Buying Hope

Jennifer Byde Myers www.jennyalice.com Lotions, potions. A special chair for eating, a special chair for learning at home. Shoe inserts, leg braces, seat cushions with no grip, a lot of grip, seat cushions with little bumps, seat cushions with little bumps and gel inside, and a backrest. Fancy forks with bendable handles, child-sized forks, spoons […]

Small white boy with short curly brown hair running through a pumpkin patch.

How to Help Autistic Kids Have the Best Halloween Ever

When it comes to Halloween and autistic kids, parents need to be clear-headed, creative, and flexible, and prioritize our kids’ needs and stamina. So, if you’re in the market for Halloweening advice, let me dump some on your head, courtesy of personal experience, friends’ adventures, and the Internet.

Understanding Autism: Gathering Autism Life Histories

Researchers from Columbia University have asked for our help in reaching out to parents on their project, which has such similar goals to The Thinking Person’s Guide to Autism. We hope that parents of children with autism who can participate, will. Thank you, -Shannon, Liz, Jen, & Emily, TPGA Editors Dear Parent, We are researchers

Autism, Apps, and Adults

Corina Lynn Becker http://autisticapp.blogspot.com/ http://nostereotypeshere.blogspot.com There’s been quite a bit of news lately about how Apple’s iPad can assist Autistic children. The stories I have heard are wonderful and hopeful, on how iPads and iPods could bring about a new era of portable supports, learning, and communicative devices, and independence. It has been pointed out

The Inclusion Dance

Susan Etlinger www.familyroomblog.com It’s official: I’m a bitch. By which I mean I’ve moved past that initial flush of optimism and teamwork and wanting everyone to feel good about themselves to disappointment, confrontation, detente, anger and now — inevitably — relentlessness. And it is relentless — for reasons bureaucratic, cultural, personal, possibly gender-determined and sometimes

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Shifting Focus: Eight Facts About Autism the Media Is Not Covering

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

We Fight the Fights That are Worth Fighting

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

The Child Can’t Spell

Elaine Park My son can’t spell. At all. I like to joke about it, because in my culture (Anglo-Canadian) making wry, self deprecating comments is how you get through things while keeping your dignity intact. For example, my favorite line is “My son spells phonetically. I’m just not sure what language it is. Maybe, Latvian?

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For the 85% of Us Who Can’t Work

Clay http://cometscorner-clay.blogspot.com I can’t say I’m surprised to learn that most autistics have a great deal of difficulty getting, and maintaining a job for more than six months. I believe it, because I know just how hard it has been for me. I saddled myself with a wife and two kids before I even got

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