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I made a comparison with other infections. With those, neither I nor pretty much anyone else says everyone with sequelae have CFS. If one treats it the same, neither I nor pretty anyone else is saying everyone with sequelae after Covid have CFS (or ME).

The National ME/FM Action Network sent an email to the people on their distribution lists asking them to share will their experiences with ME/FM and Covid i.e. lockdowns, etc. They have now shared the results on their website (see pages 2-8). I found it quite interesting...

I have now highlighted that quote elsewhere:

https://sports.yahoo.com/dr-fauci-says-covid-symptoms-110222378.html

Hear and see @Carolyn Wilshire on TV

https://www.rnz.co.nz/news/on-the-inside/426467/covid-19-s-long-shadow-the-light-at-the-end-of-the-tunnel-just-isn-t-there https://twitter.com/tomkindlon/status/1307679390000730120?s=21

https://www.dailymail.co.uk/femail/article-8739689/Long-covid-Brain-fog-constant-fatigue-Healthcare-professionals-share-symptoms.html https://twitter.com/tomkindlon/status/1307661091837751300?s=21

Sick and tired of Covid-19: The 'recovered' patients who aren't getting better 9:22 pm on 15 September 2020 By Louise Thornley*, Reporter For a subset of Covid-19 survivors, the illness has lingered. Slammed by fatigue, pain, headaches and more, they're just not getting better. What's going...

OK, I’ve replied to my tweet which many will also see

https://www.wired.co.uk/article/coronavirus-long-haulers-negative-tests-covid-19

https://www.irishtimes.com/news/health/it-absolutely-destroys-you-covid-19-survivor-five-months-later-1.4351767

This was presented at a previous IACFS/ME conference: