Jump to content

Recommended Posts

Ive had this crap for 11 years. Can someone explain to me why my visual trails have progressively gotten worse over the years at a constant pace. I used to be able to drive at night now it is getting very hard to do. During the day now i see trails on stuff that i never used to see them on. I mentally count how long i see afterimages on different things and have written it down, and they are definatley longer over the years. I have things i use to measure how long my trails are and i would say every year they get 10% worse. Is my vision goin to be one long trail in a few years?

Dp, floaters, afterimages, disequilibrium(6 years) and static also. .75mg klonopin for 6 years

Link to post
Share on other sites

Forgot to add that i dont realy get anxiety anymore, i used to get it so bad all the time, but i have conquered it mostly.

And I am i heavy computer user, especially in the winter, something tells me that the computer monitor is making my trails worse, but idk because i wont use the computer for a few days and i dont see any effect but lets say i am on the computer for 6-8 hours after i am done i will notice my trails are 25-35% worse temporaily.

Link to post
Share on other sites

I have a similar issue.... I work 8-12 hours a day on a computer. Very likely that is the problem.

Computer use made my dad short sighted, so it certainly affects the eye in a big way. My computer use is related to work, so I minimize computer use outside of that (not easy!)

Link to post
Share on other sites

I didn't even realise i had trails or what i think is trails till i found this site. For me if I'm in a dark room and wave my phone screen across my face it leaves a trail for properly only quarter to half a second. If i wave my hand in front of my face and don't focus on it the trail is even less its just like motion blur from a photo. I have never seen trails on any thing els and i really hope i don't start to. How would you describe your ones? Last much longer? Do they leave after images?

My job I'm not on a computer at all so I don't know if that has any thing to do with it.

Link to post
Share on other sites
  • 3 weeks later...

Ive had this crap for 11 years. Can someone explain to me why my visual trails have progressively gotten worse over the years at a constant pace. I used to be able to drive at night now it is getting very hard to do. During the day now i see trails on stuff that i never used to see them on. I mentally count how long i see afterimages on different things and have written it down, and they are definatley longer over the years. I have things i use to measure how long my trails are and i would say every year they get 10% worse. Is my vision goin to be one long trail in a few years?

Dp, floaters, afterimages, disequilibrium(6 years) and static also. .75mg klonopin for 6 years

Are trails the only symptom getting worse?

Is Klono the only med you are using?

How about alcohol use?

Link to post
Share on other sites

Join the conversation

You can post now and register later. If you have an account, sign in now to post with your account.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

  • Similar Content

    • By AntoCVSS
      Hey guys,
      I started taking Clonazepam in a really small dose (0,2mg per day) 3 days ago, and yesterday evening I started getting possitive palinopsia and hard afterimages.
      Is it possible that Clonazepam induced me this?
      My psychiatrist prescribed it to me for Sertraline and Lorazepam withadrawl, for not getting too much abstinence (I am currently on Sertraline 50mg and Lorazepam 0,5mg and going down every week step by step)
    • By terye90
      In 2011, during a month, I developed a lot of neurological symptoms (I was 20 and then only marijuana several times in my life) - visual snow, palinopsia after images, floaters and tingling of the whole body (24/7), muscle fasciculations.
      In 2011-2014 I was diagnosed comprehensively (MRI, cerebrospinal fluid, evoked visual potentials, blood etc.). It only turned out that I was infected with Bartonella. I treated myself for several weeks according to ILADS, but finally I gave up. I have learned to live with these symptoms since accepting treatment failure in 2014. Now some of the symptoms are gone, some are still present (like VS, body tingling).
      Now to the point. A week ago I had the opportunity to take half a pill of ecstasy/mdma (it was my first time in my life, I only thought that LSD can cause permanent vision problems, so under the influence of alcohol I took half a pill). That night I also drunked a loooot of vodka and beer. And I don't remeber second half of the night.
      The next day I sobered up and read that MDMA may also cause/worse with HPPD/ VS. I got stressed and think my visual symptoms have got a little worse. But I wonder if it's not that under stress and paying attention to visual snow, palinopsia - I just see them more...?
      1. Is there anyone here who caused (or worsened) visual snow, palinopsia - after images by ONLY ONE (1st) USE ecstasy / mdma ? I took a half a pill and drink a lot of alcohol (Does alcohol weaken the effect of ecstasy in the brain?)
      2. Does it pass someone or is it permanent forever?
    • By Allen85
      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.
    • By Lizord
      Hi all, long time reader, first time poster.
      I got a mild case of HPPD from a six month weed bender. There were like five MDMA rolls and three mushroom trips also. I realized i didn't feel myself and stopped smoking weed, using mushroom and MDMA. This happened about four years ago. My symptoms at their worst during that time was mild VS, mild after images(barely noticeable, but they existed), depersonalization and brain fog. 
      So, up until recently, the DR, DP and brainfog have really lifted. I barely have any problem with them. I had used some drugs sparingly on the weekends. Stuff like 3-fpm, Hexen, and some others. I'm not proud of this, but my visual symptoms didn't change from what I could discern, so i thought, why not? 
      One day, I tried a compound I've never had before called 4-mpd. I snroted 30 mgs and went for a jog. When I got back in the house, I realized something was off. My visual snow was a couple levels stronger now. It now climbed freely on the walls with the lights on, and before it didn't. Everything was giving me an after image also. Any light, no matter how dim, caused an after image that would flash for a second of two before fading. I also have illusory palinopsia now; waving my hand causes it to blur across my field of view. 
      It's been a few months since things have gotten this way and nothing has improved. I wanted to hear any thoughts on this situation. 
      I quit all drugs and I mean ALL. I run daily and eat reasonably well. I'm just shocked that my visual stuff got so much worse when it seemed like nothing could make it change before. I'm guessing this will probably never get any better. Wanted to share this experience as sort of a warning. Leave the drugs alone. Ask me any questions, no matter how old the post is, I'll keep up as much as I can. 
    • By Patthebat88
      I cant take these fucking afterimages and trails anymore. Im sorry I cant do it. I fucking dont deserve this. I smoked weed one time in 2008 and had HPPD for about 3 months. Then I was completely normal. I never touched a drug after that. Recently I worked out a little and all the symptoms came back but the visuals are terrible. I see afterimages after 1 second and trails of everything moving. Also floaters and light sensitivity. I have been seeing these for 7 months. I feel fucking hopeless and do not deserve this, smoking weed must have dont something to my nervous system. 
       
      I do not want to die but I cant live my life like this. Im sorry. My plan is to get completely over this is to go on a 14 day water fast at a medical facility. Doing this cleans your nervous system as well as your entire body.
×
×
  • Create New...

Important Information

By using this site, you agree to our Terms of Use.