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    Drug Discussion


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  • EADD Moderators: Shambles

What drugs have you tried & which do you still want to try?

Forgot: loprazolam, methocarbamol.

And god knows how many others, I've sampled plenty of oddball herbs and chemicals.

Should be fly agaric season soon. I can't wait to go out picking this seasons harvest, theres a forest with a golf course local to me
with a good many silver birches growing on the golf course that reliably yields a good few pounds of fly agaric per year.
 
Limpet... you wanna try desomorphine?... go ahead... give me a report, heard it's pure in Russia

That list looks like a .Bat file
 
And yeah, I didn't think much of the synthacaine, shot my way through the gram I bought to try, and was glad I'd got some ethylphenidate at the same time so I had something decent to bang afterwards. Can't say as I'd bother with the synthacaine again.

As for the diphenidine, well, I just like dissociatives in general. Only ones I've ever encountered that I didn't think too much of were DXM and 3-MeO-PCP (the latter was pleasant enough, but seemed a lot less safe than 4-MeO-PCP by comparison, triggered seizures more than once. 3-OH-PCP was a gem though)

Desomorphine, I'd love to try, but not that revolting sounding krokodil mixture the russki addicts cook up.
Thankfully my chemistry skills are a bit better than you would expect from the inhabitants of a russian squat.
 
What about its chlorinated homolog? or methoxphenidine?

They look kind of interesting to me largely due to the similarity to both lefetamine, and it kinda reminds me of a bridgeless, ring-opened MK-801, and MK-801 is one I've always thought sounded interesting.
 
Never tried methoxphenidine. Don't particularly want to, given that consensus says it's not much better than diphenidine, if at all. Probably more dangerous too.

Plenty of things look interesting, but are ultimately disappointing. Have you ever read Kafka, for example?
 
I found 2-MeO-Diphenidine (methoxphenidine)to be rather miss... I just felt a little warm, with a mood lift, up until I vomited (something which seems to happen rather often with me & dissociatives) & then it had an insightful clearheaded phase that was akin to MXE.
 
I'm on methiopropamine atm, had it before. Not too bad.

Instead of plugging meth, why not bang it. meth, and MPA both pack quite a rush that way.
 
I smoked meth, blowing huge clouds of vapour felt good mang. Rolling that blob in a meth pipe is rewarding. I also rate MPA to a certian extent, not in to taking stims to be fuctional, but found it really pleasant with MDAI.
 
^ Smoked some meth for first time in many a year or late... is good when it's good. Not especially impressive when it isn't. Causes immense comedowns either way :!

What did you think to kratom? How did it compare to the heroin?

Weaker (by some considerable distance) but really quite pleasant too. That doesn't apply to all drugs in such a position so is not as much of a throwaway comment as it initially seems.
 
Kratom ain't too bad in my experience with it. The full-spectrum alkaloid isolates I've tried have generally been the best preparation.
Not terribly strong for me, having been on pain meds of one kind or another (morphine/oxy combination currently)

Tolerance is a bitch.

I need to remind my doc about the research papers I gave him a while back to read up on low/ultra-low-dose naltrexone protocols to inhibit and reverse tolerance, to see if I can pursuade him to let me give it a shot. At least it wouldn't cost the NHS too much, seeing as how a typical dosage unit is 25-50mg, and dose ranges for this use range from a few hundred nanograms up to a couple of uG.

Reports from people that have tried it look impressive to say the least, one paper I read had someone taper off from 60-something mg hydromorphone per dose right down to really low levels, barely noticing if at all any W/D.
Not that I'm looking to lower my dose, as my knee and hip are still buggered up, but gaining more bang per buck would be a good thing, as the low oral BA morphine has more or less means I need to shoot or plug it to get sufficient effect.

Not to mention that it would give me some substrate to work with so I could get to trying out iBnTXa, that splice-variant selective MOR1 agonist.
 
Yes, thats true, but absorption is much faster, leading to a greater rush. Plugged MPA or meth compares to my experience of accidentally shooting a shot of MPA subcut, earlier today.

Yes, it will produce a rush, but the speed of onset is slower and the rush is less than with IV administration.
 
And after all these years even Limpy comprehends what the effect of plugged drugs is with only minor 'need' for side-faff.

Are you really arguing the toss about rushes of rectal injection vs intravenous injection, Limpy? You ever tried doing the same for IV vs IM? It's much of a muchness. There are good reasons for all three all the same.
 
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