Jay1

I'm pretty open minded about the supernatural, but on this one, i'd say a definite no.

Great, thank you!

3rd day taking P5P (150mg, once in the morning). Nothing noticeable yet (good or bad), with the exception of feeling nauseous for a few hours after taking it.

I also had some form of hppd at around 14-15 too... VS and moving objects... Sadly, i thought it was cool and a "free trip" Purple Ohms, Strawberries and Raving test tubes for me! The microdot I had a glastonbury 95 was what finished me off, they were about 10x the strength of anything i'd taken before and made my visuals what they are today

Welcome and thanks for sharing. I fear we are seeing the first ripples of a tsunami of HPPD cases brought about by this type of therapy. I hope you are doing ok

It's a really complex situation. We are the obvious example of very severe "side effects" of these drugs. But the legit treatments are certainly helping a lot of people too and they are generally doing it in the safest manner possible (pure drugs, eye mask, minimising stimuli). I think the practitioners need to give serious thought to this sort of treatment though, especially when treating mental health issues. HPPD will happen to some of the patients and they need to be upfront about such life changing risks. As for the trolls, don;t give them any oxygen... I'm sure most of us were in denial of any risks too, when we took drugs.

Hi Helena, welcome to the forum and thanks for sharing. I would say that your case is more likely to be VSS and I think you will have more success with doctors if you describe it as such. There is a case to be made that the ADHD med caused this though, amphetamines could potentially cause HPPD, though it seems rare (anecdotally). From what I have read though, the treatments, triggers and overall advice seems to be pretty much the same for VSS and HPPD, so the info you find on the forum will be relevant. And yes, it can definitely go away... There are plenty of success stories on this site, and I get a lot of DMs letting me know that people have got better over time. It's something that often seems to go away after a few months.

Thanks for the update, i'll give it a try! Anything that could help ease my dpdr would be priceless

There are three things that can really screw with my hppd 1) Drugs, 2) Stress 3) Lack of sleep. Lack of sleep really makes my dpdr and anxiety worse.

Hope it goes well, let us know if it helps at all

That's a good article, thanks for sharing. RIP Joey, very sad to read that part of the story.

Hi John, that's an interesting observation and one i'd never heard of before. I can only assume certain chemicals are being released during those episodes that help with visuals, (Gaba?). Hopefully some of the more scientifically minded posters can add their thoughts.

Do you mean the SSRI was what started your illness or you have now started on SSRIs to try to help the issue? If it was an SSRI that caused your issues, you could probably class that as HPPD... but really, it makes no difference what you call it.. The treatment, things to avoid etc are all the same, from what I have read.

Sadly, probably not. The only test i've heard of to show anything is a qEEG (not a normal EEG). The only success I ever really get with doctors is to calmly explain what hppd is, show them research from other doctors and try to guide them to the correct conclusion (basically letting their ego think it's done some of the work). It's a fucked up system, but it is where we are currently at, in the UK at least.

Yea, there's a few of us from the UK here... I'm from the midlands Welcome to the board