Emma

📢 #CallForPublicHealthAction

I’m also demonstrating for the right to
- #CleanAir
- #InfectionControl
- adequate care & biomedical research for #LongCovid/#MECFS

Please make your voice heard for those who are too unwell to protest.

#CovidIsNotOver

They should call it post-exertional deterioration instead of post-exertional malaise. ‘Malaise’ makes it sound like merely an unpleasant feeling rather than an actual physical blow to the body.

Persistent attenuation of lymphocyte subsets after mass SARS-CoV-2 infection Growing evidence suggests that lymphocyte subsets are declined in COVID-19 patients, but it is unclear if these alterations persist after widespread e…

Not to ruin any good vibes, but this ongoing mass infection thing isn't great, is it?

#CallForPublicHealthAction
www.sciencedirect.com/science/arti...

Hej! 🤗👋

"So currently, we are protecting HCWs and their patients against a droplet in an ocean of aerosols. This inadequacy would not be tolerated in any other industry — nor should it be in healthcare."

Exactly.

Protection from airborne disease is a workers' rights issue.

#CallForPublicHealthAction

ME/CFS study among the 2025 NIH Research Highlights 👍

Thank you!

Thank you so much! This study seems to focus on the risk of developing LC in the first place, though? I may not have expressed myself very clearly, but I’m actually looking for studies showing that patients who already have ME/LC face a risk of deterioration if they catch new infections. Know any?

I’m seeking official or scientific sources stating that reinfections (or infections in general) are a risk factor for deterioration in #MECFS or #LongCOVID. Any tips would be appreciated! 🙏

Please sign this petition even if you're not a Swedish citizen! Our very bad national treatment guidelines for #LongCOVID, #MECFS and other post-infectious illnesses need to be withdrawn!

There's an English description on the petition web page, and you can sign no matter your nationality.

🫶💪

The last post Megan shared was a petition to get safe air and masks in NZ healthcare.

Anyone anywhere can sign it.

Source post from Twitter: x.com/rhirhiarhii/...

Vad roligt Nasrin! Lycka till med utbildningen! 🤗

🫂

📣 #callforpublichealthaction

Virtual demonstration for #cleanair + medical care for #PAIS + #ME/CFS!

week 5️⃣0️⃣ ❗

Journalism must stop promoting false, outdated medical knowledge about #PAIS and #ME/CFS from dogmatic medical professionals through false balance!
This destroys medical progress!

Alison Hume MP shares an account of severe #MECFS and warns that many healthcare professionals lack understanding of severe ME — especially its hallmark symptom, post, exertional malaise PEM — and that patients are too often pushed into pathways that simply aren’t appropriate.

💕

And so are you! 💪

Thank you Malin, I hope so too 🫂

🫂

COVID-19 is “Airborne AIDS”: provocative oversimplification, emerging science, or something in between? COVID-19 caused by SARS-CoV-2 is often compared to other pandemics for its societal and global health impact, with some commentators drawing parallels to HIV/AIDS due to the immune dysfunction caused ...

Here's just one of the reasons we keep demonstrating for clean air, evidence-based infection control and public education on COVID-19 👇
The science grows clearer by the day — we just need to act on it.
#CovidIsntOver
📢 #CallForPublicHealthAction

www.ajpmfocus.org/article/S277...

Well, it doesn't have to be like this. This is a choice we're making by not cleaning the indoor air or informing the public about the need for infection control.

Moreover, these numbers also mean a new, year-round baseline of chronic illness.

This is not sustainable!

#CallForPublicHealthAction

📢 #CallForPublicHealthAction

I’m demonstrating virtually for the right to
- #CleanAir
- #InfectionControl
- adequate care & biomedical research for #LongCovid/#MECFS

#CovidIsNotOver
#MaskUp
#CovidCautious

🙏

📣 #callforpublichealthaction

Virtual demonstration for #cleanair + medical care for #PAIS + #ME/CFS!

week 4️⃣6️⃣

While governments, for capitalist reasons, fantasize that ME/CFS care is "comprehensively secured," the reality for ME/CFS sufferers is completely different.

Support us with Reskeet! 🤍

... pure hell in itself, and being disbelieved and neglected by healthcare and government certainly doesn't help. We desperately need a diagnostic test to escape the gaslighting -- and then we need a cure.

... without suffering for it afterward. I still work part-time from my bed, but that's basically all I can manage, and with my health being so fragile, I live in constant fear of becoming even worse or losing my sick pay and not having the energy to fight for it. The disease is...

Thank you so much for writing about this 🌸 I became ill in early 2020, and my life has been destroyed. I worked full-time
at the university, enjoyed my social life, did all kinds of sports, and had many other hobbies too. I'm housebound now, and can't even shower or walk around inside the house...

Scientists develop first ‘accurate blood test’ to detect chronic fatigue syndrome Research could offer hope for ME patients – but some experts urge caution and say more studies needed

ME/CFS is a devastating condition that has long been denied, dismissed, psychologised and underdiagnosed. Research is at last starting to catch up with it, with glimmers of hope for those who have been left untreated for so long.
There's a huge BUT coming ...🧵
www.theguardian.com/society/2025...

Always better to leave some room for doubt, right? We wouldn’t want people to start demanding clean air in schools or something.