As for me, I am left with restless body syndrome at a level that makes it necessary to take methadone 3 times a day for my aches, which generally takes away about 70% of symptoms. The other 30% I live with or smoke weed for, depending on the moment and how bad it gets.
I smoke and vape mostly Indica cannabis with kushy, musty, nutty, grapey, piney, honey-like, and creamy flavors, and mango flavor can be good too. Those are also the flavors I would search for. Garlic and Lavender also come to mind.
Pineapple and other exotic Sativa oriented strains can cause an increase in my symptoms but it’s strain and dose dependant. Amajikoym is a great Sativa strain for me, but with flavors of tree fruit rather than exotic fruits. Banana is an exotic fruit that usually IS ok flavorwise.
Flavors and scents, terps, for nervous conditins in general, should all be soothing, warm, balming, instead of energetic and fresh. Citrus can go both ways depending on the other notes present.
Sandalwood (the warm woodsy resin rich balsam kind, not the soapy cheap soapy smelling sandalwood) is another warm note that would do ppl with nervous conditions much good.
But don’t just tell him to look for scents in weed.
Also have him check out essential oils like Sandalwood (SantalumAlbum) and Lavender, oils that relax the mind and the body.
Those can be very helpful at night, when all you want is sleep but your meat puppet decides it’s time to jerk 20 different directions every 2 minutes.
Another very helpful tool in that regard, is Reiki. I had been initiated long before I got health issues, but even more helpful is that my wife had been initiated long before too, her mother being a 3rd degree Reiki master. The only sleep I got for months, was when my wife would hold her hand atop my head sending Reiki through my spine. She’d fall asleep but keep her hand there and those would then be the only hours I got to sleep that night. If she turned and her hand wavered, it would take but a few minutes for my entire body to start flexing entire muscle groups again, causing my body to arc up like a bridge standing over water, and that would happen about 3 to 5 times before it would wake me up, due to the sheer exhaustion my body and mind were subject to.
An interesting bit is how it all started. I had always had benign restless legs syndrome, a very mild variant that never bothered me much, or so I thought. Then I was talking with my buddy about quitting smoking tobacco and I found out that the intense sensations I got inside of me, that told me to smoke a cig, were not normal at all, and not at all a part of normal nicotine addiction; neither was the feeling of being ready to split skulls if anyone were to stand between me and my cigarette.
So I got myself onto vaping nicotine, for a month, all the while tapering the strength down with small steps, and then I quit. Second day of no nicotine I broke and bought nicotine patches, slapped on a whole, got a headache, decided a whole one was too much, and then I cut 1 patch in ever smaller pieces, so I could patch a smaller patch each and every day. 10 days later I was off the patches.
In period before that, I had had a neurological mishap happening that looked like an epileptic attack, so to investigate, I booked an appointment with a neurologist. One EEG later he decided it wasn’t likely to be epilepsy, but nothing seemed wrong so he wanted a “sleep deprived EEG”, where I couldn’t eat or sleep (or smoke, but I had already just quit “luckily”) for 24 hrs before the test. The test was done, the neurologist nowhere to be found, and there, during the test, laying on a cold bed with wires attached to my head, I experienced a tugging and pulling in my legs that was far from pleasant. The neurologists assistant asked me if I was alright as my legs and arms were pulling and twisting and turning, and I replied I thought I was gettting some intense nerve pains. She didn’t respond, nor did anyone check up on me further.
After that the previously benign restless legs syndrome that had never really bothered me, had turned it’s ugly head around, and it would be growling at me from that moment on. The neurologist would wave it away as a small thing that he certainly had nothing to do with, and he went on to offer me a variety of drugs that are given to Parkinson’s patients. I was livid. I already knew these medications, and what they did to the people that got suckered into taking them, leaving them crying in despair only 5 years later, begging to be taken off, but with no way to do just that.
Have your friend look into Iboga ceremonial or therapeutic use.
Really.
That’s the 1 single most restorative thing that your friend can do, but he’ll have to be 2 weeks clean off all meds. But Iboga can fix things medicine does not yet understand, and it would not be the first time it fixes a motor neuron disease.