Choosing one of the compounds of Kambo is a great idea but maybe there is a synergy here like the "totum" (french word) of a plant which is the synergy of the active subtances.
Anyway Hip, have you tried this again?
I agree there may be some synergy, but I mainly decided to try just one of the compounds within kambo because I did not fancy making little burns of my skin in order to administer the kambo (this is the only safe mode of kambo administration), and I certainly did not fancy the
extreme vomiting and diarrhea that kambo induces. However, if you don't mind things like this, then fine; kambo may be worth cautiously experimenting with.
Also, I wanted to biochemically explore what active principals within kambo might have caused the very significant improvements in ME/CFS that Jox reported immediately after taking kambo (and this was not a one-off improvement, because the improvements appeared each time Jox took kambo, and I believe he has taken it every week since 2012).
I think it is irresponsible not to follow up on a fellow ME/CFS patient's observations of significant improvements from some unusual treatment (provided the treatment appears safe); if you don't follow up, you may miss a very valuable remedy. Imagine if nobody had followed up on the improvements observed from rituximab, for example.
My hunch was that the
dermorphin component of kambo plays the major role in creating the ME/CFS improvements Jox observed. Dermorphin is a potent mu-opioid receptor agonist, about 30 to 40 times more potent than morphine. This hunch was based on the fact that beta endorphin (a mu-opioid receptor agonist) has been shown to be low in ME/CFS; it was also based on the fact that low-dose naltrexone, which acts on mu-opioid receptors, can be beneficial for ME/CFS.
This hunch appeared to prove correct, as I noticed substantial symptomatic improvements to my ME/CFS after taking a single 100 microgram dose of dermorphin intranasally. So potentially, intranasal dermorphin could be a valuable and effective treatment for ME/CFS.
The reason I have not personally repeated my dermorphin experiments is because after several days of much improved ME/CFS symptoms from this single dermorphin dose, I then suffered one day of mild psychosis with severe emotional flatness, as a sort of finale to my several days of significant improvement, which was a very unpleasant final day. I detail all this in the first post of this thread.
However, I think this negative side effect of dermorphin I experienced will likely not appear in other ME/CFS patients. This is because the virus that triggered my ME/CFS also caused me to develop chronic anhedonia, emotional flatness and (in the past) some mild psychosis. So I am prone to these symptoms, and somehow dermorphin triggered them, albeit just for one day (there is a recognized condition of opioid-induced psychosis). But I imagine that other ME/CFS patients will be fine.
I am not suggesting that anyone else should try dermorphin, though. First of all, dosing is difficult, because you need a tiny amount: 100 micrograms (about the weight of a grain of sugar). If you get your dose calculation wrong, and you take more than say 1000 micrograms taken intranasally, it may kill you. You are dealing with opioids here: think heroin overdose. So this dose calculation is definitely not good to do when you have brain fog! I actually quadruple-checked my dose calculations before proceeding, as I was really concerned my brain fog would make me screw up.