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Myalgic Encephalomyelitis and Chronic Fatigue Syndrome Support
Fibromyalgia | Last Active: 1 day ago | Replies (7)Comment receiving replies
I have been following the research and evolution of the understanding of Long Covid for several years. There are many parallels between symptoms of ME/CFS and Long Covid, and the thought is that both are still somewhat mysterious responses to the body's assault by infectious agents. I recommend visiting the Bateman Horne Center, which has been doing research in ME/CFS for years, and is now one of the leading educators and resources for Long Covid. They have excellent resources for both patients and providers. Here's the link: https://batemanhornecenter.org
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@kcp4321 Thank you for the suggestion, I have just been diagnosed and am searching for all the info I can find. I am, apparently One of the lucky people that doesn't have a severe issue, but is sure is very impactful on my life. I am still hoping for confirmation that CF is truly my diagnosis and would love a second opinion. But an not sure where to go for that. I feel that the doctor has simply given up and is just putting a name to something he is not certain of and it was a convenient way not to delve into the problems I have. If it truly is CF than I know what I am battling, but am worried it might be another issue , that , if not treated, might worsen without treatment.