psood0nym
Bluelighter
I see. I have one foot in the other camp in spirit. There's just little I can talk about sensibly there right now.
So, at least in my experience, the qualitative differences between oral synthetic and plant-based oral DMT may have little intrinsically to do with the source and more to do with digestive dynamics.
how it works, so it seems ignorant/arrogant to say that it's not possible - there is different shit in plants than just the DMT and the MAOI so why would it be impossible for it to affect the brain differently? It makes perfect sense to me.
Yes, it is very different. If nicotine were an effective replacement for cigarettes there wouldn't be so many smokers![]()
No, but I've always been curious to try "pharmahuasca" (never enough to actually go out and find it, though). Harmala works fine for me, and it's cheap and plentiful. I know it's supposed to be the rue or caapi that causes the nausea with ayahuasca, but I've taken up to 8 grams of ground and encapsulated harmala and never experienced any nausea. The nausea always comes after taking whatever DMT plant I'm using.Have you tried using moclobemide with oral DMT? How did it compare with the rue/caapi? I tried rue once - just took a small dose to see how it felt and felt so sick I didn't want to take that into a DMT trip with me.
I don't have much experience with DMT any form, but I know people who have extensive experience and they all say that the plant-based experience is more complex with more nuances.
Difficult to decide whether that's genuine or simply placebo tho. If I gave you a capsule and said "That's synthetic DMT" and I gave you another one saying "That's boiled down mimosa direct from the amazon" you'd probably "sense" a difference.
But if I gave you them blindfolded and didn't tell you which was which I'm not sure you'd be able to tell the difference.
Well, if you could post some studies proving this, I would be happy to consider your idea.
SourceIf a psychedelic is taken several days in succession, some degree of tolerance (failure to produce a trip) develops. If a different psychedelic is then taken and this also fails to produce a trip, the two compounds are said to produce cross tolerance, which strongly indicates that they act in the same way and create roughly the same kind of trip. LSD, mescaline, and psilocybin (and probably the hallucinogenic amphetamines) all produce cross tolerance, and there are some studies which indicate that people are unable to tell them apart.
SourceMany users claim that the problem with methadone is that it lacks heroin's
intensity. It doesn't give you the same rush when injected and many users
believe that the high is inferior compared to heroin. How much of this
resistance to methadone is psychological is unclear. Many users become
obsessed with the rituals of drug use - cooking up a hit, or rolling a bead
around the foil.
In blind trials, users who were given both drugs orally were unable to
distinguish between the effects of the two drugs. Where heroin does have a
real advantage over methadone is in withdrawal. Withdrawal from heroin
should be over after seven to ten days. Withdrawal from methadone though,
can take up to a month or even longer.