Jump to content

therocknamedwonder

Members
  • Content Count

    22
  • Joined

  • Last visited

  • Days Won

    3

therocknamedwonder last won the day on January 14 2019

therocknamedwonder had the most liked content!

Community Reputation

7 Neutral

About therocknamedwonder

  • Rank
    Member

Recent Profile Visitors

346 profile views
  1. All finished! I hope everyone who is able to complete this study takes the opportunity to do so. Here's to hoping it'll lead to future studies on HPPD!
  2. Wow, thank you so much! That's very helpful. I really appreciate that, that makes me feel better. Thanks MadDoc! ((:
  3. Are you sure your symptoms couldn't have been enhanced by the joints? And doing 24 whippets? Because that sounds like a lot of extra stuff that I don't plan on doing. Weed is what triggered my HPPD to go into full blown hppd, so I'm not going to touch it until at least two years after my symptoms go away. I really hope you're doing okay, that's a whole lot of drugs in a very short span of time. I used to be a moderate user of quite a few things, so I can't really scorn you. But my personal recommendation would be to stop doing drugs (especially ecstact, K, and weed, which have all been kn
  4. I've read on countless posts that exercise has helped a lot of people. But for me, exercise makes my symptoms MUCH worse. Both visually and mentally. Even on a brief walk, my symptoms increase exponentially and I get that 'heat wave' effect in the middle of my vision, which I find the most distressing. It's almost completely stopped me from skiing, which Ive grown up doing, because it gets so bad. Is there any types of exercise that might not aggrivate it so much that would be beneficial for me? That might stimulate brain growth and make me healthier? Thank you so much!
  5. I've already tried kratom a few times before I had HPPD, I'm more concerned about how it'll affect my symptoms now that I have HPPD. It was helpful for my chronic pain, but I'm concerned it might aggravate my hppd or make it worse! Ive never tried valerian, thanks for your insight! I've been sober for over 6 months of all drugs (i used to be a user of more than a few of them) except for the occasional drink and my nicotine addiction LOL. Meditation doesn't seem to help me at all, only makes it worse )): Thank you so much!
  6. My dentist reccomended I get my wisdom teeth removed when I went in for my appointment today. I know it's necessary, but I'm scared that the drugs they give me during/after the procedure will make my HPPD much worse. Wether that's permanently worse or temporarily. There's the anesthetics they use during the procedure & the pain killers after (one is ibprophen and the other is an opiate.) Should I be concerned? My hppd is mild-moderate, but it already interferes with my life quite a bit and I'm rather scared that the drugs could make everything worse. I'm terrified of it reverting bac
  7. Has anyone had any positive effects OR negative effects with kratom or valerian? Specifically red vein kratom. Does taking either of these plants affect your HPPD? In what way? Thank you! 🙂
  8. Hi there! It definitely sounds like you have HPPD. Welcome aboard. I've also had HPPD for around 5/6 months now, and I know how tough the first few months are. You can feel really scared and alone, and before I got used to it I didn't know what to do. Thats where the forum comes into play. People on here can really help you feel better but also just... less alone. And that's important. My first bit of advice is to just stop smoking weed (if you are still doing that). It's a drug that does not mix well with HPPD, and can not only trigger it (it triggered mine) but make your symptoms m
  9. From everywhere I've read, SSRI's usually make hppd worse )): Klonopin seems to help some. People with hppd usually try to avoid SSRI's as a treatment for HPPD/depression/anxiety. As much as the general public would have you believe, doctors don't know everything. YOU are your best advocate, period! If your doctor is ignoring your symptoms/thoughts/feelings, especially concerning a medication, that's a red flag for sure. Doctors should always have your care in mind, and unfortunately some do not listen. Not saying that is the case, but even before I had hppd I had a doctor like this. My
  10. Good luck! If your son is looking for immediate but short time relief, I've read that benzos ( like xanax or something like that ) can help with that. Unfortunately they're rather addictive if you use them all the time. Best bet would be to see a psychiatrist if you're looking for medication. Again, does not work for everyone, but might be worth a try if he is really suffering. If they don't believe your story, keep looking or try to explain. It's hard to find doctors who know a lot, if anything about HPPD. DO YOUR OWN RESEARCH! You are your sons best advocate! Look at possible treatments
  11. I'm sorry to hear your son has very serious hppd. It's a hard thing to deal with & ik it can be super rough, especially if your symptoms are not easy to ignore )): I am unfortunately not in Australia, I'm in america. I can't speak for others on the forum. I think stress & exhaustion make symtoms worse for everyone across the board, so most people try to remove both of those as best to their ability. I've found if I push myself too far, either sleep wise or work wise, my symptoms get way worse /: Many people on this forum recommend meditation, reducing anxiety, maintaining a
  12. I developed hppd over 2 months ago. For a while, it seemed to be getting better -- but now i seem to be on the decline. Everyday I wake up & my visual snow is even worse than the day before. I woke up today and the whole room seemed as if it was vibrating. When I first developed hppd I didn't even have visual snow, now I can't even go outside do to night blindness. I keep developing new symptoms... Does that happen??The only difference is that recently I have upped my dose of lamictal of 25 mg to 50 mg, and I am currently taking 0.15 mg of clonidine a day, as well as a benadryl at night to
  13. I would say even drinking should be avoided. You should give your brain its best shot to heal, and drinking is pretty awful for you all around. Most people have mild hppd & then it gets triggered by something... Not always just out of the blue. It's happened, but I don't think that's always the case. From what I gather, most people's permanent & major hppd was triggered by SOMETHING. Drugs, stress, etc. Try not to focus on the negative what-ifs, that will just increase your anxiety around your symptoms as a whole. Sometimes people wake up with new symptoms or find its worse, but from w
  14. If you do have HPPD, it sounds rather mild. My best advice is to listen to your body. I would stay away from all drugs, especially psychoactive ones like MDMA/LSD/mushrooms/weed. Yes, even weed... But all in all, don't do ANY drugs. In my experience, the more you focus on your symptoms, the more apparent they become. Anxiety around your symptoms can also make them worse -- it's a vicious cycle, but at least in my experience, focusing on your symptoms & having anxiety around them just makes both the symptoms & anxiety worse. Just stay away from drugs & I'm guessing you'll eventually
  15. My symptoms were very very mild before the full blown hppd. Slight trails, halos. However, whenever I would smoke weed I would basically start to full on trip -- I had visuals similar to a low dose of mushrooms. I even had mild auditory distortions. Yes, I was smoking weed before the 'full blown hppd'. I only have moderate hppd I believe -- and for that i'm grateful. I didn't know I had hppd before I had my acid flashback smoking weed. I read your introduction post & in my opinion if you do have hppd, it's very mild. Stay away from all drugs, even nicotine if possible, and I'm
×
×
  • Create New...

Important Information

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