buc.ci is a Fediverse instance that uses the ActivityPub protocol. In other words, users at this host can communicate with people that use software like Mastodon, Pleroma, Friendica, etc. all around the world.
This server runs the snac software and there is no automatic sign-up process.
I have set up a fundraiser for the SequenceME genetic research project into #MECFS and #LongCovid. I'd be hugely grateful for contributions and shares.
*Whether or not you're looking for a Covid Safe Date, please share this post. Because it's super difficult for people who avoid Covid to find love online.*
Covid Safe Date is now a feature full online dating website for adults of all genders and sexual orientations around the world who take #Covid avoidance seriously.
We have a few dozen members already, join us!
You may have Long Covid or you may be Novid.
You may have been engaging in consistent Covid safety practices since 2020, or you may have just started properly avoiding Covid recently.
You may have a shitty job that forces you to be maskless in order to stay employed. You may share a household with people who don't avoid the plague like the plague.
But as much as possible, you wear a respirator mask in public. People thinking you look weird or peer pressure isn't enough to make you go maskless. You would only risk another infection with a possibly permanently destructive virus if you feared losing your income, or feared violence, or had to get a medical procedure where you couldn't be masked the whole time.
You absolutely would never go inside a restaurant to eat ever again. Restaurant food can be takeout or delivery. Food can be cooked at home.
Whether you've been infected several times or never, you know the best course of action is to avoid as many infections in the future as possible because the harm is cumulative.
Whether or not you keep vaxxed, you understand that the vaccine doesn't stop infection, you still must wear a respirator mask.
You understand the importance of good indoor ventilation and filtering, but you know a public place with a good air quality rating doesn't mean it's safe to take your respirator mask off. You know people get infected outdoors too if they're very close to other people.
When I tell you that Dr. Hoerger's data shows there's more Covid spreading now than at any point in 2020, you're saddened but you're not shocked. You know Covid is far from over.
And if this applies to you and you actually avoid the plague like the plague, chances are dating websites will be hostile to you if you mention Covid safety.
People have anecdotally had a hard time finding romance on CovidMeetups, because it's not really a dating website but a better place to meet friends or find dentists.
That's why Covid Safe Date exists. It may be the only dedicated part of the internet specifically for Covid avoiders to date and possibly fall in love.
Our services will always be 100% free-of-charge. There's no "premium" tier, all features are available to all users.
And for that reason, Covid Safe Date needs donations from people who can afford to do so, so I can keep paying for web hosting and paying my developers who have Long Covid and are struggling generously for their labor.
https://covidsafedate.com/we-need-your-financial-support/
I'm also the founder of Stop Gen AI, so you'd better believe that there is absolutely zero AI on Covid Safe Date. Our web platform and service is completely human crafted and maintained.
We are a space that's LGBTQIA+, neurodivergence, disability, and poverty inclusive.
And I'm a cybersecurity specialist who takes responsibility for your cybersecurity and privacy seriously.
https://covidsafedate.com/privacy-policy/
Here are screenshots from the newly relaunched Covid Safe Date. You can see my profile, I'm looking for love too!
*Whether or not you're looking for a Covid Safe Date, please share this post. Because it's super difficult for people who avoid Covid to find love online.*
RE: https://m.ai6yr.org/@ai6yr/116253659630051645
Not just in the US. Also seriously downplaying and underestimating #LongCOVID #MECFS so we can pretend it is not a devastating global problem.
Death toll at start of Covid-19 pandemic likely higher than US count, study says
https://www.theguardian.com/us-news/2026/mar/18/covid-19-pandemic-death-toll
Check out the new #LongCOVID treatment guide from
PLRC & RTHM The guide features 24
medications, & select supplements, procedures, etc.
The guide aims to provide more clarity to patients &
clinicians around the evidence behind potential LC
treatments, in one place.
Link to guide: https://www.rthm.com/treatmentguide
Ach, schau mal einer an. Da hat die Doro Bär immer den Eindruck vermittelt, sie nähme #MECFS & Co. wirklich ernst und hat die "Dekade der postinfektiösen Erkrankungen" und die damit verbundenen 500 Mio. Forschungsförderung als ihren Erfolg verkauft. Am Ende waren es doch eher "Forderungen von Interessenverbänden bzw. aus dem Außenraum". Immerhin heißt das, dass öffentlicher Druck der Betroffenen und ihrer Angehörigen wirkt. #liegenddemo #longCovid #mecfs
@Lstn2urmama
Unless you get #LongCovid, you'll have time to sign after you recover. There are various events located according to location.
Long COVID awareness is growing thanks to researchers, clinicians, advocates, and people sharing their experiences online.
This carousel highlights a few posts helping people better understand the scale and impact of Long COVID. The more people who understand Long COVID, the more support, research, and prevention efforts can grow.
Take a moment to explore the accounts featured here and learn more from their work.
Well, if it's long COVID awareness day, I'll add my ten cents.
I was one of the first to contract it in the UK, and have had it as long as anyone, since 2019. Reclusive even then, I was lured out to help a relative who was essentially dying with a heart condition, when his visiting grandson who's father has been working in Saudi passed it to me, and frankly finished him off.
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 Canadian* medical system.
If this sounds like you too… know that you’re not alone. I see you.
#LongCovid #MECFS #POTS #LongCovidAwarenessDay
*added for clarity. I also do not currently have any spoons, I’m minus spoons and bed ridden, so I cannot reply to DMs.
Vic Greens health spokesperson Dr Sarah Mansfield posted on Instagram for Long Covid Awareness Week 👏🏻
@broadwaybabyto Thank you for advocating for the disabled. #LongCovid, #CovidIsNotOver, #disabilityjustice
This Long Covid Awareness Day let us remember the millions who've been disabled by the virus.
The people who've been forgotten and left behind.
The folks who have to hide their diagnosis because of the stigma attached to it.
You think you don't know anyone with Long Covid?
I promise, you do:
https://www.disabledginger.com/p/long-covid-awareness-day-2026
#longcovid #longcovidawarenessday #COVIDisAirborne #CovidIsNotOver #sarscpv2 #disability #ableism
To mark International Long COVID Awareness Day
ME/CFS = Myalgic Encephalomyelitis/Chronic Fatigue Syndrome
LC = Long Covid
PEM = post-exertional malaise
Wir sind noch meilenweit weg von einer anständigen Behandlung der mindestens 80'000 #LongCovid erkrankten in Österreich.
Quiero hacer este hilo para referencia futura. Son articulos de long covid en Puerto Rico
"El Covid persistente tiene cara en Puerto Rico. Y es predominantemente de mujer" - Periódico La Perla
'Landmarks from around the world will be lit up teal to bring attention to #LongCOVID. It has been 6 years since the beginning of the COVID pandemic.' #PASC #MECFS @openmedf.bsky.social @njbbari3.bsky.social @zalaly.bsky.social @longcovidsos.bsky.social
https://www.longcfoundation.org/lit-for-long-covid?utm_source=substack&utm_medium=email
It's Long Covid Awareness Day, so here once again is my own post on a Long Covid experience - from November 2025, about 3 years after being infected.
"This is to reflect on the illness, the slow journey of mostly-recovering, and the nature of that time."
Love to everyone still dealing with their own version!
https://www.uncharted-worlds.org/blog/2025/11/marking-an-anniversary/
It’s #LongCovidAwarenessDay . I’m in a huge flare so I don’t have a witty message.
But if you haven’t, I would be thankful if you checked out my art blog, @illmarks or maybe shared it with a friend (especially off fedi!).
Many of us w/ chronic conditions struggle to articulate the diversity / severity / scope of our symptoms, or be heard to when we do. That’s why I use creativity to show what I cannot say. Thank you for listening.
Heute ist "International Long COVID Awareness Day"
Thema 2026: "Impacts of COVID & Long Covid on the cardiovascular system"
https://www.longcovidawareness.life/
Weiterhin elementar: Infektionsschutz zur Vermeidung von Infektionen mit SARS-CoV-2: Clean Air, Masken 😷, Tests, Isolation bei Infektion
#LongCOVID #LongCOVIDAwareness #COVID #COVID19 #LongCOVIDHeartbeats
Recapitulando:
Long Covid es una enfermedad que ocurre después de una infección con covid19. Ocurre semanas después de una infección inicial.
Cada infección de covid19 aumenta las probabilidades de Long Covid.
Long Covid se evita al prevenir enfermarse de covid19
#LongCovid #CovidPersistente
Los síntomas entre personas con Long Covid pueden ser totalmente distintos.
No existe una cura. Solo tratamientos a diferentes síntomas.
Todavía hay mucho por descubrir del Long Covid. Se necesita invertir en investigaciones.
A 6 años de la declaración de pandemia, millones de personas han sido expuestas a varias infecciones de covid19, aumentando el riesgo de sufrir Long Covid.
Por eso hoy intentamos concientizar sobre esta condición.
@longcovid The new @patientled #LongCovid Treatment Guide is out!
——
About the Guide:
This guide is meant to spark meaningful conversations with patients and their clinicians about potential treatment options. It is not an exhaustive list, nor is it intended as individualized medical advice. Instead, it offers thoughtfully selected options clinicians and patients can explore together, based on the unique symptoms, needs, and goals of
each patient.
The treatments focus on options that have shown moderate to substantial benefit in at least 20% of individuals with Long COVID in the Harvard/ Stanford TREATME Study (PMID: 40627388 ), that show meaningful promise in clinical practice, or that have shown benefit in other infection-associated chronic conditions.
The guide is focused on medications, but does include a few supplements, procedures, and lifestyle strategies to reflect the diverse nature of Long COVID care options.
Today is #LongCOVIDAwarenessDay.
For more than six years i suffer from this insidious disease. Some symptoms have gotten better, others worse, even others have only recently developed (looking at you gastritis).
But the world has moved on, now pretends that #COVID is over and that i as someone with #LongCOVID do not exist (i must be a "trigger").
No one ever asks, how are you doing. All the care work falls to one person, who has zero support for this burden. I have never felt so alone.
Not only on #LongCOVIDAwarenessDay, please reach out to those you know who have #LongCOVID.
Stay informed on the wide range of disease clusters that can occur.
Look out for friends with "strange" and persistent symptoms, they might have LC.
And spread this excellent PDF with known treatments for specific symptom clusters:
https://www.rthm.com/resources/blogs/long-covid-treatment-guide
It's Long Covid Awareness Day. But we need to talk about willful ignorance.
CW: this post is pretty bitter
@janet reminded me it was #LongCOVID awareness day.
I got caught in the first wave in March 2020. Here we are six years later still sheltering in place......
This is one of the reasons my @cobbles blog exists.
Here's a COVID post from 2023 I wrote:
RE: https://spore.social/@yoginho/114167335227617941
Today, we remember the disappeared that are still here: millions of people suffering from #LongCovid worldwide.
My own condition has improved since last year, even though symptoms returned this winter, but only mildly. Nothing I couldn't control with a dose of antihistamines, and the right kind of pacing.
Life goes on. But I could do without the recurring post-exertional malaise (#PEM), tremors, or the new allergies that came with this...
Yogi Jaeger boosted
The impact of testing positive versus negative for COVID-19 on health-related quality of life: cross-sectional evidence from the Alberta post-COVID-19 follow-up survey
https://link.springer.com/article/10.1007/s11136-026-04174-3
Screenshot from Science for ME weekly update
Hashtags:
@longcovid
#LongCovid #PASC #PwLC #postcovid #postcovid19 #LC #Covidlonghaulers #PostCovidSyndrome #longhaulers #COVIDBrain #NeuroPASC
#Coronavirus
#COVID19 #COVID #COVID_19 #COVIDー19 #SARSCoV2 #auscovid19 #CovidIsNotOver
From Sweden 🇸🇪 :
Work ability and associated factors among individuals with Post COVID-19 condition- a cross-sectional study
https://link.springer.com/article/10.1186/s12889-026-26771-0
Screenshot from Science for ME weekly update
Hashtags:
@longcovid
#LongCovid #PASC #PwLC #postcovid #postcovid19 #LC #Covidlonghaulers #PostCovidSyndrome #longhaulers #COVIDBrain #NeuroPASC
#Coronavirus
#COVID19 #COVID #COVID_19 #COVIDー19 #SARSCoV2 #auscovid19 #CovidIsNotOver
Today is Long COVID Awareness Day and I wanted to write something positive — something like: we’re not weak, we’re fighters.
But honestly, today I don’t have the energy. Sometimes the fight feels almost impossible, and the grief doesn’t go away.
To everyone living with Long COVID or another PAIS: wishing you strength.
And to all caregivers: a sincere thank you.
@longcovid
#LongCovid #PAIS #niethersteld #LevendVerdriet #CovidIsNotOver #LongCovidAwarenessDay
📅 Tomorrow March 15 is #LongCOVIDAwarenessDay
Across Canada, events are being held in Vancouver, Calgary, Toronto, and Montreal to amplify the voices of people living with #LongCOVID. 😷
These gatherings will feature clinicians, researchers, and people with lived experience sharing stories and insights to raise awareness and push for better support and research.
🔗 See the full list of events organized by the Canadian Covid Society and ways to get involved: https://covidsociety.ca/priorities/long-covid/events-lcad-2026/
#LongCOVIDAwareness #WearArespie #MaskUp #LongCovidResearch #LongCovidSupport #LongCovid
This year International Long Covid Awareness Day is March 15
More info:
https://www.longcovidawareness.life/
#LongCovid #CovidIsNotOver
To mark International Long COVID Awareness Day on March 15
From Kornelia Paulsen (who no longer seems to be on social media)
Long COVID awareness is powered by community.
Around the world, organizations, advocates, researchers, and patient groups are creating powerful resources to educate others and push for better understanding of Long COVID.
To help make these materials easier to find and use, we’ve created a “Shared by Our Community” page highlighting resources from across the broader public health movement.
Explore the resources and discover work being done around the world:
https://whn.global/shared-by-our-community/
Long COVID can affect anyone — regardless of age, health status, or how mild their initial infection seemed.
Preventing infection and reinfection of COVID-19 is the best way to avoid Long COVID.
If you’re living with Long COVID, how has fatigue affected your daily life?
Share your experience in the comments.
#LongCOVID #COVID19 #PublicHealth #InfectionPrevention #CleanAir #COVID
Well happy I just got four official diagnoses day to me, I guess.
The following are now actually on my records as diagnoses so hopefully DSA, PIP and co will believe that I am disabled:
Long covid
Fibro
PoTS
Hyper-mobility
COVID infections are not harmless. Research shows that initial and repeated COVID-19 infections can increase the risk of long-term health problems affecting multiple organ systems. Preventing infection and reinfection helps reduce these risks.
#COVID #COVID19 #LongCOVID #InfectionPrevention #PublicHealth
Long COVID can affect many systems in the body. Researchers have documented more than 200 symptoms, ranging from fatigue and brain fog to heart, lung, and neurological problems.
The symptoms shown here are only a small sample. Preventing infection helps reduce the risk of Long COVID.
#LongCOVID #CleanAir #PublicHealth #COVID19 #COVID #InfectionPrevention #LongCOVIDAwareness
New resource for those who suffering from #longCOVID:
The Long COVID Treatment Guide comes from a collaboration between RTHM and the Patient-Led Research Collaborative.
Even one COVID infection can have lasting impacts on the heart, brain, and blood vessels. Prevention is long-term health care.
#LongCOVID #CleanAir #PublicHealth #COVID19 #InfectionPrevention #COVID #MaskUp
RE: https://forall.social/@whn/116187867031213902
Long COVID Awareness Month
#LongCOVID #LongCOVIDAwareness #COVID #COVID19 #Corona #CovidIsNotOver
Elana | אילנה boostedMillions of people around the world are living with the lasting impacts of Long COVID — a growing public health crisis that continues long after the initial infection.
Long COVID can affect the brain, heart, lungs, immune system, and more, making it harder for people to work, study, care for families, and participate fully in daily life.
This Long COVID Awareness Month, we must bring visibility to the millions of people affected and accelerate research, prevention, and support.
From a randomised, placebo-controlled trial of Nirmatrelvir/Ritonavir:
"no virological or immunological evidence supports [Paxlovid] as a treatment for Long COVID."
https://www.medrxiv.org/content/10.64898/2026.02.24.26347001v1
Screenshot from latest Science for ME weekly update
Hashtags:
@longcovid
#LongCovid #PASC #PwLC #postcovid #postcovid19 #LC #Covidlonghaulers #PostCovidSyndrome #longhaulers #COVIDBrain #NeuroPASC
#Coronavirus
#COVID19 #COVID #COVID_19 #COVIDー19 #SARSCoV2 #auscovid19 #CovidIsNotOver
https://gillianlevine.com/reasons-to-mask-in-2026
I'm THRILLED to have such an amazing resource to share with folks who don't get it. Might need to print copies of this zine to leave around the neighborhood, too!
#covidisntover #LongCovid #COVID19 #pandemic #coronavirus #MaskUp #publichealth
When these protections are used together, they help reduce transmission and protect both individuals and communities.
#LongCOVID #COVIDPrevention #CleanAir #Ventilation #MaskUp #InfectionPrevention #PublicHealth #COVIDSafety #COVID19
Q for folks who read a lot of #LongCovid studies-- do you know of any meta-analysis about the very diverse rates of long covid that are reported (1-40%)? Specifically I would love to see an analysis of what factors in the design of a long covid study lead to lower or higher reported rates
Long COVID isn’t rare.
According to the WHO, about 15 in 100 people still have symptoms 12 months after COVID-19 infection.
Prevent infection. Prevent reinfection. Protect your health.
News Release 2-Mar-2026
"Study identifies molecular cause of taste loss after COVID"
"Research links persistent loss of sweet, bitter and umami taste to reduced levels of key taste-cell protein"
https://www.eurekalert.org/news-releases/1118387
Hashtags:
@longcovid
#LongCovid #PASC #PwLC #postcovid #postcovid19 #LC #Covidlonghaulers #PostCovidSyndrome #longhaulers #COVIDBrain #NeuroPASC
#Coronavirus
#COVID19 #COVID #COVID_19 #COVIDー19 #SARSCoV2 #auscovid19 #CovidIsNotOver
[ She is back !!! Wonderful!!! ]
[[ Please check her out, she is an amazing science communicator that got completely wiped out by #LongCOVID for years. ]]
This image shouldn’t be possible
#PhysicsGirl
Mar 3, 2026
How is it possible that this photo was taken at night?!
Support Dianna and the Physics Girl team at patreon.com/physicsgirl
long covid is sooo fucking dumb, I swear to fuck
really, though, being an artist and watching other artists, whether they're friends, acquaintences, or total strangers, doing art is a complex feeling... on one hand, it not only helps me get through the day, I'm also genuinely happy when artists are able to art whether that's half a poem, a little sketch, funny comic voice overs, 3 hour long lore essays, or a whole game
but... there's also a part of me that feels the pain of being bedridden, being unable to even voice call my partners because talking is exhaustng, of being unable to do my art all the more keenly each day is another day that passes me by is another that I don't get to truly live...
I somehow survived past 30 waiting for something I couldn't identify until I finally realised I was trans, only to get one or two years before society's unability to act on empathy shrunk my world to my bed, my microwave, my bathroom, and the stairs between them... I have all of the tools I need for two of my arts (violin and voice) including a computer put together in secret by my friends, yet all I can do most days is watch those wonderful tools gather dust... tools that I would have given a leg for, yet here I am with both my legs, all of the tools, and a neural system so damaged that it can't use the body I have
I feel like a person in a do or die situation whose self-preservation limiters have been turned off my bones and muscles can handle and do so much, but using any more than a sliver of that ability borrows my ability to function for the next few days or even weeks, and all the while, I can give nearly nothing back to the people that help me survive
so I'm here with others whose bodies have been ravaged by long covid and mecfs, watching people build their futures, feeling like I'm hardly living...
people talk about hell in terms of fire and pain and torture, but if you're going to build a hell, that's probably a waste of perfectly good workers compared to just giving the torturees severe mecfs and leaving them
tired... I'm tired... and frustrated...
p.s. send this to your friends that don't mask or get vaccines, I guess, even this suffering might as well be educational for someone
I haven't watched this myself so far but have been generally impressed with media interviews Dr. Binita Kane has done
https://www.youtube.com/watch?v=pk00btt7CVs
Hashtags:
@longcovid
#LongCovid #PASC #PwLC #postcovid #postcovid19 #LC #Covidlonghaulers #PostCovidSyndrome #longhaulers #COVIDBrain #NeuroPASC
#MEcfs #CFS #PwME #MyalgicEncephalomyelitis #ChronicFatigueSyndrome
@mecfs
37-minute video: "The Biology of Post-Infectious Chronic Illness" with Dr. Anthony L. Komaroff
https://www.youtube.com/watch?v=u282aUTpyIA
I haven't watched so far but he is usually good in these videos
#LongCovid #MEcfs #CFS #PwME #MyalgicEncephalomyelitis #ChronicFatigueSyndrome @mecfs @longcovid
1/
New:
-Chaos at the CDC (again)
-ACIP announces meeting on #LongCovid and vaccines*
-Covid ⬆️ in US, AU, UK, NZ
-Christina Applegate goes on Jimmy Kimmel while infected
-A fab look at treating Covid safety like STI prevention
-A free ‘zine you’re going to love, plus more!
Link: https://www.patreon.com/posts/covid-february-151686773
· SARS-CoV-2 reinfections significantly increase the risk of #LongCOVID in children, a new National Institutes of Health (NIH) RECOVER study found
· A large cohort study found further evidence that people with #HIV have a significantly increased risk of Long COVID following SARS-CoV-2 infection
· An in-depth whole genome sequencing study called Sequence #MECFS and Long COVID is seeking to raise £20 million ($23.6 million USD) in funding
https://thesicktimes.org/2026/02/24/research-updates-february-24/
I, personally, don't think the author goes hard enough on the guy (and the industry he's in) selling "think positively" as a treatment for #MECFS
Especially considering she admits that the "brain retraining" took about as long to work as *not* doing that (ie, a placebo), and the guy she paid for that placebo was an engineer, not a medical professional.
But still an ok read of what ME/CFS can be like.
Original post I saw this:
https://mastodon.ie/@swoonie/116130323587022897
Article without the "accept all cookies or pay for a subscription" wall:
The Disabled Crone on why "personal risk" isn't enough when it comes to wearing a mask or respirator to protect against Covid.
"I’ve noticed an uptick in large accounts, mostly PhDs in something relevant such as immunology or virology, explaining why they aren’t masking as much (or at all) anymore."
"As an autoimmune person with multiple post viral chronic illnesses, I have to weigh in."
I know it's been a long time, but Covid is still here, still everywhere, still causing lasting immune issues, disability, and death. Pretending it's gone not only risks your own health, but also that of everyone around you.
#Covid #CovidIsNotOver #WearAMask #LongCOVID
https://nannyogg63.substack.com/p/assessing-your-personal-risk-isnt
News Release 25-Feb-2026
"Tulane study reveals key differences in long-term brain effects of #COVID_19 and flu: Disruption of serotonin & dopamine signaling pathways could explain why some feel 'brain fog' after being infected by #COVID19"
https://www.eurekalert.org/news-releases/1117501
Hashtags:
@longcovid
#LongCovid #PASC #PwLC #postcovid #postcovid19 #LC #Covidlonghaulers #PostCovidSyndrome #longhaulers #COVIDBrain #NeuroPASC
#Coronavirus
#COVID #COVIDー19 #SARSCoV2 #auscovid19 #CovidIsNotOver @novid #novid
📺 https://peer.adalta.social/w/kqRH8K2ZTgjShFoaNHUR1g
🔗 [🇩🇪🇺🇸🇫🇷](https://p4u.xyz/ID_5UF0567O/1)
🔗 [ℹ️](https://anzmes.org.nz/wp-content/uploads/2025/07/Hospital-Care-Plan-for-Severe-Very-Severe-ME_CFS-and-long-COVID-1.pdf")
La publication d'un plan de soins spécialisé marque un tournant dans la prise en charge de ces pathologies invalidantes.
"New Catalyst Awards to Accelerate ME/CFS and Long Covid Breakthroughs"
https://solvecfs.org/february-2026-catalyst-awards/
“Solve M.E. is committed to putting patients at the center of scientific progress. These Catalyst Award-winning studies not only push the boundaries of ME/CFS research but also ensure that patient voices guide every step. We believe these projects will bring us closer to answers, hope, and better lives for people affected by ME/CFS and Long Covid."
"Six years in, mental health care providers are still uninformed on Long COVID. And it’s making the crisis worse"
“I’d heard from people that they were being told things like they ‘identified too much with their illness,’ which is one of the most invalidating and dismissive things I could imagine”
Source: https://archive.md/ktfd3
Der schwerst an #LongCovid #MECFS erkrankte Samuel wählte an seinem 21. Geburtstag den assistierten Suizid. Im Sinne seines letzten Wunsches, dass sein Tod "nicht umsonst" gewesen sein solle, erzählen seine Mutter und sein behandelnder Arzt über ihn und über die Versorgungsmängel bei ME/CFS.
From 🇬🇧
Multimodal imaging suggests potential immune-vascular contributions to altered regional brain perfusion and oxygen metabolism in Post-COVID-19 Syndrome
https://www.sciencedirect.com/science/article/pii/S088915912600228X
Screenshot from latest Science for ME weekly update
Hashtags:
@longcovid
#LongCovid #PASC #PwLC #postcovid #postcovid19 #LC #Covidlonghaulers #PostCovidSyndrome #longhaulers #COVIDBrain #NeuroPASC
#Coronavirus
#COVID19 #COVID #COVID_19 #COVIDー19 #SARSCoV2 #auscovid19 #CovidIsNotOver
it's been sort of strange thinking about the ergonomics of being bedridden over the last half a year the stressors my body faces every day are quite a bit different from those I faced when I was mostly performing violin for a living, and also different from when I became unable to perform outside but could still stream
during the streaming heavy year, I did have to worry about my elbows, wrists, and hands, but they did not have endure the stress of being at sharp angles nearly as much as when I use my phone or read a book while sitting propped up in bed the inside corners of my elbows have especially been in danger and I have had to take extra care to both take stress off when I can as well as making sure that they get to be straight and unstressed while asleep
trying to find proper back support and a position that would avoid giving myself a headache a day was another issue I had to work on, and unfortunately, failure means I have to spend the rest of the day rather miserable and un more pain than I would otherwise have to endure
and then on top of that, learning how to hold my tools like my phone or tablet over long periods of time without stressing a single muscle or muscle group has felt like a nearly impossible task
News Release 19-Feb-2026
New single-cell transcriptomic clock reveals intrinsic and systemic T cell aging in COVID-19 and HIV
https://www.eurekalert.org/news-releases/1117098
"Immune aging increases susceptibility to infection, cancer, and chronic inflammatory disease."
Hashtags:
@longcovid
#LongCovid #PASC #PwLC #postcovid #postcovid19 #LC #Covidlonghaulers #PostCovidSyndrome #longhaulers #COVIDBrain #NeuroPASC
#Coronavirus
#COVID19 #COVID #COVID_19 #COVIDー19 #SARSCoV2 #auscovid19 #CovidIsNotOver
@novid #novid
Ventilation plays an important role in preventing airborne infections. Opening a window helps, but real ventilation is about consistent airflow. CO₂ monitors can give a simple signal of how much shared air is building up indoors.
Share to help raise awareness. 💨🌿
#CleanAir #CO2Monitor #Ventilation #PublicHealth #LongCOVID #COVID19
· A large study recently connected “chronic absenteeism” to pediatric #LongCOVID, further disproving the “immunity debt” talking points from pundits earlier in the pandemic
· A small mechanistic study in Brain, Behavior, & Immunity – Health found that immunoglobulin G (IgG), isolated from people with #MECFS, can destroy mitochondria in endothelial cells
· ADDRESS-LC has opened two more study sites: a new one in California and one in Connecticut
https://thesicktimes.org/2026/02/10/research-updates-february-10/
· New review in Dovepress states that #LongCOVID, #MECFS & #POTS should be classified as neuroimmune disorders.
· Wearable activity tracker notifications may not be a reliable way to mitigate or reduce PEM, new study in Nature Communications
· Small, phase one study is recruiting in Sacramento & San Francisco, CA to test advanced techniques in total body imaging to improve understanding of “tissue-level immune dysregulation” in the disease
https://thesicktimes.org/2026/02/17/research-updates-february-17/
“[In] music spaces, the denial is huge,” phytocene said. “Because I think if musicians were to admit that every day they put themselves at risk, they wouldn’t be able to do that career.”
Covid cautious folks…. I’ve got a dilemma. I’m sick and throwing up so it’s hard for me to mask.
I’ve had a plumbing emergency and someone will be in my unit for approximately 2 hours tomorrow. They will wear an N95 and be in bathroom with exhaust fan on. I will be in bedroom at opposite end of apartment.
I’ve got multiple air purifiers and will open the window in the main living space.
Would you be comfortable not masking under those circumstances? I will mask to let him in obviously.
It’s Been a heck of a 24 hours and I highly doubt I would be able to keep the mask on sadly. My face is too swollen to tolerate it at all right now.
Any tips appreciated!
From The Sick Times:
“Invisible Illness” could have been transgressive. Instead, it minimizes Long COVID.
"The book fails to convey the severity of infection-associated chronic conditions, demands for treatment, or importance of infection prevention."
#LongCovid #PASC #MEcfs #ChronicIllness #CovidIsNotOver #Books #BookReview
Hospital acquired Covid has a 10% fatality rate.
It’s almost completely preventable with respirators and clean air, but healthcare facilities have chosen a policy of forced infection instead.
Let this case set a precedent & start forcing hospitals to adopt airborne precautions!
#covid #COVIDisAirborne #covidisnotover #sarscov2 #LongCOVID #disability #healthcare
clean air is a human rights issue
clean air is an accessibility need
a decade or three from now, this reality will be so painfully clear to you in so many ways. now would be a GREAT time to stop pretending that the pandemic won't follow you for the rest of your life.
https://www.tiktok.com/t/ZTrWpA7gS/
#covid #covid19 #longcovid #covidisntover #disability #disabled #ableism #access #accessibility #humanrights #cleanair #maskup
Highly recommended household items for my fellow #ChronicIllness baddies:
1) A bed desk / Reading pillow / Bed Wedge (take your pick)
2) A weighted blanket
3) A bedside/portable basket for your essentials
4) A 1L insulated water bottle
5) Dimmable lights (IKEA’s system is quite affordable)
6) Honourable mentions: fidget toys, plushies, blankets, and other cozy items.
@keithwilson.eu Link to last year's @patientled #LongCovid Fact Sheet: https://patientresearchcovid19.com/storage/2025/03/Long-COVID-Awareness-Day_-2025-Fact-Sheet.pdf
Maryland may soon become the first U.S. state to directly support Long COVID research and development
https://thesicktimes.org/2026/02/06/maryland-considers-long-covid-innovation-bill/
Screenshot from latest Science for ME weekly update
Hashtags:
@longcovid
#LongCovid #PASC #PwLC #postcovid #postcovid19 #LC #Covidlonghaulers #PostCovidSyndrome #longhaulers #COVIDBrain #NeuroPASC
#Coronavirus
#COVID19 #COVID #COVID_19 #COVIDー19 #SARSCoV2 #auscovid19 #CovidIsNotOver
At parts of the Winter Olympics in Italy, COVID precautions remain, grounded in the reality that airborne infections are still circulating. When your body is your livelihood, prevention is part of performance.
#COVID #COVID19 #PublicHealth #InfectionPrevention #Olympics #LongCOVID #MaskUp #N95
That moment when you have to admit defeat and medically withdrawal from University due to the compounding effect of multiple disabilities/illnesses. 😞
I tried, friends.
For two years, I gave it my all.
Now, I’ve got at least 3-6 months off to focus on trying to stabilize my health. I’d like to return for spring/summer, but it’ll likely be in the fall.
(cont. on second post)
#medical #ph #disability #disabled #mecfs #pots #autoimmunity #LongCovid #Accessibility
Ask your doctor which infectious disease might be right for your child. /s
#Covid #Rsv #MIS-C #CovidIsntOver #LongCovid
For anyone still not talking covid seriously, I really, really need you to read this...
https://eldritch.cafe/@TheSunnyOne/116031331726013783
This isn't a one-off, it isn't a part-time thing For those of us heavily affected by long covid, this is our reality day in and day out.
Our bodies look like they exist in their entirety. I'm not missing limbs, I still have my sight and hearing, but the systems that allow us to use them are broken, and our lives become our beds.
I can't even talk to my partners withy voice except once every week or two for maybe 2 hours tops because talking puts a drain on my stamina, and if I go over my capacity, my max stamina *decreases*
Even petting my cats is draining, and so is having any of them on me, as much as they want to be.
By not bringing covid to heel, this is what was inflicted on millions of people. We lose our professions, our passions, our friends, and even the little comforts, and our existence shrinks down to trying to make sure we don't just shrivel up and die while fighting desperately to keep the will to live and keep fighting burning.
And what's worse? We don't know if we'll recover. Some seem to after a handful of years. For me, I've simply gotten worse and worse over the last 3. I've watched one thing after another slip through my fingers. Now, I'm finding that I need compression on my wrists and hands or they're too painful to sleep with
Please stop making even more people experience this hell. Please mask. Please stop throwing giant events without masking.
I don't know how to end this. My hands hurt and my brain feels too fuzzy to think properly.
In case you missed this big, exciting news:
Germany Declares 'National Decade Against Post-Infectious Diseases'
From February 2026 Massachusetts ME/CFS & FM Association newsletter
https://massme.monkeypod.io/mailcoach/webview/campaign/05601954-e0f2-44eb-af44-5aca96c2b253
#MEcfs @longcovid
#LongCovid #PASC #PwLC #postcovid #postcovid19 #LC #Covidlonghaulers #PostCovidSyndrome #longhaulers #COVIDBrain #NeuroPASC
#CFS #PwME #MyalgicEncephalomyelitis #ChronicFatigueSyndrome
@mecfs
I really wish I knew how much of this is lc/mecfs and how much of this is depression in order to even have a hope.of not worsening things let alone recovering, I have to gauge what my actual, real stamina capacity is so I don't strain it and break it even more, but it feels like that's getting harder and harder to do
To Ground Research in the Lived Experience of Patients and Caregivers, Give Us a Voice!
Screenshot from February 2026 AMMES newsletter
https://www.annfammed.org/content/23/6/570
#chronicillness #Spoonie #MEcfs #CFS #POTS #LongCovid #hEDS #CCI @mecfs @longcovid @pots
"Pacing in the Real World"
Another blogpost I liked a lot by this OT who specialises in ME/CFS & long Covid.
Contains lots of practical tips. As she says, an emphasis is harm reduction rather than perfection
https://onelifelivedwell.substack.com/p/pacing-in-the-real-world
#MEcfs #LongCovid #CFS #PwME #Pacing #MyalgicEncephalomyelitis #ChronicFatigueSyndrome @mecfs @longcovid
Give me hope & help me escape #abuse & finally get out of here.
Please help by hitting 🔄 #BOOST 🗒️ QUOTE & 💸 GIVE IF YOU CAN. Please #share on all social media platforms you’re on. I can’t get to all.
🚨### Urgent Appeal: Help Anna #Escape #Abuse – Time is Running Out! 🚨
https://chuffed.org/project/161937-help-anna-escape
Thanks so much for reading! 🙏
#MutualAid #Narcissist #NarcissisticAbuse #Crowdfund #pwlc #chronicillness
#LongCovid #MyalgicEncephalomyelitis
#MECFS #PWME #SevereME #ChronicPain
@mecfs
@mutualaid
RECOVER Research Review Webinar: Long COVID trajectories in adults, February 10
Links:
https://rtiorg.zoom.us/webinar/register/WN_N2vZj5WDQzyTJ0qmjXm0LA#/registration
https://recovercovid.org/r3-seminar-series
From February 2026 Massachusetts ME/CFS & FM Association newsletter
https://massme.monkeypod.io/mailcoach/webview/campaign/05601954-e0f2-44eb-af44-5aca96c2b253
Hashtags:
@longcovid
#LongCovid #PASC #PwLC #postcovid #postcovid19 #LC #Covidlonghaulers #PostCovidSyndrome #longhaulers #COVIDBrain #NeuroPASC
#Coronavirus
#COVID19 #COVID #COVID_19 #COVIDー19 #SARSCoV2 #auscovid19 #CovidIsNotOver
Long COVID is not psychosomatic. It is a complex, multisystem condition with physical causes documented across growing bodies of research. Preventing COVID-19 infections remains one of the most effective ways to reduce long-term harm.
Shared from the WHN Voices section — reflecting an individual’s lived experience and review of current research. Read full post here: https://whn.global/long-covid-is-not-psychosomatic/
#LongCOVID #LongCOVIDAwareness #COVID19 #COVID #PublicHealth #InfectionPrevention
Dieser Text schaffte es auf die Titelseite von @derStandard
Geschrieben von der stellvertretenden Chefredakteurin.
Da versuchen wir seit Jahren, durch medizinische Aufklärung ins kollektive Bewusstsein zu bringen, dass es nicht gut ist, wenn Leute krank in die Arbeit, in die Schule, in den Kindergarten gehen. Nein, der Glaube, dass Kinder krank sein müssten, um gesund zu bleiben, ist grundfalsch.
Durch viel Aufklärung und oft persönliche schlechte Krankheitserfahrungen hat sich bei vielen Lehrenden durchgesetzt, dass kranke Kinder ernst zunehmen sind. Zum Wohle der Kinder und zum Wohle der Lehrenden. Immerhin sind sie -noch vor den Gesundheitsberufen - die Berufsgruppe mit dem höchsten Anteil an #LongCovid und anderen postakuten Infektionssyndromen (PAIS).
Aber wenn die Kinder zu Hause halt zu mühsam sind...
· A treatment for cats with a #COVID19-related infection may help advance #LongCOVID research
· The supplement Oxaloacetate may help reduce fatigue for LC, but it “did not reach statistical significance,” according to a new study at Bateman Horne Center
· A new prospective cohort study in JAMA Oncology of 1,572 participants with cancer found that COVID-19 had a “significant impact” on these patients, incl. hospitalization, treatment disruptions, death
https://thesicktimes.org/2025/07/22/research-updates-july-22/
· Two studies on potential biomarkers for #MECFS were published this month
· Stellate ganglion blocks, a procedure where an anesthetic is injected into nerves in the neck, may help reduce the severity of some symptoms of #LongCOVID and ME
· An observational study is recruiting 40 people in Boston, Massachusetts to test for defects of air and blood flow in the lungs in people with Long COVID
https://thesicktimes.org/2025/07/29/research-updates-july-29/
· A drug originally developed for celiac disease was found to be safe and effective in treating a post-COVID syndrome in children
· “Dormant cancer cells are like the embers left in an abandoned campfire, and respiratory viruses are like a strong wind that reignites the flames,” said one of the authors of a new study in Nature
· An upcoming at-home clinical trial program for #LongCOVID, run by Scripps Research, is seeking participants
https://thesicktimes.org/2025/08/05/research-updates-august-5/
· People with myalgic encephalomyelitis (#MECFS) have significant genetic differences in their DNA
· A very small clinical trial of the infusion drug BC 007 published in eClinicalMedicine found “significant improvement” in fatigue in people with #LongCOVID
· A phase 2 clinical trial testing the monoclonal antibody sipavibart is recruiting in Fort Lauderdale, Florida
https://thesicktimes.org/2025/08/12/research-updates-august-12/
· A new preprint from the National Institutes of Health (NIH) RECOVER study found that #COVID19 reinfections may increase risk of #LongCOVID by about 35%
· A new review article in Ageing Research Reviews found that persistent infections from viruses, bacteria, fungus, and parasites can accelerate human aging
· A new Long COVID clinical trial to test the immunotherapy drug Anktiva was announced this week by the Chan Soon-Shiong Institute for Medicine
https://thesicktimes.org/2025/08/19/research-updates-august-19/
· Metformin may help reduce the risk of #LongCOVID, according to two new studies
· A Phase 2 clinical trial is studying the drug vidofludimus calcium (IMU-838) for Long COVID
· The National Institutes of Health’s second RECOVER-Treating Long COVID workshop is happening next week, September 9–10
https://thesicktimes.org/2025/09/02/research-updates-september-2/
· A medium sized study in Saudi Arabia found that 29% of participants who were infected with SARS-CoV-2 developed #LongCOVID
· In a small case series, a combination of three antivirals was effective in improving symptoms in participants with Long COVID, according to a new preprint
· The Food and Drug Administration (FDA) accepted the drug application of a potential oral therapy for the prevention of #COVID19 following exposure
https://thesicktimes.org/2025/09/09/research-updates-september-9/
· An estimated 36% of people with a documented SARS-CoV-2 infection worldwide have experienced #LongCOVID, according to a new systematic review
· New funding will help advance a potential low-cost diagnostic test for myalgic encephalomyelitis (#ME)
· The SPEAR study group has proposed a potential Long COVID clinical trial with the company’s next-generation monoclonal antibody, VYD2311
https://thesicktimes.org/2025/09/16/research-updates-september-16/
· Two recent studies found limitations of the drug Paxlovid for protection from #LongCOVID, contrasting prior studies that suggested the antiviral drug might help prevent the disease
· Long COVID may increase menstrual bleeding, according to a new survey study published in Nature Communications
· A new clinical trial is testing the supplement Mitoquinone in combination with “exercise rehabilitation” (which may be detrimental) for Long COVID
https://thesicktimes.org/2025/09/23/research-updates-september-23/
· Researchers in Spain assessed over 190,000 participants, found that #LongCOVID prevalence was three to 10 times higher in individuals with three or more reported infections
· A new RECOVER study published in JAMA found that olfactory dysfunction, or changes to sense of smell, occurred in people after SARS-CoV-2 infection
· A behavioral trial at Columbia University (LONG-CALM) is assessing a vague “mindfulness intervention” for Long COVID
https://thesicktimes.org/2025/09/30/research-updates-september-30/
· A review paper summarizes the vast global costs of #LongCOVID, it is estimated to have an average annual burden of at least $1 trillion globally per year
· A small study in Nature found SARS-CoV-2 in the organs of fetuses from people who were infected with the virus while pregnant
· The National Institutes of Health’s RECOVER-Treating Long COVID initiative released a draft of its protocol for the low-dose naltrexone trial for people ages 6-25
https://thesicktimes.org/2025/11/25/research-updates-november-25/
· Large retrospective cohort study of over 18,000 births found infants exposed to #COVID19 during pregnancy were more likely to have adverse neurodevelopmental diagnoses as 3 years olds
· Another study has found that common diabetes drug metformin may help reduce risk of #LongCOVID
· NIH is recruiting for a small observational study to understand if people with neurological symptoms of Long COVID have inactive [?] remnants of SARS-CoV-2 in their bodies
https://thesicktimes.org/2025/12/02/research-updates-december-2/
· A new study in the International Journal of Infectious Diseases examines how #COVID19 impacts the immune system
· German government announced just over €500 million ($582 million USD) in funding for infection-associated diseases, including #LongCOVID & #MECFS
· A preprint using data from the DecodeME study found more than 250 genes associated with ME, 76 of which were shared with Long COVID
https://thesicktimes.org/2025/12/09/research-updates-december-9/
· New study in Cureus found veterans diagnosed with #LongCOVID at 34% higher risk of visiting emergency department 6 months after infection
· “Our data demonstrate that [LC] is characterized by chronic inflammation, immune exhaustion, & metabolic dysregulation,” scientists conclud in new study published in Nature Immunology
· U.K. charity ME Association awards £1.1 million in funding to the Imperial College to study immunological profiles of LC & #MECFS
https://thesicktimes.org/2025/12/16/research-updates-december-16/
· Two recent studies state that #LongCOVID is an occupational disease.
· Vanderbilt researchers are conducting an immune profiling study on people with Long COVID and postural orthostatic tachycardia syndrome (#POTS)
· A new phase two remote clinical trial was recently announced for myalgic encephalomyelitis (ME) #MECFS
https://thesicktimes.org/2025/12/23/research-updates-december-23/
· 43% of Latino people reported symptoms of #LongCOVID in a new survey study published in Journal of General Internal Medicine
· A case series for Long COVID using a combination of Paxlovid, valacyclovir (Valtrex) and celecoxib (Celebrex), was recently published in Frontiers of Immunology
· A new phase II clinical trial for Long COVID was recently announced in the Netherlands
https://thesicktimes.org/2026/01/06/research-updates-january-6/
· A large, electronic health records study published in JAMA Internal Medicine estimated that over 100,000 Americans died each year between 2022 and 2024 from #COVID19
· A new study published in Molecular & Cellular Proteomics found further evidence of abnormalities in post-exertional malaise #PEM
· A small phase two clinical trial is testing #Ketamine for #LongCOVID fatigue and cognitive function
https://thesicktimes.org/2026/01/13/research-updates-january-13/
· A new study in eBioMedicine found neurological #LongCOVID symptoms were associated with increased pTau-181 levels, a marker of brain inflammation tied to Alzheimer’s disease
· A new “state-of-the-art” review on #POTS highlighted that the multisystemic condition is disabling, causes societal & economic withdrawal
· A phase II clinical trial testing efficacy & safety Uplizna (Inebilizumab) in LC & #MECFS recently announced by German Ministry of Research
https://thesicktimes.org/2026/01/20/research-updates-january-20/
· A large prospective cohort study published in Infectious Diseases found that a majority of people with #LongCOVID did not recover
· Some researchers in Australia are getting a small boost in Long COVID funding
· The biotech company Invivyd is advancing research of a #COVID19 monoclonal antibody called VYD2311, designed to improve upon the currently-available Pemgarda
https://thesicktimes.org/2026/01/27/research-updates-january-27/