Hi everyone. I'm wondering if anyone in the UK has had a diagnosis from a doctor of CCI? I was diagnosed with ME because of disabling PEM. However,after a few trips to an osteopath that worked on contractures in the sub occipital area, I found my symptoms improved massively! I am interested to hear if anyone has experienced anything similar. Thanks!
Posted by rosier11 at 2022-05-04 19:09:25 UTC