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Beiträge, die mit pandemic getaggt sind


#h5n1 #hpai #press #news #vogelgrippe #avianflu #geflügelpest #avianinfluence #usa #pandemic

"Diese Ergebnisse deuten darauf hin, dass das #Virus das Potenzial hat, in naher Zukunft von einer #Epidemie zu einer #Pandemie zu werden."

https://etidioh.wordpress.com/2024/11/09/large-scale-computational-modeling-of-h5-influenza-variants-against-ha1-neutralizing-antibodies/


“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


Tick tock⏰... Bird flu begins its human spread, as health officials scramble to safeguard people and livestock.

BREAKING: @CDCgov study finds undetected human cases of bird flu on dairy farms.👇 My new piece @ Fortune Thanks Amesh Adalja & Richard Webby.

https://fortune.com/well/2024/11/08/bird-flu-human-spreadsafeguard-people-livestock/ #birdflu #pandemic #press


Tuesday’s silver lining: the risk of #civilwar in the near future was diminished by virtue of undermining the premise of a stolen election.

The next very dark cloud: any #pandemic would leave us helpless, even one that really was made in a lab in China this time.

Not to mention the impending cumulative and overlapping climate-related storm damage response, and eventual relief shortages.

ref: https://mastodon.social/@rexi/113411373849934676
Fans of #civilwar as a modern political solution:

Please know this: peer-reviewed science states emphatically that your entire accrued personal wealth, and that of your children, will likely disappear forever as a result.

Most of the world’s poorest nations have civil war to thank for their present economic woes.

So, if you don’t care about human suffering, maybe you do about your own pocket-book.


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


I wish we'd see more ads going after #DonTheCon on the #economy.

He inherited a great economy from #Obama and destroyed it (BEFORE the #pandemic.)

He ignored #Covid and killed more Americans in 11 months than every war since WWII. Which destroyed the #SupplyChain and caused #inflation to skyrocket.

I refer to it as: "The house was still standing when he lit the match" paradox.
Empty shelves as panicked shoppers stocked up on everything they could get before a National Lockdown was issued in a desperate attempt to stop the spread of Covid.


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


A few months ago a friend told me I needed to stop “being a burden” on those around me & find somewhere with round the clock care to live & accommodate my disabilities. Knowing no such place exists for someone like me - I gave them a challenge.

I told them that I had looked for such a place many times - and I’ve come up empty because people like me (relatively young with unstable chronic illnesses) fall through the cracks. We aren’t considered when care homes are being established.

We have homes for the elderly, rehab centres and hospices but almost nothing for a young person who isn’t imminently dying but also has no expectation of improvement. I challenged this friend to find me a place - within a reasonable budget - and said if they did I would move.

Of course they were unable to find anything - and in fact even when they tripled their budget they came up empty. There was one contender that provided a brief glimmer of hope - but as soon as they discovered my heart condition they said no.

The reason? “She’s too unstable and we don’t have adequate monitoring. She should be in hospital or try hospice.” Most chronically ill people know that hospitals are short term solutions & will often discharge you before you’re strong enough to be on your own.

And hospice? You can’t enter hospice unless you are imminently dying. So around & around this friend went… hitting all the same roadblocks I’ve hit time and time again. Finally they asked if I considered private in home nursing?

In home nurses where I am start at around $36/hour. If you need round the clock care that’s just over $6000 a week. Clearly not an option for the vast majority of people.

Finally my friend conceded that I was right and there was no magical place where I could have round the clock care & cease being a “burden” to those around me. They were flustered and apologetic & kept saying “I just assumed you hadn’t really looked”.

Therein lies the problem for so many of us - our friends & family always seem to assume they know better and/or that we have simply failed and not “tried hard enough”. The reality is we often spend all our energy looking for solutions - but those solutions simply don’t exist.

I thanked my friend for apologizing & for their efforts in trying to find a place - but I also asked them to consider how it feels to be called a “burden” just for needing support to survive. To be told you needed to go away & stop “bothering” friends & family?

Of course my friend didn’t have an answer - just uncomfortable silence followed by some muffled apologies. I share this story to implore people to stop assuming disabled people haven’t already tried the things you’re suggesting.

This doesn’t mean it’s wrong to make suggestions. But if we tell you we’ve already tried it and it’s not an option - believe us. It’s exhausting spending your days dealing with chronic illness - we don’t need to be explaining ourselves to people who should have our back.

Lastly - disabled people are NOT a burden. There’s nothing wrong with needing help to survive. Telling someone they should feel bad about receiving that help is an unkind thing to do. Please offer help or keep quiet. Most importantly - believe us when we say we’ve tried.

#CovidIsAirborne #CovidIsNotOver #CovidCautious #sarscov2 #maskup #WearAMask #CleanAir #Pandemic #Disability #accessibility #DisabilityRights #N95s #Ableism #CommunityCare #Eugenics


New study: "The #OpenScience, #patent-free nature of the project enabled a large number of collaborators to provide in-kind support…By making all #data immediately available and ensuring that all compounds are purchasable…without the need for materials transfer agreements, we aim to accelerate research globally along parallel tracks…We hope that this can serve as an alternative model for antiviral discovery and future #pandemic preparedness."
https://www.science.org/doi/full/10.1126/science.abo7201

#COVID #COVIDMoonshot


#BBCNews - #Covid Inquiry focuses on government as stakes rise
https://www.bbc.co.uk/news/health-66951800
Decisions made by #Boris #Johnson , his government and his team of scientists in the early days of the #pandemic are to come under intense #scrutiny as the second part of the #CovidInquiry begins.