This has nothing to say on the matter of reversing LTC-like phenomena... Why are you talking of a switch from "normal" (whatever your normal is) to an alpha state when we are talking about trying to go from an LTC to normal... An example would be trying to mindfulness your way through a mental illness that made mindfulness incredibly difficult. That is great that you can do meditation when you're in a biological state that is conducive to meditation though

But I'm not saying that correcting aberrant activation/dysfunctional deactivation of the default mode network for example isn't a therapeutic target. Its a therapeutic target for ruminating depression as well, but it just doesn't make any sense to label these as psychosomatic disorders when there is a root biological cause, just as there is with MDD.
We're not speaking of 5-HT depletion or receptor homeostasis issues, we're speaking of neuroplastic adaptations that are downstream of MDMA's effects, encompassing all effects, everything from the acute cortisol increase to a7 nicotinic partial agonism. In the majority of cases the time course of what I'm calling an LTC is ~ pills - horrible symptoms - googling - bluelight. NOT ~ pills - mild symptoms - googling - bluelight/studies - rumination - horrible symptoms.
Anyways to be honest I still don't know why you continually cite something that supports the notion that SRAs and direct agonists aren't completely cross tolerant but you seem to take it as meaning something else...
This isn't the first time you've disagreed about something strongly with several people but failed to produce sound logical reasoning or evidence.