Has anyone else seen an Osteopath for EM? I started seeing one about a month ago. I was having 20-30 flare ups every day in my hands, feet, legs and ears and after seeing her I’m down to about 5 a day.
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No, but it’s crossed my mind. What kinds of things does your osteopath do?
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Would like too know too. Are you sensitive too touch at all? I have CRPS too. Feel at this point nothing or noone helps
The one I go to focuses on the connects in the brain related to EM and resets them. I was very skeptical but she managed to stop a flare up while it was happening and I’ve been doing so much better since seeing her. I was barely getting through a day at work before I started seeing her. She honestly only softly touched me, no pain compared to any other kind of treatment I’ve tried.