This study underscores the importance of ruling out other conditions before giving a #MyalgicEncephalomyelitis diagnosis. This study used the Canadian consensus criteria.
I have had vit D deficiency. Getting that addressed improved several symptoms but did not touch the underlying ME.
I have had vit D deficiency. Getting that addressed improved several symptoms but did not touch the underlying ME.
Reposted from
thetranscendedman
Hyogo, Japan: 28 ME/CFS cases after COVID-19 vaccination.
27 had low vitamin D. After treatment, 82% no longer met ME/CFS criteria.
Biggest improvements: sleep (71%) and autonomic symptoms (68%).
Trial planned to confirm.
www.sciencedirect.com/science/arti...
27 had low vitamin D. After treatment, 82% no longer met ME/CFS criteria.
Biggest improvements: sleep (71%) and autonomic symptoms (68%).
Trial planned to confirm.
www.sciencedirect.com/science/arti...
Comments
the 2021 identifying and diagnosing ME/CFS paper at Mayo Proceedings lists several things to test for and treat or rule out. It was *so* helpful for me and my doc, and my records.
https://open.substack.com/pub/colleensteckelmeiccinfo/p/myalgic-encephalomyelitis-ic-primer?utm_source=share&utm_medium=android&r=deavh
it was a real help having it all documented, when i applied for disability, too.