#disability abuse laws

[zylomarshall]

Zylo Marshall - Disabled Rights Advocacy & Awareness

Website: https://www.zylomarshall.com

Zylo Marshall's website is a platform dedicated to addressing the challenges and injustices faced by individuals with disabilities. With over forty years of personal experience in traumatic brain injury and neurological brain damage, Zylo Marshall provides a unique perspective on the struggles of disabled individuals. The site emphasizes the importance of treating disabled people with respect and equality, and aims to raise awareness about the exploitation and discrimination they often face.

Facebook: https://www.facebook.com/zylomarshallstory

Keywords: brain injury awareness month disability rights advocate brain injury rehabilitation near me brain injury rehabilitation centers near me disability inclusion in the workplace abuse of disabled adults disability abuse laws traumatic brain injury awareness ribbon traumatic brain injury awareness disability awareness games for adults disability awareness campaigns disability awareness activities for the workplace brain damage recovery chances disability advocacy training free disability awareness training advocacy for parents child protection brain injury awareness facts disabled welfare association learning disability social worker role disability awareness programs best disability campaigns self advocacy learning disabilities brain rehabilitation therapy learning disabilities advocacy groups disability advocacy resources brain injury awareness activities disabled rights movement methods disability discrimination awareness advocacy services communication physical disability advocacy brain injury awareness week 2024 brain injury awareness day 2024 neurological causes of brain damage activist for disability rights disabled rights activist dies disabled civil rights activist disabled animal rights activist disabled civil rights activists equal opportunities for disabled students signs of disability abuse abuse of intellectually disabled disability challenges awareness in school disability awareness programs for students disability inclusion efforts in the workplace

[vividstardustrevolution]

Disabled people (both people with physical disabilities and people with psychological disabilities) should be able to get housing, food, medical needs, etc met without having to work or stay in school. ...Okay, really, everyone deserves access to free or affordable housing, food, and medical care, but disabled people ESPECIALLY deserve it because if I, a law student with "low support needs" autism, depression, GAD, OCD, and ADHD, cannot afford to take a break from school and take a semester off because I'd have to start repaying my loans because I had to drop down to three credits last fall and because I would have to get a job, so it wouldn't really be a break (which, I have had one job in my life, and I'm not fully convinced it wasn't a fluke, and also, trying to maintain a job when you have disabilities is difficult), I can only imagine that disabled people with higher support needs are even more fucked than me when it comes to being able to get housing and food and medical care without much, if any, funding.

Yes, Medicaid, Medicare, Food Stamps, and housing programs exist in the US, but, uh, I hate to break it to y'all, but that doesn't fully fix the problem, at all. There are a lot of old apartment complexes that are straight up inaccessible if you use a wheelchair. I'm living in one now. Applying for Medicaid and other programs can be a pain in the ass, especially when you're disabled.

"Just live with your parents!" My parents were emotionally abusive and emotionally neglectful, transphobic, and they literally harassed me so much during my 1L year that I still have nightmares.

"Live with a roommate!" I tried to. It went fucking terribly.

"Are you really disabled if you're able to be in law school?" YES. YES I AM.

Actually, on that note, law schools and the law profession need to become more accommodating for disabled people ASAP. Buck v. Bell needs to be overturned. Courts should be wheelchair accessible. Having to get past seven plus different forms of ableism just to graduate and pass the bar is ridiculous. Seriously, can we get some resources for disabled people in law school and the law profession, please?

Disabled rights matter, and we have every right to be able to live in peace and get our needs met, regardless of our support needs, disabilities, or anything else.

[creature-wizard]

You did not "manifest" poverty into your life.

You did not "manifest" abuse into your life.

You did not "manifest" illness or disability into your life.

Anyone who tells you differently is victim blaming, and you should not be listening to them.

[cookie-waffle]

“people need a psychological evaluation before being allowed to have kids!”

Or… you could advocate for better mental health care, family resources, addiction rehabilitation, and public education on childhood trauma and development instead of advocating for eugenics

[charismaticwanderer]

We are organizing this fundraiser with a few friends because this person needs as much help as they can get. The story in the description doesn't even scratch the surface but that is as many details as can be safely given without them getting forced to take down the gofundme again. If this comes across your feed, you can help. Even if you can't donate. You can not only reshare but copy the link and directly ask friends and family who have money to help. If there is ever a time you wanted to get involved and help stop trans genocide now is the time.

[vtforpedro]

update- TWs in tags

Thank you all very much for your replies to my last post. I’ve had zero energy this past week and yesterday was a very hard day. Got my decision in the mail and wow, they sure are long. It’s not good, folks!!! Not good at all. This guy is an SSA shill and I’m flabbergasted. Hopefully my attorney gets back to me next week asap because not only do I have grounds for an appeal, I believe I’ve been denied my rights by law. Some highlights from his decision. They’re very painful to read and my case manager way back in November of 2021 said that they love to tell people they’re disabled but here’s why you can work. Basically what this dude did but I’m seriously confused and angry. I think it also speaks to the type of person and biases he has. -I meet the disability insurance thing, as in he considers my record to start back in October 2015, which is how my attorney laid it out. And it’s true because that’s the last time I was able to work. -I am severely limited and cannot perform the work I once did. The work I once did was, uh, retail/customer service, and a ‘stay at home’ job if you will by being a caregiver to a veteran (my ex). -My disabilities as the SSA listed them: chiari malformation, leukemia, major depressive disorder recurrent, severe, PTSD w/dissociative affects, headache, s1 radiculopathy (nerve damage), and idiopathic intracranial hypertension (IIH, my number one enemy) -Chiari and leukemia aren’t considered disabilities, which I knew they wouldn’t be. I’m in remission and people often work with debilitating cancers even tho they should absolutely not have to. Let’s begin with what he got wrong lol -He dates that I got an EMG done in March of 2022 before the lumbar puncture. I did not get an EMG until September of 2022. The LP was in April of 2022. -Nerve damage. I have zero evidence of nerve damage in my medical record, according to him. Zero. I do not have a single symptom to suggest nerve damage and I need at least one from both ‘categories’ the SSA lists. But I have none. I was bedbound for eight months because of nerve damage. I had noted swelling (with pictures) of my paraspinal muscles which might have contributed. I had an EMG because of nerve pain. My dr ordered an EMG because of nerve pain. Shooting pain down my leg and numbness/tingling. Also the severe pain in my lower back causing me to not be able to sit up or walk without excruciating pain 💀 I was referred by my neuro to a pain specialist who really wanted to do steroid shots in my lumbar region FOR NERVE PAIN. I was in physical therapy for months to relearn how to like walk and sit up but also for NERVE PAIN. Legit have no words. It’s noted in my neuro’s and his PA’s file about the radiculopathy explaining what happened to me finally. Hhhhhh. -MDD/PTSD/suicidal ideation. I have extensive medical records going back to 2015--NPs, therapists, my psychiatrist, and the neuro psych eval I had in Sept of 2021 + more since. The eval is one of my most important medical documents. He said the medical evidence did not support major depression/anxiety/PTSD for 2+ years with no improvement, which is not factual. My medical records from my NP in 2015-2017 show how many medications I was on that did not work. How long I was in therapy because it did not work. My current psychiatrist is on my side and tells me every time I see him that I’ve been on everything and we’re limited lol I believe this summer I will be with him for two years alone. The judge notes I have no medical evidence of panic attacks despite them being listed in my medical record. At most of these places. Again. Plus the ER at the very beginning discuss panic attacks. This man read my neuro psych eval where she diagnosed me with those MH disorders (beyond already being diagnosed elsewhere). This is an intimately personal document because it details a SA that occurred in 2012 plus the abuse my ex put me through for 2yrs, which made me unable to work starting in 2015. She noted high concern for my well being as my suicidal ideation is, uh, high lmao and the effects of PTSD from multiple traumatic things. He said there is no evidence in my medical record beyond a depressive and anxious mood which do not fit the bill for MH disabilities. He completely ignored the neuro psych eval (and everything else) so I think that speaks volumes of the type of person he is. -IIH. This is where I get very angry. He lists it as something I was diagnosed with and it was in consideration, yet he completely fails to consider it. He considered ‘headaches’. Not IIH, not multi-feature chronic migraines that are well documented, not the recommended brain shunt by my neurosurgeon if pressure was high, which it was. He is, by SSA law, supposed to argue for/against the conditions listed. He didn’t. -Allegations. He says that the “allegations” I have made don’t completely match my medical records by, like, existing or severity. Except the things that he says I alleged but are not supported are because of IIH. Which he had plenty of medical evidence of + the burden of deciding I meet criteria for disability is on the SSA at this point. He has to by law complete my medical record himself once it goes to him (almost a year ago) so he has the entire picture to make an accurate and fair judgment. He says I allege symptoms not endorsed by medical record but they are symptoms of IIH lmao -He implies I lied (”allegations”). He said that in my records it has been noted I stopped driving once all this happened (dec 2019) and have not driven since. It is noted *everywhere*. But he says that I indicated I drove one (1) time in December 2021. Obviously, this is not true and I have no idea where he got this from. My mom was pissed because she has driven me everywhere for 3+ yrs lmao I have a feeling someone misheard me say dec 2019 for dec 2021, so the judge thinks this makes me a liar. He completely ignored the vocational expert’s testimony in the opposite way I have read happens--narrowing me down to 1 job, then 0, but deciding himself I could perform jobs like ‘mail clerk, router, or marker’ whatever the fuck those last two are. A dr who reviewed my case (I didn’t even know they did lkafaja) said I could only have occasional interactions with people. The judge said that he felt that was not true and increased it to frequent. I don’t trust people. At all. I never want to make friends irl again because it feels way too fucking vulnerable. This is in my medical records. Anyway. I truly believe I have grounds for an appeal b/c of mistakes he made and I hope my attorney agrees with that. The judge is not supposed to fuck up dates or ignore medical evidence entirely in his judgment. BY LAW. Angry, hurt, tired. Why does this keep happening to me lol why can one thing not go right but instead everything always gets worse. I feel like I try to put good out into the world when I can but it spits on me in return. I want to give up.

[nicolodine]

[nobody-cared-then-either]

Did you know that if you have more then $2000 and you have been disabled longer than you have been employed, you are legally too rich to be disabled in the USA?

[nando161mando]

Review details NDIS commission's failures on autism program | ABC News

[starblaster]

"but if you're pro-union, why are you anti-cop-union?" because cops are not laborers. what cops do is not labor. they are enforcers of the laws that oppress laborers and exist solely to protect capital. don't bother me with stupid questions.

🛑 STOP asking me to make the post rebloggable. i refuse to let a bunch of anticommunists, libertarian anarchists, neoliberal spooks, and other pro-cop fascists pass around their bad-faith additions on a post if i can help it (which i can, by disabling reblogs) while others of you are saying some really misguided, off-topic shit, and it’s pissing me off.

please get your facts straight before embarrassing yourselves on the internet. for fucking ONCE in your lives.

i am not “redefining labor” i SAID that cops are not LABORERS (EXPLOITED WORKERS) unionizing to receive better working conditions for the betterment of their fellow workers. they participate in collective bargaining with the express goal of subjugating and abusing the working class by protecting their fellow cops who harass, brutalize, stalk, rape, and kill the poor, homeless, working class, and other marginalized people. OTHER, ACTUAL LABOR UNIONS also use collective bargaining power to protect their members. if you argue otherwise, i’m sorry but you need to get serious and examine not only the truth about what a labor union is and does but why our purposes and missions and goals as unions are what they are. clarification aside, here, that wasn’t the fucking point of this post! the derailing and misunderstandings of what a LABOR UNION IS that occurred in the short time this post was rebloggable was too insane not to shut off reblogs!

COP unions, LIKE I SAID IN THE ORIGINAL/ABOVE POST, ARE UNIFIED IN DIAMETRIC OPPOSITION TO THE LIBERATION OF WORKERS, AS IN PEOPLE WHO DO LABOR (WHICH DOES NOT INCLUDE THE LITERAL ARMED PROTECTORS OF CAPITAL)

NO OTHER UNION BASHES, KILLS, OR ARRESTS STRIKING WORKERS LIKE COP (OR PRISON GUARD) UNIONS DO.

if you agree with the post so much that you NEED it on your blog or whatever, post a screenshot of the original post with this part cropped out and leave me the fuck alone! THANK YOUUU!!!!!!!

and to the wiseasses saying screenwriters and actors "aren't laborers, either," are you just fucking stupid actually? you think artistic labor isn’t labor? shut the fuck up.

[apas-95]

'ohh if i was a horny mech pilot and you disabled my mech would you abuse me' no i would treat you as a prisoner according to the laws of war. i would not cut your sexy bodysuit off because it is a crime to strip a POW of their clothing and personal effects other than explicit combat equipment. i would not hurt you with my big boot & would instead render medical aid unto you. i would carry out political education to you and set you free as soon as possible according to the strategic and logistical situation

[medicinemane]

I don't know... just the utter insanity of being like "I don't trust the government" only to put your full faith in the government cause you've decided that this punitive law is one you like and could totally never be used in an inappropriate way

Never trust the government man

Government needs to be forced to have full transparency and accountability and have a boot kept on it's neck at all times to make sure it's doing what we need it to... and we're not there yet, not even close. DOD can't even pass an audit man, and so many of the governmental systems as so clearly just kind of broken

So why on earth would you ever trust some new law to only be used in positive ways and not as a tool of suppression?

And part of it is about looking at laws, looking at what they say and do, looking at their scope. Like yeah, I'm pro right to repair laws because they mostly say companies can't stop me from fixing my own shit and need to make parts available (which they demonstrably don't do otherwise, which is the only reason I even want a law about it)

But like... there's a bit of a difference between the scope of a right to repair bill vs something on surveillance, or banning something like tiktok, or making it so police can arrest you for something new... never trust that stuff's going to be applied how they say it will, assume they've slipped massive overreach in the fine print, and assume that even if it's technically the most restrained bill that the feds might ignore that and use it as an excuse to trample all over your rights despite technically not being allowed to

Doesn't matter if the cop technically isn't supposed to arrest you for it, we see cases all the time where cops do shit they're not supposed to do and go after people not doing anything wrong

[you-can-face-this]

somehow found a way to make one of my final papers about britney spears so i’m actually kinda excited to write this one 

[five-thousand-loaves-of-bread]

autism awareness & autism acceptance not either or. not mutually exclusive. can coexist. need coexist.

“there enough awareness for autism already 🙄 we need acceptance”

ok. you aware of high support needs autism? aware what that even means? not “need reminder take meds need remind take shower” “high” support needs autism, but “need full physical help do bADLs lack danger awareness may accidentally hurt self or even kill self without support” high support needs autism? not just higher support needs people who can be independently online do advocacy, but those who need help from others even be online, or those who cannot be online at. all.?

aware of nonverbal nonspeaking people? not just nonverbal nonspeaking people who can write grammatically correct cannot tell apart base on writing. not just nonverbal nonspeaking people who can be online who can advocate online.

aware of nonverbal nonspeaking people who cannot communicate in way that easily understood, either for now, or ever? aware of nonverbal nonspeaking people without functional communication, aware of how without functional communication, how that drastically limit communication, even though behaviors are valid communication? aware of nonverbal nonspeaking people who may never use AAC fluently even with best support?

aware of technically verbal but very limited verbal autistics who may only able say wants & needs but not other things and certainly not online advocacy, “despite being verbal”?

aware of just how much our life depends on caregiver/carer/PCA/etc? aware how vulnerable that make us? aware of abuse from caregivers? aware of caregiver burnout from lack of support for caregivers, & how that impact our care we receive? have you even heard of term respite care? aware of those of us who cannot separate ourselves from caregiver? aware of those of us who cannot participate in autism community without caregiver?

aware of visibly autistic people? aware how we not automatically believed? aware how we often bear blunt of violence because we most easily identified target because we visible? aware visible =/= get support, aware that many those diagnosed severe who now adult so no longer qualify for services under 21 year old, languish in hospitals because nowhere to go? aware how long life saving necessary waitlists are? aware that even to this day parents have to fight school fight day service fight government fight insurance for them give their nonverbal nonspeaking child AAC & be properly taught how use it? actually, are you aware of how properly teach AAC to nonverbal nonspeaking, developmentally delayed child who may or may not have intellectual disability?

actually, aware of autistics with (correctly diagnosed) intellectual disability & how they make up big amount of autistic? aware of institutional systemic & legal impact of mental [r word] right & the human rights abuse justified using r word right? wait, you aware that r word come from old term for intellectual disability, that, actually, still in many laws because no one bothered updating, right? aware of what severe profound ID look like? and aware they real and they still human deserve education deserve life deserve care, yes?

aware of early diagnosis 20 30 or even 10 years ago, not same as now, even less resources & knowledge about autism now? aware that while gender race class 1000% impacted diagnoses, a lot of early diagnosed people early diagnosed because… they die without support unlocked by diagnosis, right? but also, aware that in old times, early diagnosis often did mean doom, not because autism bad or anything, but because severe lack of support & diagnosis can literally bar you from so many things including basic education?

aware that for many people in special education, which impact specific group of autistic people, they not get degree when graduate high school, they just get certificate, which limit their educational & employment opportunities & others?

aware of life saving importance and necessity of masking for autistic of color especially Black autistic people, despite stress inducing traumatic? aware that live in broken system be victim of hate crime & police brutality just as traumatic often even more traumatic than masking? aware that many Black & other parents of color forced to teach their child masking because of this?

are you aware of most marginalized autistic people? aware of leadership of most impacted?

aware you can and need to care about autistic experiences & form of autism you not experience? aware that you can and need to do that without try twist your experience into our experience into our words our community?

aware that advocacy goes beyond about you?

aware that you can’t speak for all autistic? aware that you shouldn’t speak for all autistic?

are you aware of when you need to stop talking & listen & amplify others? aware of when and how to decenter self?

aware that even this long post, barely scratch surface? still so much to say?

[better worded version of original post]

[nobody-cared-then-either]

If I have to live with it so does society.