#Tag
I think 2 million Canadians with long COVID, is likely a serious underestimation. However, I’m glad to see at least some focus on this issue.
It’s Long Covid Awareness Day.
This year marks 3 years of living with it for me… and my health continues to be precarious.
I do my best to walk through life in the present and to manage what I’m able to - while relentlessly advocating for myself in the medical system.
If this sounds like you too… know that you’re not alone. I see you.
It’s Long Covid Awareness Day.
This year marks 3 years of living with it for me… and my health continues to be precarious.
I do my best to walk through life in the present and to manage what I’m able to - while relentlessly advocating for myself in the medical system.
If this sounds like you too… know that you’re not alone. I see you.
I think 2 million Canadians with long COVID, is likely a serious underestimation. However, I’m glad to see at least some focus on this issue.
"LongCovid is new"
Post-viral diseases aren't new.
Dysautonomia isn't new.
ME/CFS isn't new.
Endothelial dysfunction isn't new.
MCAS isn't new.
Auto-immune issues aren't new.
Chronic inflammation isn't new.
POTS isn't new.
PEM isn't new.
Blood clots aren't new.
Tinnitus isn't new.
Mitochondrial dysfunction isn't new.
Migraine isn't new.
"LongCovid is new"
Post-viral diseases aren't new.
Dysautonomia isn't new.
ME/CFS isn't new.
Endothelial dysfunction isn't new.
MCAS isn't new.
Auto-immune issues aren't new.
Chronic inflammation isn't new.
POTS isn't new.
PEM isn't new.
Blood clots aren't new.
Tinnitus isn't new.
Mitochondrial dysfunction isn't new.
Migraine isn't new.
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