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#ableism

24 posts18 participants0 posts today

This is horrifying and blatant misogyny and discrimination.

A woman in Tennessee was denied prenatal care because she wasn’t married.

The doctor said it went against their “Christian values”

This in a so called “pro life” state which has enacted an abortion ban as well.

It was never about life, it’s always been about control.

They want people procreating, but they want it to be those they deem the “right” people.

The Christian, white, married people.

Tennessee has the worst maternal mortality in the country.

What a shocker.

open.substack.com/pub/wellsrac

TN Repro News · Exclusive: Pregnant Woman in Tennessee Denied Care for Being Unmarried (Updated)By Rachel Wells

I’m dealing with multiple severe chronic illnesses, including serious heart issues and frequent loss of consciousness.

Yet most days I feel like supply chain issues will be what kills me.

It’s terrifying to rely on medications & medical supplies during these uncertain times.

You can’t “just stock up” on medications.

Financial issues aside, there’s insurance issues and often limits as to how much a person can have.

There’s virtually no way you can “prep” for medication shortages, and it’s scary.

I spent this entire day trying to track down a medication that’s on back order.

Trying to find an alternative.

Trying to cobble together enough to survive.

People who are non disabled have no idea how scary it is to know that supply chain disruptions could quickly & painfully end your life.

We need a system to ensure medication needs are met.

Many years ago I needed an emergency hysterectomy due to extreme and uncontrollable blood loss.

I spent five days in the hospital and was discharged despite obvious complications.

My surgeon had a vacation planned and wanted me gone.

I had to go to the ER four separate times to be taken seriously, and the fourth trip required a man to advocate on my behalf.

The result? A huge internal bleed and infected abscess that required a second surgery and a month long hospital stay.

The bill? $0.

Because it was in Canada.

This is why I say healthcare is a basic human right.

The way I was treated was appalling, but let’s not pretend that patients don’t face similar barriers and misdiagnoses every day all around the world.

We should not have to suffer financial ruin because we got sick.

We shouldn’t fear bankruptcy because a doctor or hospital delayed our care.

Healthcare is a basic human right.

In urban settings, I see an almost 100% correlation between people who walk dogs on a long, retractable "clothesline" lead, and people who couldn't handle a dog safely even on a short lead.

Ironically, most of the experienced dog walkers who could handle a clothesline lead safely (e.g. keeping it retracted unless they're in an open area with no one nearby) typically don't bother using them.

Those things were terrifying on the sidewalk when I was just starting to walk again with a walker or cane. The fact I didn't get tripped and injured is thanks to the dogs' intelligence, not the humans'.

#dogs #disability #ableism

p.s. I love dogs and could spend all day with them; it's the humans handling them who sometimes disappoint me.

Covid has caused an increase in patients with Dysautonomia, a condition which destroyed my quality of life

Yet at Dysautonomia International’s big fundraiser, there was no mask requirement

Worse, they’re publicly stating masks don’t work & quoting the debunked Cochrane study

I’m generally not one to punch down on advocacy organizations because I think we need to fight like heck to lift one another up.

I appreciate that they had HEPA filters, corsi rosenthal boxes and were apparently providing free masks.
But I can’t sit silently when an organization that should be protecting people starts spouting far right rhetoric

What difference does it make if you put masks at the door when you’re telling people they don’t work?

If you’re not leading by example & wearing them yourself?
People look to these organizations to set the tone.

They assume they have our best interests at heart.

Dissuading people from masking during a pandemic is not advocacy. It’s not patient centred. It’s not leadership.
We’ve known for years that Long Covid often causes Dysautonomia/POTS.

There’s been such a significant increase in patients that there aren’t enough doctors to treat them.

Many have lost everything to the condition and are now fully disabled.
Yet this conference will end up causing more disability.

It will end up creating more patients when what we desperately need to do is stop the spread of Covid and start helping those who’ve been disabled already.

The best way to do that is to wear a mask.
Their post says: “there is insufficient evidence to show that mandatory masking in a public setting does anything to reduce COVID risk
Please read this Cochrane review, considered to be the definitive unbiased analysis of this important public health question”

That’s a lie.
They say that people feel “passionately” about the subject but then absolve themselves of any responsibility to actually protect the attendees.

They claim that doctors and Long Covid researchers agreed there was no need to mandate masks at the event.
I will be honest, I wish every indoor event and conference had mandatory masking.

I’m sick of people dying and becoming disabled from a disease we know how to prevent.

But I also recognize that almost no one is willing to require masks because we’re cosplaying 2019 “normal”
Hospitals, medical conferences and events for disabled people need to be the exception.

They need to do better.

They need to realize that they have a duty to do no harm.

They have a responsibility not to make sick people even sicker.
If they’re not willing to do that, the bare minimum they can do is not deride those who do take precautions.

They could encourage masking rather than spread lies that they don’t work.

They could refrain from sharing junk science that’s been largely debunked & discredited
We know masks work.

We know respirators work even better.

We know two way masking is better than one.

We know asymptomatic transmission is a very real threat.

We know all of this, and yet “advocacy” organizations are choosing to ignore it.

We have to push back on this. Over 400 million people have Long Covid. Many of them also have Dysautonomia.

Another Covid infection could wipe out whatever baseline they have left.

We need leaders and advocates to set the tone.

We need them to be honest about transmission

Above all else, we need them to stop the spread of Covid.

We need them to say “enough” to preventable death and disability.

We need them to wear masks and encourage others do the same.

When you know better, you do better

#Eugenics, racism & ableism define the Republican Party now.

For >10 years, the 2014 Obama-era targets led to more hiring of disabled employees, countering wage & employment gaps & bringing disabled workers more economic independence. That’s likely to change.

On July 1,🚨the #DOL introduced a proposed rule that'd end the disability hiring goal for fed contractors & the practice of collecting info about it.
#Disabled #Ableism #Discrimination #WorkersRights #Rights #USPol
motherjones.com/politics/2025/

Mother JonesLabor Department moves to end disability hiring goal for federal contractorsSecretary Lori Chavez-DeRemer plans to axe a longstanding, successful incentive program for disabled workers.
Replied to Broadwaybabyto

@broadwaybabyto

To my fellow Canucks, it won't stop at the US border, either. A fascist / autocratic US will at least bully #Canada into submission, and quite possibly simply take the country. Appeasement will backfire, but Canadian politicians will try anyway. Strength stops fascists, not shame.

"It won’t stop with immigrants. It won’t stop with autistic people.

"Fascists never stop and we must all fight back."

I got a question last night that I really appreciated, because I think it's one of those questions a lot of people ask themselves, answer themselves and never think about again. The question was "Wouldn't a blind person rather produce a podcast than a video?"
Many a person would grab the pitchforks at this point and cry #ableism, but I feel that would be supremely unconstructive so I answered the question, albeit with a minor helping of snark. This is still me, after all.
I'd be curious to hear if anyone else is willing to challenge their assumptions, so consider this an #AMA or #AskMeAnything.
Question about #blindness, how a #blind person would do X or IF a blind person does Y? Go, you shall not be yelled at. Embarrassing question? I've seen it all, DM if you're worried about backlash or propriety. And yes, asking about wiping is permitted :P

Continued thread

Disabled people make easy targets for ICE thugs.

What’s worse, the detention facilities are designed to maximize cruelty.

They worsen existing disabilities and can create new ones.

I wrote about two ICE victims, Alma Bowman and Rodney Taylor.

Both are still being held: disabledginger.com/p/disabled-

The Disabled Ginger · Disabled People are Being Mistreated in ICE Detention FacilitiesBy Broadwaybabyto

Remember when RFK Jr said he wanted to make lists of autistic people?

Disabled advocates warned that was just the beginning. That the violation of medical privacy would be used for nefarious purposes.

Today the regime announced it’s giving all personally identifiable information of Medicaid enrolees to ICE.

That’s right, ICE bullies will now have access to almost 80 million people’s personal info. This is an atrocious violation of privacy that will no doubt be used to target other groups as well.

It won’t stop with immigrants. It won’t stop with autistic people.

Fascists never stop and we must all fight back.

I can't be a good disabled and prove to you all that I deserve AND need help and am a worthwhile human being. It's an impossible task.

"The world" has decided that the only reasonable measures to measure people like me by are literally impossible and self-contradictory, and that's by design.

Besides, even trying to prove that you're human means you already lost. It's an inherently dehumanising position to be put in.

I'll be a gremlin first, before I play that role again! I need to escape that trap, it feels exactly like the trap of domestic abuse. Which is obvious since it's the same mechanisms, just on different scales. Fuck this shit. I was thrown out with the trash for being an abuse victim and I will only escape the cycle by refusing to play by ableist, classist, capitalist rules.

UCSC is Downsizing and Downgrading The COVE, a Life-Saving Resource

"The COVE has been an on-campus recovery resource for more than 10 years. It supports students affected by alcoholism, substance abuse, and other addictions. The COVE welcomes students in recovery, individuals with loved ones struggling with addiction and their allies. It also serves as a sober space for any students seeking a substance-free community."

cityonahillpress.com/2025/07/1 #NeoliberalHellhole #Ableism #Capitalism #UCAccessNow

City on a Hill Press · UCSC is Downsizing and Downgrading The COVE, a Life-Saving Resource - City on a Hill PressOver the course of four months, the COVE’s student interns wrote and released an open letter to the UC Santa Cruz administration — effectively revealing the UC Santa Cruz administration’s plans to downsize the COVE.  The COVE has been an on-campus recovery resource for more...

"It's a patriotic duty to keep ourselves healthy"

Where does this leave disabled people?
We are un-patriotic now?

This is eugenics. This is "useless eater" rhetoric thinly disguised as wellness.

He says they're "encouraging" folks to be healthy.

How long before encouragement becomes force?

#uspol#rfkjr#maga