F.U.B.A.R.
Bluelight Crew
Does the bad quality make people want more of it and make it more-ish?
Yes, because its not satisfying so you're chasing a feeling that is unattainable, no matter how large the initial dose or how many redoses you take.
Does the bad quality make people want more of it and make it more-ish?
I may have that problem.Yes, because its not satisfying so you're chasing a feeling that is unattainable, no matter how large the initial dose or how many redoses you take.
“Surely happening”?on how glycidate is easily turned to MDP2P and everything ought be sweet from there and not deal with the reality of what is surely happening.
But I thought you said “surely happening”???could make perfect MDMA if it was treated right and each product purified properly as one goes. But is that happening? Most of the time probably not but who the hell really knows.
Hear, hear.and others like it and we really need research scientists to analyse the impurity profiles of mdma samples
Are you making that assumption based on that 2016 Australian report?produced from these precursors (which are by far the most common now)
This is a six-year-old report from a geographically isolated country of 26 million reporting on data from seized ecstasy only. We cannot and should not extrapolate and extend that data to be representative of Europe (population > 747 million), North America (population > 579 million), and/or South America (population > 423 million) and the drug-taking habits therein.And if you are still not sure about this, check out this Australian illicit drug report -
https://www.acic.gov.au/publications/illicit-drug-data-report/illicit-drug-data-report-2016-17
That sounds like an unholy idea…We have talked about this before, and the clear shift from borohydride reductive amination to platinum hydrogenation. But what of this other method or methods - reductive amination “unclassified route” or routes was almost 50% of all seizures. Unhelpful but what is it. Is this in reference to the mythical “one-pot” reductive amination of PMK-glycidate to MDMA
Hear, hear.or is it something else. We need to know.
When Sasha was still alive and before the dementia sunk in, he was really good about corresponding w/people on these sorts of topics. I don’t imagine you would’ve needed to cross continents to gain knowledge from him. Many moons ago, circa 2003, I was incarcerated with someone who had a case for 5-MeO-DiPT and they had reached out to him and were in regular correspondence with him vis-à-vis the Federal Analogue Act and its different implications.Most frustratingly, since 2016, the profiling of MDMA seizures stopped so I cannot give you similar data for last five years. What might it tell us? What trends would be apparent? Which government laboratories have these answers?
If only the mighty Sasha Shulgin was still alive (may he RIP), because I for one would cross continents to hear his theories and views regarding this Meh-ss.
Well, I guess I should 'fess up then.
Recently received a diagnosis of autistic as well as ADHD/OCD.
Could be relevant to our conversation, so...there you go.
Take with a grain of salt, as I went 40+ years blending in with the neurotypical population for the most part. Only got a diagnosis because I sought it out after a family member was also diagnosed.
Curious what you are referring to as an atypical response pattern.
I would 100% participate in a MAPS study if there is one I ever qualify for.
I have been overwhelmed by stuff lately, and and am dealing today with a ton of anxiety/stress, but I don't want this to disappear without at least a placeholder comment.
I could talk a lot about late diagnosis. That's probably outside the scope of this thread.
The vast majority of MDMA users take it seeking a "good/happy feeling." (How's that for generalization?) I've had conversations and seen interviews/videos with autists re MDMA, and a lessened/missing "good/happy feeling" is surprisingly not uncommon. That's the atypical response I referred to. There could be a lot of reasons for that (including "What is wrong with the MDMA available today"), and of course what's going on would vary by individual case, but the MAPS study would shed light one way or the other.
In my case (which seems really complicated with a lot of potential factors/reasons), I have never gotten the "good feeling." Very interestingly, I have seen therapeutic benefit. Increased (or renewed) interest in communication with others and less anxiety about that. Also, I am definitely tracking a longer-term increased awareness (maybe even more control) of my emotions. Seems to me there are clues about neurological circuitry and receptor subtype function in there if the autistic population contains a statistically significant atypical response. To say nothing of active-mind modeling and analog blending of different circuits via signal modulation (up/down receptor regulation).
And re that last bit (neurological circuitry and receptor subtype function), I believe that's exactly where Matt Baggott and Tactogen are engaged studying various molecules/substances to find effective therapeutic solutions that are "gentler" (their words).
Thanks for the personal details re typical/atypical. As for a separate thread, I'm honestly very skeptical given the lack of comments/feedback on just about everything I've posted anywhere near the topic.I definitely had the good/happy feeling in my early years of use, through 2005 or so. More than just good and happy though...profound, enlightened, open, aware, in-touch, divine...I could go on and on.
This probably deserves a separate thread, honestly.
I have recently wondered if the dopamine response of an ADHD individual is one reason why MDMA always helped me to hear more detail in music. Possible that the dopamine release simply allowed me to focus more. Would I have a similar response from ADHD meds? I don't know as I have not tried any.
Good MDMA will definitely help me to communicate more and with less anxiety. However, some of the Meh batches have had the opposite effect and made me not want to talk AT ALL, and just wish everyone would leave me alone.
I agree that there is a lot to unpack with all of this, and many routes of study. I am hoping if the FDA approves MDMA for PTSD it will at least open the doors on additional research regarding response, magic, loss of magic, etc.
Thanks for the personal details re typical/atypical. As for a separate thread, I'm honestly very skeptical given the lack of comments/feedback on just about everything I've posted anywhere near the topic.
I won't derail further, and sorry for the interruption. But one more thing, because I do think it's relevant to the thread topic generally.
https://phys.org/news/2022-06-scientists-breakthrough-serotonin-receptors.html?utm_content=212062120
I will say the crystals do look quite clean, but it's only 50 mg in that capsule. And also it's in Raleigh-Durham, North Carolina, and while this could be worse, no disrespect to the Cackalackas, but I'll pass, lol.https://www.drugsdata.org/view.php?id=13264 this MDA looks like the magic
. And when that set was done, back to deep-heady-droning hip-hoppy beats, which is still nice, but the energy was gone again, as soon as it started. I've discussed this with a few of my closer friends and they experienced the same thing this weekend.Can't remember if I posted before, but i've set aside the prettiest crystals of what I believe to be highly pure MDMA. When crushed to a powder, there is a light MDMA scent.
To my knowledge, it was made in Canada and the source says made w/ safrole in a less than large operation. Take that with 2 romantic grains of pink salt, but to me nothing seems untrustworthy about the finer details that I won't share here.
Obviously looks are meaningless and counter to harm reduction if actual testing hasn't taken place, but with those boxes checked I'm always on the lookout for stuff that looks like this. I always window shop the MDMA of dealers that come by trying to sell to our festival campsites, this is not a common form & have not come across it this way (granted dealers often get the product crushed already).
Apologies if I'm breaching any sourcing stuff
Yes, been taking 100mg doses of this same MDMA for like 2 years, 6 times i think? Works great, I would consider it the magic stuff, but it doesn't miraculously work for ppl in my group who have trouble with MDMA working "properly", which has led me to be skeptical of this dichotomy between magic & meh. Myself as a test subject, the same 100mg dose is not the same each time, and feels highly influenced by set & setting, the roll is subdued to varying degrees if things are less than ideal. I do wonder how crazy i'd get from 125mg; the time i rolled the hardest ever I didn't have the pleasure of weighing out the cap myself or confirming its weight.You tried it though?
I tend to think of drug-induced euphoria as falling into one of three overall categories:MDMA never blew me away though, especially not in the sense that I've seen others roll. I don't get too lovey and for sure don't experience pure "euphoria". But others do, on the same MDMA.
Yeah, I've never experienced any real euphoria from serotonin releasers, I enjoy them, of course, and have really tried, but by now I just know very well what I'll get from the ones I know at least. Never tried methamphetamine, but these days my main hope is on MDA which does sound like it has massive recreational potential and like something that I'd enjoy more than MDMA. Very rare in Europe though...I tend to think of drug-induced euphoria as falling into one of three overall categories:
- Numbness euphoria – from drugs that numb the mind and body, offering relief from pain as well as anxiety. I include opioids, barbiturates, benzos and “z-drugs” like Ambien. Also, dissociatives have one foot here and the other in psychedelics. The common thread is the numbness and detachment from certain feelings.
- Stimulant euphoria – from stims that hijack dopamine and adrenaline. Sometimes serotonin comes into play with the heavy-hitters like MDMA and methamphetamine, both of which can be profoundly euphoric but come with some risks. This stands in contrast to the aforementioned numbed euphoric state – the user is placed deeply and firmly within their own bodies with heightened senses as opposed to feeling numbed, sleepy, dreamy, dissociated and/or detached.
- Psychedelic euphoria – This is not for everyone, and it’s perilous hiking the side of this particular, steep mountain into nirvana. It takes practice, discipline, courage, and a willingness to place oneself in a state of vulnerability in order to achieve higher states of consciousness. In the lower states of psychedelic euphoria, the experience is in the body with heightened senses sort of over-stimulated in a way, producing psychedelic effects. At highly increased doses, or in the case of certain compounds like n,n-DMT, the user can undergo ego death and feel completely detached and dissociated from their corporeal body. There is a great deal of insight to be had by visiting these states in one’s mind’s eye, so to speak. But again: it isn’t for everyone, unfortunately.
That's a shame. MDMA euphoria is unique and intense. MDA comes close but is more psychedelic, grittier, and less empathogenic, less anxiolytic. In my opinion, 5- and 6-APB and their n-methylated structural analogues get close to MDMA's euphoria, too, and are enjoyable, but still aren't quite MDMA. There's also 4-FA which isn't bad, and methylone, which some people like and others loathe, but both these drugs are in the MDMA ballpark, at least. You've got 3-MMC and 4-MMC, but they're like if MDMA and Cocaine had a baby and it grew up to be a drug…Yeah, I've never experienced any real euphoria from serotonin releasers, I enjoy them, of course, and have really tried, but by now I just know very well what I'll get from the ones I know at least.
Yep, recreational potential confirmed. I think I like it better than MDMA, but they each have their place. MDMA has a worse hangover to me, though. Also, I can take and enjoy MDA by myself, but MDMA is lonely without some company, something that is somehow both a merit and a demerit depending on circumstances. Either way, MDMA is too social to take alone, for me, but I don't feel this way about MDA (or virtually any other drug for that matter).but these days my main hope is on MDA which does sound like it has massive recreational potential and like something that I'd enjoy more than MDMA. Very rare in Europe though...
Depends what you're into. Different strokes for different folks.Recreationally, psychedelics are indeed unmatched.
Even Dr. Shulgin advocated what he called "piggybacking"—what many people today call "candy-flipping"—with his suggestion being to go from MDMA into 2C-B, dropping the 2C-B just after the MDMA peak, one fading into the other. I like to candyflip LSD. The MDMA tends to give the acid trip a warmer, brighter character wherein my social skills and language abilities are not compromised as much as they typically are while tripping. So depending on the mood, set, setting, company, and other factors, it sometimes makes more sense to candyflip as it lengthens the overall trip/roll time, lets me trip without communication issues, and gives me plenty of energy to pull an all-nighter (which I typically do when I candyflip (unless there's K involved, then I'm crashing into a couple k-holes and passing out)).I've actually never combined a psychedelic with MDMA, as far as I recall right now, intuitively it feels like I'd be muddying the waters too much but what is my intuition in the face of mountains of anecdotal evidence