I’ve have most of those symptoms and they have developed after 60. Slowly over time.

and are saying they did about 10-15 years earlier than would otherwise be expected, based on their current health. Which is another way of saying that most of the people who died were not young.

there will be a lot of people experiencing post-virus issues. They will be put in the same category, medically speaking, as chronic fatigue syndrome, fibromyalgia, etc. I asked if Covid group group will be marginalized like the other conditions, and he said that remains to be seen. I have a hard time believing the "it's all in your head, psychological" explanation will fly much longer.

but is it permanent? No one knows at this point...

Looks more like Medicaid for all.

"Everything is going to shit isn't it." He nodded slightly.

My CFS began decades ago after my "recovery" from an unknown viral infection.

The internal med specialist I saw at the time said I seemed to have contracted a malaria type of illness - this was in the 70s.

He was the one doc at that time who refused to go to the "it's all in your head" excuse. I was grateful. Since then, I've found a few docs who accept the facts of my illness and thankfully, although untreatable, my symptoms have lessened over the decades.

what he was saying. If this does come to pass I sure hope that marginalization by the medical mainstream ends.

Good article

Don't know if permanent (that's scary).