the only reason i have not said anything in this thread yet is because when i read it it seemed to sum things up well, sometimes you want CO2 sometimes you want steam distilled its all about what constituents you are looking to get and what to avoid.

if you put on a nicotine patch for like 10-15 minutes then take a puff of a cigaret and lay down for a nap, well basically the grade at witch real life feels real RIGHT NOW is equal to how real the dreams are when you do this real life like dream and they are almost 100% all super nightmares. now that i know how to learn from what my dreams mean i see great things to be gained from facing these terrors specifically because the details all record as good or better than waking reality meaning all the things that i can learn from all the little details will be amplified.

thanks for the thing about throwing up, i will probably put my first 2 dots next to my nipple and make sure to avoid things that prevent nausea and instead use things that induce vomiting. one thing i KNOW i will be using is the singing bowl i got, everyone be careful i cannot remember if i gave the message over here as well but singing bowls are not for playing with they are comparable to 5MeO-ahuasca when your ringing it you feel the need to vomit strongly after a little bit, this is because the bowls vibrations are balancing the frequency of the organs causing the organs to activate the their cleansing mechanism i am sure if i were to vomit on singing bowl vibrations i would probably vomit all bile because its not like i ate a toxin or it made my food into toxins it made the organ healthy then the organ expels what i had the whole time that was not healthy.

it does not feel like 5HT3 nausea it feels like movement sickness.

its possible if i purged enough toxins out with this method and others combined it would stop making me feel like i need to vomit and instead do other things once the toxins are expelled.

thanks for making this thread KP it is a great idea i love it, in fact i cannot thank you enough because reading this makes me courageous to delve into what i have on hand as far as kissing death (:

it might be better for individuals to take part in kambo and similar practices that cause strong short lasting death feelings before trying iboga this would allow them to get a feel for how to accept and assimilate the experience of dying, and if done right an individual might be able to come out of a iboga experience with much more learned from the love.

i could see iboga slow long death beings harsh without preparation, that's why i think preparing by taking part in others that are shorter but harsher will allow them to learn to change the way they identify the FEELING of dying.

i am working to test how to get the system to be upregulated with as few mechanisms as possible.

i think D2 agonism upregulates Kappa receptors and D1 receptors.

i think Mu and Delta agonism upregulates Kappa receptors.

i think Kappa agonism downregulates Kappa and upregulates Delta and Mu and D2.

so

you chronically take high dose menthol for Kappa agonism, at some point it downregulates Kappa to the point ware you no longer get the upregulation of Mu, Delta, and D2.

then you dose agonist for either D2, Delta, or Mu these will cause Kappa to be upregulated

so

menthol -> Kappa agonism -> kappa downregulation -> upregulation of D2, Delta, Mu

agonist for D2 or Mu or Delta -> upregulation of Kappa -> downregulation of D2, Delta, Mu

with this info alone you can do amazing things all we need to do is remember that the end goal is to get Mu, Delta and D2 upregulated as high as possible, it would involve finding out when kappa agonism starts to stop working from tolerance and find out how small an amount of a D2, Delta or Mu agonist would be needed to put Kappa back in large enough amounts to agonize further.

i think depending on the substances used and the dose you can create a compound that upregulates D2, Mu and Delta without downregulating Kappa its about balancing the ratios of Kappa agonism with D2, Mu and delta agonism to get a net gain.

the idea here is for endogenous functioning of Delta, Mu and D2 to be improved long term.

it has nothing to do with if you think your a drug addict or not, if blue lotus does not have you ranting and raving yet then you did not take it for enough nights in a row, you still have tolerance to work through.

i will repeat it again, YOUR ENDOGENOUS SYSTEM CAUSES SELF TOLERANCE. if you have not been taking drugs very often at all then you probably have a endogenous system that produces self tolerance very rapidly, THIS is why blue lotus is so amazing because if everybody takes it for long enough it will level out their endogenous systems unbalances and bring your body and mind to its true potential.

if it has not turned your weaknesses into strengths yet, you have to keep taking it more you have not had enough yet.

instead of "i am not an addict" you should go "i feel like i am not an addict because of all these things i don't do, but am open to learning why i might still be an addict and not aware of it"  you see blue lotus lets you see how addicted you are to all the things you don't consider drugs the things you have been addicted to since far before you started using what we consider "drugs" this part of blue lotus makes it unfathomably valuable.

"vitamin B6
vitamin E
zinc"

these are prolactin inhibitors they give you more electromagnet energy, its important to take at least these 3 chronically because they will DRAMATICALLY reduce how taxing on your entire system it is every time you have an orgasm, this is very important, for many reasons one large one is that the sex system is heavily interlaced with the addiction regulation system.

you want to take MUCH more than the daily recommended dose for all 3 of these.

Could someone explain exactly what cycling is in simple terms (for those of us who don't have a PhD in Biochemistry...!).

A. insert compound that is an aldehyde or alcohol or one that can be metabolized into one.

B. make sure Aldehyde dehydrogenase is inhibited.

C. supply piperidine or dimethylamine for the aldehyde to condense with and make a new highly active compound from.



piperidine metabolites have usually very long durations (multiple days)  and are often more potent.

Reading through this again, I realize I'm slightly confused.  Are you saying the CYP2D6 inhibitors (on the list) will facilitate Noribogaine or Ibogaine?  Somehow I'm scratching my head on this...

Quote

the more CYP2D6 enzyme present in the stomach the less ibogaine you will get and the more Noribogaine you will get below is a list of inhibitors for that enzyme witch will cause ibogaine to be active alone taking much longer for the enzyme to recover and turn ibogaine into Noribogaine.

these induce more CYP2D6 this means more of the enzyme becomes present, inhibitors suppress the enzyme, the other longer list are inhibitors.

inhibitors for CYP2D6 will prevent Noribogaine from forming until the inhibitors wear off.

the inducers listed below will cause Noribogaine to be more likely to be made. 

"CYP2D6 INDUCERS

Valerian root
Valerian root EO: 2-5 drops"