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…
Hi all, I wanted to share this post from a fellow autism parent and blogger. I read his posts often and rarely has something resonated so deeply with me. Click to read Losing Hope Is Not A Bad Thing by Autism Daddy. When people ask me if I think Cooper is going to talk one day I used to say….YES. And then slowly I switched to MAYBE. And lately I say a no. People usually look at me with a weird look or scold me or tell me to be…
This. Always this. I do not gift you with clever conversation, cute remarks to be laughed over and repeated. If you allow me, I will teach you what is really important in life. I gift you with my innocent trust, my dependency upon you. I teach you giving. Most of all, I teach you hope and faith.
I have been blogging about Cooper for a few years now. Since the beginning I’ve received more emails than I can count from autism parents who have teenagers. The emails always start the same way. They say they have a teenager who was just like Cooper. And they tell me about the diagnosis and the process and the where they are currently in the journey. And then they go onto tell me that their daughter or son started hitting and kicking and exhibiting really aggressive behaviors. I’ve read enough of…
I stumbled across a post today on Facebook titled, ‘My Son Has The Kind Of Autism No One Talks About-Term Life’. “Because for every boy with autism who manages his high school basketball team, there are 20 boys with autism who smear feces. And for every girl with autism who gets to be on the homecoming court, there are 30 girls with autism who pull out their hair and bite their arms until they bleed. And for every boy with autism who gets to go the prom, there are 50…
This image has been going around Facebook for a few weeks now with the following caption: Disabled people in US: 19% Transgender people in US: 0.03% THIS is the bathroom issue I am more concerned about. Having a private place to change my beloved son with dignity, privacy, and cleanliness…not on a dirty bathroom floor with a large cot I have to carry everywhere with us. We consider ourselves “fortunate” when we can find large private family bathrooms like the one pictured…but most places are stalled restrooms where even the…
Hi all, I wanted to share a video of Cooper’s talking device. Cooper has been using it at school for a little over 3 months and we are just starting to use it at home. Much like everything else I find it to be a little overwhelming. Sometimes I feel like it’s just ‘another’ thing we are trying. But in saying that his speech therapists are RAVING about his successes with it. He can say up to 6 word sentences. An example would be: ‘I want to eat yogurt please.’…
I am so glad I saw this today. On the way to work this morning I was thinking about how hard it is to raise babies. It’s exhausting and challenging and tiring and wonderful and amazing. For any of you that know me you probably saw on Facebook that Sawyer put sand in my lawn mower gas tank last night. And then stripped down naked and ran around my front yard destroying plants. As I chased him around my yard screaming I had a silent chuckle at the neighbors watching…
I found another amazing article about autism! While I am struggling to write about our own journey it appears that autism is becoming more and more popular in society. YAY! Every time I open up Facebook I see another article or blog that is changing lives and perceptions. Gordy, a nonspeaking, autistic teenager, wrote an incredibly, profound letter explaining autism….one letter at a time. See his letter below. Here is a link to the full article. What touches me the most is how he talks about the reasons autistic people…
I say the words ‘nonverbal autism’ daily. Cooper isn’t just autistic…he is nonverbal. It adds another layer. A really difficult layer. It adds severe frustration. It adds yelling and screaming and sometimes scary, loud noises. It adds a lot of head hitting. And mostly it removes a lot of layers of simple every day interactions. I will spend minutes staring at Cooper and wonder what he is thinking. Wondering if he is happy. Wondering what he would say to me if he could. Wondering if he understands me. Talking devices…
