Autism Representation – Daniel Tiger to Introduce New Character

I can vividly remember taking my autistic son, Johnny to the park when he was four years old. As I pushed the double stroller with him and his baby sister through the park entrance my heart sank as our usually pretty empty park was full of children and parents.  Johnny was excited, and there was no turning back. I had to let him play for at least a little while. As he darted off to play I quickly strapped the baby to me and followed him like a shadow. Sometimes…

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It’s Not That I’m Not Happy For You

I need to be real for a minute. It’s not that I don’t want to be around you. It’s not that I don’t like your kids. It’s not that I don’t love watching your kids grow up from afar. It’s not that I’m not happy for you. It’s just too hard. It’s too hard to see your children developing at a normal rate. There’s no speech and language delay. There is no vocal stimming. There are no show stopping meltdowns. You have kids who have a typical path to follow.…

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The Power of Words

“I’m so tired of hearing about special needs kids. They’ll be fine. They were retarded before Covid they’ll still be retarded after. So let’s just keeps those kids at home and when this passes they can come back to school. Do you really think they’ll be any different after a year of staying home with their parents? Sounds like someone doesn’t want to deal with their special needs kid. Sorry you fucked got pregnant and had a retarded kid. Your problem not mine…” [sic] These words were written on Facebook…

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Why Can’t You Be Normal?

Why can’t you be more, well, normal? Have fun for a change! Blow bubbles in the summer breeze and chase waves in the ocean and jump into big piles of autumn leaves. Make friends.  Go to birthday parties and sleepovers and on camping trips. What if I can’t, he asked.  Try harder, they answered. Try bigger.  Try with everything you have.   I am trying.  I am all the time trying. Be a normal kid. Say hello when someone talks to you. Shake hands. Hug people good-bye. What if hugging makes…

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We are Raising Him to be Proud of Who He Is

Every morning I wake up to messages from people. Most are well-meaning. Many are kind. A few are awful. Some are bizarre. And some, tell me how to raise my son. And how I’m doing it wrong. They tell me what I should be doing, how I can do it better, and what I can and cannot say about him. I’ve gathered a list of what I cannot say. I cannot say he has autism. Or is autistic. I can’t say he is nonverbal or nonspeaking. I can’t say he…

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He Was Always Him

January 16, 2017 It’s been 4 years since my son Stalen was diagnosed on the autism spectrum. He was 21 months old. I remember he was wild in the room as we waited for the doctor to come in and speak with us. He was throwing toys and picking crumbs from the carpet. He was pulling single plastic gloves from a box hanging on the wall. I was trying to hold myself together with strict composure but could feel the lump in my throat and the anxiety deep in the…

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An Open Letter to Those who Bully People With Special Needs

Dear Bully, When I was in public school I used to be bullied by people like you. You would see me in the corner, usually trying to keep to myself and wonder why I was there. Other times you would see me having issues reading out loud in class and snicker while I tried to pronounce different words. You’d take my inability to understand sarcasm as a way to get me in trouble. Worst of all, you’d make me feel like an outsider when more than anything I wanted to…

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I Don’t Mind You Staring At My Brother’s Disability

Living 36 years of my life having a brother with a disability has made me embrace the things I can’t change.  Being the sibling of a brother with a disability has taught me many life lessons, and one of those lessons I’m sharing today in this blog.  There is one thing that all families who have a child/sibling with a disability have experienced more often than not…….People who stare.   When they notice a difference in the people around them, they stare.  When they observe or hear a different form of…

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Light at the End of the Tunnel

The comment read, ‘for some families, there is no light at the end of the tunnel.’ I thought about it all night. And when my toddler woke up at midnight for a hug, and then again while I drank my coffee and watched the news. I thought back to our hardest days when there was no apparent light at the end of the tunnel. Our autistic son didn’t sleep longer than 45 minutes at a time and we started every day at 3 am. We lived in this place of…

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Raising a Child With Autism; You Are Not Alone

During the years surrounding my son’s autism diagnosis, I could barely say the word “autism” out loud.   I thought I would just break down every single time and, frankly, I didn’t have time for that. To be clear, this had nothing to do with shame.  Not one day has gone by that I am not immensely proud of this boy. It was about fear, worry, the unknown, and all the other bumps along the road to acceptance. All a parent could ever want is for their child to be…

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