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CFS Like Symptoms After COVID-19

CFS Like Symptoms After COVID-19

Article, very detailed, describing symptoms of CFS after COVID-19.

Please read!!

PS: this is tragic news but there may be a silver lining. I think since these debilitating symptoms affect a significant portion of the population and has such an intense focus WORLDWIDE by epidemiologists, virologists, etc, etc, that it MAY create more research and a treatment plan for us with identical or similar symptoms.

Please read and see the experts drawing parallels with CFS and… read more

A MyFibroTeam Member said:

🙋‍♀️ @A MyFibroTeam Member ... what a great idea you have to open specialized medical centers for CFS, Fibro, COVID or any post-viral symptoms!! Brilliant!

I hope that that even small clinics and hospitals do that asap.

Truly, you have a brilliant mind Olga and I hope that someone pivotal in the medical community begins a world focus on doing just that.

And I hear your deep frustration at your 2 year wait list just to be seen for competing care in a city with 6mill population. It's mind boggling, especially considering the widespread magnitude of these conditions that have existed pre-covid and will now exponentially explode, post-covid.

edited, originally posted 1 day ago
A MyFibroTeam Member said:

My fibromyalgia and cfs all started after having pneumonia and has continued ever since! I had a full on physical job so therefore thought alot of my tiredness mild ache's and pains ect were due to that but then I had flu chest infection which led onto pneumonia and from then on after getting over the initial illness itself developed into cfs and a 2 year elimination process of a diagnosis of fibromyalgia! I never suffered any of the above until being struck down with pneumonia although was an asthma sufferer before that!

posted 3 days ago
A MyFibroTeam Member said:

It is a great article and one that certainly sounds very familiar with its long term symptoms after initially recovering from the covid virus! Fingers crossed it gives us fibro cfs/me ect suffers some sympathy and understanding of what can be our daily chronic symptoms too!!..

posted 4 days ago
A MyFibroTeam Member said:

Great article. Let’s hope this will prompt research and open clinics specializing into post viral chronic illness/CFS/ME. 🙏🏻🙏🏻 I’m waiting at the very least 20 months for the only clinic in our area that specializes in FMS, CFS/ME and other illnesses caused by environmental factors such as chemical or electromagnetic exposure. I live in an area with 6 mil people in the greater metropolitan area....to put it into perspective.....crazy!

Have a great day 💕🤗

posted 4 days ago
A MyFibroTeam Member said:

Another article on this specific topic...

https://www-telegraph-co-uk.cdn.ampproject.org/...(Phone number can only be seen by the question and answer creators)&csi=1&referrer=https%3A%2F%2Fwww.google.com&amp_tf=From%20%251%24s&a...

posted 6 days ago
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