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National Council on Severe Autism

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For Our Children with Severe Autism, Speak Loud, Speak Proud

March 12, 2019 Jill Escher
My fifteen-year-old severely autistic son Justin enjoying two of his favorite pastimes, his toys, and anything related to Halloween.

My fifteen-year-old severely autistic son Justin enjoying two of his favorite pastimes, his toys, and anything related to Halloween.

By Kim McCafferty

A couple of weeks ago while procrastinating from what I should have been doing and scrolling through Facebook I saw a post that immediately caught my interest. It was from the National Council on Severe Autism (NCSA) which I had never heard of, and the title read “Suffering in Silence: The Dark Side of Autism.”

I actually put down my chocolate for better scrolling access, and I never put down my chocolate for anything.

I read the article by a mom out in California who spoke about an incident she had lived through with her eleven-year-old severely autistic son, one which culminated in the California Highway patrol pulling up behind her as she parked her car on the highway and hoped to quell the rage her son was displaying toward her so she could safely leave. Both her love and fear for her son came through in every sentence, as well as her heartache in knowing that an attempt to take him ice skating could end this way.

I personally have a 15 year-old severely autistic son with accompanying OCD, tics, and intellectual disability. Justin and I have a profound connection — this is a child who kisses me even when he doesn’t want anything and hugs me on a frequent basis. We have a bond that through insomnia, aggression, refusing to eat, soul-sucking OCD, and last year also a terrible movement disorder, has remained true and strong.

I write a blog about him, Autism Mommy-Therapist, because I want the world to see him as I do, a kind-hearted, intrinsically happy almost-man, despite his challenges. And yet I also share about his incidents of aggression, the fear I’ve felt when dealing with my son’s meltdowns, my anxiety for his future. I do this in part so that some other parent out there going through this will not feel so alone. I also do this for my own mental health, because it’s important that I have an outlet to share my experiences with my severely autistic child.

And I do this in the hopes that more parents will share their stories, and this underserved segment of the autistic population will finally get the attention, and the services, they deserve.

“And I do this in the hopes that more parents will share their stories,
and this underserved segment of the autistic population
will finally get the attention, and the services, they deserve.”

Stories of high-functioning autistic children and adults are easy to find. As the mother of a twelve-year-old on that end of the spectrum I want him represented too. However my eldest son is nothing like the protagonist on “The Good Doctor,” yet he also deserves to have his story told as well. The public badly needs exposure to this segment of the autism population, the one that nobody writes the “feel-good” stories about. The one that makes some of us uncomfortable. The one that will never star in a television series.

Autism acceptance is not just for the high functioning. Those of us with children and adult children on the more severe end of the spectrum need to tell their stories and have them be heard. Many of our children are silenced by the inability to speak or communicate through a device.

Their realities should not be silenced too.

I am thrilled with the creation of the NCSA. This is a platform for families with severe autism to finally have a strong voice. I am actively for any organization which can help my kids, and hopefully with time we will see NCSA as a major contributor to the goal of realizing safe, happy and productive lives for those severely affected.

Kim McCafferty is the mother of two sons with autism. She lives in New Jersey.

← I’m 80 Years Old and There’s No Post-Mom Transition Plan for My Severely Autistic Son“Hit Me With Your Best Shot”: A Story of Severe Autism on Public Radio →
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