the toad
Bluelighter
That order I was worried about showed up this morning 

No, he's just incapable of realizing the issues as of now. Which (please don't get me wrong) isn't meant as a personal insult ofc. It still does seem arrogant I guess, but everyone with a little drug experience at hand will know what I'm talking about. Some consequences, especially when it comes to the effect on things like personality developement and true addictive potential can only be evaluated after quite some time or some damages can never directly be related to the compounds because of the temporal distance between their manifestation and the drug abuse (abuse is the right word here I'd say). Physical damages often are compensated and therefore not apparent at all for a while, especially if the subjects are still relatively young.missimoo --- you really have no serious issues with 500-1,000mg per day usage?
Fortunately you haven't done the stuff as early in life as you've done tea and cannabis and not at the same frequency either because in that case things might look different.hardly any noticable craving. i probably crave tea more often in a day. cannabis far more. will be dosing tomorrow when home from holiday, am curious to see if tolerance has changed in 8...will be 9th day.
That order I was worried about showed up this morning![]()
same here lolhavent had any MXE for months.... very tempted to buy some again. even though i said to myself i wouldnt bother with it again due to the weirdness of that shit
No, he's just incapable of realizing the issues as of now. Which (please don't get me wrong) isn't meant as a personal insult ofc. It still does seem arrogant I guess, but everyone with a little drug experience at hand will know what I'm talking about. Some consequences, especially when it comes to the effect on things like personality developement and true addictive potential can only be evaluated after quite some time or some damages can never directly be related to the compounds because of the temporal distance between their manifestation and the drug abuse (abuse is the right word here I'd say). Physical damages often are compensated and therefore not apparent at all for a while, especially if the subjects are still relatively young.
First and foremost I'm almost certain that changes in personality are very hard to avoid with chronic use of dissociatives. I don't want to get too fair into detail, because that'd mean either becoming very autobiographical to a point I'm uncomfortable with or vastly generalizing my own experiences. From both my own experiences and what I could observe in heavy users though and also from what is to be guessed when looking at the role of nmda receptors in the brain, there will be personality changes that might be evaluated as negative by a lot of people in contact with the user.
I just hope that you are aware of the fact that this pattern of use can usually not be kept up with the same benefits, eventhough I do hear you when it comes to the outstanding potential as short term antidepressant drugs this class of drugs possesses.fter I began using mxe, I am more outgoing and feel much better about life. I am no longer depressed, my anxiety is (finally!!!) under control, and I can go out in public without worrying what other people think of me. MXE has truly saved my life.
I have been using it daily at about 85-100mg's.
It has changed my perspective on life and pulled me far away from the edge. I am so grateful for it. This is a drug that I will control as I do not want to lose the effects it has given me. I just need this in my life right now to help me get myself back on track, and hopefully afterwards I can slowly let mxe go and continue on and use what it has shown me to better myself.
While I agree wholeheartedly with your words of caution, I personally have never experienced an anti-depressant effect from either Ketamine, PCP or DXM at non-dissociating dosages, eventhough I'm well aware of studies claiming otherwise. Maybe I'm just looking for excuses to get blasted though. :DLegitimate benefits from NMDAR antagonism come from sub threshold doses which don't have dissociating effects, which prevent LTP (long term potentiation) from taking place for your NMDARs. Low doses have been seen to prevent LTP decay (increasing LTP duration) with some NMDAR antagonists, but studies show recreational or anesthetic doses to stop LTPs and have cognitive impairment. The anti-depressant effects of ketamine has been seen with low to sub-threshold doses, so high doses aren't necessarily needed for lasting anti-depressant effects.