u/Exact-Carpet1364

Advice for those who cannot break through using 5-MeO-DMT

​Six months ago, I posted on a forum asking for help because I couldn’t achieve a breakthrough no matter what I tried—I had attempted 37 mg rectally, as well as 20 mg and 10+ mg via inhalation. I still haven't broken through yet, but I have discovered two methods.

​The first method is taking MAOIs. I do not recommend this; it is very dangerous. However, after taking an MAOI on one occasion, I took just a small hit of 5-MeO-DMT—my goodness, just a tiny hit, and I nearly broke through! But I don't dare try it again because of how dangerous it is.

​The second method happened two weeks ago when I was with a friend. I took a big hit of 5-MeO-DMT, held it in for a bit, and exhaled. As expected, I didn't break through. Annoyed, I picked it up and took another deep hit, holding my breath. At that moment, I suddenly felt a bizarre, wonderful sensation. I quickly lay down and felt my body dissolving. Regrettably, I still didn't break through, but I am convinced that just a little bit more would have done it.

​This experience gave me an idea: for non-responders like me, perhaps the trick is to take a big hit, hold it briefly, exhale, and then immediately take another massive hit—holding the second one in as long as possible. That might make breaking through much easier.

​Also, I have a question: after using 5-MeO-DMT a few times, I no longer experience any uncomfortable sensations—no tension, consciousness collapse, or fear whatsoever. I feel very calm now, even quite comfortable. Is this normal? Does everyone experience this?

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u/Exact-Carpet1364 — 13 days ago

书内直接储存的B+孢子——污染概率和存活性

最近一个朋友给了我一些 B+ 菌丝,但他们没有做一个正规的孢子印,而是把生孢子直接倒在一本普通书的页面上。这些孢子已经在书里放了很长时间,考虑到书页的环境不干净,我猜它们被细菌和霉菌严重污染了。

在我浪费时间和材料之前,我想问一下:

用培养基从这样的样本中分离出干净的菌丝的成功率到底有多高(假设进行多次转移)?

这样的努力现实中值得吗,还是说概率低到我可以直接扔掉,然后找一个干净的孢子印/针吗?

我感谢任何实际的反馈或建议,看看能否挽救它。谢谢!

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u/Exact-Carpet1364 — 21 days ago
▲ 0 r/DMT

First time attempting A/B extraction and failed. Where did I go wrong?

Hi everyone,

​I just tried my first Acid-Base (A/B) extraction, but it ended in a total failure. After leaving it overnight, there was absolutely nothing at the bottom of my glass dish. Here is the exact procedure I followed:

​* Material: 200g of bark powder (supposedly high quality).

* Acid Stage: Boiled the powder with 100ml of vinegar for 4 separate rounds, 1 hour each round.

* Filtration: Combined the liquid from all 4 rounds and filtered it using a French press.

* Salting & Basing: Added 200g of coarse salt to the filtered liquid, then added Sodium Hydroxide (NaOH) until the pH reached 12.

* Result: Placed the liquid in a glass dish and left it overnight.

​This morning, the bottom of the dish is completely empty—no crystals, no precipitate, nothing. Even if the bark quality was subpar, I expected at least some minimal yield, but I got absolutely zero.

​Does anyone know what might have caused this? Did I miss a crucial step, or is there a glaring issue with my ratios/process?

​Any insights or advice would be highly appreciated. Thanks in advance!

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u/Exact-Carpet1364 — 1 month ago