Has anyone tried PEMF therapy for their Parkinson’s symptoms (or anything else for that matter)? I have had non Parkinson’s friends recommend it but haven’t talked to anyone who has PD yet. Any info, opinions would be welcome.
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Hello @maggiemsy and welcome to Mayo Connect. I have spoken with anyone who has had this therapy but I did find some information on it on the NIH's website. Here is a link to that information, https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4562205/#:~:text=PEMF%20therapy%20improves%20PD%20symptoms,session%20%5B161%E2%80%93163%5D.
If you are able to share more, how long ago were you diagnosed with PD? What other treatments have been tried (i.e, meds, physical therapy, etc.) What symptoms are most difficult for you right now?
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Did my reply go through ? I think it may have disappeared before it should have.
I don't see your reply. Perhaps you need to send it again.
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