Why is he the Hardest One?

‘Mama, I want to get a bait caster. It’s for fishing. Then I can catch huge ones like dad.’ Pause. Silence. ‘Mama, when you chew gum and then drink water, does it feel weird in your mouth?’ ‘Sometimes I guess.’ ‘Yeah, I don’t like it one bit. Maybe I won’t chew gum anymore. But I like gum. Maybe I won’t drink water. Yes, that’s a better idea.’ Giggle. Pause. Silence. ‘Mama, what is 6 plus 6?’ ’12 buddy.’ ‘Oh, what’s 12 plus 6 because that’s how many bait casters that…

Read More

I Will Not Miss my Son’s Life being Sad

There are a lot of things I allow on this page. Healthy debate for one. Constructive, respectful criticism for another. Why? Because that’s how we all learn. We only know what we know. And let’s be honest, most of us are living in parenting bubbles. I am not at an expert parenting level yet, even with three boys. But, there is one thing I do not allow. It’s pretty simple really. It’s criticizing the value of my child’s life. Or any other life for that matter. Autistic or not. Sick.…

Read More

When People Stare at you

I used to get so upset when people stared at you. You’d be flapping. Or making happy noises. Screeches. Grunts. High pitched screams. One second you’d be on the floor and the next running only to drop to the ground, roll, laugh and pat the ground. Or you’d be melting down. Screaming. Either way it almost sounds the same. Loud. I’d look around. Make eye contact. And look away. I’d think in my head, stop. Stop Cooper. Stop drawing attention to yourself. To us. Everyone knows. But it’s not for…

Read More

What it Could Be

A long time ago, back before the diagnosis, before autism was a word in our vocabulary, I had a little boy. He was two years old. He had blonde hair and hazel eyes. He was busy. So busy. He never stopped moving. Sometimes not even when he was sleeping. He was rarely happy or content. He screamed in the car. He screamed when we were outside. He screamed in restaurants and stores. No matter what we did, he wasn’t happy. I knew something was wrong. But I didn’t know what…

Read More

You See a Boy and a Baby

You see a boy and a baby. It’s so much more than that. I see an 8-year-old boy and a 9 month old baby. Brothers. The boy is sitting in his driveway. Outside. Near a road. Safely. Sitting. He isn’t running. He isn’t eloping. He is calmly sitting. Next to his baby brother. A baby brother who is touching him. Leaning into him. Reaching for his tablet. Touching his arm and his leg. If you could hear you would hear Barney singing the ABC’s. The boy is babbling about the…

Read More

Living our Kind of Normal

I was on YouTube the other day during one of my many research missions about autism and I came across a video. The lighting was poor and the camera angles were even worse. It made me a little nervous at first since you never really know what will pop up during a search, but the caption insisted it was an “interview with autism parent” so I kept watching. On camera was this person, who I can only assume was a reporter, and he was interviewing a distraught mother with a…

Read More

If it Never Gets Any Better…

Part of me started to believe it was going to be really hard forever. Part of me started to only know how to live in the intensity. The chaos. I learned how to manage. How to react. I found happiness there. It was my normal. I could handle it all. The running. The self injuring. The screaming. I perfected ‘first-then,’ token boards, timers, a speech device, therapy, calm body-calm hands, family skills…you name it. I could do it all. I made your happiness the center of my world kid. Willingly.…

Read More

Coping with Autism

I’m an optimist at heart.  I really am. So, when I got the diagnosis of autism for my daughter  I remained hopeful.  She was two then. I had actually known she had autism since she was 10 months. At 10 months Antoinette never looked at me when I made a sound.  She never made eye contact.  She never cried. Crying is a form of communication.  She  wasn’t communicating. I watched my daughter and thought to myself “she’s a genius, that’s what this is.”  I told myself that daily. Three years…

Read More

No Talk All Action

The red shirt that Brian has worn everyday for the past 5 years (we have 4 of them) says “No Talk All Action”. It is not just a slogan, it is how he lives his life. My younger daughter Catie was upset one night last week and was in tears sitting on the couch between me and my husband. Brian appeared from the other room and came over to Catie, wiped off the tears on her face, and hugged her until she stopped crying. He would not leave her side…

Read More

Sometimes I Forget

Sometimes I forget. I know I shouldn’t. I mean, come on, it’s been 8 years. This isn’t necessarily new. And it’s been a long 8 years at that. It’s been so much trial and error. We’ve moved. We’ve seen countless doctors, therapists, and educators. They all say the same thing. Autism. And then severe autism. After that nonverbal autism. Level three and then level four and back to level three. Apraxia. Severe intellectual disability. Anxiety. In a way it’s like our life became checkboxes. Words on an evaluation. I always…

Read More