If abnormalities found in ME/CFS are found in clearly defined (post-)Covid-19 patients, that could be convincing for some people in the medical and scientific communities.
Well I'm sorry if I misrepresented what you believe/said. I highlighted the bit I was referring to and believed that's what you were saying.
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Here are the paragraphs in question:
Anyway, it doesn't look like my and other people's public challenging of him has had any negative effects...
You are entitled to your opinion but I don't know how you or others can be sure it isn't a postviral fatigue syndrome with a similar mechanism to ME/CFS/PVFS. As many others with ME/CFS have said, their symptoms at the start continued. There are 60+ day COVID groups.
Dr Garner said the most...
Anil van der Zee started this:
People could also do it on other social media platforms such as Facebook and Instagram.
People can also make posts here if they wanted.
Lots and lots of people have responded under Anil's post
It would definitely give useful data. However, if it wasn't part of her initial plans, it might add a lot to the costs.
Anyway, I don't think I will get involved in passing on specific suggestions to her, at least at this stage. I think you are on Twitter, so you could always reply to her under...
Another way of looking at this is that warning people that they could be left with long term problems like ME and that they need to consider that pushing themselves or others could make things worse for the individual is not necessarily unethical.
I think if an infectious disease doctor makes...
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