plumbus-nine
Bluelighter
Because the doc liked it, I guessWhy were you put on it??

Because the doc liked it, I guessWhy were you put on it??
Doc prolly got a nice kickback for it, i'm sure. lolBecause the doc liked it, I guessI have neither of said disorders either and wasn't just on one but oh almost all of the antipsychotics. Edit: Yeah, add-in treatment resistant and it makes sense.
I've surprisingly been on bupe about 5 years & have normal testosterone. Although bupe is it's own beast and loses effectiveness, plus can make things worse with it's long ass half life.Oh, hypomania is actually nice. If you're lucky you get it from some arylcyclohexylamine dissociative.
It's not just the docs but approval guidelines tell them they need to have a one pill fits all sort of thingy. Opioids work until they wreck up your hormones, been there, done that and stims are somehow similar in that they don't tend to last but I don't get who abandoned stims for psychiatry, they work better than what we have now.
Similar here!! I thought it had to be some weird RC interaction which made me truly manic but it might as well just have been the breakup. Sometimes these things don't work as expected. Oh and I was on memantine, that shrink decided not being able to continue prescription for it and put me on sodium valproate, with which the diagnosis was set in stone.think i've been manic once in my life. After a breakup. I went pretty crazy. Stopped eating & sleeping really and just partied like crazy. But it died down after awhile. Doctors seem to think I must be 'bipolar' if that happened, but I'd say 1 episode of acute mania is not enough IMO to label some one "bipolar". It's only natural to go crazy after something like that after all anyway.![]()
I was doing lots of DXM around this period too and had some really life-changing experiences.Similar here!! I thought it had to be some weird RC interaction which made me truly manic but it might as well just have been the breakup. Sometimes these things don't work as expected. Oh and I was on memantine, that shrink decided not being able to continue prescription for it and put me on sodium valproate, with which the diagnosis was set in stone.
Fuck that's a lot of similarities here! I was doing too many dissociatives anyways, methoxetamine back then but DXM too, and they certainly turned me from a socially awkward person into somebody actually enjoying interaction. Was in my early 20s as well.
Difficult to say because dissociatives (NMDA antagonists) as such already are a broad spectrum. Probably you'll have heard of the plateaus of DXM and that they are attributed to different receptors/systems but I and some people found this to be not the complete truth; all dissociatives exhibit all the plateaus, just to varying degrees. The clearest distinction maybe is that DXM is also a powerful SNRI, while some of the other dissos are NDRI/triple reuptake inhibitors but that also doesn't cut it. I found DXM to possess very weird psychotomimetic (psychosis mimic) features which also were attributed to NMDA - we have this theory of NMDAr hypofunction being responsible for schizophrenia, and while there might be a possibility that some of this is true, for me it doesn't fit because DXM and DXM alone induced so-called positive symptoms in me (hearing voices to be specific) while more potent, PCP-based dissociatives didn't do that. A friend suspect it might have to do with receptor sigma (subtype 1 or 2) but that one's weird, we have agonists and antagonists under approved drugs which aren't psychotomimetic and the selective agonists noscapine and pentoxyverine did nothing at all for me in severe overdose.How would you compare DXM to other dissos? I've never had a chance to try ketamine or any of the research chems/dark net type of dissos & have always wondered.
Remarkable. I never ever managed to catch a true "hole" type experience off any dissociative, while some people seem to be able to get it readily. There's definitely the need for more research (as in real, scientific research as well as research done by us research chemical users). I left my body, at least the sensation of it, quite some times but I never went though hole type paranormal stuff and mostly I would just pass out, going from "plateau 2:" to full anesthesia without any transition. This led me to thinking that I could have over-active NMDA receptors but it's a plain guess. At least the anesthetic effects of ketamine seem not to be dissociative based while dissociation certainly is anesthetic and analgesic - etc.There were a handful of times I reached a "state" out of hundreds and hundreds of times I've used DXM and in these handful of times, it felt like I left my body.
It felt like all my organs were shutting down and all I could feel was a weird sensation deep down in the bottom of my stomach, almost by my spine.
Difficult to say because dissociatives (NMDA antagonists) as such already are a broad spectrum. Probably you'll have heard of the plateaus of DXM and that they are attributed to different receptors/systems but I and some people found this to be not the complete truth; all dissociatives exhibit all the plateaus, just to varying degrees. The clearest distinction maybe is that DXM is also a powerful SNRI, while some of the other dissos are NDRI/triple reuptake inhibitors but that also doesn't cut it. I found DXM to possess very weird psychotomimetic (psychosis mimic) features which also were attributed to NMDA - we have this theory of NMDAr hypofunction being responsible for schizophrenia, and while there might be a possibility that some of this is true, for me it doesn't fit because DXM and DXM alone induced so-called positive symptoms in me (hearing voices to be specific) while more potent, PCP-based dissociatives didn't do that. A friend suspect it might have to do with receptor sigma (subtype 1 or 2) but that one's weird, we have agonists and antagonists under approved drugs which aren't psychotomimetic and the selective agonists noscapine and pentoxyverine did nothing at all for me in severe overdose.
DXM is dirty. Dirty as in that it his many receptors, but also dirty as in dirty feeling. Every now and then sombody brings this topic up, the most recent occurance was "sinister dextromethorphan" about the sinister vibes which come with this molecule and some speculate that, according to the NMDAr hypofunction stuff, this is an inherent property of dissociatives but I doubt it. Also, the only reason we see K used as an antidepressant nowadays isn't because it would be super good at it but because the approval work was already done, and it's the only dissociative currently approved at all (besides memantine, this is a weird one too, its almost world wide only approbation is for Alzheimer's, where it is of questionable efficacy while the effect against opioid/stim tolerance is well established but seldomly used).
Remarkable. I never ever managed to catch a true "hole" type experience off any dissociative, while some people seem to be able to get it readily. There's definitely the need for more research (as in real, scientific research as well as research done by us research chemical users). I left my body, at least the sensation of it, quite some times but I never went though hole type paranormal stuff and mostly I would just pass out, going from "plateau 2:" to full anesthesia without any transition. This led me to thinking that I could have over-active NMDA receptors but it's a plain guess. At least the anesthetic effects of ketamine seem not to be dissociative based while dissociation certainly is anesthetic and analgesic - etc.
Some times I would drift away from my body though, and sometimes this was a pretty wild ride and stuff which doctors would certainly count as out of body experiences, but to me there was the real "heck-I-just-forgot-my-body" lacking. It always was conscious.
I was always interested in out of body experiences and paranormal stuff, and the possibility to experience such things with next to no physical danger on dissociatives appealed to me but I can't get there readily. Some people get a full out of body experience the first time they try K. But then we have to question what is a real out of body experience - is it losing sense, touch, control, remembrance of/with your body? But remarkable that you associate the remaining .. point.. of body with this position down the bottom of stomach and not, as one could imagine, the brain/eyes etc. I had some similar experiences but they remain too far and non-specific to really grasp them. Maybe I should have used more THC, this indeed seems to greatly potentiate psychedelic as well as dissociative experiences but to me THC alone is very dysphoric so I stood clear of it.
Dissociative + DMT (which seems to be dissociative on its own) is on my list though, pretty high on top if I could find the right people and substances. Also strangely has been shown to mitigate excitotoxicity. DMT containing trees are abundant here so that's not the problem.
Did you read the full DXM FAQ by W. White? He wrote a full chapter about paranormal experiences on DXM, and some of them are linked to temporal lobe abnormalities. Which answers next to nothing of course. Somehow I love the thought that not everything of psychedelic/paranormal/spiritual experiences can be explained purely by a neurochemical model because this leaves room for some weird trippy sci-fi fantasy stuff but I also like to know what's possible and going on.. we definitely need more research.
My coordination was very difficult on it. What you describe sounds like a familiar sensation I had. It was almost like vertigo, but different. I felt like I was all over the place in terms of my physical & spiritual body.Vraylar does some weird things to the energy body.
Sometimes I'll be out walking and my body is obviously just going with the motions of walking but Vraylar can make my energy body feel like it's doing cartwheels and falling over and getting hit by cars and rolling under buses, all while I'm just trying to mind myself and where I'm going.
I often feel similar and I know that not all psychiatrists want to act in this fashion. I consider myself rather fortunate, or proud, in that I am able to go above and beyond despite these hardships.I'd say it's almost like the poisons these institutions throw at us are just messing me up more and creating more "problems" for them to "fix"..
Thank you for the update mate. It's great to hear you're improving, and I hope it continues that wayToday marks my biggest stride in my recovery from Vraylar.
A large amount of pressure, built up on my right side, suddenly released while I was out driving and the result was phenomenal, considering. My energy now moves normally. No more of that "twisting rebar" feeling in my back.
Ever since about 6 months or so off vraylar, my thoughts have been pretty bizarre, up to the point I even began hearing voices (which I've never experienced before including off drugs). It seems that every thought I would think would consequence me severely, even it if was positive. I fucking hate this drug, but at least that part of me is almost fixed.