My POTS is gone—was it angioplasty? Uh, no.
POTS, one aspect of dysautonomia is GONE for me. Working with the root of the problem (as opposed to treating the symptoms via salt-loading, etc) may be the key for many of us with dysautonomia (EDS, chronic fatigue, fibromyalgia, M.S., chronic Lyme, etc). Setting up clinical trials now. If interested, please send your contact information to "volunteers@Prettyill.com". If you'd like to help, please let me know!
Is it POTS or Dysautonomia?
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