Missjess

Thanks for ur response...I didn't think a local anesthetic would have any affect.

I also am able to take a ventolin puffer for my asthma thankfully ...I do get a delayed reaction to it but it's nothing serious like if I was to drink alcohol or take a medication that affects my brain.

And did it have any affect on ur vision ?

I strongly think that this may be multiple sclerosis

For me

Does anyone else have a sensitivity to hot and cold weather ? In summer I had to be mostly in air con otherwise when I was out my vision would go more blurry and I would feel a sort of inflammation happening and now it's winter time and the winter is affecting me much more worse then summer..it seems the cold air has an affect on my sensory nerves and my vision feels like it's geting worse and more inflammation again..

Oh god this is the worst part of hppd ..the mental shit. I always get jumbled up thoughts and auditory hallucinations it's like ur mind is one big jumble of mess

Are u located in Australia by any chance ? I am actually looking to find some fresh lions mane mushrooms for myself to try!

Does anyone in Australia know where to buy fresh lions mane mushrooms? I'm located in Perth but I don't know where to find the fresh mushrooms to eat, I can only find supplements.

I've just ordered some lions mane mushroom supplements for myself has anyone got some more information on them please ?

Thanks

Yes and the doctors are not helping me at all...So screw them

Oh well it sounds like u got the normal hppd style jagermeister

Yes there is a chance of full fuking recovery !! So far I have done my venous blood has tests...liver functioning and metabolic. Just left is arterial blood gas testing then results will go to my doctor. I know I have a probly with my oxygen because of wat happened in Brazil and then it clicked when I typed in environmental sensitivities and multiple chemical sensitivity on google

Carbon monoxide may be a cause for many ppl with hppd honestly... But of course there are probly many others too but if ur super sensitive to everything such as supplements, electromagnetic fields and the extreme weather conditions like I am then deff get checked out for muses syndrome

So after typing in on google ...multiple chemical sensitivities and environmental sensitivities I came across this article about carbon monoxide poisoning and it's affects on the sensory nerves!! Obviously this may not be the cause for everyone and I do beleive my case of hppd deviates away from the norm but what we all share is extreme sensitivity too almost everything (not all of us obviously) I know I cannot take anything and react badly to everything including weather extremes...

It's called muses syndrome ...here is an article http://www.mcsrr.org/poe/cohome.html

http://www.breathing.com/articles/mcs-muses.htm

I am in the process of doing all the testing but they have already found something wrong in my oxygen levels ....my theory is Iboga caused my body so much stress and in order for my body to get rid of the Iboga it was under so much stress and produced carbon monoxide which flooded my sensory system and gave me hppd .....i rlly feel like I found good information for my style of hppd!!!

Just thought I'd share

I would like to know if I share this in common with anyone else...

so I arrived in brasilia a couple of weeks ago...it was very hot and humid...i didnt know it was wet season..4 days later my stupid brain started getting aggitated and started to react to the air and possible humiditity ...i had to leave brasilia and when i did my hppd started to worsen...i was dehydrated to fuck and thought i was gonna die ....am now hanging out in são Paulo and waiting to try a dehumidifier to see if that was the actual problem and to see if it will help....usually i cannot sleep a wink at night and my brain starts reacting etc

am i really odd in this symptom and alone in it??

thank u !...i have run into some bad luck tho....ive had to leave brasilia because of extreme humididity that was actually making my hppd worse i wwnt in wet season this time apparently...so am hanging out in são Paulo and waiting to get a dehumidifier and go back in dry season.

does anyone elses hppd brain react to the environment and mold and high humiditity ???

david b

I had the same experience with lamictal...the longer i took it and when i tried to move up the dose my hppd went 100 times worse and i had to stop

i cant take anything...drugs..supplements and anything that alters the brain chemistry in any way

I also reacxt very badly to smells, unclean air, high humidity....its fuking awfull!!!

im in brazil again waiting to go to brasilia in march for my second trip back to John of god

jay

i cant seem to like ur posts!! but i started laughing lol

of course i didnt get cured with ayahuasca!!

Ibuprofen is a fairly benign drug.  It's similar to taking an aspirin, tylenol, or naproxen.  Like people do for headaches.  Worth looking into Jess.

Well so far every supplement I have taken fuks me up, every drug I have taken that gets processed thru my brain fuks me up, I have also got multiple chemical sensitivities now since getting brain damage from Iboga. That's why I'm scared to take anything else

I must say I find this post interesting....I do believe in my case of hppd that there is some sort of brain inflammation going on....I'm way to scared to try to take another drug tho

Good luck

Hmmm it's hard to differentiate that with plain old Dpdr

Aside from the visual shit...what type of mental symptoms does everyone suffer with? I'll start with mine:

Severe cognitive impairment

Unable to register shit thru my brain

Trouble with judging distance when driving

Never feeling like talking

Shit memory

No sense of time

Random meaningless thoughts or scenarios sometimes go thru my head

Hard to control impulses

Extreme mental slowness

Unable to learn new shit especially motor skill activities

Poor body coordination in relation to other people

Clumsiness and frequently bump into things

A sense of being in another planet far far away from reality and people

The cognitive dysfunction is the worst shit ...but I also despise dp I guess coz I has dp for 7 years before I got hppd...but now my dp perception is 20 times more fuked with hppd

I rlly rlly want my cognitive functions back I'm sick of feeling like a fuking retard

Yes ur taking a huge risk...honestly I don't think it matters what drug u take...every drug, supplement even fragrance has done the exact same thing to my hppd!!!!

It's best not to take ANYTHING!!!

Jay....I rlly feel sorry for u

All of that sounds absolutely terrifying and fuked up !!