Long Covid Awareness Day 2026

Post from Solve ME for Long Covid Awareness Day:

Solve ME said:
Every year on March 15, our community pauses to recognize Long Covid Awareness Day—a day to acknowledge the millions of people whose lives have been changed by long-term illness following infection, and to reaffirm our commitment to research, advocacy, and support.

Long Covid has affected people of all ages and backgrounds. For many, it means navigating persistent symptoms that disrupt work, family life, and everyday routines. For others, it has been the start of a much longer journey with infection-associated chronic conditions, including illnesses like ME/CFS and related disorders. Behind every statistic is a real person—and often an entire family—working to adapt to a new and uncertain reality.

Includes this list of resources (Google doc):

 
News article from the Austin American-Statesman:

For many, the pandemic feels like it's over, but for some people "the pandemic never ended. COVID never went away," said Katie Drackert, co-founder of Clear the Air ATX, a group committed to raising awareness about long COVID and providing public spaces and residences with HEPA filters to mitigate the spread of viruses in the air.

One in 19 people in the country is living with long COVID — a disease with more than 200 symptoms that can develop after an infection and currently has no known treatment or diagnostic test.

On Thursday, Austin City Council declared March 15 Long COVID Awareness Day. The action serves as a reminder that an estimated 42,000 people in Austin have long COVID, while also encouraging funding of long COVID treatment programs and support groups and promoting COVID-19 precautions.

"The pandemic is not over," said Dr. Desmar Walkes, public health authority for Austin and Travis County. "There are still people day after day contracting COVID-19."
 

Long Covid – the fight for justice​

Dr Murray-Cavanagh added: ‘We cannot – we will not – allow Long Covid to become the next ME or chronic fatigue syndrome: poorly understood and stigmatised. This is an occupational disease. The evidence is there. We must make the call for change. If the BMA won’t stand up for doctors disabled by their work who will? It’s not just the right thing to do, it's the very least we can do for our colleagues.’

Long Covid – the fight for justice
 
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Long Covid Advocacy posted a short video (30 seconds) on Bluesky:



Main text of post (in case Bluesky embedding has problems)
⚡️The power of medical education!

30% of clinicians thought Long Covid wasn't real.
After 90 mins of Putrino Lab (@putrinolab.bsky.social) class
0% thought it wasn't real!
 
Dr Murray-Cavanagh added: ‘We cannot – we will not – allow Long Covid to become the next ME or chronic fatigue syndrome: poorly understood and stigmatised. This is an occupational disease. The evidence is there. We must make the call for change. If the BMA won’t stand up for doctors disabled by their work who will? It’s not just the right thing to do, it's the very least we can do for our colleagues.’
Well this is an all-caps ironic but, uh, too late for that. It's here, it's done, because it's a lot of the same thing. Coming from the BMA, this is frankly ridiculous. They won't do a damn thing here, who the hell are they even kidding?

I still find the idea of making this a health care occupational illness appalling. So much wrong here. It's still infecting people. The entire population has had it many times. Not a damn competent thing is still being done and the medical profession is almost entirely to blame for this.
 
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