by Adam Strauss
The following article was originally published on Psymposia.
There’s a new article in The New York Times, entitled Can Psychedelics Be Therapy? Allow Research to Find Out.
While I’m a strong supporter of psychedelic research, and have donated a large portion of all proceeds from my show The Mushroom Cure to the cause, this article is just dead wrong on every significant point.
First, the entire premise—that Schedule I status is the primary obstacle to research—is flat-out wrong. I know because I also once assumed this. Then, in writing my own opinion piece for Huffington Post, I corresponded extensively with the folks at the Multidisciplinary Association for Psychedelics Studies (MAPS), who clarified that schedule status is no longer a significant barrier—the FDA is now approving all legitimate psychedelic research.
The obstacle now is simply getting funding for research. That the author so completely misses the fundamental issue at hand demonstrates a lack of both basic understanding and even the most cursory research.
Second, the article states psychedelics “are illegal in the United States because they carry a high risk of abuse.”
Two huge inaccuracies in this one statement.
First, there is virtually no risk of abuse, at least not in the classic sense of daily use, physical dependency, selling worldly possessions to get a fix, associated spikes in crime, etc. (As anyone who’s done psychedelics too frequently will attest, these drugs will tell you pretty unambiguously if you’re pushing it too far too fast.)
Second, their alleged abuse potential has nothing to do with why they’re illegal. A full historical accounting is beyond my scope here, but suffice to say the prime motivating force behind the state and federal bans of 1969/70 was criminalizing a social movement that opposed Vietnam and the status quo in general. It was about power and politics, not public health (which some courageous politicians, most notably Senator Bobby Kennedy, recognized and tried to counteract).
Third, this: “They can also cause harm. The best-known adverse event is persistent flashbacks, though these are believed to be rare. More common are symptoms like increased heart rate and blood pressure, anxiety and panic.”
“Flashbacks” (really, the author means HPPD; flashbacks are defined as transitory, while HPPD is long term) are unheard of in any sort of responsible use context, while the other “harms” cited are all transitory—that is, they last only while one is experiencing the acute drug effects (and rarely last the entire duration of the experience). Twenty minutes of elevated heart rate or anxiety may be unpleasant, but they hardly qualify as harmful in any meaningful sense.
Finally, this piece massively understates the incredibly positive results obtained in recent research. With PTSD, addiction, end-of-life anxiety and other conditions, we’re routinely seeing massive effect sizes that dwarf anything seen—ever—for any other class of psychiatric medication. And the scientific studies establishing this are generally tracking results for anywhere from six months to several years after the administration of the drug, while pharmaceutical studies rarely collect data for more than a couple of months.