morbide

Well now you're not lost anymore LostGirl, welcome to the forum! As a matter of fact i suffer from each and every one of the symtoms that you listed, though not as extreme as you describe them. Some users report allevation of visual symtoms and dpd/drd with antiepileptical benzos such as keppra and klonopin (kepora can be a lifetime option and klonopin may only be used on occasions where you really need to be on your a-game) There is a huge amount of good information on this forum so read up and listen to and share experiences!

New party trick maybe?

Oh i see! The spasm has died down now It suddenly moved up in my right ass-cheek and my ass was wobbling like crazy, friends and my gf thought it was hilarious since you saw it through my jeans...

What is IBS?

I am getting more and more certaim that i have rls, the muscles on the back of my right leg have been jumping and vibrating like hell lately. Right now my leg is living it's own life... I might buy some iron and vitamin-b supplements, if that don't do the trick i will go to a doctor and maybe get ropinirol prescribed, would be interesting to see how that would affect hppd.

Damn most of the newcomers are reckless, let me put it like this: Recreational drugs gave you hppd in the beginning, why would you even consider to keep doing them? You only live once, give yourself an endurable time whilst you are still living, i am saying this out of my own experience. I read about hppd when i experienced warning signs but i keot on drinking and toking and here i am, my walls are moving, geometrical patterns are forming in the static and my afterimages and traces are horrible.

All the time man, all the time... Done is done though, no reason to dwell on it imo :/

This really bugs me, i am seriously considering getting klonopin prescribed but only to use once or twice a week for study/reading sessions, work interviews etc. Would it be ok to use it like that and not everyday?

If it's like a an impenetrable black courtain that doesn't go away then it's retinal detachment and then you must go to the doctor But almost only old geezers get this so no worries

Great post james! That is all

It seems that you are going through the same phases as i have, the only thing we can do is to adapt even more, i move really slow when i'm at home couse my arms leave really long traces... Oev's are really terrible at night too, straight trippin...

This is really amazing but wow, when i think about how complex and voulnerable the brain is my head really hurts... But wouldn't this suggest that taking lyrice whilst having hppd is a good thing?

I'm feeling kinda lucky that i've had starbursting since i was little and i'm used to it!

I would be so happy if my vs went away, and when i think about it the shady stuff you see instead of vs, i defenitely think it was my first symtom. On the few of my good days i've had post-hppd i have also seen it, the vs covers it up atm. And now i haven't been drinking for four days and i really notice a change in all symtoms! And since you're not drinking it's maybe obvious that you're improving. I'm gonna try to have some months without being drunk but no alcohol at all will be hard

It's impossible to not drink during summer bbq only fits with beer or red wine

E seems to be mixed with 2-ce, 2-cb way too ofteb and come on, if you really are taking hppd serious you must cut the drugs. It's not like you don't have any choice and you WILL get messed up if ou keep doind mdma and heavy shit like that, why make it worse than it already is?

Hi, since you haven't had it for a long time yet you have a good chance of recovering. Don't freak out about your symtoms, new ones will certainly pop up but keep in mind that they are certainly 100% normal and you are just starting to pay attention to them (like flosters and streetlight halos), i myself've had bad starbursting ever since i was a toddler. Stay strong and we (us?) here on the forum are always here fo support and advice!

Warning signs at 17 but it really hit me at 18.

For your anxiety maybe klonopin? It also reduces some visual symtoms from what i've read.

Haha a fucking doctor I'm sorry but i couldn't resist.

My hppd kicked in ~a month after a trip on ~70mg of 4-ho-met, just like wham! The white room i am sitting in today was filled with static and the walls started moving and it has ever since. More and more symtoms have of course showed up since the onset. Dp/dr were the first symtom to dissapear.

It's not worth the trip man, you should take hppd more seriously and cut out on ALL drugs except maybe alcohol.

Wouldn't we feel dizzy and tired all the time if we had cerebral apoxia, physical activity would then make us pass out no? I think someone on the forum had hyperbaric oxygen treatment without any results. Although it makes a little sense that our brains doesn't get as much blood and oxygen as it should becouse it does missinterpret visual stimuli and Maybe our brains runs on a higher rate to make the most of it ?

This is so weird, i'm pretty hungover and now my symtoms are really mild... Why can't hppd make sense?