Chavisory www.chavisory.wordpress.com I got to open my presents early for Christmas this year, as my mother was going out of town to see family. I told her I hadn’t had a chance to wrap hers yet, so she could open it when she got back Christmas night. We didn’t get to finish opening presents that night. We had a yelling match about the true nature of the autism spectrum. I was diagnosed with Asperger Syndrome a year and a half ago (though I’d known the truth for several years previously), which I guess that most people in my life probably know by now because I decided that it was part of my life that I wasn’t going to make any particular effort to hide, because I had nothing to be ashamed of. I really have no idea what people think of me as a result, because I stopped concerning myself…
Tag: self-advocacy
Julia Bascom juststimming.wordpress.com Our Story: The Loud Hands Project is a publishing effort by the Autistic Self Advocacy Network. Currently, we are raising money towards the creation of our first and foundational anthology (Loud Hands: Autistic People, Speaking) and accompanying website. Loud Hands: Autistic People, Speaking features essays, long and short, by Autistic authors writing on autism acceptance, neurodiversity, Autistic pride and culture, disability rights and resistance, and resilience (known collectively by the community as having loud hands). Questions posed to the contributors might include what does autism mean to you; why does Autistic culture matter; what do you wish you had known growing up Autistic; how can the Autistic community cultivate resilience; what does “loud hands” mean to you; and how do you have loud hands? The anthology is the first of a projected series featuring contributions from Autistic writers stressing the preservation and celebration of Autistic culture and…
Lydia Brown autistichoya.blogspot.com At the Adult Services Subcommittee’s final meeting in late July, much to do was made about semantic disagreements — “ASD individual” versus “individual with ASD,” and of course, the dreaded “person with autism” or “person who has autism” versus “autistic person.” These issues of semantics are hot button issues, and rightfully so. Words and language are powerful tools by which an individual can express ideas, whether abstract, actionable, or concrete. As a writer and editor, I know firsthand that language and the meanings we attach to words very much impact, influence, develop, and change the attitudes that we have toward the subjects of discussion. That is why people are easily insulted or upset by word choices. Changing a phrase — even if it holds the same literal meaning — alters the subtle connotations and nuances of the speech, and communicates a different meaning and context than the…
Four weeks ago, Syracuse University hosted its first regional Neurodiversity Sypmosium, with Ari Ne’eman as the keynote speaker. Mr. Ne’eman is President and co-founder of the Autistic Self-Advocacy Network, as well as a presidential appointee to the National Council on Disability. He spoke both fiercely and wittily about both neurodiversity and self-advocacy in the past, present, and future. TPGA is publishing a series of excerpts from Mr. Ne’eman’s talk. This is part three. Part one was published two weeks ago, and focuses on the history of the disability rights movement. Part two centers on power and perception, about how “…in the autism world, what autism is — and what we should do about it — is very much under conflict.” In part three, Mr. Ne’eman talks about the divorce of the autism conversation from the larger developmental disability conversation, the tyranny of “normal” expectations for Autistics, and the shared hopes…
Three weeks ago, Syracuse University hosted its first regional Neurodiversity Sypmosium, with Ari Ne’eman as the keynote speaker. Mr. Ne’eman is President and co-founder of the Autistic Self-Advocacy Network, as well as a presidential appointee to the National Council on Disability. He spoke both fiercely and wittily about both neurodiversity and self-advocacy in the past, present, and future. TPGA is publishing a series of excerpts from Mr. Ne’eman’s talk. This is part two. Part one was published one week ago, and focuses on the history of the disability rights movement. Part two centers on power and perception, about how “…in the autism world, what autism is — and what we should do about it — is very much under conflict.” TPGA was given an audio copy of Mr. Ne’eman’s talk by journalist Steve Silberman, who is currently researching a book about neurodiversity. Thank you, Steve. A couple of years ago,…
Two weeks ago, Syracuse University hosted its first regional Neurodiversity Sypmosium, with Ari Ne’eman as the keynote speaker. Mr. Ne’eman is President and co-founder of the Autistic Self-Advocacy Network, as well as a presidential appointee to the National Council on Disability. He spoke both fiercely and wittily about both neurodiversity and self-advocacy in the past, present, and future. TPGA was given an audio copy of Mr. Ne’eman’s talk by neurodiversity-immersed journalist Steve Silberman, who said it needed to be shared. This will be the first of three posts covering the talk; this excerpt focuses on Mr. Ne’eman’s coverage of the history of the neurodiversity, self-advocacy, and disability rights movements as civil rights movements, as well as “…the peculiar concept that people with autism could be a minority group like any other.” — I see this symposium not only as the beginning of a process that’s being going on some time…
Kerry Magro KerryMagro.com Kerry was recently featured in a story that ran in the Orlando Sentinel and the L.A. Times which shared his transition to college life and the skills he gained there as he became a self-advocate. He has since graduated from Seton Hall. -The Editors Hello, my name is Kerry Magro and I have autism. I just recently learned about The Thinking Person’s Guide to Autism from a truly outstanding individual, Laura Shumaker, who is a remarkable advocate for those of us who are on the spectrum. Once I looked at the website, and read some of the essays, I knew I was hooked. Regardless of what I took from the essays, I wanted to help in any way I possibly could. This gave me the idea of posting one of my own personal works about coming out about being on the spectrum. Below you will find…
I met Carol Greenburg last summer at the BlogHer conference in New York. Her confidence, humor, and commentary made her instantly appealing, but her kindness, fierce intelligence, and advocacy skills make knowing her both a luxury and a necessity. She is the executive director of Brooklyn Special Needs Consulting, and serves as the East Coast Regional Director of the Autism Women’s Network. She joined the Thinking Person’s Guide to Autism’s editorial board in January, where she adds her depth of knowledge as an advocate, parent of a special needs child, and an adult on the spectrum. ~Jennifer I’ve joked with you before that you really “have it all.” You’re an adult with Asperger’s syndrome, the mother of an autistic child, and an advocate in the autism community. Do you have trouble switching hats? Do you compartmentalize? I try to compartmentalize. I think that’s the only way to really do it.…
Holly Robinson Peete www.hollyrod.org Over the years many parents have reached out to me for emotional support after their child was diagnosed with autism. I particularly remember getting Jenny McCarthy’s phone call shortly after her son’s diagnosis. Like most moms and dads, she needed to connect with somebody who knew first hand the swift gut-kick of this difficult diagnosis, somebody who had been in the trenches for seven years already. We cried. We cussed. We even managed to laugh. We spoke for eight hours. She was naturally frustrated with the lack of answers about autism. I was there for her as I’d be for any parent, and I told her she was blessed to get such an early diagnosis. Her passion was palpable and I could tell she was going to grab autism by the horns, making it her mission and focus. I knew she’d help spread autism awareness like…
Elise, A.K.A. aspergers2mom asd2mom.blogspot.com Fifteen years ago, my oldest son was diagnosed with PDD-NOS (Pervasive Developmental Disorder, Not Otherwise Specified). At the time, we had no idea what kind of future he would have — if he would have at a future at all. Autism was not even a word on anyone’s lips at the time; no one was talking about it and no one was even acknowledging the epidemic that it was becoming. Luckily, I had a cousin whose son had been diagnosed years earlier and I called him for some advice. The best thing that he ever said to me and what I pass on to others is: Do not project the future for your child. Take each day, each moment if necessary, and do what needs to be done at that time. Then one day you will look back and see how far your child has come.…