are there any covid cautious, contagion cautious, virus vigilant, still masking, etc kind of hashtags that are not for PSAs or vent posts? I would like the ability to see more posts that are covid safer or from masking folks but are about joyful things rather than The Horrors™️

P (he/him): I’ve started the #maskedupsluts hashtag and it would be great to find more tags to follow like that, or accounts to follow that are covid cautious but not full of doomposting or calls to action

#PandemicIsNotOver #maskssavelives #n95ssavelives #communitycare #LongCovid

Mit 500 Mio€ fördert der Bund in der #Forschungsdekade 10 Jahre Forschung zu #LongCovid #MECFS #PAIS, Ministerin Dorothee Bär präsentierte das wie ihre Initiative. Dokumente zeigen jedoch: Ihr Ministerium wollte das nie - es sollte viel weniger Geld geben. Weiter Streit gibt es über die Ausrichtung der Dekade. Experten und Patientenorganisationen wie Nicht Genesen drängen auf Therapiestudien, das Ministerium will v.a. auf Grundlagenforschung setzen. Mehr @riffreporter: https://www.riffreporter.de/de/wissen/forschungsdekade-long-covid-mecfs-ministerium-dorothee-baer-pais-bund-foerderung
Forschungsministerium wollte gar keine „Forschungsdekade“ für Long Covid, ME/CFS & Co.

Der Bund fördert Studien zu postinfektiösen Erkrankungen, mit 500 Millionen Euro über zehn Jahre. Nun zeigen interne Dokumente: Das Forschungsministerium wollte nicht annähernd so viel Geld investieren.

RiffReporter

This is my favourite podcast on complex chronic conditions so far:

🎙️Make Visible: Chronic Illness Explored

Homepage:
https://madevisible.podbean.com/

Themes included:

ME/CFS
Long Covid
Ehlers Danlos ( #EDS )
#Fibromyalgia
#POTS
Mast Cell Activation Syndrome ( #MCAS )
Chronic Lyme
Infection Associated Chronic Conditions ( #IACC ) and more.

#mecfs
#postcovid
#LongCovid
#postvac
#podcast
#makevisible

Make Visible: Chronic Illness Explored | Visible with Emily Kate Stephens

Shining a light on invisible illness.<br /><br />Emily Kate Stephens, journalist and Long Covid sufferer, discusses the latest research and insights with the world’s leading experts, scientists and healthcare professionals.  Including ME/CFS, Long Covid, E...

La mitad de los pacientes con covid persistente (#LongCOVID) continúan sin tratamiento 6 años después de la pandemia: “Nos buscamos la vida como podemos” | vía Infobae
https://www.infobae.com/espana/2026/03/11/la-mitad-de-los-pacientes-con-covid-persistente-continuan-sin-tratamiento-6-anos-despues-de-la-pandemia-nos-buscamos-la-vida-como-podemos/
La mitad de los pacientes con covid persistente continúan sin tratamiento 6 años después de la pandemia: “Nos buscamos la vida como podemos”

El sindicato CSIF ha presentado su encuesta sobre las secuelas del covid persistente, que denuncia el abandono sanitario y laboral de los afectados

infobae
Up to 60% of health care workers may have #LongCOVID 4 years after infection | CIDRAP
https://www.cidrap.umn.edu/covid-19/60-health-care-workers-may-have-long-covid-4-years-after-infection
Up to 60% of health care workers may have long COVID 4 years after infection

CIDRAP

Hello 👋

Welcome to the new Mastodon account for the Science for ME forum. Migration to the new server appears to have succeeded and most followers have been transferred.

Our forum is an independent, patient-led, international forum for people with ME/CFS or Long Covid and the carers, clinicians, scientists and advocates who support us.

Anyone can read the public posts on the forum but to join the discussion you must become a forum member.

You can learn more about our forum here:

https://www.s4me.info/threads/welcome.38181/

If you have any questions, just ask! 😁

But please note that this account is run by volunteers who have ME/CFS so replies may be delayed.

@mecfs @longcovid

#MEcfs #LongCovid #MedMastodon #Introduction #Science4ME

Welcome

A warm welcome to the Science for ME forum! We’re glad you found us. Science for ME is an independent, patient-led, international forum for people with ME/CFS and the carers, clinicians, scientists and advocates who support us. ME/CFS is a debilitating disease or group of diseases, often...

Science for ME

Today's small pleasure is finishing my little todo notebook. I actually used it! Turns out I was right: having a couple cute pens and a very bright notebook does help me remember to make plans and check them through the day

#LongCovid #brainfog #planners #notebooks

Long Covid & ME/CFS – Blackbox der Pandemie

Die Pandemie ist für die meisten vorbei, aber für über Hunderttausende in Deutschland ist sie es nicht. Sie leiden unter den Spätfolgen ihrer Corona-Infektion.

ZDF

“Ja je ziet me even niet op m’n best…”
“Dit is eigenlijk normaal.”
“…want ik had nogal een intense week…”
“Zoals zo goed als elke week.”

De huisgenoot deed aan ondertiteling om het bezoek een realistisch beeld te geven ondanks mijn pogingen tot bagatelliseren.

Maar nu heb ik schoonzusknuffels gehad dus morgen ben ik beter.

#LongCovid

TWiV 1306: Clinical update with Dr. Daniel Griffin

YouTube