Flux Health Forum

Advice for mitochondrial/neurodegenerative disorder

Hello! I was injured by the C vaccine almost 3 years ago. I am not able to walk more than 50 feet. I have motor and sensory loss and it seems like demylination of the spinal cord, internal tremors, dysautonomia etc… When I touch my spine I get worse paraesthias in my lower legs/feet. A Nutreval test shows severe mitochondrial dysfunction and oxidative stress. Unfortunately I can’t get any help in BC and still waiting for a nerve conduction study test! Anyways… I am wanting to try this therapy and wondering which device to use and how to use it. I open to other pemf suggestions as well but I am not sure I trust the other devices out there. Thanks!

Just an opinion, not medical advice, based on no data, just my best educated guess:

Model A9 with a 2x2 coil array, placed directly over the most severe problem area of the spinal cord. Start setting on LOW (L), test yourself for a short period, maybe 10 minutes, then work up from there.