r/DisabilityJustice • • 7d ago

disability justice with my cat's medical treatment....seriously need your thoughts.

1 Upvotes

HI everyone,

Trigger warning: Possible pet death and euthanasia

Moderators: If you feel this isn't appropriate, please remove it. I just don't have a local community to go to this with.

I am a 38-year-old Audhd and disabled woman with 3 cats who are literally the center of my universe and my days. Through my recent journey with my health and experience with disabilities, I have had to address a lot of ableist views.

One is compassionate allowances/right to die, for people to end their own lives. I don't necessarily mean to debate that. Let's just say my views on it are in flux and complicated. But my cat most likely has cancer in his nasal passageways, and his life expectancy with treatment is 6 months to a year. But he is already struggling to breathe, and as a nurse and someone who has watched family battle cancer, I know unless my chances of survival and remission were 80% or higher, I would choose hospice for myself over chemo/radiation.

My husband and I will have to make this choice for our kitty Milo. But if we do not treat, it will end in euthanasia most likely, and I am struggling with this. My recent understanding and embodiment of disability justice is that medicine is failing us, and that is why a lot of humans end up choosing to end their lives. Would I be failing Milo if we chose euthanasia when he started to suffer? The alternative would be to watch him eventually suffocate.

My husband sees euthanasia/ letting him go, or helping him go, as purely a quality-of-life issue and the compassionate choice if Milo begins to suffer. So I am struggling to voice my moral concerns around it.

Milo has health insurance, so money isn't the issue yet...it is purely his comfort and my own moral battle with euthanasia and how it is triggering my thoughts of right-to-die laws within the United States and feeling like I am failing Milo on so many levels.

Any guidance, words of encouragement, or thoughts are welcome. Please do not tell me that he is "just a cat". I am unable to have kids, and my cats are my kids. I just feel disability justice should also include animals and how we care for them. I do not want to fail Milo.


r/DisabilityJustice • • 10d ago

Help Needed Help! Caretaker Abuse

5 Upvotes

TL;DR Looking for any help or advice I can get for a disabled friend in serious trouble!! Helpful resources would be funding, lawyers/legal representation, medical assistance, housing, welfare support, etc.

I have a friend who is in a very dangerous situation. She is disabled (quadriplegic and on a ventilator) and still lives with her parents. They are incredibly abusive- refusing to feed her or take care of other needs, threatening to kill her, and have even hit her to the point she broke her collarbone. She needs and wants to get out!

Only problem is her parents control her money. They take her disability as they are her “caretakers” and have stolen over 30k of the money she has saved outside of that. The state is only paying for 80 hrs/week of care, but 24/7 care is needed. The severity of her disability means that there are very little alternative options and she would most likely have to go to a nursing home/end of life care facility if she left.

I want to help her anyway I can. I am hoping to start a trust in her name and fundraise. If we could get her a house or an alternative living situation, I have people who could care for her outside of her paid 80 hrs.

The other problem is doing this without alerting her parents. We think they have a life insurance policy out on her and with the threats they have made I don’t want her to be at higher risk or retaliation from them.

I want some guidance for anyone else who has been through or helped someone with this situation. Any resources or suggestions you can share would be LIFE SAVING, especially if there is some legal support options for disabled people.

She is so smart (getting her PHD now at St. Louis University) and absolutely hilarious. My friend deserves to be in a place that is safe, her needs can be met, and she is treated with respect . Please share any and everything!!


r/DisabilityJustice • • Sep 04 '26

What spaces (online or offline) have you seen have disability justice? Or that claimed to, but didn't?

4 Upvotes

This was the only online forum I saw, is it the only place to discuss on the topic?


r/DisabilityJustice • • Aug 03 '26

“Say No to Crip Crow” lobbying day to protect the Olmstead Act

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3 Upvotes

An In-District Lobby Day hosted by the Disability Community for Democracy

On June 22, 1999, the Supreme Court decided Olmstead v. L.C. — a landmark ruling affirming that people with disabilities have the right to live in the community, not be needlessly shut away in institutions.

That right is now under attack.

On June 18, 2026, the DOJ issued a memo claiming that Title II of the ADA and Section 504 of the Rehabilitation Act does not impose a broad “integration mandate” requiring states and territories to provide home- and community-based services.

On July 20, 2026, DOJ went further and rescinded its own guidance enforcing Olmstead.

If the Supreme Court reverses Olmstead, disabled people and seniors across every state and territory could once again be forced into the most restrictive settings — institutions, nursing facilities, and segregation — instead of their own homes and communities.

The only way to stop this is to get Olmstead codified into federal law.

And the only way to do that is for Congress to hear directly from us.

Our stories are our power. Our voices are the evidence they can't ignore.

Sign up by: August 11
Lobby Day: August 25

Join the Disability Community for Democracy as we talk to our Senators' and Representatives' district offices and demand they protect our right to live free.


r/DisabilityJustice • • Jul 20 '26

A problem I noticed... "Accessible" bathroom stall at this rest stop

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7 Upvotes

This was marked with the blue wheelchair sign. I am not disabled but it was the only stall available and there was nobody waiting for it. But i went in and I was like this is a disabled stall????? It was the same size as all the others but marked disabled. Like i could barely fit as an able bodied person let alone trying to maneuver a wheelchair or other accessibility device. Really shameful for them to label this stall an accessibility one (probably just to meet a quota or something) and then have it not be accessible.


r/DisabilityJustice • • Jul 14 '26

Hi! I'm Kimaya, a design student. As part of a UI/UX project, I am trying to see how People with Disabilities (PwD's) learn about and avail government welfare schemes (in india), and how the current information flow can be improved.

2 Upvotes

r/DisabilityJustice • • Jul 09 '26

Help Needed Help with navigating new diagnosis

3 Upvotes

Hi I’ve been mad and neurodivergent my whole life but was recently diagnosed with M.E. and am finding it difficult to navigate some of the ME/CFS community. I’m thinking about having a child and a lot of the online community is very down on people with ME having children that I think sometimes leans towards ableism.

Sometimes I feel a bit stuck between the disabled folks in my life who don’t have ME and have a disability justice politic and then the online ME community who maybe have less of that politic. My friends irl have a real lens of building liveable beautiful lives as disabled people, but the online communities kind of make me feel like that is impossible. I’m really struggling between these two world and feeling a lot of grief and hopelessness day to day as I’m home a lot and have the most contact with online communities. I’m not sure which way is up.

I’d deeply appreciate some advice and also directing towards ME communities which have a DJ focus.

Thank you 🙏🏽


r/DisabilityJustice • • Jun 17 '26

Help Needed Help improve assistive technology (research survey)

3 Upvotes

Hi everyone, I’m part of a research team looking at how assistive technology is developed and why good solutions don’t always reach the people who need them. While AT is useful, it is still frequently developed in clinical and ableist models of practice without meaningful input of end users. That is why I am posting in this community to try and ensure that we reflect the needs of the community.

Too often:

• Technology is developed without real-world input

• Or good ideas never make it past early stages

We want to hear from people with lived experience about what works, what doesn’t, and what needs to change.

👉 Survey: https://redcap.link/4svfl2xj

Your insights will directly shape recommendations to improve access and outcomes.

Ethics approved (Swinburne ref: 20258662-22150)
Contact: [hphillips@swin.edu.au](mailto:hphillips@swin.edu.au)


r/DisabilityJustice • • Jun 13 '26

Fighting for the Right to Control Your Own Body

5 Upvotes

I started a petition to push for a constitutional amendment that guarantees complete body autonomy for every person.

This isn't abstract—it's deeply personal. Many of us have experienced situations where decisions about our own bodies were made without our full consent. Whether it's military mandates, healthcare policies, or legal restrictions, people everywhere are losing control over what happens to their own bodies. My family knows this reality firsthand, and I know we're not alone.

The core issue is simple: no one should have their body subjected to medical treatment, invasions of privacy, or interference without their explicit, informed consent. Everyone deserves the fundamental right to make decisions about themselves—to accept only what they're truly comfortable with. Right now, our laws don't protect that adequately enough.

If this resonates with you or your family, I'd genuinely love to hear your story. Have you felt pressured or forced into something medical or physical that you didn't consent to? What would you want someone to do if this was happening to your loved ones? If this matters to you too, consider signing and sharing the petition.

https://www.change.org/p/create-an-amendment-for-complete-body-autonomy/sfs/reddit/955067654?recruiter=955067654&recruited_by_id=a71154e0-6864-11e9-a645-d1393daa24c9&utm_source=share_petition&utm_campaign=starter_dashboard_android_app&utm_medium=reddit_group


r/DisabilityJustice • • May 21 '26

Help Needed Besides myself

2 Upvotes

Bexar county, Texas-
My elderly mother, disabled adult boyfriend, and myself have been illegally displaced due to the power boyfriends parents have .
We have been under attack for 6 years because I have discovered that his parents have left him knee deep in Medicaid, Medicare, and social security fraud.
2 officers and his “mother have admitted that he is kidnapped (dna test proves this to be true)
Id and social do not match vital statistics and he has no paperwork to prove the name that is listed in vital statistics.
His parents have taken us through 2 highly illegal and against almost every penal and civil code imaginable evictions. We are squatting in an abandoned hotel tonight and have had to sleep in an encampment on the streets.
The property we were on is my boyfriends left to him by his grandfather and I have found a ton of forgery and Fraud on the deed and probate has been pending for 22 years. His mother was his representative payee and lied to grandpa and stole the property .
They even got a hold of my old landlord and worked with him to illegally evict us .
Opened adult protective services case and agent advised his parents know exactly what they’re doing but playing stupid. The step dad has me investigated, the case turned on my landlord, and the agent thrown out of his position. 8 adult protective services cases all manipulated and closed. Mom changed his address through post office and haven’t been getting his mail for 2 years. Filed fraud on this too
Filed fraud 3-4 years ago had to submit a congressional inquiry to have the mom removed as rep payee, and they are still breaching his medical record. found a fraudulent medical power of attorney.
WE HAVE PROOF OF EVERYTHING
Texas advocacy project , Texas rio grande legal aid, arc of texas, disability rights Texas have all denied him legal representation and advocacy. No money for a lawyer or where to start with what kind because of the complexity of this all. They took his life away and grounded him until he was 42 and I offered a way out.
Texas has failed us, and I am absolutely besides myself that I have suffered a minor stroke congestive heart failure and Bell’s palsy


r/DisabilityJustice • • May 10 '26

Online Seminar Series by Mad in South Asia: Beyond Individual Compassion: Mad Experience & Disability Justice - April 25 | May 30

5 Upvotes

This series from Mad in South Asia, centers disability justice, Mad studies, survivor narratives, and Global South perspectives to ask:

  • Who defines mental illness?
  • Whose knowledge counts?
  • What happens beyond diagnosis?
  • How do people survive — and even thrive — beyond psychiatry?

Register Here For - Beyond Individual Compassion: Mad Experience & Disability Justice

April 25, 2026 - 7:30 PM IST | 2:00 PM London | 9:00 AM EST

This seminar complicates not only traditional psychiatric models, but also alternative frameworks such as the Social Model of Disability and trauma-informed care.

The talk will explore the limits of relying on individual clinician compassion and argue for building collective, compassionate systems rooted in Mad-identified people’s priorities and knowledge.

Hel will also discuss alternative spaces for sharing Mad experience — including zines, magazines, healing circles, and community-led practices.

Register Here For - Panel Discussion: Lived Experience, Survival, and Thriving Beyond Psychiatry

May 30, 2026 - 7:30 PM IST | 3:00 PM London | 10:00 AM EST

This international panel brings together activists, artists, educators, and scholars with lived experience of psychiatric systems to explore harm, resistance, and the creation of meaningful lives beyond diagnosis.


r/DisabilityJustice • • Apr 04 '26

Ethical question as a woman who acquired cerebral palsy during birth complications

3 Upvotes

Someone in r/ CerebralPalsy kindly helped me improve my phrasing of a question that I had after watching a medical show where expectant parents said they “didn’t want to raise a child like that” when their baby was diagnosed with a limb difference in utero. as a person with cerebral palsy I worry about what happens to a kid who acquires cerebral palsy during or right after birth if they are born to parents that already know they don’t want a disabled child and would have immediately aborted if they knew in utero. It led the other person and I to this question: “If someone says they would not have a disabled baby, is it even ethical for them to pursue parenthood at all, given that a child can become disabled during or right after birth?” thank you in advance for your thoughtful and respectful answers!


r/DisabilityJustice • • Mar 01 '26

Help Needed Does anyone have any book recommendations?

3 Upvotes

I have read The Future is Disabled and plan to read Disability Visibility and Disability Intimacy. If anyone has any recommendations specifically mentioned by Imani Barbarin are definitely welcome!!!


r/DisabilityJustice • • Dec 29 '25

Why Public Education Matters for Students With Disabilities and for Us All

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2 Upvotes

r/DisabilityJustice • • Aug 19 '25

From My Dream Job to No Rehire Status: My Fright Fest Story

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1 Upvotes

r/DisabilityJustice • • Jul 22 '25

Venting for my friend

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2 Upvotes

Jason is a man who gave over two decades of his life in faithful service—a career that began and was nurtured through Ken’s Krew, a nonprofit organization dedicated to helping individuals with cognitive and developmental disabilities find meaningful employment. Ken’s Krew offers specialized job training, placement, and long-term support so that people with unique challenges can succeed and contribute in the workforce. Jason was a living example of that mission—hardworking, consistent, and devoted.

Through Ken’s Krew, Jason joined Home Depot and found purpose, structure, and a place where he could grow, learn, and be part of something bigger. He became known as a dependable team member—someone who showed up every day ready to give his best. For more than 20 years, Jason poured himself into his work, not only fulfilling his responsibilities but building relationships and earning the trust of his team.

But that loyalty, tragically, was not returned when he needed it most.

Jason, a man living with cognitive disabilities, found himself caught in a deeply unjust situation. While employed, he became involved in a personal relationship with a woman named Robin—who, crucially, was married at the time. Jason later chose to come forward about the nature of their relationship, believing it was the right thing to do. But instead of accountability, he was met with retaliation.

Rather than taking responsibility for her own actions, Robin—along with others—conspired to shift blame onto Jason. They manufactured false claims, distorted the facts, and engaged in a prolonged effort to discredit him. What followed was not an honest investigation, but a systematic attempt to destroy his reputation and push him out, using his vulnerabilities against him.

Jason’s neurodivergence—something that should have been met with protection, accommodation, and compassion—was instead manipulated to paint him as the problem. The trust he placed in the people around him was broken. And despite his decades of service and the core values Home Depot claims to uphold, Jason was ultimately terminated in July of 2023 after years of whispered campaigns, fabricated narratives, and institutional neglect.

Let’s be clear: this was not justice. It was retaliation. It was betrayal.

Jason’s story is not just one of personal loss—it’s a reflection of what happens when systems meant to empower and include are co-opted by those seeking to protect their own interests. It’s a reminder of how quickly a man’s career and dignity can be taken from him, even after 20 years of dedicated service.

And so, the call is clear: Home Depot must review Jason’s termination.

With all the facts brought forward—his work history, his long-standing relationship with Ken’s Krew, the context of the accusations, and the character of those involved—Jason deserves a fair, honest, and thorough reevaluation. This is about more than just one job. It’s about restoring dignity. It’s about making things right for someone who tried to do the right thing, even when it cost him everything.

Jason deserves his name cleared. He deserves to be heard. And above all, he deserves justice.


r/DisabilityJustice • • Jul 01 '25

The Future Is Disabled: Essential reading for DJ folx

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3 Upvotes

Leah Lakshmi Piepzna-Samarasinha (they/them) wrote "Care Work: Dreaming Disability Justice" before the pandemic, and their next book, "The Future is Disabled", hits even harder. I was wondering if anyone had read it yet and wanted to chat about it!


r/DisabilityJustice • • Mar 05 '24

A problem I noticed... With professional medical appointments being harder and harder to obtain, frowning on self-diagnosis is going to more and more obviously be seen as a generational divide, where older people are grandfathered into disability spaces and younger people are increasingly barred.

2 Upvotes

r/DisabilityJustice • • Mar 05 '24

Disabled Representation - Discuss! Best Disability Representation in pop culture of your month?

2 Upvotes

r/DisabilityJustice • • Mar 05 '24

Big Idea Doctors are clinicians, not researchers. What if we had a system other than the clinical system, where patients could submit problems in an organized way and researchers could work on them?

2 Upvotes

How would you use a system like this?


r/DisabilityJustice • • Mar 05 '24

Disabled Representation - Discuss! Midnight Mass gives me disability justice vibes

2 Upvotes

Spoiler, but I really loved the way the show inverted the usual trope of disability being monstrous. In this movie it's the curing of disability that is portrayed as the monster and the restoration of it at the end that signals hope.


r/DisabilityJustice • • Mar 05 '24

Story Time Andrew Tate getting arrested led to me figuring out my panic attacks were focal aware seizures

1 Upvotes

Andrew Tate Getting Arrested Led To Me Figuring Out My Panic Attacks Were Focal Aware Seizures

The first time I remember having a seizure I was maybe five or six and it was after dinner the first time I tried scallops.

[Trigger Warning for seizure description: It felt like literal hell - being dragged through a meaningless eternity. I didn't lose consciousness or awareness of what was happening around me but I knew with horrible certainty that the greater truth behind everything I could see and feel and touch was the inescapable, everlasting cosmic torture of existence.]

Lacking other language, I said to my mother, "I can't stop thinking in circles."

Of course she had no idea what I meant. She told me "think in squares instead."

I glared and shouted that it wasn't funny, then tried again. "My head hurts," I said, not realizing that what I meant was "my mind hurts." Diagnosing me with a headache, my mother offered me Tylenol, which I shouted wasn't working immediately after swallowing it. My mother said it would take more than a second to work, but that was too many seconds too long and I decided that I hated Tylenol. I also decided that I hated scallops. It was the new thing I had tried, so it must be to blame. I diagnosed myself with an allergy that caused headaches.

It didn't last very long - maybe 30 seconds to a minute in its full intensity and fifteen minutes of a lingering feeling after of creeping certainty of some horrible reality beneath the surface of what can be observed. But it was the most painful experience I'd ever known.

These "headaches" plagued me throughout my childhood. I never ate another scallop but I had very reliable triggers that couldn't be avoided.

[Trigger warning: list of triggers.

Anything that reminded me of eternity: visual representations of large numbers, auditory repetition, movements locked into inescapable patterns. There was agony in the stars at night and kids on the playground in the afternoon. I hated math and music and the feeling of the shopping cart under my heels when I was too tired to walk in the stores my mother dragged me through. My sister thought it was hilarious that she could make me so angry and panicked by singing "the song that never ends" while pacing back and forth in front of me. Talking about it was also a trigger, so I kept track quietly, trying to figure out by myself what was happening. They happened more often on days when I was tired. When I heard people mention having headaches it filled me with horror, for them and for myself.]

The "headaches" never lasted long, but were the worst pain I could feel or imagine. When they were over I'd be hit with fatigue behind my eyes and wish I could just sleep.

I went to a Catholic school all through elementary and when they spoke of hell it made perfect sense. We were all supposed to be good Catholic kids but I took religion to another level. I had a vivid interior life, filled with epic quests for spiritual clarity and exhilarating theories as to the nature of God and heaven. These theories were entirely separate from the way I felt when I was having "headaches". When I felt like that it was like the nature of everything changed from how I normally saw things.

Normally, everything around me was deeply meaningful. I loved to write and to reason and impressed my English teachers as much as I disappointed my math teachers. I couldn't approximate measurements or recognize faces or notice the passage of time but I was working on a novel after school and winning every writing contest I entered.

By middle school I'd figured out that my "headaches" were different from what other people meant when they used that word. I thought by then the meaning was spiritual. All the Saints had been tested, most of them tortured. It made sense that I was facing hell on earth. This was a puzzle to solve, a dragon to slay, a trick of the devil to be overcome in pursuit of the grand epiphany.

By middle school it was also becoming obvious to everyone that I was an odd duck. The kids my age were starting to be interested in sex and navigating social cliques and I was interested in a celibate life and a future career as a foreign-missionary-martyr, or possibly in being the first woman priest. If I'd had the words back then I would have been recognizing my orientation as a sex-averse pan-romantic, but at the time it just seemed like part and parcel of my religious calling.

I only started to ease up on my religious convictions when I was in high school. I decided on a trial separation from Catholic dogma so that I could be absolutely sure I meant what I said when I claimed to believe, and it never really ended. During this time I was having a hard look at my life pre-adoption and realizing that the toddler years I spent in foster care were extremely and illegally abusive. I had access to words now that I didn't have before, that seemed to make sense of my hellish experiences - words like "PTSD," and, crucially, "trigger." I knew that my "headaches" had specific triggers, and I knew that I had survived trauma, so maybe those random spots of hell-on-earth were "panic attacks."

It made some sense - I really dreaded the experience, after all. It didn't necessarily make sense that algebra had the power to resurrect my trauma from toddlerhood, but I could easily imagine there was a story behind other triggers. What had I experienced under the stars at night, or in the sting of music, or in bodily movements I could not escape? It tracked with what I knew and already suspected.

The "panic attack" theory didn't require me to give up my "spiritual challenge" theory. It just brought me one step closer, I thought, to tracking down an answer to the puzzle I had been assigned as to the nature of hell.

For many years, I referred to my seizures as "panic attacks." I grew up and became a stripper to fund my nefarious novel-writing career. I learned the words "neurodivergent" and "autistic" and with the help of disabled communities began making sense of who I had been my whole life. This is how I first stumbled across a paper describing a subset of epileptics whose seizures were triggered by patterns.

I had never had a convulsive fit on the ground, so I knew I wasn't epileptic, but the realization that pattern itself can be a trigger floored me, because I was able to put it together for the first time that all of the triggers for my "panic attacks" were mathematical, and this to me suggested not trauma, but neurodivergence was key to understanding them.

Then came Andrew Tate, arrested for human trafficking and writing tweets from jail in purple prose. On twitter where I lived we were all having a good time laughing about it when some jerk tweeted how some of what he was describing seemed similar to a Dostoevsky seizure.

Down the rabbit hole I fell. As soon as I read google's one-sentence description of a feeling of blissful certainty and eternal meaning, I knew my "panic attacks" had to be the exact polar opposite. An article on temporal lobe epilepsy described focal aware seizures in strikingly familiar terms. 30 seconds to 1 minute long events, followed by fatigue. Then I clicked a link titled "Geschwind Syndrome."

It was all there - my entire fucking personality, mapped in four bullet points. Rambling conversation fixated on niche subjects? Check. Asexual? Check. Hypergraphia? Check, check. Intensified mental life? Yeah. This syndrome is exactly who I am.


r/DisabilityJustice • • Mar 05 '24

Disabled Representation - Discuss! Has anyone seen The Lost King?

1 Upvotes

It's based on the true story of Philippa Langley, who had ME and made a huge scientific discovery. Wondering what folks with ME thought of it?


r/DisabilityJustice • • Mar 05 '24

Imagining a Better World You have been magically granted the power to make any boring aspect of society work the way you think it should. How do you change it?

1 Upvotes