FAQ/Help |
Calendar |
Search |
Today's Posts |
![]() |
|
Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS) |
|
Thread Tools | Display Modes |
![]() |
#1 | ||
|
|||
Junior Member
|
I am seriously considering trying palmitoylethanolamide (often referred to as PEA). I know it is now much more readily available in the U.S. whereas in the past it often had to be imported from the Netherlands & other countries.
Has anyone had experience with PEA? Was it helpful (in what way?), made little or no difference, or had adverse side effects? How many milligrams did you take for the loading dose? How long did you take the loading dose before you began to feel its effects and were able to reduce the number of capsules? Perhaps, most importantly, what brand did you find most reliable and that worked best for you? Good customer service? There does seem to be a wide variance in prices. Any insight you can give me would be most appreciated. Thank you!! Brightcloud |
||
![]() |
![]() |
|
|
![]() |
||||
Thread | Forum | |||
Our "Tips" and "Laws" for the Parkinson´s. 25 years of experiences (1994-2019). | Parkinson's Disease | |||
Can the antibiotics "Ceftin" or "Flagyl" cause a temporary spike in Small Fiber pain? | Peripheral Neuropathy | |||
So which "existing" diabetes drug turns the PGC-1 Alpha "Master Switch" back on? | Parkinson's Disease |