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#ableism

25 posts18 participants0 posts today

When I had my hysterectomy, I was told recovery would be quick because I was young, fit & otherwise healthy.

They were wrong. The surgeon made an error and despite signs of post op bleeding, discharged me & went on vacation.

When I returned to the ER, I was ignored & gaslit

They told me it was “normal” to be in more pain 8 days after surgery than on day 1 (it’s not).

They said “what do you want us to do?”

They refused to run any tests beyond basic vitals, and scolded me for wasting their time

I knew something was wrong, but I was young and hadn’t yet learned how to advocate for myself.

The pain, swelling and bruising were getting worse with each passing day. I was dizzy, listless and had no appetite.

I slept ALL the time.

I was not getting better

I did what anyone would do, I went back to the ER. Surely this time they would take me seriously?

They didn’t. They made no attempt to hide their frustration that I had returned”. They made misogynistic comments about how “sensitive” I was & that being in pain was normal

I went home feeling completely dejected and disrespected, but also starting to gaslight myself.

Maybe it wasn’t that bad. Maybe this was normal pain. Maybe I did need to suck it up.

I tried to force myself to eat and go for light walks. I tried to play through the pain.

I was vomiting everything up and frequently collapsing from fatigue.

I could not suck this up.

My boyfriend had to carry me into the ER for a third attempt to get help

They did the exact same thing. Asked what we expected them to do. Told us the pain was normal. Refused to call a consult or run tests.

Thankfully my boyfriend believed me over them. He was certain if I went home, I wouldn’t make it through the night

He refused to let them discharge me. He told them, loudly and sternly, that he was not taking me home to die. That they needed to do their jobs.

They threatened to call security but he did not back down.

Thankfully a doctor overheard him and decided to look in and see if he could calm the situation.

When he saw me, half unconscious and white as a ghost, he immediately ordered tests. He told the triage staff not to call security and to take me into a private room

It turns out my boyfriend was right. Had I gone home that night, I wouldn’t have made it to morning.

I had a massive internal bleed and a giant infected abscess which had been growing since the surgeon sent me home.

I was rushed to another hospital for emergency surgery and given 50/50 odds of survival. I spent over a month in the hospital, developed a second hospital acquired infection, and needed 11 months to fully recover.

I survived due to luck & privilege. Had my boyfriend not believed me, I wouldn’t be here. Had he not been a white man? He likely would have been removed & I would have died

This is medical misogyny. They didn’t listen because I was a woman. They thought I was being dramatic

I tell this story because of what happened to Adriana Smith. A young black woman in Georgia who tried to get medical care for severe headaches, and was dismissed and gaslit instead.

She suffered brain death at home because no one believed her. Because of misogynoir.

To make matters worse, she’s been turned into a medical experiment because she was nine weeks pregnant and living in a state with an abortion ban. She’s on organ & tissue support being treated as a human incubator.

No care when alive & forced “care” when dead

Misogyny in medicine kills. It maims. It disables and traumatizes.

Women are frequently treated as hysterical and not given the medical care they require.

We often need a man to accompany us just to be taken seriously.

It’s not right and it needs to change

I will forever deal with medical PTSD because of what I went through, but at least I survived.

Adriana wasn’t so lucky, and no one’s survival should ever be based on luck, privilege or their ability to find a man to speak for them

I survived due to luck and privilege, Adriana didn’t.

What’s worse, due to abortion bans and dangerous forced birth policies, her body is kept alive on organ and tissue support without her family’s consent.

We must do better:

disabledginger.com/p/adriana-s

The Disabled Ginger · Adriana Smith, Misogyny and the Cruelty of Forced BirthBy Broadwaybabyto

Having your concerns dismissed in the ER is nothing new to most of us, especially women and marginalized individuals. Misogyny, ableism and discrimination are far more rampant in healthcare settings than we want to believe.

It’s even worse if you’re black. Misogynoir, which is the term given to the sexism and racism experienced by black women, is a serious issue in America. Black women are three times more likely to die in pregnancy because their pregnancy related concerns are frequently dismissed.

This intersection of sexism and racism creates an exceedingly dangerous situation, and it only gets worse in states with abortion bans.

My latest article is about Adriana Smith, abortion bans, Medicaid cuts and autonomy.

The patriarchal and misogynistic culture of medicine ends lives.

Abortion bans end lives.

We can and must do better:

disabledginger.com/p/adriana-s

The Disabled Ginger · Adriana Smith, Misogyny and the Cruelty of Forced BirthBy Broadwaybabyto
Replied in thread

@MyView

Hold on. Are you saying the disabled couple, who are claiming they were discriminated against, are ostracising somebody?

That comes across as some weird, victim blaming, anti disability, shit.

And saying people change laws, when the voices of disabled people are continually muted or ignored, is a real head in the sand attitude. Mostly, news grabbing stories are what change these laws. For disabled people, this is usually when a celebrity with a disability comes forward, or a particularly nasty incident happens. It would be great for once if an alpaca shook up the laws that need updating.

Adriana Smith was failed by the medical system. She attempted to access healthcare for severe headaches, and the ER sent her home. They dismissed her, as they’ve done to countless other women.

The next day she was pronounced brain dead, and due to Georgia’s strict abortion ban, placed on organ and tissue support without the consent of her family.

My latest looks at this medical experiment and why it’s a gross violation of ethics, the duty to ‘do no harm’ and bodily autonomy.

We must end the cruel policy of forced birth. Abortion bans don’t save lives, they end them.

disabledginger.com/p/adriana-s

The Disabled Ginger · Adriana Smith, Misogyny and the Cruelty of Forced BirthBy Broadwaybabyto

If you’re disabled in the US and rely on a caregiver, this is a must read article.

The fascists are trying to limit Covid vaccine access. Only those who are over 65 or have ‘preconditions’ will be eligible.

While that means many disabled people will still be able to be vaccinated, their caregivers won’t qualify.

Caregivers are a lifeline to those of us living with disabilities. I need help with almost all my activities of daily living.

They’re also one of our biggest risks. We need them to take precautions and protect their health so that they don’t infect us.

This is yet another example of cruel, ableist policies that will harm the most vulnerable:

motherjones.com/politics/2025/

Mother JonesFDA to cut Covid booster access, excluding in-home carersBy restricting vaccinations, "the FDA creates a dangerous public health gap."
#fda#uspoli#fascism
Replied in thread

@tazgetroete
Edit: das Titel wurde geändert nachdem wir unser Kommentar in eine Email geschickt haben. Danke für die Bereitschaft, dazu zu lernen. Gerade zeigt bei uns die Vorschau zum Artikel hier noch das alte Titel aber auf die Seite ist es jetzt angepasst worden.

Die Kommentar an sich ist in Ordnung aber bitte setzt euch damit auseinander aus was für eine ableistische Sprache ihr reproduziert mit diesen Titel vom Text. Da solltet ihr besser wissen, bitte überarbeiten, das ist einfach beleidigend. Was hat jetzt Friedrich Merz und die ja schrecklichen Umgang der deutschen Regierung Israel gegenüber nun mit blinde und taube Menschen zu tun? Reflektiert euch bitte etwas.
#Ableism #Ableismus

Wheelchair user misses train and branded ‘rude’ by station staff after they refused to get ramp
independent.co.uk/travel/news-

It is insane that it's 2025 and wheelchair users are still unable to use a significant chunk of our national transport infrastructure

The Independent · Wheelchair user misses train and branded ‘rude’ by station staff after they refused to get rampBy Rebecca Whittaker

As the fascists move to slash Medicaid, claiming it’s full of “waste and abuse”… I beg you not to lose sight of who these cuts actually impact.

Disabled people. The elderly. Those living in poverty. Disabled and poor children.

Sarah is telling the story of a disabled child who will literally die without their Medicaid.

Why? So the billionaires can become even richer.

They are willing to sacrifice the lives of innocent kids who can’t vote, can’t fight back and who don’t get a say.

It’s eugenics. It’s a cull. It’s greed.

We can’t let it happen.

When mask mandates were enacted to try and save lives, the right screamed about freedom.

When mask bans were passed? They celebrated. Because it’s not about freedom.

With vaccine mandates, they screamed about autonomy.

When vaccines get restricted, they cheer. Because it’s not about autonomy.

It’s about control. It’s about perpetuating the illusion that Covid is over. It’s about eugenics. It’s about thinning the herd but culling the weak & vulnerable.

And for many, it’s about payback. They haven’t dealt with their own trauma from the early days of Covid, and like bullies do, they’re taking it out on the most vulnerable in society.

These decisions cost lives. Criminalizing masks and restricting vaccines will kill and disable people.

Speak up. Call and email elected officials. Tell them to vote No on mask bans, Medicaid cuts and restricting vaccines. Tell them to do better.

Excellent article by Violet Affleck about COVID, climate change and social justice.

She articulates what many of us have been saying for years… the pandemic didn’t end because the threat passed, it ended due to public pressure and denial:

“Public impatience, misinformation about the nature of COVID’s spread & corporate influence over institutional public health, meant that, rather than mitigate ongoing risk by demanding clean-air & accessible healthcare, our leaders announced disabled people would have to fall by the wayside”

She’s an incredible advocate. At the tender age of 19 she’s using her platform and privilege to advocate for the most vulnerable in society.

She fights for the disabled, elderly, children, the marginalized, those living in poverty and imprisoned.

She’s one of the few people consisting calling for clean air in prisons as well as schools and hospitals.

Until we recognize that Covid is a social justice issue, we won’t ever beat it:

yaleglobalhealthreview.com/202

Yale Global Health Review · A Chronically Ill Earth: COVID Organizing as a Model Climate Response in Los AngelesBY VIOLET AFFLECK I spent the January fires in Los Angeles arguing with my mother in a hotel room. She was shell-shocked, astonished at the scale of destruction in the neighborhood where she raised…
Replied in thread

@MyView

I hope it ends when the needs of people with a disability are taken seriously and society generally doesn't keep excluding them or making their lives more difficult.

In the meantime, I guess people with disabilities and illnesses will have to do the best they can, with the obstacles others put in front of them, and the stigma that is attached to disability and illness.

UC Access Now was far from the first group of disabled people in higher ed fighting to dismantle ableism.

Apple TV is apparently showing "Deaf President Now!", about the activism at Gallaudet to get their first Deaf president.

yahoo.com/news/gallaudet-four- #HigherEd #Ableism #Audism #History @academicchatter

Yahoo News · The Gallaudet Four Demanded a Deaf President. Their Legacy Transformed Disability RightsBy Michael Natale
Replied in thread

@MyView

I hope they win their case. Tasmania is the only state which doesn't recognise assistance animals, other than seeing and hearing dogs.

Disabilities comes in a vast range and if an animal can assist, that should be legally recognised. Otherwise, we're just promoting ableist crap.

RFK Jr says only the “sick children” should die of measles.

Dr Oz says that Medicaid and Medicare aren’t “getting their money’s worth”

Casey Means (nominee for Surgeon General) is a wellness influencer who claims that “good energy” can heal chronic illness.

They’re eugenicists. They’re dismantling social supports and conditioning people to blame the disabled for being sick. They’re training you not to care about us.

Next up is Medicaid. Trump’s “Big Beautiful Bill” Aims to slash Medicaid funding.

Medicaid currently provides care to a third of disabled children and 7 out of 10 poor disabled children.

It’s a cull. They see us as “undesirables” so they’re going to eliminate us.

Please fight back. Speak up. Tell your elected officials you do not support ANY cuts to Medicaid.

Continued thread

What’s worse, Adriana tried to get medical care for her headaches. She knew something was wrong. Despite being a nurse, she was dismissed.

When I had my hysterectomy complication, I was sent home 3 times from ER. Gaslit & told I was fine

I survived based on luck because I had a man to fight for me:

disabledginger.com/p/my-most-d

The Disabled Ginger · My Most Dangerous ER Experience and How My Advocate Saved My LifeBy Broadwaybabyto

When I was in my twenties, I was repeatedly denied a medically necessary hysterectomy because I might “meet a man who wants kids”.

I was left completely disabled, forced to undergo six surgeries, multiple blood & iron transfusions to preserve a diseased uterus for a HYPOTHETICAL child.

This happened in Canada, where we tend to be more Liberal than our neighbours to the South.

I was cishet and white, so faced less barriers to care than marginalized people do.

I still wasn’t permitted to make a decision about my own body.

Wasn’t trusted to know my own mind

I had zero quality of life. There was no way I could have been a mother even if I HAD wanted to (which I didn’t).

Yet a hypothetical future husband’s needs and desires were repeatedly put before my own.

I was told I would feel differently once I was “in love”. That my dream man would leave me

Basically imagine every misogynistic and patriarchal nonsense you’ve ever been told… I heard it all.

I watched my twenties slip away from a hospital bed, confused and disheartened by the fact that I couldn’t convince any doctors to let me make the choice that was best for my life & body

I eventually did get the hysterectomy, but only because I was literally bleeding to death.

What could have been a planned & controlled operation was done as an emergency and left me with tons of complications.

Autonomy doesn’t exist for uterus owners. And we’re losing more each day

I tell this story because I feel sick over what’s happening to Adriana Smith in Georgia.

She was a black nurse who tried to seek medical care. She was dismissed and it cost her life.

Now because of an abortion ban her body is being kept alive for a 9 week old fetus.

Her family had no say in the matter. She’s been turned into an incubator by the State. Had “care” forced upon her despite the fact that she couldn’t access proper care when she was alive.

The same day I found out about Adriana, I discovered that police in the UK are being given guidance on how to search a woman’s home & devices for any reference to abortion after a pregnancy loss.

Choice is an illusion. So is autonomy. And it shouldn’t be.

I don’t know where we go from here, but I do know that if I faced a battle to obtain a hysterectomy, more marginalized people living in less Liberal areas have it far far worse.

We need to tell our stories. I’ve told this story before, and I’m going to keep telling it until none of us suffer this way.

For the Adriana’s who can’t tell their story. For those we’ve lost and will lose. For the next generation.

We need to keep fighting for true autonomy. We need to support each other.

We need to make it clear that we do not agree with patriarchal fascist means of controlling our reproductive organs and by extension, our lives.

When we share stories, we help others know they aren’t alone. We educate people on how far we are from equality. We change hearts and minds

Continued thread

I'm feeling like no one actually sees my posts or else most don't care

Only those struggling most have been sharing

Those who are #disabled, in #poverty, facing dangers of #racism, #ableism, #sexism, #bigotry

People talk of the #middleclass growing ever smaller

Yet those who are struggling most are increasingly condemned to die

Meanwhile #consumerism continues

A new #Nintendo Switch dropped & I'm sure those who "can't help" will get one