the group shares up-to-date information on the resources available and the latest research on the topic. it also gives people a place to share their frustrations with the lack of care and, often, express their worries and concerns about their own health.
“what if my condition is permanent?” wrote one member this week. “and if i never get better … how will i live?”
mcginn, 39, contracted covid in december 2020 and continues to deal with a long list of symptoms. they include brain fog and crushing fatigue, as if she was “wrapped in a lead blanket all day.”
she referred to the few quebec doctors providing care on their own time as “angels,” but said it’s unacceptable the province has yet to put something more structured in place.
people are doing their best to navigate the system themselves, she added, going from family doctor to specialist and back again. but the lack of co-ordination is an added frustration on top of everything else they’re already dealing with.
she believes if the government doesn’t do more to address the issue soon, it’s only a matter of time before it comes to a head.
“there’s going to be a tsunami of disability coming from people like me, people who were in the prime of their lives — healthy, happy, parents, workers,” mcginn said. “now we’re at home, we’re ill, and we have no care or help or support from the government.”