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Beiträge, die mit longcovid getaggt sind


New: the week's #Covid news and new resources in one easy, free digest. US faces "quindemic," babies under 6 have highest hospitalizations, David Tennant's Macbeth cancellations, new black masks, and more.

Link: https://www.patreon.com/posts/pandemic-roundup-115966923

#publichealth #LongCovid #journalism #prevention


A new Tour de force review of #LongCovid by Antar & Cox in Science.

The authors discuss poss mechanisms of Long Covid including viral persistence, autoimmunity, endothelial activation, microbiota dysfunction, etc & review some trials that are underway.
https://tinyurl.com/2p8jnrrz #press


“If you’ve been fighting for Covid mitigations for the last five years - you more than likely saw this coming. It was painfully obvious when the great unmasking occurred that many people on BOTH sides of the aisle didn’t care about the “vulnerable”. Didn’t care about community or protecting their neighbours. Didn’t care about anything other than their own ability to go to brunch, travel, socialize and get ‘back to normal.’

I’m not saying people should have shuttered inside their homes forever. None of us are. But they should have kept masking. There was no reason to stop. Respirators are highly effective at stopping the spread of Covid. The vast majority of people CAN wear them. We have mask blocs all over the world to provide masks to people who can’t afford them. It’s a simple thing you can do to protect yourself and - perhaps more importantly - protect others.”

If you missed my latest - it’s about the U.S. election, disability rights, eugenics, fascism and how we got to where we are. Perhaps more importantly - it’s about what comes next.

https://www.disabledginger.com/p/how-did-we-get-here-and-what-comes

#CovidIsAirborne #CovidCautious #CovidIsNotOver #CleanAir #WearaMask #Disability #LongCovid #Ableism #Denial #CleanAir #Pandemic #PublicHealth #InfectionControl #Eugenics #SafeHealthcare #N95 #Respirators #MasksWork #MaskUp #Spoonie #Discrimination #Dysautonomia #mecfs #pots #mcas #communitycare #wearamask #chronicillness #keepmasksinhealthcare #MaskBans #NoMaskBans #fascism #election2024


#IDMastodon #molecular_biology #MolecularMedicine #Publichealth #LongCovid & Mitochonrial Dysfunction.This study distinct mitochondrial structural abnormalities in LC patients,notably incl significant swelling, disrupted cristae, & an overall irregular morphology, which collectively indicates severe mitochondrial distress.
the altered levels of assessed mitochondrial biomarkers in PC patients suggest mitochondrial malfunction and disrupted mitochondrial dynamics, potentially underpinning the persistence of post-COVID symptoms


People spend their lives running from suffering. Doing whatever they can to avoid feeling pain. The idea of “forever suffering” is terrifying to them. I think this fear is behind a lot of the disdain we see directed at disabled people.

We remind others that suffering can be permanent. That it can’t always be outrun.

We exist in the grey. Our illnesses won’t kill us - but they also won’t ever get better. There’s no cure on the horizon. No “are you better yet?”

This reality scares the crap out of people.

As such - they pull away from us. They abandon us or treat us with such disdain that we walk away from them. The ones that stay often expect us to hide how sick we are. To plaster a smile on our face and say we’re “fine” so that they don’t have to feel uncomfortable.

When they ask how we’re feeling or if we’re “any better”… they don’t want to hear the truth. In fact - if you tell them the truth you could find yourself facing a lecture on “positive thinking” or how you just need to “try harder” and you will suddenly overcome your illnesses.

People are unable or unwilling to face the realities of chronic illness - so they make it harder for us to face it as well. They treat it like it’s our fault. Like we did something to become ill or like we could get better if we “really wanted to”.

They will push our boundaries, gaslight us and yes - put us at risk for covid. So this is your reminder that it is ok to set and hold boundaries. It’s ok to protect yourself. If someone won’t be there at your worst - they don’t deserve you.

https://www.disabledginger.com/p/we-dont-do-sick-if-you-cant-hide


#CovidIsAirborne #CovidCautious #CovidIsNotOver #CleanAir #WearaMask #Disability #LongCovid #Ableism #Denial #CleanAir #Pandemic #PublicHealth #InfectionControl #Eugenics #SafeHealthcare #N95 #Respirators #MasksWork #MaskUp #Spoonie #Discrimination #Dysautonomia #mecfs #pots #mcas #communitycare #wearamask #chronicillness #keepmasksinhealthcare #MaskBans #NoMaskBans


This study is from 2022 but I'm just discovering it now, and .... Jeesh #covid #brain #viralpersistence #longcovidkids #longcovid

https://www.nature.com/articles/s41586-022-05542-y?fbclid=IwY2xjawGWUbpleHRuA2FlbQIxMQABHbkPu6ANFSZS8SoQnpQDja0R2JeJTcd5Ua2kXs-cuRLoIMFFzkHUI-NIXw_aem_qEEbP_evBb03neU41y78JA





What It’s Like to Have Long COVID As a Kid.

"I used to be a person who pushed myself academically, athletically, and personally. But with Long COVID, that only made me sicker"

"With chronic illness, slowing down isn’t quitting—it’s survival."

"Chronic illness changes you. It forces you to slow down, rethink what success looks like, and find new ways of measuring progress."

Source: https://archive.md/J0b5U

#LongCOVID @auscovid19
What It’s Like to Have Long COVID As a Kid

5 minute read

Cyndi Monaghan—Getty Images Ideas

By Alana KaufmanNovember 4, 2024 10:29 AM EST
Kaufman is a high school senior in Anchorage


So basically treat everyone driving as if they are driving drunk. That's what I've been doing. I look both ways while driving through a GREEN light. I've seen more people drive through a 🚦 red light recently than I have the entire rest of my life!

"The OR of car crashes associated with COVID-19 was comparable to driving under the influence of alcohol at legal limits or driving with a seizure disorder."

(I believe "OR" stands for Odds Ratio?)

#Covid #LongCovid

https://www.neurology.org/doi/10.1212/01.wnl.0001051276.37012.c2


REAL TALK
had i not had #LongCovid and #cancer, i would probably be freaking about now, but am surprised with myself that am relatively calm.

i've been +20 years marginalized for blogging about American fascism. what has me calm is that even back in January a lot of mainstream journalists and the whole Democratic Party leadership still refused to acknowledge Trump is running on fascism.

the fact that just days ago NY Times had to acknowledge it?

FUCKING FINALLY.
🧵

#USpol #2024Elections
Amid Talk of Fascism, Trump’s Threats and Language Evoke a Grim Past

Plenty of presidents have been called dictators by their political opponents, but none until now has been publicly accused of being a “fascist” by his own handpicked advisers.
Trump at the Garden: A Closing Carnival of Grievances, Misogyny and Racism

The inflammatory rally was a capstone for an increasingly aggrieved campaign for Donald Trump, whose rhetoric has grown darker and more menacing.


More proof of #covid and #longcovid damaging the heart. We know COVID causes serious heart conditions, heart attacks, etc., we have so many studies and stats, why this isnt important to the majority of people, why this us not leading to infection control measures like masking, is something I will never understand. But I'll be continuing to #maskup as I know #covidisnotover and #longcovid is a dice roll away, increasing chances each infection.

https://www.news-medical.net/news/20241101/Elevated-cytokines-found-in-the-blood-of-long-COVID-sufferers-explain-heart-problems.aspx
Screenshot of text in link


People are angry that hospitals are bringing back mask mandates due to COVID outbreaks.

Patients like me are angry that we have to risk infection to get medical care. Some of us have died due to hospital acquired COVID.

Masks make sense in hospitals - why oppose them?

I’ve yet to hear a decent argument against mask mandates in hospitals.

The people who oppose them are almost always the ones screaming about how strong and healthy their immune systems are - so theoretically they never spend any time IN a hospital. Why do they care?

Inevitably people just trot out the tired “if your mask works then no one else needs one”… which just highlights that they’ve never spent any significant time in the hospital.

If you’re sick enough to need the hospital there’s decent odds something might prevent you from masking.

Even if you CAN mask - if you’re admitted what do you do when you need to eat, drink or brush your teeth? What if you require oxygen, having vomiting or airway complications?

The responsibility to stay covid safe shouldn’t be left to the patient.

It’s cruel and unusual punishment.

Mandatory masks mean that patients are protected by those around them - which is how it should be.

No one should have to risk covid to get care - and the normalization of hospital acquired covid needs to stop.

If you’re someone who opposes masks in healthcare - or who doesn’t understand WHY they’re necessary - please read my plea to healthcare workers.

Vulnerable patients feel unsafe. Expendable. Terrified.

Needing the hospital is scary enough - we shouldn’t have to worry about forced infection too:

https://www.disabledginger.com/p/a-plea-to-maskless-healthcare-workers

#CovidIsAirborne #CovidCautious #CovidIsNotOver #CleanAir #WearaMask #Disability #LongCovid #Ableism #Denial #CleanAir #Pandemic #PublicHealth #InfectionControl #Eugenics #SafeHealthcare #N95 #Respirators #MasksWork #MaskUp #Spoonie #Discrimination #Dysautonomia #mecfs #pots #mcas #communitycare #wearamask #chronicillness #keepmasksinhe


From ME Research UK:

"Estimating ME/CFS prevalence in individuals with long COVID"

During the early phases of the COVID-19 pandemic, as the term ‘long COVID’ first emerged, Dr Anthony Komaroff raised a crucial question in an article:

"Will some people who get COVID-19 subsequently develop ME/CFS? … many people with ME/CFS say that their illness began with some kind of infection: a virus, a flu, a bad cold."

@longcovid @mecfs

#LongCovid #MEcfs #PostCovid #PASC #LongHaulers
Key points

- Long COVID and ME/CFS have overlapping symptoms, yet many studies overlook the proportion of individuals with long COVID who meet ME/CFS criteria.

- Improving on previous research, Dr Leonard Jason and Joseph Dorri’s study reveals that 58% of their long COVID participants met ME/CFS criteria. Nevertheless, the authors acknowledged the study’s limitations and emphasise the need for long-term follow-up.

- To improve future long COVID studies, symptom questionnaires such as DSQ-PEM could aid in determining the proportion of participants meeting ME/CFS criteria.

- Given the predicted rise in disease burden and economic costs linked to ME/CFS as a result of the COVID-19 pandemic, thorough investigation is imperative.