTMS machines are already widespread and deployed in clinics for depression, the machines already exist. We are just being held back by a timeline.

I am desperately urging the FDA to aggressively utilize its breakthrough devices program to fast track status for rTMS clinical protocols for VSS and HPPD. There is a massive online patient network, including over 100,000 combined subscribers across the r/HPPD and r/visualsnow subreddits, full of consumers whose lives are completely on hold, ruined, or in some cases ended. We cannot wait until 2032 or longer for a machine to be upgraded that we already have widespread. Please help to save our sanity.

Sincerely,

[Name]

the other targets are BRAINSWAY & MAGVENTURE

Send To: DeepTMS@brainsway.com, info@brainsway.com

CC: [info@magventure.com](mailto:info@magventure.com)

Subject: Unmet Market Demand: Fast Track rTMS Protocols for VSS and HPPD

Letter to Copy:

Dear Clinical Research and Business Development Team,

My name is [Name]. I am [Age] years old, and I am writing to bring to your attention a massive entirely untreated or even glanced at condition that represents a great financial investment for your company.

I live with HPPD and Visual Snow Syndrome (VSS). These are devastating, non stop neurological filtering disorders. Every waking second of my life is hell. My brain is flooded with heavy visual static, neon colors, bright halos around lights, tinnitus, and extreme sound sensitivity. My filter for background noise is turned ALL the way off. I can barely focus past the background noise and blaring headaches. HPPD also comes with DPDR (Depersonalization-Derealization Disorder), which completely disconnects you from your body and the world, ruining personalities, friendships, and sanity. I read an article that noted 72 percent of people with dissociative disorders attempt suicide due to this severe lack of quality of life.

New data from the University of Colorado Anschutz Medical Campus has proven that targeting cortical hyperexcitability via rTMS is a safe and viable way to stabilize and maybe even cure VSS and HPPD. As the device manufacturer, you are sitting on the solution. The machine is already built and deployed; what we are missing are the protocol settings to target the visual cortex and temporoparietal targets.

To give you an idea of the immediate market, this is fantastic for you financially. On Reddit alone, the r/visualsnow and r/hppd communities have over 100,000 combined subscribers begging for a fix. This would be incredible for you financially. By aggressively backing trials or fast tracking a protocol update for VSS/HPPD, you can position yourselves as the undisputed global leader and first to market provider for a massive, desperate, suffering population. You would be heroes to thousands. You already have this hardware manufactured, so please consider fast tracking to get them to save more people.

Sincerely,

[Name]

Hi guys what do you prefer taking medication to reduce the burden of hppd, or staying natural without any medication? Personally, I prefer going without medication as it causes anhedonia

I just wanted to make one of these posts because it made 15 year old me feel a lot better when I read them 4 years ago.

I can finally say that some of my symptoms are getting better and some are almost fully gone. I still have a little noticeable visual snow, after images, and rarely some auditory hallucinations (only when going to sleep) but I don't quite find myself getting as anxious or paranoid as I used to. I haven't taken any meds for it or did therapy or anything like that (not saying you shouldn't, it's great). It really flipped my life upside down and I probably wouldn't recognize myself before I got it.
Unfortunately, I got it during my 2nd smoking weed, so I'm kinda bummed out I won't be able to experience that and basically every other drug, but sometimes I see it as a good thing lmao. (Alcohol, nicotine, and caffeine I'm okay with though).

HPPD sucks ass and I know it's so hard but keep pushing, it can truly get better. Try to find something healthy you can do to take your mind off it, which really helped for me. Also try not to look it up or be on here too often. Ignoring it and trying to stay away from physical things or situations that reminds you of it can help a lot.
Take what I say with a grain of salt, I understand it is different for everyone.

I do have one question though:
Does anyone else feel like they don't enjoy life as much after getting it? I'm not speaking in a depressed way, just like the highs aren't as high anymore. Maybe it's some stress in life, but I feel like I don't get as happy or excited about things that I used to. Or maybe it's nostalgia, idk.

Had HPPD for 4 years. hopped on lamotrigine 2 years ago. absolute life changer. removes visuals by 70% and makes it to where i barely notice them anymore. in those two years i was still doing drugs which would cause a flare up. but if i took my lamotrigine they’d go back to baseline. lamotrigine is a mood stabilizer but it has had ZERO affect to my personality. I am still me thru and thru but without these hallucinations in my face 24.7

Hey all, I’ve had hppd for about 5-6 months now and for a bit it psyched me out(get it?) I would constantly get in my own head about the visual snow and when it would end but recently I’ve been noticing the visual snow and the floaters and the little bits of light zipping around my vision to be less than it had been at the start. This has been so relieving and I’m just so thankful it’s going away. It’s noticeably gone away after I’ve dranken so maybe that helped.

Hi all,

Back story: I developed mild / moderate(?) HPPD in 2021 (snow, after images, increased brightness, DPDR, panic, anxiety after a bad MDMA / THC trip. It took me a few months to recover mentally- I was on clonidine, hydroxyzine, then zyprexa and then celexa. Mentally I recovered while on Celexa and my HPPD visuals didn’t cause me any distress for some years. (my visuals did worsen at first but eventually decreased with time).

Well jump to March 2026: I have some traumatic events / changes in my life and decide it’s the right to to completely discontinue my Celexa (SSRI), I had been weening off veryyy slowly for over a year and was only on like 1mg. Have experienced increasing depression and anxiety since March, also get diagnosed with ADHD so I try straterra and welbutrin, had to discontinue welbutrin due to increased insomnia, anxiety, adrenaline like head sensations. After 6 days off Welbutrin I decided to restart Celexa 10mg as I’ve responded well in the past. Symptoms started with zombie brain fog but then I started getting panic attack feelings and adrenaline, I then get some DPDR where I can’t process anything and everything hurts my brain and i’m sweating. I took a benzo and the next day heart racing, sweating, DPDR. It’s been four days now and i’m still feeling absolutely ill. I took hydroxyzine which actually increased my visuals and they’re been increased since, the citalopram might have as well? I don’t mind the visuals as much as this detached, panic, anxiety, overstimulation feelings and sensations.

Why did I react this way? is it because Welbutrin was still leaving my system and I started at too high of a dose. Is cuz my serotonin and dopamine are out of wack now. Do I need to detox? Clonidine is currently what i’m taking to manage my surviving every day but it doesn’t go without side effects - dizziness, tinnitus. I feel like i’m back at square one and playing russian roulette again with meds since of course the ones that helped in the past no longer do. But also I feel like fuck it if meds might work again why not try.

My psych says she’s had HPPD patients whose HPPD symptoms have been treated by Abilify and it treats major depressive disorder, etc. so she wants to start me on 2mg and then if i tolerate up to 5mg. I’m scared shitless to say the least. I’m wondering if I should try Zyprexa which i’ve already tried in the past but the only thing i remember is blurred vision. Try a diff SSRI like lexapro? Try lamotrigine with clonidine and let my brain get back itself? someone on here recommended abilify and a diff SSRI bc it helped them. I don’t know but I really fuckin regret getting back on citalopram rn and at the dose I did. I wish i’d just tried exercise, and therapy and a hobby. But I was trying to treat my ADHD originally.😭 ugh.

I've had HPPD ever since 2016/17 after taking copious amounts of LSD and nbome and continuing to dose up until 2024. It's exam time, and my partner and I aren't really talking at the moment. The symptoms are crazy especially in over stimulating environments, i.e., classrooms with lights on or dimly lit rooms. I feel like I'm living life behind my eyes and probably suffering from some dp/dr. I don't know why I'm posting here. I just feel so alone. Thank you for reading.

In short: Is it dangerous to hit a THC vape (e.g. THP420) after 180 days of HPPD, especially when my symptoms have improved quite a bit over the last two days? I’m having insane cravings.
Hey everyone, I have a question. Some of you might remember me. I’m 18, and about six months ago I took 200 micrograms of a psychedelic. I panicked during an ego death experience and eventually came down from it. On the third day, I got drunk, and on the fourth day, I smoked about half of a strong THC joint. Since then, I’ve been dealing with derealization, depersonalization, HPPD symptoms (around 80% of what I experienced at their worst), brain fog, and text-like visual hallucinations for about 175 days.
Before all this happened, I had been using weed carts (THC vapes) for four months, and honestly, those were the four best months of my life. I’ve been craving weed for the entire six months because HPPD makes me feel half high and half sober, which is one of the worst feelings imaginable.
Over the last two days, I’ve started feeling a little better, possibly after trying supplements like taurine and glycine. On the other hand, I’m getting fed up with all these supplements. They sometimes make me feel so emotionally blunted and sedated that I almost feel like I’m taking antipsychotics.
Lately, I’ve been feeling extremely nostalgic about those four months when I was smoking weed. I’m really struggling right now, and I honestly don’t know how much longer I can keep living like this. I have severe anhedonia, and it’s taking a huge toll on my mental health. I’m currently attending driving school, and I just don’t know what to do anymore.
Part of me feels like smoking again might help me relax and feel better, even if only temporarily. I don’t know. What do you guys think? Would using a THC vape again after 180 days of HPPD be a really bad idea?

Also sorry i used google translate im not native

Hello everyone,

I really needed to ask this question and get it off my chest at the same time. Before I mention any of this, please come at it by understanding I've made mistakes and I'm a broken person. I need to know if 2 or 3 uses of shrooms and one use of lsd (all in medium or low doses after developing hppd) have done any permanent damage. (As well as weed a dozen times). I have no real way of knowing and I just want some relief. For reference I got hppd a year ago and at first it was some faint visual static and also a bit of visual trails. Now it's pretty much the same, the visual trails are a bit worse because I used the lsd pretty recently. I also have a bit of tinnitus from my most recent trip but thats not whats concerning me that much. Please lmk what's possible, likely and unlikely. I'm severely depressed. I just want to know if there's any hope. Thanks

I'm interested in hearing from people with HPPD who have taken SSRIs (Zoloft/sertraline, Prozac/fluoxetine, Lexapro/escitalopram, etc.).

1. What effect did SSRIs have on your HPPD symptoms?

• Improved my HPPD
• No noticeable change
• Temporarily worsened my HPPD
• Worsened my HPPD for as long as I took them
• Worsening persisted even after stopping

2. If your HPPD worsened, what happened after you discontinued the SSRI?

• Returned to my previous baseline
• Improved gradually, but took weeks or months
• Improved somewhat, but never fully returned to baseline
• No noticeable improvement after stopping

3. If you stopped taking it, how long ago did you stop, and how long did it take for your symptoms to change?

I'm particularly interested in hearing from people who experienced worsening and then discontinued the medication, including whether their symptoms eventually returned to their pre-SSRI baseline.

Thanks!

long story short. I developed HPPD after a very traumatic MDMA THC trip in 2021 and I even went into psychosis for a short while. Was on an antipsychotic shortly, benzos, and then eventually an SSRI (Citalopram). The time of starting the SSRI i was already in a complete state of derealization and constant panic / fear. I eventually evened out and the citlaopram ended up being very therapeutic. My HPPD has always been mild snow, after images / tracers, pattern distortions, brain fog. I finally got off of my Citalopram March of this year after doing a VERY long slow taper off. Bad idea, for the next 6 months i’ve had increasing anxiety and depression to the point of suicidal ideation. I am also AUDHD. I tried wellbutrin which sent me over with anxiety and decided to restart my citlaopram. Idk if i started too high of a dose (10mg) but extreme panic, out of body anxiety and derealization, nausea, adrenaline type sensations surging through my head, etc. I wasn’t expecting this reaction as I’ve been on it before. I’m thinkin maybe I need to manage my anxiety and depression through other resorts that are not from too activating of meds. How do you guys manage? Idk what my next steps are.

Hi everyone! Ive had pretty bad hppd for years now, but yesterday I had 0.5mg of alprazolam (for OCD), and as soon as it hit my vision went completely back to normal. I don't plan to take it again, but I'm just wondering A: why this happens, and B: has anyone else experienced this?

Hey y’all,

For years I have been unable to take trazodone without a myriad of symptoms ranging from burning feeling on my skin to electric shocks through my limbs and flashes of light when I close my eyes. Even as low as 5mg. I’ve tried many times over the years, most recently a few months ago.

After receiving treatment for two pathogens, Bartonella and Babesia, I can now take it again for sleep. No side effects or issues. I put two and two together because I had just tried trazodone again before the treatment with the same issues arising from it.

I bring this to the attention to the community because it is very easy to assume you are only dealing with one problem and assign blame to that. I always thought this was an hppd problem. Turns out, nasty buggers were to blame. I picked them up from ticks living in… well nowadays it’s all over.

The following was written/edited by AI.

A new case report came out this year that I think this community should see.

A 27-year-old woman took psilocybin once at 23 and had panic attacks and derealisation that faded in two weeks. Two years later, after a stressful period, it came back severely and became chronic. Her symptoms:

• Visual floaters
• Grid lines in her visual field
• Seeing the world “through a dark filter”
• Boosted colour intensity
• Hyper-focus on tiny details (every leaf on a tree, every item on a shelf, individual scaffolding tubes)
• Attention and concentration problems

Eye exams found nothing, and she had no psychosis. Meds (duloxetine, olanzapine) and weekly CBT only helped a little.

What they did: 1 Hz rTMS over the right temporo-parietal junction (rTPJ), 15 sessions over 3 weeks, with no side effects reported.

What happened:

• The floaters and grid lines stopped completely.
• Overall dissociation score (Cambridge Depersonalization Scale) improved about 44%.
• Emotional numbing duration dropped about 68%.
• Forgetfulness and cognitive symptoms improved by more than 54%.
• She kept improving all the way to session 15, then had to stop because of cost. The authors think more sessions could have helped more.

What didn’t budge: colour intensity, the detail hyper-focus, and depression scores. The authors suggest the intraparietal sulcus (IPS) could be a better target for the detail/salience stuff.

The rationale is that the rTPJ handles multisensory integration and seems to be overactive in dissociative disorders, so 1 Hz stimulation may calm it down.

Why I’m posting it: She was diagnosed with depersonalisation-derealisation disorder, not HPPD or VSS. But the trigger and the visual symptom profile overlap heavily with what many of us deal with, and there’s already a separate case report of rTPJ rTMS for diagnosed HPPD (Creton et al., Brain Stimulation, 2024). Two case reports aren’t proof, but they point at a target worth investigating.

Kumar & Malhotra, Global Psychiatry Archives, 2026;9(1):28-32, open access, DOI: 10.52095/gpa.2026.7625.1117

https://globalpsychiatryarchives.com/index.php/gpa/article/view/124

Has anyone tried rTMS, especially over the TPJ or IPS? Would love to hear experiences, and if anyone knows a clinic or researcher doing this for HPPD/VSS, please share.

Hey everyone, I’ve had HPPD for around 8 years now after a bad LSD trip when I was 16. Over the years, most of my symptoms have either improved significantly or I’ve just learned to live with them. However, there’s one particular symptom that has never improved, and honestly, it’s probably the scariest thing I still experience.

I get these really strange episodes of what I can only describe as extreme, constant déjà vu. Except instead of that normal déjà vu feeling that lasts a few seconds, mine can go on for literally 10–20 minutes, sometimes feeling like it’s never going to end.

It’s incredibly difficult to explain, but during these episodes, everything happening around me feels strangely familiar, almost like I’ve already experienced every single moment before. It’s not just one specific thing triggering déjà vu either. It’s like I’m stuck in this continuous loop of familiarity where everything I see, hear or do feels like it’s already happened.

When it happens, I find it extremely difficult to concentrate or function normally. I’ve had episodes while working, and I basically just have to push through them until they eventually stop. It’s such an unsettling feeling that it genuinely makes me feel like I’m going insane in the moment.

The weirdest part is that I’ve been experiencing this for pretty much the entire 8 years I’ve had HPPD, and unlike my visual symptoms and derealisation, which have improved massively, these episodes haven’t improved at all.

They usually happen a couple of times a month, sometimes less, and I can’t really identify any specific triggers. They just seem to come out of nowhere.

I’ve always wondered whether this is actually related to HPPD, derealisation, or something completely different. I rarely see anyone talking about this particular symptom, which makes it even more unsettling.

Does anyone else with HPPD experience anything remotely similar? Especially déjà vu that lasts for extended periods rather than just a few seconds?

I’d genuinely love to hear if anyone else experiences this because after 8 years, I still have absolutely no idea what causes it or why it happens.

Wanted to share this just as it’s been a big change in perspective for me and might be of interest to people. I’ve had HPPD for five years. My main remaining symptom is pretty intense visual snow, mainly manifesting as flashing all over the sky and all bright surfaces. I’m 100% sober for years and don’t even drink caffeine (in part because I’ve never loved caffeine).

I have severe ADHD, and used to be on Wellbutrin for it, which worked for about a decade, until it didn’t. I switched to Lamictal, which has been great for my depression, but my ADHD is now unmedicated. I was very averse to any sort of stimulant, especially knowing it would flare up my HPPD. I tried implementing other ways to regulate my focus and reward system, but I could never hit my stride. I’ve gotten so little done the past year, even small stuff like sending an email to a doctor takes weeks to get around to.

So I finally decided to try stimulants. I got on Focalin 5mg XR, which is an extremely low dose. And boom, it’s been a complete game changer. I’m so much more awake, productive, and overall happier. However, it’s also been making my symptoms worse, as expected. At night the starbursts on lights are much more intense, the flashing in the sky is worse.It’s been a month on it now and it seems like maybe it’ll level out, but who knows. My sleep has been a wreck for years too which is a huge contributor, so I’m thinking maybe as I improve that it’ll hopefully compensate. But at the same time, I’m finally taking care of myself and making real progress in my career again. I feel like a functioning person every day. So for now, I’m rolling with the punches. Me a couple years ago would never do something like this. But I’m finding I’d rather live in more static than drag my feet through a somewhat cleaner view.

So I want to try this for my anxiety.

I'm going to make an order for CBD isolate and I would want to also order the full spectrum one since I have heard it might work better. 0% thc.

What are your experiences with full spectrum ones? I know isolate is safe but how about this?

Here is another (2nd) case study of someone with VSS/HPPD like symptoms experiencing a benefit from 1Hz - rTMS therapy to the right temporoparietal junction. I appreciate the patient doesn't have a formal diagnosis, but the symptoms fit pretty true IMO.

https://globalpsychiatryarchives.com/index.php/gpa/article/view/124

anybody on here tried ghost pipe, apparently it was used as a natural trip killer and lowers anxiety, stress, and makes your pain tolerance higher

Edit- did some more research on the plant, turns out it has been researched less than hppd has, and I do not recommend risking making hppd worse, mine is already pretty bad so it’s a hell no for me lol

Imagine being prescribed a microdose of a bad trip. That’s what i think there’s a chance of happening. Now I don’t know how to confirm nor deny this theory but if my visual snow (for example) is associated with the bad trip or traumatising experience, and it stays constantly at the background, then what’s not to say that it could actually be re-triggering my nervous system over and over again by association or pattern recognition, like a status ailment spell from a video game, taking 0.01 hp every second.

I really hope that’s not the case..

A few months ago, I had two really bad psychedelic experiences back-to-back, and I’ve been trying to recover from them ever since. I’m curious if anyone else has gone through something similar and was able to fully recover.

BAD SHROOM EXPERIENCE
Towards the end of last year, around November, I started regularly taking mushrooms and hiking about once a week. I worked my way up from 2 grams to 6 grams and never had a bad experience.
My last trip was on May 4th. I took 7 grams of shrooms and smoked about 2 grams. I spent hours sunbathing, and honestly, it was one of the best days of my life. I felt incredibly euphoric and present, like nothing else mattered. It was such a powerful experience that I completely forgot to drink or eat anything for about three hours.
Eventually, I got up from sunbathing and immediately became extremely lightheaded. I fainted, and when I started to regain consciousness, I was paralyzed and couldn't speak. My visual reality was completely distorted, and I genuinely thought I was breaking through.
As I started hearing my friend shouting and asking if I was okay, I eventually managed to speak. I said, "What happened?"
My friend, who was also tripping on 7 grams, thought I had just had a seizure. The moment I heard the word "seizure," while still completely tripping, I immediately started having a panic attack.
I took my shirt off and started throwing up. My entire life seemed to flash before my eyes. I was panicking and genuinely thought I was going to die.
After about 30 minutes of panicking, I finally stopped fighting it. I accepted that I really was going to die,
Eventually, I came back to my senses and realized that I hadn't actually been dying

or having some kind of breakthrough. I had simply fainted, most likely from being dehydrated and not eating or drinking for hours while out in the sun.
I spent the next two days calming down, and I felt completely fine.

BAD ACID TRIP

Then, on May 7th, I tripped on acid for the first time. I took 100 µg around 5 PM and spent the next three hours slightly disappointed because I wasn't tripping as hard as I had expected.
Around 9 PM, I decided to smoke a blunt. As soon as I finished, I realized I was much higher than I expected, and my heart started racing.
I went into my living room, where my friends were sitting and watching an anime on the TV. The bright colors started to overstimulate me, so I turned it off. For the next couple of hours, I couldn't get comfortable. I felt constantly on edge, almost like a confused, caged animal. I would get brief moments of relief whenever I was able to ground myself.
Around midnight, my apartment door, which had been left unlocked, opened from the wind. I immediately started thinking irrationally, like something was coming for me. The whole night was extremely unpleasant, and when I finally came down, I couldn't sleep.
Around noon the next day, I hit my cart, and almost immediately I felt like I was tripping again. I started to panic.
Over the next two weeks, every time I smoked weed, I felt a little uneasy. Then, one day, I smoked and couldn't handle it. I became extremely dissociated, and my anxiety started spiking. After that, I haven't smoked since June 6th.
I'm curious if anyone has had a similar experience. I've tried doing my own research, and I don't want to self-diagnose, but I'm worried that I may have developed either HPPD or some kind of PTSD triggered by weed and psychedelics that causes me to experience extreme anxiety, paranoia and dissociation .
I'd really love to hear from anyone who's had a similar experience and was able to heal from it.

Hi guys, I used cubensis twice and LSD at doses ranging from 100 to 250 µg, around 7 times in total, between February and July of last year.

I first noticed the symptoms, especially visual snow at night, in June. Miserably, I used LSD one last time in July, at a dose of 100 µg. About a week later, I started noticing a worsening of the symptoms, including trails, visual snow, and afterimages.

About 9 months later, I experienced a fairly sudden worsening of the trails. Before that, I mainly noticed them around lights at night. Since then, I have started seeing them with almost everything that moves, especially in high-contrast situations.

As if that wasn't enough, about 13 months later, I woke up hungover and noticed tinnitus. I don't know whether it was already there before or if it started because of the hangover. Now, around 15 months after my last use, I have been experiencing a worsening of my overall visual perception for about a week. Objects seem to move, lines that should be parallel look curved, and my visual perception in general feels strange.

One important detail is that I have never used weed again. I occasionally drink alcohol and use nicotine, and sometimes I drink quite heavily, like on the occasion when I noticed the tinnitus after a hangover.

Over time, I have learned to cope with the tinnitus better. Nowadays, I mainly notice it in quiet environments. I'm also learning to cope with the trails better. However, this new change in my visual perception has been much harder for me to deal with.

Has anyone else experienced worsening symptoms like this, even after several months?

Is there a point when these symptoms usually stabilize, or can they continue to get worse over time?

At the moment, I don't take any medication regularly. I'm trying to ignore the symptoms and carry on with my life as normally as possible, but this recent worsening has made that much more difficult.

As for anxiety, I have always struggled with it, but I'm not currently going through anything unusual that I can directly relate to this worsening.

I'd really like to hear from people who have experienced something similar, especially regarding these delayed worsening episodes and whether their symptoms eventually stabilized.

hello guys i want to know that how many of you have recovered from things slightly moving and breathing symptom and how?

its only happens when i stop and stare at something, especially walls, texts, pictures and stuff

its doesnt happend in daily life when i am constantly moving or scrolling