Mr Blonde
Bluelighter
Ok, a little background info first:
I usually get affected more by psychoactives then other people. I have a relatively low BMI, not that much muscle mass
( ), plus when it comes to codeine I have the suspicion that I might be in that small percentage of the population that has slightly more of the enzyme that converts codeine to morphine.
I was going through a bad place a while back, and picked up a codeine addiction. At the peak of this addiction, my tolerance was over 800mgs. I was only getting the effects I used to get at 240mgs, plus I was keeping withdrawal at bay.
However, codeine is supposed to have a ceiling effect; over a certain amount, your liver can't convert any more of a dose into morphine.
My question is: how did I get such a high tolerance when there is a ceiling effect? When I was increasing doses and my tolerance wasn't so bad, I was noticing better effects at say, 600mgs then at 400mgs.
Could my liver, adjusting to the physical addiction, have begun converting more of my dose into morphine?
I usually get affected more by psychoactives then other people. I have a relatively low BMI, not that much muscle mass

I was going through a bad place a while back, and picked up a codeine addiction. At the peak of this addiction, my tolerance was over 800mgs. I was only getting the effects I used to get at 240mgs, plus I was keeping withdrawal at bay.
However, codeine is supposed to have a ceiling effect; over a certain amount, your liver can't convert any more of a dose into morphine.
My question is: how did I get such a high tolerance when there is a ceiling effect? When I was increasing doses and my tolerance wasn't so bad, I was noticing better effects at say, 600mgs then at 400mgs.
Could my liver, adjusting to the physical addiction, have begun converting more of my dose into morphine?