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marce

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Posts posted by marce

  1. On 5/7/2018 at 11:16 PM, Onemorestep said:

    Many people with hppd say SSRIs make them worse. This was the case with me. I was on SSRIs most of my life and went off of them right before I got hppd. When I gave them a shot again I tried a low dose of escitalopram for 7 months. I came off of it due to sexual side effects and noticed that I immediately started feeling better. I was able to fully withdraw in a weeks time which, in my past experience, would normally be too fast and would send me into a depressive episode. I don’t think I was permanently hurt by trying them though. 

     

    On the the flip side, there are people with hppd that SSRIs have helped. My understanding of the mechanism is it is the eventual downregulation of certain serotonin receptors such as 5ht2a that cause a big part of the antidepressant effect. That and increased bdnf after sustained use. This does take time, however. One to two months on the drug. Before that, many “normal” people can even experience feeling worse. If you think it is worth it to try, give it a shot. Otherwise discontinue and try something else. There are plenty of things that can help reduce 5ht2a and raise bdnf that aren’t SSRIs. I believe selfhacked has an entire page about the receptor and how to influence it—I like the page but it should be cautioned that some things they talk

    about are not safe for those with hppd such as using psychedelics to downregulate. Also feverfew. Don’t take that. 

     

    Hope le you find some relief soon.

     

    oms

    Thank you for your insight, im doing better now. I have since stopped taking zoloft, i was also experiencing sexual side affects and they have since ceased. No long term issues were caused by zoloft im doing well. Ill check out selfhacked sounds interesting!

  2. My symptoms are, I guess in relation to others' VS is mild. I've only had hppd since April, but regardless I experience dp/dr quite a bit, and I have a tinnitus like ringing in my ears that is pretty loud and can only really be drowned out with constant music. I also have a bit of a foggy mind as if I'm still high, and my reaction time has slowed down, as well as my eyes feeling like they roll very slowly in my head. Also I cant see shit at night, the VS makes me almost night blind. Best wishes to everyone here.

    -marce

  3. Im curious to know if alcohol worsens hppd and if that only applies to getting shitfaced or does it apply to light drinking too? Also i smoke cigarettes, does nicotine affect hppd in any way? Im fine with no more drugs but id be pretty sad if i couldnt drink or smoke cigs anymore. And one more thing, ive been sort of been hearing that hppd gets worse througout the years, is this true? how many people does it get worse for? the majority? im scared of it getting worse im 17 and dont want this to affect me any worse than it is already.. sorry for all the questions 

    thanks for reading,

    -marce

  4. thank you for the advice, i've started working out and going on runs, and i feel great but i noticed that my tinnitus like symptoms as well as my visual snow gets worse when im extremely exhausted from say running, is this a good thing? and i have also found that distractions help me ignore it more easily than not.

  5. I do smoke often and it doesnt make visuals intolerable but it definitely makes them stronger and the ringing in my ears gets almost unbearably loud. Ill take a break for a while and stay hopeful thank you for the support and advice

  6. Just found this site and I think itd help me cope better with hppd so here's how Ive been affected. I'm not super expreienced with psychedelics Ive probably only dropped acid about 12 times, shrooms once, and ecstasy once. It was after my fourth trip that I developed visual snow, and only off of 2 tabs, so naturally I panicked thinking I was perma-fried, but it was very minor so I didnt really care. I kept taking acid and it progressively got worse as I'm sure you all know and now I havent dropped in 2 months probably and I dont plan to drop anytime soon. My visual snow is super bad now with flashing of light, small visuals, and some pretty bad night blindness. I have also developed the tinnitus like ringing in my ears, and experience dissassociation and derealization time and time again. I have also noticed a slowing of my reaction time and find it harder and harder to remember things and pay attention, I am also very restless now and find it hard to sit still. Sometimes I feel like I'm losing my mind and that nothing is real, but I can usually reassure myself that of course reality is real its reality right? Ive had hppd since April of 2017, so not as long as a lot of you here but hopefully it gets better, thanks for reading.

    -marce 

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