Finally, a cure.
vlcfa.org/viewtopic.php?f=8...
I've read about this before, for Multiple Sclerosis. First I've read about Mito-Q helping Adrenomyeloneuropathy. Doesn't surprise me. I've read a lot of good things about Mito-Q
Finally, a cure.
vlcfa.org/viewtopic.php?f=8...
I've read about this before, for Multiple Sclerosis. First I've read about Mito-Q helping Adrenomyeloneuropathy. Doesn't surprise me. I've read a lot of good things about Mito-Q
Hello there! I know this is an old post but I Just stumbled upon some info about Mito Q lowering the neuro damage in worms with a gene similar to ALD. Was curious if you tried it and if it helped you in any way?
Also read a study about it possibly being toxic to certain kidney cells. (Sigh)
Trying to decide whether to dole out the money to try it. My symptoms in my back and legs are worsening and I’m getting frustrated 🙁
I never did buy any. The operative word is "buy". I'm spending a fortune on drugs as it is.
I like the look of this, but then again, I've heard nothing of any value from the MS community. So, I don't really know.
Thanks for getting back to me! I ordered a bottle and will start today. I’ll let ya know if I notice anything. It’s not cheap and like you I have cabinets and boxes full of medicines and supplements (that either didn’t work, gave me bad side effects, or I’ve forgotten about in some corner somewhere!)
The worm study with it specific for AMN/ALD caught my attention. And I am intrigued by Dr Wahls work on nutrition to rev up and maximize the mitochondria (but cannot follow that strict diet right now...may try it when I’m an empty nester down the road). Theoretically the MitoQ sounds hopeful...but so have so many other things I’ve tried 🤞
Fingers crossed!