Martin aka paused||M.E.
Senior Member
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Theoharides has an own formulation, NeuroProtek, which you can buy to see if it helps with any symptoms. While it's an interesting hypothesis, I remember reading about this idea over five years ago. Curcumin and luteolin are easy to obtain and test for anyone, but I have yet to hear anyone getting cured or improving remarkably from taking them. It does seem obvious there is some brain inflammation going on in ME/CFS, but how to treat it is another matter, both curcumin and luteolin made me worse.
depends on what you expect... I’m a big fan of Youngers work and so came the idea to do a cortisone shock therapy with 1000 mg methylprednisolone (at my own risk - legal almost impossible in D). My doc wanted to start “carefully” and Gazve me The fırsat ınfusıon with 500mg. Then we had a day off to see how my body reacts. No side effects BUT after a few hours my brain fog was GONE next to my blurred vision and for the first time in many (7?) I didn't feel like having the flu (I tell ya it was great). Three infusions with 1g let the headaches disappear, the sensitivity and boys and girls I'm righting this text WITHOUT Ativan. Last week this would have been unthinkable (I'm very severe) I'm on
- Mizellen-Curcumin (don't know, in English perhaps Micell? My autocorrect purposes microphone-Curcumin but I guaranty you, I'm an expert in studio gear and it's NOT a mic!!!!)
- zystrosetea (still experimenting with the dose)
- LDN (3 mornings, 3 middays, so the 6 mg approach
- Rhodıola (makes me dizzy, but not too bad,
- St Johns wort.... tried every AD, the only one that worked is a mixture of two SSRI citalopram and megivenafucktralin... Kills your libido (bad, having a new GF) and even worse (your noodle stays where it has been when you really want)
- pro-/prebiotics bc I'm a tube user (read a book by Stanford researchers: when you can eat, eat things for your gut.... Don't buy pills)
That's a lot. But I want to erase the inflammation
Martin