Dopamine agonists, which treat RLS may also treat MECFS
https://forums.phoenixrising.me/threads/how-i-solved-my-neuroinflammation.81625/
https://forums.phoenixrising.me/threads/how-i-solved-my-neuroinflammation.81625/
CONCLUSIONS:
There is a higher prevalence of RLS in POTS patients compared to controls. This association may have to do with shared increased inflammatory/autoimmune load and autonomic dysfunction.
I'm thinking now that this is a milder version of the bone crushing feeling I get in my lower legs and hands when in PEM.
Time to try that spoonful of marmalade ...I get this for a few weeks in the summer, usually when it's very warm at night. It stops me sleeping. I'll try a spoonful of marmalade next time, if I remember.
My sister had RLS back in 2012 when she came to visit and we tried to get to the bottom of what was causing it. She had low ferritin and was later diagnosed with Hashimoto's. She is being treated for HD, and when her iron levels were brought up to normal range her RLS went away.
My sister had RLS back in 2012 when she came to visit and we tried to get to the bottom of what was causing it. She had low ferritin and was later diagnosed with Hashimoto's. She is being treated for HD, and when her iron levels were brought up to normal range her RLS went away.
powdered cockroach
I'm nicking that!