A new study urges trials of MDMA to treat anxiety in autistic adults
thedailybeast.com
thedailybeast.com
Its so funny, every time links like this gets posted I just nod and think "Poor bastards, they haven't figured it out yet?"
It's been 8 years since I did MDMA, so far no negatives as far as I can tell. Obviously, as with any strong drug/psychedelic, you will be a different person after the trip, what you take from that, is up to you. It is not for everybody, and especially if you feel you are prone to something like schizophrenia do NOT do psychedelics.
Secondly, what evidence is there that psychedelics cause schizophrenia?
Second, NO, psychedelics absolutely do NOT cause schizophrenia in my opinion, BUT people who have underlying symptoms or are prone to it, for them it can very much act like a trigger.
[1]http://www.sciencedirect.com/science/article/pii/09209964940...
[2]http://europepmc.org/abstract/med/17007222
[3]http://schizophreniabulletin.oxfordjournals.org/content/38/2...
I think the reason people are socially anxious is not because they think people 'give a fuck' but rather because they're confused by social signals / body language / verbal cues and that sort of thing. They don't know how to mesh and mingle properly with a crowd.
From what I read is that MDMA will help the autistic increase their emotional IQ and "fit in" better. Not because it will help them ignore what other people think of them.
From my experience, MDMA eases the mind, and fills it with empathy, love and connectedness to others (or release the molecules necessary for this). Under this state, it's not hard to see how one could temporarily break free of their 'normal anxious' state.
I now also have generalized anxiety. While I doubt it has anything to do with MDMA, I would strongly caution people to not self administer substituted amphetamines for psychiatric disorders.
Anyone who studies the history of science should be worried by the amount of power that politicians currently have over what scientists can and cannot study. There was a time after the renaissance when universities in Europe where granted almost total independence from the state. My university had its own police force and jail, at one point. This was a time when civilization advanced rapidly, and many of the ideas that we take for granted now were explored.
Now universities are very much part of the system. I am afraid that we are entering the high-tech dark ages.
I had the complete opposite experience. It took my social anxiety to another level after one use. Took about a year for me to get it back to where it was before (manageable).Obviously I can't say for sure it was the drugs fault but I'm convinced of it enough that there is no way I would try it again.
In other words people have different experiences with things like this. Just because it had such a good impact on you doesn't mean it won't have the complete opposite effect on someone else.
The studies on humans that are often cited are typically unscientific because they're inclusive of individuals who also use other substances that are known to be neurotoxic such as alcohol or even methamphetamine. Also more importantly these recreational users are not given a supply of pure MDMA so it's safe to assume that some percentage of them are actually ingesting a cocktail of MDMA adulterated with other substances.
With all of this said, the verdict is still out on whether or not this is neurotoxic in human at normal doses.. there definitely is a long term tolerance that builds up to the effect of the drug but this alone does not prove anything about neurotoxicity.
Psychopharmacology (Berl). 2007 Jan;189(4):407-24. 3,4-Methylenedioxymethamphetamine (MDMA) neurotoxicity in rats: a reappraisal of past and present findings. Baumann MH, Wang X, Rothman RB. Free full-text: http://www.ncbi.nlm.nih.gov/pubmed/16541247
It has been previously claimed that overdoses of MDMA caused structural damage to serotonin axons ('axon pruning'), but there has never been any good evidence of this. Most evidence points to modulation of expression of serotonin transporters without damaging the axons themselves:
The Nature of 3, 4-Methylenedioxymethamphetamine (MDMA)-Induced Serotonergic Dysfunction: Evidence for and Against the Neurodegeneration Hypothesis. Biezonski DK, Meyer JS. Curr Neuropharmacol. 2011 Mar;9(1):84-90. Free full-text: http://www.ncbi.nlm.nih.gov/pubmed/21886568
It is definitely neurotoxic -- I could tell that the first time I took it -- but in my experience, the noticeable effects are temporary, being mostly gone in a couple of weeks and quite undetectable after a couple of months. As a software developer who works in a fairly technical field, I'm quite sensitive to how well my brain is working on any given day. I did not notice any long-term falloff in my abilities as a result of MDMA use.
All that said -- it does invite abuse, and I was abusing it. In 1990, my then-SO left me, and I realized I had to quit.
I wouldn't worry about occasional, supervised, therapeutic MDMA use by healthy individuals.
Doses in the 0.1-0.2g range would leave me fairly slow the next day, but that's it. With heavier doses I'd see after-effects for about a week (like reaching for my phone and pulling a lighter from my pocket, disconnecting in the middle of a conversation, losing track of time)
The only time it took a long time to fully recover (5-6 weeks, progressively) was after taking some twice in 2 consecutive days. Quantities weren't big, maybe 0.5g total, but the effects lasted really long.
I did that twice and was getting vertigo for a week after. Same with my friends.
I'd say fair amount per night is 2x0.1 grams per night.
I've had pure MDMA several times (tested). I've supplemented with 5-HTP and antioxidants, made sure to eat, and even then I've often had issues where it left me depressed and anxious for days afterwards. My friends, who never supplement, do not experience such a crash. At this point, I generally avoid MDMA because the crash is too painful to be worth it.
I've recently had my genes sequenced and found out that I have a slow variant of the TPH2 gene. This gene encodes for the enzyme (tryptophan hydroxylase) which makes serotonin. It's normal that I have more aftereffects after MDMA use, because my brain is probably 2-5x slower at replenishing serotonin. No amount of supplementation will fix this, because tryptophan hydroxylase is the bottleneck.
Brains are more unique than faces. Pretty much every protein involved with monoamines has multiple common genetic polymorphisms. You really shouldn't expect MDMA or any drug to have the exact same effect on everybody.
People on the spectrum often have trouble reading emotions, people that use empathogens often feel enhanced abilities for similar tasks.
Who knows if it will pan out, but it would change many directions in research.
EDIT: Hmm. If you are talking about things like aspergers and other "mild" autism diagnoses then I can see your point since I personally see them more as personalities. I don't see it as treating however I more see it as elevating downsides of an "autistic" personality.