Tag: Lydia Brown

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Disability

How to Plan Events That Prioritize Accessibility

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Color Communication Badges by Button Justice League, on Etsy [Image Description: Three 1.5 inch pinback buttons each with a vivid color, a bold black word and a black shape underneath the text. From left to right: a “Red” button with a octagon, a “Yellow” button with a triangle, and lastly a “Green” button with a circle.]  Lydia X. Z. Brown @autistichoya [Note from Lydia: This originally appeared on Twitter as a thread on 4 June 2018, and is an incomplete list of suggestions.] Some tips on access-centered event/program organizing/planning (some are mine; many I learned from other fabulous folks): (1) When you put information about the event online, whether on (a) a website, (b) in email announcements, or (c) social media, only include images if you include alt-text and text-only captions. (2) Don’t rely on online/email/social media to get the word out. Call people too. Many comrades with intellectual disabilities…

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Book Review-And Straight On til Morning : Essays on Autism Acceptance

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And Straight On til Morning : Essays on Autism Acceptance edited by Julia Bascom Published by the Autistic Self-Advocacy Network  We want April — Autism Acceptance Month — to matter, to help further acceptance and understanding of autistic experiences, happiness, and rights for autistic people of all ages and abilities. We will be publishing your Autism Acceptance posts and pictures all month long. If you want to participate, contact us at thinkingautism at gmail dot com. -TPGA Editors In keeping with Autism Acceptance month, there probably isn’t a more appropriate book to share than And Straight On til Morning : Essays on Autism Acceptance, which contains the work of wonderful Autistics and allies, including Zoe Gross, Shain Neumeier, Lydia Brown, as well as Kassiane Sibley, and Shannon Des Roches Rosa from TPGA.  Julia Bascom edited the collection, and in its current  format, an ebook, it is available quickly, and very…

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Disability

2012 at Thinking Person’s Guide to Autism

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2012 was an eventful year at Thinking Person’s Guide to Autism: Our book drew much acclaim, three new editors joined our team, we featured more than 30 profiles of Autistic kids and adults for April’s Slice of Life series, we went to the International Meeting for Autism Research in Toronto, our Facebook community hit and surpassed 10,000 members while remaining a nexus for thoughtful autism news and conversation, and we were cited and our editors were interviewed frequently — especially whenever autism made headlines. We also continued to publish thought-provoking and educational essays and interviews on this site, and all enjoyed and learned from the ensuing discussions. The 15 TPGA posts (with excerpts) below were 2012’s most popular — meaning hotly debated and/or praised — and give a sense of what we in the Thinking Person’s Guide to Autism community had on our minds these past twelve months. Thank you…

Disability

Recognizing Ableist Language in the Autism and Autistic Communities

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Lydia Brown autistichoya.blogspot.com It’s everywhere. “Autism isn’t mental illness. We’re not like those people.” “It wasn’t an autistic person who would commit mass murder. Only people with actual mental illness, like psychopaths or schizophrenics do that kind of thing.” “Those ideas are insane!” “Autism Speaks’s idea of representing Autistic people is absolutely crazy.” “People who want to give their kids bleach enemas are just nuts. Their ideas are nuts.” It comes not merely from Autistics and non-Autistic parents and professionals and researchers but also from Autistics and non-Autistic parents and professionals and researchers who are disability rights advocates and activists. Take the humble pill, recognize your own strands of ableism, and stop using the ableist language. It is not okay to refer to ideas and people with whom you disagree as ‘insane’ or ‘crazy’ or ‘nuts’ or ‘loony,’ because those are hateful and hurtful words just as much as the…

Disability

Person First: An Evolution in Thinking

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Jess at Diary of a Mom www.adiaryofamom.wordpress.com If you were to sit down and read my blog Diary of a Mom from its inception back in 2008, I’m sure  you’d notice some pretty dramatic changes. Many of the words I use and the way I use them have changed. And the change in verbiage is reflective of a change — an evolution really — in my understanding of autism. When Brooke was first diagnosed, I bristled at the word ‘autistic’ when it was assigned to her in conversation. I actually found it offensive. “Person first!” I would shout in my head as I calmly responded, “my daughter HAS autism,” emphatically yet (theoretically) politely ‘correcting’ the perceived gaffe. And then, somewhere along the line, I read THIS: Jim Sinclair’s Why I Dislike ‘Person First’ Language. And something shifted. I had never considered the words nor what they represented from the inside…

Disability

The Dangers of Misrepresentation

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Lydia Brown autistichoya.blogspot.com Anders Behring Breivik, the Norwegian terrorist gunman who killed seventy-seven people in one day last summer, appeared in court yesterday morning as a psychiatrist declared that he likely “suffers” from Asperger syndrome and Tourette syndrome. One news article claimed that “Asperger’s is a developmental disorder on the autistic spectrum that often is characterized by a lack of empathy.”1 Another article paraphrased the psychiatrist and wrote that “Norwegian mass killer Anders Breivik has a rare, high-functioning form of Asperger’s that has left him incapable of empathy or real friendship.”2 Although even a peer-reviewed paper published as early as 19913 found no evidence for any correlation between violence and Asperger Syndrome — further finding that the incidence of violent behavior in those with Asperger’s is lower than the incidence in the total population — the media has continually and repeatedly conflated being Autistic with a propensity toward violent or…

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For Autistic Teens Feeling Doomed or Broken

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You are not alone. Many teens who receive an autism diagnosis feel broken, and suffer from pain of acceptance — even to the point of suicidal thoughts. And the resources you need are not easy to find. So we asked several adult autistics who were once autistic teens themselves: If you were in this headspace, how would you feel, what would you want people to say to you, what could possibly help? These are their replies. Karla Fisher I was angry the day I received my diagnosis. At first it just made me feel “broken.” People tried to tell me that I was the same person I was before. But those words did not make me feel better. Reaching “acceptance” of my label took me around eighteen months. There is very little written about this process that pertains to autistic people as our emotions do not neatly lineup in the…

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Disability

Lydia Brown and Autism Acceptance Month

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We’re featuring “Slice of Life” conversations with Autistics of all ages — kids through adults — throughout April’s Autism Acceptance Month. Today we’re talking with Lydia Brown, who is eighteen, attends Georgetown University, and is an intern at the Autistic Self-Advocacy Network‘s national office. What is your name? Lydia Brown Do you have a website or are you on Twitter?  www.autismeducationproject.org & www.autistichoya.blogspot.com What would you like a one-sentence description of yourself to say? I am a neologist, a writer, and a student who gorges frequently on hot chocolate. Do you have any autistic superpowers? What are they? I have very hypersensitive hearing, and I also learn languages very quickly. Not so fast as to be on par with Daniel Tammet, but much more quickly than the average person. According to some native Spanish speakers, I’ve lost any trace of an American accent in my spoken Spanish. I can also…

Disability

“Don’t let your children grow up in a world where society devalues their lives.”

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Lydia Brown  autistichoya.blogspot.com To the parents of Autistic children: We need you. Sometimes in public discourse, Autistic adults and non-Autistic parents disagree over very important issues that affect each of us personally. Sometimes this disagreement is spectacularly explosive. But there is no way for the autism and Autistic communities to move forward without creating some type of group cohesiveness. Yes, that means that we will have to enter into painful dialogue and discourse, and yes, that means we will have to accept the validity and legitimacy of the ideas and feelings of people with whom we may disagree. It does not mean that we have to set aside all of our differences, because that would make us self-deceivers. But it does mean that we have an obligation to each other and to ourselves to recognize what Dr. Martin Luther King Jr. called “inescapable mutuality.” Every Autistic child, youth, and adult…

Disability

Tired (of Autism Misrepresentation)

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Lydia Brown autistichoya.blogspot.com From the editors: We hope that even veteran autism parenting advocates and self-advocates will consider this post part of their neurodiversity education, along with Todd Drezner’s recent HuffPo article Nickels, Dimes and ‘High-Functioning’ Autism — and that it leads to productive reflection and discussion. From the author: Trigger warning: This is mostly about ableism and a response to other, very triggering things, as well as including lots of direct quotes of ableist stuff. An accessible audio recording: Tired – Autistic Hoya by autistichoya I’m tired of being misrepresented. I’m tired of seeing the principles of self-advocacy misrepresented. And I’m tired of seeing the autism rights movement misrepresented. Let me be clear. I’m not talking about allies, or about people who were just thrust into Autismland and don’t yet know much, if anything, about the constant conflicts that erupt here. This isn’t about you. This is about people…