@notanautismmom@VaHouse@autismspeaks@CASProviders@CASP & @AutismSpeaks are cogs in the 22 billion dollar ABA industry wheel. Nonspeakers are some of their best clients. Accommodate nonspeakers & that’ll take a bite outta that 22 bil sweet cash. What’s their objection to nonspeakers being accommodated? Cash flow problems for ABA
@notanautismmom@VaHouse@autismspeaks@CASProviders@casp@NCSAutismOrg@autismspeaks never mentions the fact that 65% of incarcerated minors were students w/IEPs, many are neurodivergents. At the intersection of race & disability comes the school to prison pipeline. Fail to support NDs, and incarceration is how it often ends
@notanautismmom@VaHouse@autismspeaks@CASProviders@casp@NCSAutismOrg And just like that, after the bill was tabled, Amy Lutz from @NCSAutismOrg, another hate group, left a comment opposed to HB 2047. It’s clear she hadn’t read it, was just sticking w/all the talking points of the other haters. Their big beef is with letter boards and spellers
@notanautismmom@VaHouse@autismspeaks@CASProviders@casp@NCSAutismOrg Let me first post a video that shows facilitated communication or letter boards to which all the autism profiteers so object. RPM and facilitated communication are miraculous for some nonspeakers. I know 2 people who it’s changed them entirely
@notanautismmom@VaHouse@autismspeaks@CASProviders@casp@NCSAutismOrg For some people, it’s the only communication modality they are able to use or they choose. For my nonspeaking son, he preferred American Sign Language over all others. His choice of communication modality was not supported. School decided he needed a PECS, which he hated
@notanautismmom@VaHouse@autismspeaks@CASProviders@casp@NCSAutismOrg PECS is an ABA-based communication system. I realized after he was so miserable in ABA, and later found out PECS is taught via ABA, that’s why he rejected it. And later he rejected devices w/the same icons. I think they reminded him of PECS and he was stridently disinterested.
@notanautismmom@VaHouse@autismspeaks@CASProviders@casp@NCSAutismOrg He now is able to use minimal speech to communicate, mixed with ASL, and a text device. He always 100% rejected the picture devices and PECS. The point is, because communication is a human right, the modality he chose should have also been his right.
@notanautismmom@VaHouse@autismspeaks@CASProviders@casp@NCSAutismOrg This is where social model v medical model come into play. Medical model folks see disabled ppl as broken, needing to be fixed, forced to comply at all costs, (behaviorism) Hence, the concept of their choosing their own modality isn’t accepted as valid, because they aren’t valid
@notanautismmom@VaHouse@autismspeaks@CASProviders@casp@NCSAutismOrg Medical model adherents want to make all choices for disabled people. And yes, there are many disabled people who have very high support needs and need help with some or almost all decisions, but offering them choices still matters, even if small choices.
@notanautismmom@VaHouse@autismspeaks@CASProviders@casp@NCSAutismOrg Choosing a communication modality is a big choice. I taught my son ASL, despite what school did; he flourished and still uses a lot of ASL. We changed more to finger spelling when he started showing interest in a text device, to get used to the concept of spelling to communicate
@notanautismmom@VaHouse@autismspeaks@CASProviders@casp@NCSAutismOrg High support needs disabled people are not broken. Social model adherents believe greatest barriers for disabled people are denial of personhood, supports, care, basic human rights. We are human beings. Our abilities/disabilities should have no impact on respect for personhood.
@notanautismmom@VaHouse@autismspeaks@CASProviders@casp@NCSAutismOrg But it’s really not about RPM or FC because nothing in HB 1047 mentioned a thing about these communication modalities. These are people who seem terrified of respecting personhood of high support needs disabled people, or nonspeakers. They infantilize them.
@notanautismmom@VaHouse@autismspeaks@CASProviders@casp@NCSAutismOrg They dehumanize autistic adults, undermine their concerns, dismiss their lived experience. Why? Bc they don’t see them as sentient human beings. I will end this rant w/Mel Boggs, a nonspeaker, who illustrated precisely why all people deserve personhood.
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@ekverstania@notanautismmom@VaHouse@autismspeaks@CASProviders@casp Linked to 3 bil dollar restraint/seclusion industry, which must exist as part of behaviorist infrastructure. They claim it’s all positive now, which begs the question, if it’s all positive, why over 1 mil incidents of restraint/seclusion since 2012 in US?
@ekverstania@notanautismmom@VaHouse@autismspeaks@CASProviders@casp Nonspeakers are not only 1 of groups most subjected to ABA, but also restrained & secluded in highest numbers. A$, NCSA, all these autistic hate groups, support ABA vociferously, and of course restraint and seclusion, as necessary parts of any behaviorist infrastructure
@AutismSpeaks killed a bill for nonspeakers in Virginia today. They parked their BIG grifter arses atop a great bill that made inclusion of nonspeakers in GenEd possible. It would have eliminated IQ testing being a determinant of AAC access. If you think A$ sucks, please RT
I’ve spent 3 years as an anti-restraint/seclusion activist angry @autismspeaks refuses to intervene on the pervasive restraint and seclusion abuse of autistics. Their silence is DEAFENING. But then I saw what happens when A$ decides they must kill a bill today and am grateful
@AutismSpeaks didn’t loudly try to kill our work against restraint and seclusion. Although, their silence on it is tacit support for restraint and seclusion of our most vulnerable. Maybe they need to rename themselves Autism SCREAMS.
Gov @GlennYoungkin of Virginia, by repealing mask mandates in schools, has proven he’s pro-DEATH of children and staff who are medically fragile. Their only choices now are DEATH or segregation. Oberti v Board guarantees the right to a fully accommodated inclusion education. 1/7
In 1993, Oberti v. Board established inclusion w/supplementary aids and services as the presumption because it is “a fundamental value of the right to public education for children with disabilities.” Oberti v. Board of Education, established inclusion as a right 2/7
Oberti mandated that if placement outside the classroom is necessary, the school district must then include the child in as many school programs w/abled children to the maximum extent appropriate.” Removing masks denies schools the ability to include medically fragile kids 3/7
I love the brazen hypocrisy of Gov @GlennYoungkin of VA claiming he’s pro-life as he removes mask mandates, placing lives of medically fragile kids, teachers, staff in grave danger of COVID death. He wants to save embryos, but God help them if born w/complex medical needs 1/6
The entire anti-mask movement is ableist. Removing mask mandates in schools makes inclusion of kids and staff with complex medical needs impossible. This population will face forced segregation and denial of their fundamental, and ADA enshrined right to inclusion 2/6
From Section 504 of Rehabilitation Act of 1973: No otherwise qualified individual w/ a disability in the United States, as defined in section 705(20) of this title, shall, solely by reason of her or his disability, be excluded from the participation in, be denied the benefits 3/6
My disabled 15 year old son still sometimes needs help in the bathroom. We are constantly harassed and attacked when I bring him into the ladies room, but that started when he was 7. All this bathroom hate is also impacting caretakers of disabled people of the opposite sex.
He’s autistic with audio sensory issues and I’ve had women scream at me or worse, at him, about being in the women’s room. It’s gotten so bad, I’ll often just drive all the way home from wherever we are to let him use our bathroom rather than risk being yelled at by strangers.
He doesn’t need as much help with toileting now, but is often afraid to go into a crowded mens’ room alone and wants to stay with me. I go into the ladies room or locker room and tell women I’ll be bringing him in. Some are very understanding. Some are just vicious about it.
Parents Defending Education is a dark money funded right wing group that is very ableist, with an ableist, medical model agenda. If your child is disabled; this group does not see them as fully human. Their answer for disability are segregated private schools w/little oversight
Also, the silence of PDE on restraint and seclusion bans of disabled kids is deafening. But they know the private schools they pimp for aren’t IDEA or ADA compliant, can assault kids in 48 states with no federal oversight on disabled abuse.
We hear a lot from PDE about library books, nothing from PDE about ND abuse. For example, Judge Rotenberg Center, who still routinely subject NDs to shock torture; where’s the outrage?JRC is a private school who refuse to comply w/ADA or FDA on shock abuse