Items tagged with: disability

Search

Items tagged with: disability


When I started The Disabled Ginger I sent it to my friends and family … as most of us do.

I was proud that I was finally standing up for disability rights. That I was taking my pain and putting it on the page in an effort to help others. That I had found something that lit a spark inside me.

Unfortunately, many of my friends didn’t feel the same way.

My disabilities are invisible, and I had become very good at hiding them. Apparently that’s what people expected of me, as they didn’t like this “new” version of Kelly.

Almost none of my friends subscribed. What’s worse, many stopped talking to me. Or would only reply in brief texts.

It’s almost been a year since I launched, and my circle is noticeably smaller. Many people I thought I was close with haven’t reached out for nearly 6 months.

When you find your purpose and your passion, it’s an incredible feeling. Hopefully people support you.

Not everyone will. And that’s ok.

It’s painful seeing so many relationships fade away. It hurts knowing they don’t see the value in me now that I’m “officially” disabled.

As painful as it is, it’s also a perfect example of why I became an advocate. Ableism is a huge problem. Being disabled can be incredibly lonely. I wanted to give a voice to those who haven’t yet found theirs.

In the process I’ve met incredible people from all over the world who inspire me to keep going. Who give me a reason to write every day. Who remind me of the compassion, love and goodness that’s still out there.

Thank you to each and every one of you. I couldn’t do this alone.

My latest looks at the reasons we hide, and what would happen if we all decided to stop hiding and show the world the realities of chronic illness:

disabledginger.com/p/why-are-c…

#chronicillness #longcovid #mecfs #ableism #disability #disabilityrights #eugenics







Most of the time, I don't care about being #blind. I don't dwell on it, and I just go on about my business, dealing with the unique aspects of life that come up when you have a #disability. But I can't help the frustration that comes when I've just spent the last four hours doing something a sighted person could do in five minutes.


Okay, this is just stupid! One of the benefits of having a #website is that people can access your services at any time, day or night, right? Well, I just went to the #SocialSecurity website to try and get a benefit verification letter, which I need because I'm trying to reestablish a #VocationalRehabilitation case. I clicked "Sign In" and was greeted by this message:

This service is not available at this time.
Please try again during our regular service hours (Eastern Time):

| Day | Service Hours |
|-----|--------------|
| Monday-Friday | 4:15 a.m. - 1:00 a.m. |
| Saturday | 5:00 a.m. - 11:00 p.m. |
| Sunday | 8:00 a.m. - 11:30 p.m. |
| Federal Holidays | Same hours as the day the holiday occurs. |

If you need immediate assistance:

  • You may call us Monday through Friday: 8:00AM - 7:00PM at: 1-800-772-1213
  • If you are deaf or hard-of-hearing, call our toll-free TTY number: 1-800-325-0778


This of the website limitation is especially frustrating for me because I have a #Non24HourSleepWakeDisorder and an unpredictable schedule. It feels like the website is designed without thinking about people like me who need flexibility.
Has anyone else out there had similar issues with government services or other websites?
#Vent #Venting #Disability #ChronicIllness #Accessibility #DisabilityRights #InclusiveDesign #GovernmentServices #PublicServices
@disability@a.gup.pe @disability@beehaw.org @disabilityjustice @accessibility @chronicillness @spooniechat @spoonies


Top Tech Tidbits for Thursday, February 27, 2025 - Volume 1004 ♿️
toptechtidbits.com/tidbits2025…

The Week's News in Access Technology
A Mind Vault Solutions, Ltd. Publication
#news #technology #accessibility #a11y #disability #blind #deaf #deafblind #toptechtidbits

Top Tech Tidbits. The world's #1 online resource for current news and trends in access technology.

Subscribers: 36,455 🔢️ subscribers were sent this issue via email.


If you think mask bans are “no big deal” because there’s medical exemptions, please consider the following:

😷 Police are not doctors
😷 Many disabilities are invisible
😷 Disabled people don’t live in a bubble. I need my friends and caregivers to mask to protect me
😷 Everyone should have the right to protect their health, you shouldn’t have to already be sick to be permitted to mask
😷 Criminalizing masks sends a message that maskers are “bad”. It emboldens anti-maskers and increases odds of aggression

The reality is that mask bans are discriminatory, ableist and eugenicist. They push disabled people out of public spaces. They put marginalized and POC at increased risk of police profiling.

There’s no official policy for a medical exemption either, it’s at police discretion.

If you’re stopped and questioned, you will have to prove you’re masking for the “right reasons”

I’m more than willing to admit that if I were stopped by a cop for masking, I would appear nervous, shaky, tachycardic and probably “suspicious”.

Not because I’m doing anything wrong, but because my illnesses do not respond well to stress and the police are stressful.

It’s not right to put the onus on the masker to defend their right to mask. We’re still in a global pandemic. Texas has a measles outbreak. There’s tuberculosis in Kansas. Bird flu is spreading and it’s the worst year for influenza A in over a decade.

Masks are a public health tool. They’re a disability accommodation. They should NOT be criminalized.

For more on mask bans and medical exemptions, I wrote an article on the Nassau County ban here:

disabledginger.com/p/nassau-co…

#nomaskban #uspoli #texas #northcarolina #maskban #disability #uglylaws #publichealth #ableism #eugenics #h5n1 #measles #longcovid #covidisairborne


🆕 article from @TetraLogical

Meet Josh: a sportsman who has Spinal Muscular Atrophy

"The missing piece is usability testing with disabled users. Even with good intentions, accessibility efforts can fall short without real user involvement."

#disability #a11y

tetralogical.com/blog/2025/02/…


I do not owe anyone my #disability positivity. I am not a walking advocacy campaign, but a human being living the rollercoaster that is #disabled life, that is life itself.

I will have good days and bad, most will be mixed, all will come with challenges. I cannot demand the standards of myself that the wider non-disabled world asks of me, but I can be more gracious in my assessment of my abilities.

I will complain without solutions, celebrate with enthusiasm tinged with frustration, choose the parts of myself I share sometimes with care and sometimes without.

You will deal with it, or not; it makes very little difference, other than when it makes all the difference.


Someone plays music in the background during a meeting. They ask if it's bothering people. Neurotypical folks on the call quickly speak up and say it's fine.

The autistic person on the call (me):

1. has extreme difficulty participating in or even following the meeting due to the inability to separate foreground from background noise

2. experiences distress from sensory overload

3. spends the whole meeting stressing over how to bring it up in a side channel without taking the wrong tone and offending the person due to social communication difficulties

4. questions whether it should even be brought up, or if they're just being "too sensitive" due to a lifetime of conditioning to treat their own needs as invalid just because they're aren't "typical"

Meanwhile, no one on the call even realizes something is wrong or that the autistic person just got screwed over, completely by accident.

#Disability
#Accessibility
#AccessibilityMatters
#Autism
#ActuallyAutistic
@actuallyautistic


In the hospital for cardiac testing & there’s a mask mandate in place.

My chart says I’m high risk.

Tech comes in with mask under her nose.

Me: “Can you please pull up your mask I’m immune compromised.”

Her: Big sigh, pulls it up “You’ve got some serious Covid anxiety eh?”

Me: “not anxiety, I’m being rational. Colds have put me in the hospital.”

Her: Another big sigh

As I’m leaving I say: “It seems really quiet here today.”

Her: “Yeah half the staff are out sick. You’re actually lucky they didn’t cancel your appointment.”

Me: Internal shrieking

#ableism #eugenics #covidisairborne #covidisnotover #wearamask #sarscov2 #disability #keepmasksinhealthcare


This is a great initiative to help advance accessible sports: derekriemer.com/posts/2025/01/… While this is an inspirational idea for now, it definitely deserves sharing around. #accessibility #sports #disability


Tomorrow will be a dark day for many.

For disabled, marginalized, LGBTQ+ folks & women. For anyone who still cares about others

The disability community saw this coming. It’s important we listen & understand that labelling people as expendable for 5 years leads nowhere good

Since November we’ve watched hate win over and over again.

We’ve witnessed the emboldening of those who think they’re superior to others.

We’ve seen an increase in misogyny, bigotry, ableism, racism & discrimination.

Disabled people begged the Left to pay attention. We begged you to keep masking, to push for clean air, to demand accountability from government.

We implored you to realize that our lives are not less important than your ability to go out for brunch.

Unfortunately, the vast majority of people on both sides of the aisle decided that mitigating COVID was “too hard.”

They accepted repeat infections as inevitable so they wouldn’t have to adapt their lives in any way.

They threw away people like me.

We let hate win. And now we’re going to see the consequences of that decision.

Disabled people weren’t surprised in November, we’ve been living in what feels like an alternate reality for years.

But I suspect others are about to feel our pain.

If you’re feeling scared or angry right now, know that you’re not alone. There’s a community standing with you.

I don’t know exactly what comes next, but I do know we have to keep up the fight.

disabledginger.com/p/how-did-w…

#disability #COVIDisAirborne #covidisnotover #uspol #ableism #eugenics #trump #pandemic #longcovid


Recent commentary on OpenAI's O3 large language model suggests, even to me as a non-expert, that it exhibits remarkable problem solving performance and adaptability to tasks for which it was not trained. If this line of research continues successfully, our prior assumptions about the limitations of machine learning systems may be due for revision, including our understanding of the relationship between AI and disability. The assumption reflected in the literature has been that AI systems have little capacity to respond appropriately to human diversity without detailed training in disability-related scenarios - whatever those are for the specific application. This view may soon cease to be valid, or at least not hold to the same extent as it does presently.

arcprize.org/blog/oai-o3-pub-b…
#AI #MachineLearning #disability #discrimination


I just received Testflight invitation for @surf application. And discovered that VoiceOver, assistive tech for blind people, does not read anything. Just says "bottom sheet" twice, and the app's name, then NOTHING. I hope they fix this mess, because this all means cutting blind people off. I won't keep silent in front of yet another accessibility issue. #ableism #accessibility #blind #inclusion #disability #voiceover #fediverse


How do you feel about the fact that in the United States people with disabilities can be paid a sub-minimum wage?

Today is the last day to submit a comment to the Federal Register asking for an end to this practice. Right now, people who profit off the back of this exploitation are flooding it with comments.

Allies: please don't miss the opportunity to even the score. It takes less than 5 minutes.

federalregister.gov/documents/…

#Disability #USPol #EqualRights


I will never understand why more people aren’t angry and radicalized by the events of the last five years.

The anti mask, anti-vaxx crowd are angry… but they’re also terribly misinformed and on the wrong side of history.

Those of us with disabilities are livid … but we aren’t heard. We’re treated as even more invisible now than we were five years ago. An unwelcome reminder of Covid and the frail nature of the human condition.

But what about everyone else? The anti mask crowd may be the loudest, but they’re far from the majority.

Why aren’t the rest of you angry? Why are so many people content to accept and normalize mass death and disability?

An article came out in PBS today that puts the total COVID deaths at over 20 million.

20 million people. Those are fathers, mothers, spouses, grandparents, siblings and children. Each number represents a loved one to someone else.

Where’s the outcry?

400 million are dealing with Long Covid. That’s an obscene amount of people whose lives are forever changed. Who may never again know what it’s like to be healthy or exist in a body that isn’t rife with suffering.

Where’s the rage?

We know how to prevent covid. We’ve known for years. Yet rather than adapting our lifestyle and being humble in the face of a novel virus - we’ve given it the reins.

We’ve conceded defeat before we even put up a fight. Accepted repeat infections as inevitable. Shrugged our shoulders as we report more and more deaths. Aggressively minimized and disappeared those with Long Covid.

This should make you angry. It doesn’t need to be this way.

What would success look like? What would fighting back entail?

🫶Mandatory masking in all healthcare facilities (with respirators)

🫶Free tests and vaccines for everyone

🫶Better funding of anti virals and other treatments

🫶Clean air in all public spaces with transparent data visible to the public

🫶Clean air on school busses and anywhere that children congregate

🫶Paid time off for everyone who’s sick

🫶Free respirators in public places AND freely available to anyone who can’t afford precautions

🫶A robust public health campaign about how to properly wear a respirator

🫶A brutally honest public health campaign about the dangers of COVID. We have to stop treating it like a respiratory virus and make the public aware that it’s a multi system vascular virus with immune damaging capabilities

Doing even a few of those things would make a huge difference. Doing all of them would end the pandemic.

Get angry. Get loud. Demand better. Demand transparency.

Say that 20 million dead is not “mild”. That 900 dying every week in the U.S. is not “over”. That 400 million disabled will NOT be ignored.

#covidisairborne #covidisnotover #sarscov2 #longcovid #pandemic #cleanair #wearamask #disability #ableism #eugenics


Being #blind is fun. Just encountered a visual captcha with no audio option. So I used JAWS Picture Smart to get AI to read me the text of the visual clue, which I typed in and got through. So basically I'm a human who needs a robot to prove to another robot that I am not a robot. Without my robot, the other robot would have thought I was a robot. Also I was trying to make a payment on my PAP machine, which really should in itself indicate that I am not a robot. #Disability #Disabled


🏧Aira Access at Chase Banks, Nationwide 🏦

Aira is now available at every Chase Bank branch in the U.S.! Bank customers can connect with a visual interpreter on-demand while in any branch, using Chase Bank ATMs, or when accessing online banking services. All calls are free of charge with the Chase Bank access offer.

"As a Chase customer and Aira user, I'm excited at the added accessibility this offer gives me! I love that I can call in and get the support I need to use the ATM or navigate the store on my own terms." - Aira Explorer

This full roll-out follows a successful pilot at 46 Chase Bank Innovation Lab locations as Chase expands efforts to meet the needs of its blind and low vision members.

Full Article: aira.io/aira-at-chase/

#accessibility #disability #DisabilityAwareness #inclusion #AccessibleTechnology




Before you tell a disabled person that they need to “just make the healthcare worker mask”… please understand the imbalance of power that exists in hospital settings.

We can’t “just make them” do anything. If they refuse -our options are to take the risk or go without care.

There’s little recourse when a HCW refuses to mask - there’s almost NO recourse that exists in the moment.

You can file a complaint after the fact - but if the care you require is urgent or an emergency - that won’t help you

Imagine you’re taken to the emergency room with an urgent (or life threatening) issue. The doctor comes in and refuses to wear a mask.

Do you walk out? Throw a fit? These are not good options

Even if you manage to keep your composure and strongly advocate for them to reconsider - the longer you argue the more potential virus you’re being exposed to.

The more you “annoy” the staff - the greater the odds of retaliation or reduction in care.

This isn’t like telling a friend or a colleague to mask. The dynamic is completely different.

HCWs have the ability to help you or harm you. You want them on your side.

A note in your chart indicating you’re anxious, difficult, non compliant etc can follow you around and impact all your care going forward. Getting charts corrected and notes removed is a time consuming and difficult process

As a result many patients don’t push the issue. They delay medical care as long as possible and then just cross their fingers they will get a compassionate HCW when they do finally go.

These delays can also cause harm - and shouldn’t be necessary.

Hospitals have never been terribly safe places. They’re where the strongest and most resistant bugs thrive. They’re also where the sickest and most vulnerable people are.

At least before Covid it felt like hospitals were TRYING to prevent infection.

These days it’s as though any amount of infection control is seen as weak. People are actually bragging about how many times they’ve had Covid or about the risks they’re taking with their health. Staff aren’t masking even around babies, cancer & transplant patients

We have to change course. Our healthcare systems could barely handle the amount of chronic illness they were facing before Covid - they certainly can’t handle the constant influx of disabled patients and staff that Covid is causing.

This is why we need mandatory masks in healthcare settings. The responsibility to keep themselves and others safe should NOT fall on the vulnerable patient.

Many are unable to advocate for themselves - and others are unable to mask.

Mandatory masking protects everyone

Lastly - the solution to this problem should not be “don’t go to the hospital”. It’s not right to make ANY patient feel like they’re wrong for seeking care. Like they’ve somehow “failed” if they end up with Covid.

Until you’re facing a life threatening emergency or serious health challenges - you can’t possibly know what you would do.

Is it scary to go to the hospital right now? Of course. Is it also necessary? Absolutely.

Patients should never be blamed for needing care or for being unable to get HCWs to mask. The system is failing us - we aren’t failing each other.

If you need the hospital - you have all my love & support. It’s impossibly hard - and I will keep fighting to make it better.

As long as hospitals refuse to do what’s right to prevent COVID (hello clean air & mandatory masking)… the onus is unfairly on the PATIENT to avoid COVID.

My guide offers tips to reduce your risk of hospital acquired COVID (and other HAIs)

disabledginger.com/p/how-to-st…

#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



Reading WITHOUT Sight: Challenging the Ableist Assumptions of Non-Visual Literacy

In today’s world, where accessibility is supposedly ever-expanding, comments on how blind people read – or rather, whether we “really” read – reveal a significant amount of latent ableism. When someone remarks, “You’re not really reading because you have to listen to it,” they are unwittingly touching on deep-seated biases that marginalize blind people and our experience. For me, as a blind person, these comments feel aggressive, like a slur that undermines not only my intellect but my very existence within a literate society. The underlying suggestion that my method of consuming literature is somehow less legitimate than traditional reading reflects a lack of understanding and a failure to appreciate the richness of alternative literacy.

At its core, this statement implies that visual reading is the only valid form of reading – an attitude deeply rooted in ableist assumptions. Just as the sighted world learns and adapts to new ways of accessing information, blind people, too, use technology to bridge gaps that were once insurmountable. By suggesting that listening to an audiobook or using a screen reader is inferior to reading with one’s eyes, the speaker perpetuates a narrow view of literacy that excludes anyone who does not fit their narrow definition of a reader.

The Emotional Impact of Dismissive Comments

Hearing such remarks can be hurtful. When someone tells me I’m not “really reading,” they trivialize the effort, love, and passion I pour into every book. Reading, in any form, is more than just a mechanical process; it’s an engagement with ideas, narratives, and emotions. Denying my capacity to “really” read is akin to erasing my agency in choosing to explore literature. It dismisses my experience and can feel like a personal attack, minimizing my intelligence and curiosity.

Moreover, these comments strip away the nuances of my identity and life experience as a blind person. They ignore the reality that many of us navigate systems not designed with us in mind, yet we adapt with resilience and creativity. Listening to a book, for me, is as much an engagement with its content as sighted reading is for others. This medium allows me to dive into narratives, to imagine worlds, and to connect with characters just as vividly as if I were reading visually. Such a remark does not just invalidate my experience, but it also points to a societal failure to recognize and celebrate the diverse ways people interact with literature.

Understanding the Roots of Ableism

Ableism, at its core, stems from a belief that certain abilities, like sight, are inherently superior. This mindset manifests in the way sighted people sometimes view adaptations like screen readers or braille as substitutes, rather than as equally valid methods of accessing information. This thought pattern diminishes the lived experiences of blind individuals and subtly implies that we’re only half-participating in the world of literature. The comment reflects an ideology that upholds one mode of experiencing the world as ideal, while relegating others to second-class status.

Furthermore, literacy is a concept that should not be defined by sensory modality. Whether through braille, audio, or screen readers, blind readers engage in the same cognitive processes of understanding and analying text. These methods are not merely compensatory but rather alternate pathways that lead to the same destination.

Responding Constructively

Addressing this kind of ableism requires a blend of assertiveness and education. In responding to these comments, I could say something like, “When you suggest that I’m not really reading, it feels as if you’re diminishing my engagement with the text. For me, listening to a book offers the same intellectual and emotional journey as sighted reading does for you. It’s not about the method; it’s about the experience of connecting with the material. I’d appreciate it if we could acknowledge that there are many valid ways to be a reader.”

By framing the response in this way, I affirm my own experience while gently inviting the person to reconsider their assumptions. Another approach could be to highlight the diversity of literacy methods available today: “There’s a wide range of ways people can read now, whether through audio, braille, or text-to-speech technology. These methods open up the world of literature to more people and should be celebrated rather than diminished.”

My hope is that, in responding to these comments, I can foster a moment of reflection for others. Reading is about engaging with ideas and stories, not about the medium through which we access them. Ableist remarks about non-visual reading, though sometimes spoken thoughtlessly, present an opportunity to open minds and broaden perspectives. By sharing my experience, I contribute to a more inclusive understanding of literacy and help to dismantle the harmful stereotypes that still persist.

Conclusion

Reading is not an act confined to the eyes; it is an intellectual and emotional endeavour that transcends sensory modality. For many blind people, it is the ultimate expression of our love for stories, our curiosity, and our intellect. When someone diminishes my experience as “not really reading,” they underscore a fundamental misunderstanding of what it means to be a reader. As we continue to expand our understanding of accessibility, it is crucial to challenge and reframe such biases. Only by doing so can we begin to recognize and respect the many ways in which people interact with the written word, enriching our collective experience of literature in all its forms.

#Ableism #Accessibility #Audible #Blind #Braille #Disability #Equality #Inclusion #Kindle


Ugly laws will be enforced in Louisville. Medical masks will be allowed at “police discretion”.

Police chief says: “We do have to look at behavior of person, what they're doing at time, those kinds of things."

I have a disability that makes me LOOK nervous. I “appear” like I could be doing something wrong. As a result these bans terrify me.

Disabled people have been begging others to mask for years because we were afraid of this exact outcome.

Failure to normalize masking means those of us who NEED to wear them are seen as outliers. Deviants. Possibly criminals. There’s a target on our back.

Medical exemptions are not the answer - they leave too many people behind.

Everyone should have the right to protect themselves from a deadly & disabling virus. Whether already disabled or not.

Banning masks and then saying that the police will determine who is “legit” in wearing one based on their overall behaviour? Its terrifying.

This is exactly HOW profiling occurs. These bans will disproportionately impact marginalized individuals and people of colour.

They could also impact someone with a condition like mine. I’m immune compromised and high risk for Covid complications - so I ALWAYS wear a fitted respirator when I’m outside my home.

I also have dysautonomia - a literal malfunctioning of my autonomic nervous system.

If I’m upright - I “look” nervous. I’m sweaty, shaky, twitchy and sometimes wobbling. I’ve been accused of being drunk in public on MANY occasions.

It’s not my fault - Dysautonomia means I can’t regulate my blood pressure, heart rate, sweating & even pupil dilation.

The things that cops are trained to look for and consider “suspicious” are all symptoms of my disease.

In the past - the worst thing I had to worry about was being accused of public drunkenness. Even THAT was scary for me.

Mask bans mean I could be arrested and charged with a crime. Just for trying to keep myself & others safe.

I tell this story to encourage others to speak up against mask bans. To mask up in solidarity and help us normalize them so they will be harder to ban.

To encourage people to stop assuming if you have a “legitimate medical reason” you won’t have to worry. We DO worry.

We need less judgement, assumptions and gaslighting and more allies. These laws are dangerous. They will lead to more death, disability AND division.

Many of us have difficulty convincing HCWs of our illnesses - what hope do we have with police?

Please - if you CAN mask - now is the time. You don’t have to wait for a mandate or permission. You can choose to say “enough is enough” & be part of the solution. Break chains of transmission. Protect the vulnerable. Don’t allow government to decide who is & isn’t expendable.

We all have power and agency and can choose to do the right thing. We don’t have to sit idly by and accept repeated covid infections & exclusion of disabled people from public life.

Let’s work together and stop these bans before it’s too late.

wdrb.com/news/louisville-polic…

#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 #UglyLaws


I called EMS once and police showed up before paramedics (paramedics were busy).

The first thing they said? “You don’t look sick.”

They waited for paramedics who took me to hospital - but that initial response stuck with me.

It’s why mask bans are dangerous. Police aren’t trained to make medical decisions. They shouldn’t be the ones deciding who can and can’t legally wear a mask.

Many illnesses are invisible - you wouldn’t KNOW we’re disabled to look at us.

Most of us have experienced gaslighting from friends, family and even doctors - people are quick to judge and decide you’re “not that sick.”

So are we really expected to risk criminal charges by wearing a respirator & just HOPE police will believe we truly “need it”?

Not to mention that medical exemptions leave behind anyone who wants to mask to protect and preserve their health - as well as caregivers and family of disabled people.

We rely on them to keep us safe - we NEED them masking in public.

I sincerely hope more people join the fight against mask bans soon - because if we don’t fight against them - more cities and states will pass them and more people will suffer.

A good respirator is excellent protection against covid & other illnesses.

We shouldn’t be further excluding disabled and high risk people from public - but that’s exactly what these ugly laws do.

Call your elected officials - tell them medical masks can not and should not be banned.

Don’t embrace escalating fascism and eugenics just because you don’t think it will impact you.

Don’t celebrate it because you hold a grudge about mask mandates.

It won’t stop with disabled people. Help us now & your future self will thank you.

My full article on mask bans, medical exemptions and how we’re witnessing (and even welcoming) escalating eugenics and fascism: disabledginger.com/p/we-are-wi…

#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 #bullying #CleanAirClassrooms #UglyLaws