During the last 3 months my symptoms increased a lot and I still thinking it’s because Sertraline. I’ve been taking Sertraline 100mg for 3 years now, same with Lorazepam 1g, every day during 3 years.
I talked to my med and he wants to take me off the Sertraline and change Lorazepam for Clonazepam some weeks / months. I am super afraid of withadrawl and also of still using benzodiazepines. My symptoms nowadays are: Severe VS, severe ghosting and palinopsia with afterimages, photophobia, photopsias, nyctalopia, flashes, color problems, apparent movement in objects, kind of bugs in vision, and really mild shaking vision (just on my periphery).
What I can do? Please I need help because my symptoms are so severe nowadays and I don’t want to get them worse, actually I would like they come back at least to last year were they weren’t so noticeable.
I get intrusive thoughts everyday and I need help. I’m 21 years old.
Hello all! I took high grade acid a month ago and had a good trip, although I have been dealing with some very mild static. I think it might be going away but I can’t really tell. I have access to CBD oil, would it help get rid of the symptoms quicker or temporarily? How much should I take at a time? Should I micro dose? Maybe I am impatient; I have been fasting from weed, alc, shrooms, nic, etc for the whole month haha
I’ve been suffering VSS for 2 years into mild and not too symptomatic way, but last month it became so several worse and I want to ask you something about my symptoms because I am super confused and afraid.
Let me explain my case.
About 2 - 3 years ago I tried hashis cigarette from some friends, I had a really bad trip with visual hallucinogens (something that got me super anxious and depressed, I didn’t like the effect).
After some weeks I got panic attacks and much anxiety, so my doctors prescribed me Sertraline 100mg and Lorazepam 1g per day. After some months of getting alright I started getting VS symptom, static dots in my vision like a TV. I went to the doctor but my vision was alright and my brain too, so as it didn’t bother me too much I lived with it for 2 years.
On Summer 2019 I felt so good so I stopped the medication gradually, I stopped the full medication on December 2019. Last month I got too anxious because a medical test. So my VS got worse and I started with flashes in the eyes, palinopsia and severe nyctalopia. I also had a kind of bad tinnitus so I went to the doctor and got treated with Dacortin (corticosteroids).
and also I had to start again with my psychiatrist medication because anxiety and obsessive compulsive intrusive thoughts.
Nowadays my VSS is super severe but I also have some weird, uncomfortable symptoms, and I get something new everyday, I am super afraid.
I have really severe symptoms: VS, palinopsia, nyctalopia, afterimages, really hard flashes at the edge of my vision, spontaneous and random black and bright dots that appear and disappear from the vision quickly, and also I have the perception of looking and object and the object moves so lengt but it only have a seconds duration.
Everyday from 1 month symptoms get worse and worse, I had to stop working because my world is so distorted.
Do you think it’s VSS, or HPPD??
What I can do and how I can be threated? I need help.
I saw a lot of success on Clonazepam and Clonidine or Lamotrigine. Should I go to the doctor to get a prescription of those? I am super afraid, anxious and desesperated.
I also have obsesive and intrusive thoughts about becoming schizophrenic, or suffering it for all the life. I can’t live with that, I feel like living into a psichedelic trip, and I NEVER tried LSD, cocaine, MDMA, or something like that, I have been always fear of these kind of drugs. So what do you think?
Looking for your answer, thanks for your time and attention.
Hello All, My name is Allen. I've browsed this site randomly over the past couple years but was afraid share. I'm in my 30's and have had HPPD 2 for 18 years. I was diagnosed 5 years ago after a seeing countless doctors through the years. Recently I found out my wife was pregnant and I became determined to find a treatment or, god willing, a cure. When I was in my mid teens I took lsd about 5 times and I was a chronic marijuana smoker. The last time I took lsd I smoked weed at the same time and I had the worst experience of my life: My heart began to race uncontrollably, my arms and face became numb; I saw long blury trails on everything and I felt hot and cold all at once. It was so intense that I thought for sure I was going to die. In desperation, I curled up in a ball on my couch, closed my eyes, and began to pray to god repeatedly to make it stop and let me live, until eventually I fell asleep. I woke up the next morning and thanked god I was alive. I swore of lsd forever. Unfortunately that didn't stop me from trying to party with my friends as usual. Every time I smoked weed after that I would have severe panic attacks and almost black out. When I'd drink alcohol I felt like I had a lump in my throat and couldn't breathe. A couple weeks after that horrible trip I woke up to a dull version of the same type of visuals I had the night of my bad trip, I was petrified and began having random panic attacks. I finally told my mother what I did and what happened since and she took me to the doctor. The doctor swore it was depression with anxiety and completely dismissed any lsd involvement. She prescribed me Effexor and xanax. The effexor didn't help at all and it made my heart race. The symptoms were not going away. I was afraid I damaged my brain beyond repair. Shortly after I withdrew from school and became a hermit. The xanax helped a lot with anxiety but the visuals remained. Through the years I saw about a dozen different psychiatrists and none of them knew what was wrong with me and continued me on benzodiazepines and ssri's. I lost my insurance and couldn't afford all the doctor appointments and medicine, so I began getting zoloft and Vicodin off the streets to self medicate. Eventually the visuals became less intense and my panic attacks were less frequent. Although the visuals and anxiety are a part of my daily life, I still manage to function. Some days are worse than others but I forced myself back into society and I got a good job in construction, and married my girlfriend who has been with me through this whole experience. I got off the vicodin with suboxone and continued the zoloft. With the news of our first child, I found a new determination to get rid of this horrible disease for good. I told my doctor that I wanted to try anything we can to make this stop and she agreed to start prescribing me different medications to see what, if anything, will work. She prescribed clonidine last visit and I started it 6 days ago. Unfortunately it hasn't helped my visuals at all and last night I began having strange thoughts and seeing weird images when I closed my eyes. I'll keep everyone updated on how it goes. I'm really hopeful that something will get rid of this for good. Wish me luck and good luck to all of you.
P.s. I am thankful to whomever started and maintains this site. I hope we can get this horrible disease more attention and find a real treatment for it.
June 11, 2019
SUBJ: Faces of HPPD Survey/Research Published – RESULTS!
Dear HPPD Online Community:
As a mom with a grown son with HPPD, I was so fortunate to come across this forum several years ago for information and support. David Kozin, who runs this board, is an amazing man to have created and maintained this website and kept up his work/studies over the years – all the while suffering with HPPD. I would like to thank him for this platform, and well as thank those of you who participated in the survey that I launched four years ago to collect data about individuals who had received an official diagnosis of the disorder.
Fast forward…. Here it is June 2019. Long overdue for the published report, however, I lingered – always hoping to gain a larger sample of subjects.
I am fortunate to have a PhD in psychology, experience in research, and a heart to try to make a difference. Instead of publishing a book, it only made sense to get the results in the hands of the scientists and medical professionals through scientific writing. I am so happy to tell you… the peer-reviewed medical journal, Addictive Disorders & Their Treatment, published by Wolters Kluwer publishers, has reviewed and accepted my manuscript for publication in an upcoming issue. Last week the article completed rounds of publication editing and formatting. The article is posted at their website for advance release.
Lewis, DM, Faces of HPPD: Hallucinogen Persisting Perception Disorder Patient Survey Results and a Descriptive Analysis of Patient Demographics, Medical Background, Drug Use History, Symptoms, and Treatments. Addictive Disorders and their Treatments. Forthcoming 2019.
The link is here: https://journals.lww.com/addictiondisorders/Abstract/publishahead/FACES_OF_HPPD__Hallucinogen_Persisting_Perception.99733.aspx
(NOTE: This direct link will change probably in a month or two when the article is given a print-issue date – right now, it is advance copy, undated. In the future, you can search the article at https://journals.lww.com/addictiondisorders/ .
While the article is available for immediate download, many of you know that publishers charge money for copy downloads (this one is $49), and authors cannot give away their copy. This, I know, is not a good thing for some within the community who do not have the funds.
However (here’s the good news 😉), I contacted the publisher and obtained permission to publish a summary of the results (the important data!) and I created an infographic that provides you all the results. I am including it here as a .pdf file, attached. It’s reader-friendly, and I hope it provides insight.
I want to mention some findings that particularly concern me: the high rate of suicide ideation (among other co-morbid psychological/psychiatric symptoms reported), and the significant number of individuals who reported being unable to work due to HPPD. I feel strongly that HPPD needs recognition as potentially disabling – and I believe there are some individuals who may need government assistance (eg, Social Security Disability benefits). My future work leads me in the direction of carving a path for HPPD as a qualifying mental disorder for eligibility for assistance. I will keep you posted on that.
Again, thank you so very much for those who partook in the survey.
My best wishes to each of you for good health and peace of mind,
Doreen M. Lewis, PhD
Faces of HPPD Infographic - LEWIS.pdf