▲ 23 r/cfs
Why is there still barely any research into treatment options??
I don't get it, even with the low funding in general, there is still some funding, but I can barely find any papers about LDN, LDA or similar drugs.
I know that without having any idea what causes this illness, treatment is basically trial and error, but that is the same for lots of other illnesses. And those have many studies just trying out potential drugs, I'm sure there are many of us that are desperate enough to just try anything and participate in a study.
And if by chance a drug actually helps, it could point to a potential cause..
u/ElonsBreedingFetish — 11 days ago