I Stopped Talking To Cooper A Long Time Ago

Yesterday Cooper’s Crisis Intervention Social Worker came over for our weekly visit. I have so much to write about that and will at some point. He has given me more valuable advice than any single person, blog, doctor, etc., throughout this journey. He has helped me and my family. And in turn I want to share that with you peeps. But, per the usual, I am days behind at work and working from home in a disgusting house with dirty dishes, dog hair and a pile of laundry that would…

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Trick-Or-Treating

I gave Cooper a sign for Halloween. It was simple. It said Trick-or-Treat. I gave it to him because he looks so much like a typical child and people don’t know how to react when he does things. They get nervous. I get nervous. And then Cooper gets nervous. By giving Cooper a sign I removed the guesswork and answered the questions that people have. ‘Is there something off with that child?’ We’ve all been there. You’ve all wondered it. Let’s be honest. You see a kiddo or even an…

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Fighting for an Autism Diagnosis

I thought getting a diagnosis would be easy. My son is different. He doesn’t talk. He flaps. He screeches. He hates to be touched by strangers. As a baby he never slept. Ever. He cried constantly. Endless ear infections, stomach issues, constipation, hearing problems. The list goes on. He never babbled. To this day he’s never said a word. I thought it was obvious. There is something wrong. Tell me what it is so I can fix it. That’s what you do. It’s broken and you fix it. No one…

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It's Ok To Care. Don't Forget That.

I’ve been thinking a lot about Cooper attending kindergarten next year. Right now he goes to an autism preschool at the actual elementary school. He rides the bus. Which is great. His class has 4 other kiddos in it. And every day they join the typical 4K kiddos. It is a completely controlled setting. It’s 3 hours long and Cooper has a teacher and an aide and a speech therapist and an occupational therapist. He lives in a bubble. When I went to the open house this year I watched…

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Finally, An Improvement. Thank You Sweet Jesus.

If you talk to parent’s of autistic kids they will often say that their kid goes through periods with no improvement. And often you can mix in a little regression. For example, when Cooper was two years old he forgot how to drink out of a straw. Or sleep is a big one. Cooper didn’t sleep through the night until he was 2. And then slept through the night from age 2 to 3 and then suddenly stopped again. There is no rhyme or reason. Look at your child right…

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What If I Lose Him…

One of my greatest fears is losing Cooper. He’s not necessarily a runner or a wanderer, which are traits highly associated with autism, but still….the fear is real. Cooper will most likely not call out if he is lost. Or answer to his name. Or come running. Or even recognize the fear of being lost. And Cooper looks like a completely average little boy and his disability may net even be recognized. So as Cooper has aged, his dad and I know that there will most likely come a time…

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I Don't Know What's Wrong

I made the decision when Cooper started at Fraser that either Jamie or I would pick him up 5 days a week. I did this because Cooper is nonverbal. And he is getting highly intensive therapy 5 days a week. And if I don’t pick him up I have no idea what is happening in his world. Imagine never being able to ask your kid how their day was. Or what they did. It really, really stinks. So every single day, either Jamie or I, sit in the Fraser parking…

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I Thought By Now…

I thought by now I would have mastered autism. I truly did. And that I would be the one giving advice to other mamas. I thought by now that my nonverbal boy would be talking away. And potty trained. I thought by this time we would be so much farther along. We are not. In some ways we are in the same spot. Standing still. I just spent 5 minutes scrolling through Pinterest. I entered one word into the search box…Autism. I wasn’t sure what I was looking for. Maybe hope.…

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Super Cooper

Do you know that I was actually stressed about posting that video of Cooper making sounds online. I’ve been doing this for 3 years. I’ve been waiting for the words for so long. And I start to feel like my hope is like a broken record. Even today, I regretted it. I know the comments I will hear from people now. Don’t be sad…he’s making sounds. He’s close to talking. Someday he will talk. It will happen soon. It’s almost like these videos are ammunition of hope. But what the mom inside me…

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The Sounds are Starting to Come

Jamie and I had a late night conversation last night about the nonverbal struggles. We both agree that although nonverbal is hard…it’s the delays in ‘understanding’ that is harder. There is no waiting. There is a little tiny bit of ‘first this, than that’. There is very little reasoning. And holy moly can that kid carry on. At times I am secretly impressed by his devotion to the things he loves. If only his devotion didn’t have to be so damn loud and shrill. I truly believe the language is coming. I…

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