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Beiträge, die mit CovidIsNotOver getaggt sind
I’ve had people ask me why I’m concerned about mask bans given there’s a “medical exemption”
Mask bans are a return to ugly laws that will further isolate & exclude disabled people from society.
Medical exemptions are inadequate & leave many people behind (like healthy covid cautious people)
My article goes into it in more detail - but police are NOT medical professionals. It shouldn’t be up to them to determine who’s “medically justified” in wearing a mask
Many of us have invisible illnesses & struggle to convince our doctors to take us seriously
What hope do we have with police?
Moreover - disabled people don’t exist in a vacuum. We have friends, family and caregivers who we rely on to mask to protect us. They don’t qualify under most medical exemptions.
If you’re non disabled and want to stay that way? If you’re trying to avoid covid? That also doesn’t qualify.
These bans represent escalating fascism. They’re preying on people’s hatred for the disabled as well as their anger over mask mandates and covid policies.
The best way to push back? Wear a mask. Right now.
Call local lawmakers & tell them you won’t visit any state or county with a ban.
The Governor of North Carolina vetoed the bill - but the senate super majority overrode his veto.
Right after the mask ban bill passed - a woman with stage 4 cancer was accosted for masking.
The man called her a liberal, identified himself as a conservative & coughed on her.
What’s even more appalling - is that if you read the language of the North Carolina bill - it says any OCCUPANT of a public space can legally demand you remove your mask.
Its essentially deputizing the public to enforce mask bans - and designed to dissuade people from masking in the first place
Given these bans have been pushed by Republicans - and JD Vance spearheaded the federal ban on mask mandates - it’s prudent to fight back now while we still can.
Wearing a mask in public shows solidarity. It helps normalize them as a medical device. It will make them harder to ban.
My full article on the Nassau County ban and why medical exemptions aren’t the answer is below - I just found out Facebook has removed it for “disinformation”. And we wonder why more people don’t know mask bans have already happened 😞
https://www.disabledginger.com/p/nassau-county-ny-makes-masking-illegal
#nomaskbans #maskbans #wearamask #CovidIsNotOver #covidisairborne #ableism #eugenics #discrimination #disability
Mask bans are a return to ugly laws that will further isolate & exclude disabled people from society.
Medical exemptions are inadequate & leave many people behind (like healthy covid cautious people)
My article goes into it in more detail - but police are NOT medical professionals. It shouldn’t be up to them to determine who’s “medically justified” in wearing a mask
Many of us have invisible illnesses & struggle to convince our doctors to take us seriously
What hope do we have with police?
Moreover - disabled people don’t exist in a vacuum. We have friends, family and caregivers who we rely on to mask to protect us. They don’t qualify under most medical exemptions.
If you’re non disabled and want to stay that way? If you’re trying to avoid covid? That also doesn’t qualify.
These bans represent escalating fascism. They’re preying on people’s hatred for the disabled as well as their anger over mask mandates and covid policies.
The best way to push back? Wear a mask. Right now.
Call local lawmakers & tell them you won’t visit any state or county with a ban.
The Governor of North Carolina vetoed the bill - but the senate super majority overrode his veto.
Right after the mask ban bill passed - a woman with stage 4 cancer was accosted for masking.
The man called her a liberal, identified himself as a conservative & coughed on her.
What’s even more appalling - is that if you read the language of the North Carolina bill - it says any OCCUPANT of a public space can legally demand you remove your mask.
Its essentially deputizing the public to enforce mask bans - and designed to dissuade people from masking in the first place
Given these bans have been pushed by Republicans - and JD Vance spearheaded the federal ban on mask mandates - it’s prudent to fight back now while we still can.
Wearing a mask in public shows solidarity. It helps normalize them as a medical device. It will make them harder to ban.
My full article on the Nassau County ban and why medical exemptions aren’t the answer is below - I just found out Facebook has removed it for “disinformation”. And we wonder why more people don’t know mask bans have already happened 😞
https://www.disabledginger.com/p/nassau-county-ny-makes-masking-illegal
#nomaskbans #maskbans #wearamask #CovidIsNotOver #covidisairborne #ableism #eugenics #discrimination #disability
Nassau County, NY Makes Masking Illegal - Why Medical Exemptions Aren't the Answer
Defendants of mask bans point to medical exemptions as proof that disabled people have nothing to worry about. They're wrong. A look at why bans are ableist, discriminatory and dangerous.Broadwaybabyto (The Disabled Ginger)
This week my department at the VA, many of whose employees work remotely, will be meeting in person, as we do several times per year.
I won't be there, because they refuse to take any #COVID precautions. I got COVID for the first time earlier this year from the last in-person group meeting, and I'm not going to risk that again.
I angsted over whether this will hurt my career. My boss insists it won't. I'm not sure I believe him, but I believe him enough to stay home.
#CovidIsNotOver
I won't be there, because they refuse to take any #COVID precautions. I got COVID for the first time earlier this year from the last in-person group meeting, and I'm not going to risk that again.
I angsted over whether this will hurt my career. My boss insists it won't. I'm not sure I believe him, but I believe him enough to stay home.
#CovidIsNotOver
#covid #COVID19 #CovidIsNotOver
From Mike Hoerger"s PMC #COVID19 Forecasting Model, Nov 11, 2024:
"We're starting to get our 1st glimpse of the shape of the winter wave.
- Expected transmission a month from now: 1.3 million daily infections
- Best-case: 0.7 million daily infections
- Worst-case: 1.8 million daily infections"
https://pmc19.com/data/PMC_COVID_Forecast_Nov11_2024.pdf
From Mike Hoerger"s PMC #COVID19 Forecasting Model, Nov 11, 2024:
"We're starting to get our 1st glimpse of the shape of the winter wave.
- Expected transmission a month from now: 1.3 million daily infections
- Best-case: 0.7 million daily infections
- Worst-case: 1.8 million daily infections"
https://pmc19.com/data/PMC_COVID_Forecast_Nov11_2024.pdf
“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
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
How Did We Get Here and What Comes Next?
Disabled people have been warning others for nearly 5 years that eugenicist Covid policies would lead to a rise of fascist, racist, bigoted, misogynistic hatred. It's here now. So what’s next?Broadwaybabyto (The Disabled Ginger)
Seit #corona immer das gleiche... Bevölkerung positioniert sich gegen Bedrohung bis dann schleichend eine totale Bullshit-Position so oft gepushed wird, bis die Mehrheitsmeinung fällt...
#desinformation #ukraine #israel #klimakatastrophe #covidisnotover
irgendwann werden uns die Länder ausgehen...
#desinformation #ukraine #israel #klimakatastrophe #covidisnotover
irgendwann werden uns die Länder ausgehen...
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
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
Family Abandonment During Covid Pandemic. They 'Don't Do Sick'.
A look at relationship dynamics, ableism and the importance of setting (and sticking) to personal boundariesBroadwaybabyto (The Disabled Ginger)
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
https://www.news-medical.net/news/20241101/Elevated-cytokines-found-in-the-blood-of-long-COVID-sufferers-explain-heart-problems.aspx
Elevated cytokines found in the blood of long COVID sufferers explain heart problems
University of Queensland-led research has found inflammatory markers in the blood of long COVID patients which could explain why many experience ongoing cardiovascular issues.News-Medical
I am so glad I gave myself time this morning to listen to Ed Yong's talk from XOXO. https://youtu.be/ddy5uMdzZB8?si=vT8rVEuprpgEhJi4
Huge feels that came up for me about becoming disabled, worrying about my productivity, immunocompromised life under Covid prevention denial, getting well enough to go back to producing but realizing that is not good for me and not necessary, but still some guilt.
#Covid #Journalism #MentalHealth #MajorLifeChoice #CovidIsNotOver #Burnout #ImpostorSyndrome #SelfCare
Huge feels that came up for me about becoming disabled, worrying about my productivity, immunocompromised life under Covid prevention denial, getting well enough to go back to producing but realizing that is not good for me and not necessary, but still some guilt.
#Covid #Journalism #MentalHealth #MajorLifeChoice #CovidIsNotOver #Burnout #ImpostorSyndrome #SelfCare
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
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 Plea to Maskless Healthcare Workers from Vulnerable Patients
If you see a mask - wear a mask. Better yet - wear a mask all the time and show us you understand that we're still IN a pandemic. We are depending on you to keep us safe - please don't betray that.Broadwaybabyto (The Disabled Ginger)
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
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