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Luukzorika

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Posts posted by Luukzorika

  1. We've now created a Facebook group espescially for HPPD only. 

    Everyone may join, it doesn't matter if you live outside the Netherlands, but everything will be written in Dutch language though.

    If you'd like to join:  All questions / discussions started from people outside the Netherlands will be answered in English language.

     

    Here's a link to our new HPPD related Facebook group. Feel free to join everyone!

    https://www.facebook.com/groups/HPPDNederland/permalink/103338163819960/?notif_id=1519750992673288&notif_t=group_post_mention&ref=notif

     

     

  2. Hey guys,

    Fortunately my HPPD symptoms are mostly gone (after roughly 6 years)

    I've made a facebook post, (in an anonymous group.) Apparently a lot of people were recognizing a lot of HPPD symptoms i listed into my post, without knowing they were suffering from symptoms of HPPD. The group administrator has made a Dutch related article about HPPD based on my post I've placed there. (https://changingperspective.info/drugsinfo/gids-voor-blijvende-visuele-verstoringen-na-drugs-hppd/)

    At this moment there's a huge discussion going on about HPPD in this specifically 'anonymous' Facebook group.

    Unfortunately everything is discussed and writed in Dutch language. So in case you're from the Netherlands and wants more knowledge / or discuss about hppd please join the facebook group: Changing perspective.  

     

    *This is not a group that is espescially made for HPPD. This group is based on having discussions about all sort of drugs)

    You're required to fill in some questions first before joining the facebook group, (to prevent bots from joining this group)

     

    Hope this will help some people who are still suffering from HPPD.

     

    Best regards,

     

    Luuk

  3. Hey mate,

    I've had HPPD for over 4-5 years but at this moment I am fully recovered. I focused on doing exercises and eating healthy that time.

    I continued drinking alcohol and smoking weed with no increase of my HPPD symptoms.

     

    I noticed the following HPPD symptoms when HPPD was a part of my life:

    - Brainfog

    - Visual snow (I still have VS but it's reducded by 80% or so)

    - Sensitive to lights. *Driving at night was HORRIBLE* (The same sensitive to lights you get from psychadelics.)

    - Eye pressure, for example, when I sat behind the computer I would get horrible headeaches and eye pressures)

    - Trails

    - After imagines

     

    I even continued using psychadelics and serotonin based drugs.  Luckily with no increase of my HPPD symptoms.

    I also haven't used medication to get rid of the HPPD since I wasn't depressed or anxiety.

    I literally have no idea why the HPPD did got better, but maybe this will help you going through these horrible times.

     

    Regards,

     

    Luuk

     

  4. This message is meant for dutch people only.

     

    Dear people,

     

    First of all excuse me for my English language. I tried my best writing this as good as possible for you guys.

     

    Yesterday I found a dutch talkshow looking for people to tell their story about those who got unrecovered brain damage from drugs use. Official facebook thread: https://www.facebook.com/SpuitenSlikken/photos/a.332876610099663.89909.332850190102305/1006906779363306/?type=3&theater

     

    Examples they were talking about are: 

     

    • Sight getting disturbed by vibrant images.
    • Sight getting disturbed by visual snow
    • People that experience their own body or the world as weird 

    The dutch talkshow is named ''Spuiten en slikken'' and I told them about HPPD which they are now really interested in.

    For those who are interested in being there as a quest and talk about your hppd, please just pm me and I'll give you the contact details.

     

    I'm a almost recovered HPPD person who was suffering from hppd for over 5 years.

    I quit harddrugs (except alcohol and weed) for a long time now.

    (I'm still on escitalopram for over a few years though)

    Also I don't think a lot about hppd anymore which probably helped me the most.

    I'm also focusing a lot on fitness in combination with healthy food which also is helping me a lot.

     

    The reason I'm making this thread?

    I want this hppd to be more famous so the doctors don't look at us in a weird way while we're talking about HPPD.

    For the dutch people who want to talk about this subject can take their chances right now.

    Spuiten en slikken is a famous dutch talkshow television program which will be live.

     

    In case people are interested or have more questions please leave a reaction here and I'll try to reply as soon as possible.

     

    Keep strong!
     

    Best regards,

     

     

    Luuk

    • Upvote 1
  5. Sorry for this late response. I was on vacantion for a long time where I didn't have the chance to get on this forum.

    My double vision got worser. I also got a terrible headache which started a month ago and didn't disappeared yet. Very annyoning!

    I have made an appointment with a proffesional eye docter at an eye hospital. Unfortunately the wait time contains 2 months.

    No, they can only do the prism thing with glasses.

    Have you already got glasses with the prisms? If so, do you feel any improvement?

  6. I wear contacts right now, not glasses. I've always had bad vision and I've worn contacts since I was 11, that's why part of me feels like the double vision thing might of happened whether or not I did drugs since my vision was always pretty bad. But, at my last eye doctor's appointment my doctor told me that there didn't appear to be anything wrong with my eyes physically so she was reluctant to give me the prism lenses. She just told me if the problem persists by our next visit then she would look into getting me the glasses. I'm supposed to go for a check up in December and I plan on asking for the prism lenses then. From the way she described it, they're just normal looking glasses with little things in the corner, so thankfully I won't look stupid with large over-sized weird glasses.

    But yea, it sounds like we have the same thing, which is a relief cause pretty much no one else I've talked to on these forums experiences double vision.

    Thanks a lot for your information.

    I will probably go to the eye docter next week, and I will go ask contacts with prism's if that's possible!

  7. ^^^^^It's not unfortunate, in my opinion, that nothing was found. I'd much rather not have brain damage. But, I can't say for certain whether or not drugs did it or if it's something that would of happened either way. The double vision for me didn't start until a good 6 months after the initial onset of HPPD, and at that point I had pretty much stopped using drugs. So it kinda came out of nowhere. I think drugs probably had something to do with it, but I can't say for sure. Also, does your vision correct itself if you close one eye??? My double vision disappears whenever I close one eye so I'm thinking it's some sort of convergence issue between the two eyes. It could definitely be HPPD related, but people often get it without HPPD too. Here's a link to the wiki page about it, you should check it out. http://en.wikipedia.org/wiki/Diplopia

    Hmm yea, the double vision started for me 1 month after I took 4-fmp (research chemical). It got worser every day from then.

    It seems we both have exactly the same issue. And yes, my vision also correct itself as soon as I close one eye.

    But are you wearing glasses or lens with prism now? If yes, do you feel any improvement, and after how many days did you felt any improvement?

    Thanks for the link, I will sure go check it out!

  8. I've never heard of anything like this with hppd.

    I think you should get a 2nd opinion from another doctor... I really don't think that has anything to do with hppd

    But you can get cross eye if you have brain damage / eye damage right?

    And you can consider brain damage as HPPD. So I think it is HPPD, since it all started after using drugs.

  9. Hello everyone,

    First of all, my English is not perfect, so I hope you can read my story a bit..

    I think I have HPPD for a long time now, but not the kind of HPPD you guys are talking about.

    It all started about 1 year ago, after using (only!) 300 mg's of MDMA. Visual snow started to come.

    I kept on using drugs for about a year. Drugs like, cannabis (1 time a week) , alcohol (also 1 time a week)

    and 4-fmp and methylone. (I only did that 2 times so far.)

    Now my symptoms are getting worse. I got visual snow, my eyes are very sensitive, and I got after images (a little bit)

    Now the worst thing about my HPPD is that I am looking cross eyed..

    I have never looked cross eyed before, but it started when I continued using drugs.

    As soon as I change my point of view to a different style my eye(s) looks like this:

    http://tinypic.com/r/1j7vch/6 (Looks weird right?)

    I even look cross eyed when I am writing a message on my mobile.

    I also can look through my finger sometimes, it's very hard to explain..

    My point of view gets disturbed as soon as I relax / stare with my eyes. (Like the pic above.)

    My point of view is getting disturbed, and I start looking double, it gives me a headeache.

    There was also no eye or bain damage found, so it must be the HPPD that causes this.

    Is there any type of medicine that can remove my cross eye, and maybe my visual snow?

    post-2557-0-38573400-1349919952_thumb.jpg

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