When my son was diagnosed with nonspeaking autism, or nonverbal autism, I remember being so confused by the terminology. Everybody speaks. Maybe late. But eventually. That’s what I thought. I had no idea that not speaking was even a possibility. Flash forward, he is 11 and communicates in so many different ways. Speech, typing, pointing, taking photos of things he loves, spelling, sign language, and using a speech device. He’s so unbelievably smart. If you are new to our page, please know that h
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When my son was diagnosed with nonspeaking autism, or nonverba…
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It wasn’t my son’s severe nonverbal autism diagnosis that broke me. Nope. It was the years the followed. The fighting for services and supports. The lack of sleep and self care. The isolation. The people who stopped showing up. It got real bad there for a while. And no, I didn’t handle it all that well. My friends saved me. If I can give you one piece of advice from a mom who has been living alongside autism for 14 years….FIND YOUR COMMUNITY. Make it your greatest priority. #autism @the.morethan
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In the beginning, when my son was first diagnosed with severe autism, I felt this unbelievable pressure to teach him everything and as fast as possible. That obviously didn’t work. Because he was on his own time line. I’m here to tell you that our kids are lifeline learners! We have time. So identify what’s important, break down the skills, and start practicing. And enjoy the ride. ❤️❤️ #autism | Finding Cooper's Voice
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Changing the way I thought about my son’s autism helped me not only understand him better but also helped the way we helped him. Take a listen. #autism | Finding Cooper's Voice
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