Are there any relatives of people with ME/CFS after Corona?
What are your experiences with it? Have your loved ones recovered? And how are/were you feeling about it?
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CFS ME was already in front of Corona.
On the other hand, the forums are full of people looking for help and sharing each other.
That's what happened before, I'm aware, but it's more about Corona, because my relative has it. Plus I didn't know where else I was supposed to sort it out topics. 😕
Can you recommend forums? Unfortunately, I don't know where young people can exchange relatives…
Whether triggered by corona or caused by other viruses or influences, it doesn't matter. Only through Corona it has become known in the population.
Most discussions on the topic are from a perspective on Facebook.
Yes, please
Do you like contact and more information via PM?
No, what's that?
Demand: Do you know HPU? This test should always start from my point of view. If positive, it explains a lot. However, not every doctor is open to this. I'm lucky.