Category Archives: autism

Prayers for My Oma

I have a really lovely grandmother. On the outside she is lively, humorous, interested in many things, and she enjoys life and its ups and downs. She had a big family of four children so she is forever thinking about her family, which is a lot bigger now. She is a stubborn woman too. She resists help. She fights against pity. I have seen her recover from a serious injury. At that time she really didn’t look the way she should at all. She could barely walk or talk, and she stopped acting like herself.

Then, she stubbornly recovered. In a worst case for her, to be limited is unthinkable. She gets motivated by challenges. I would like to have more of her fighting spirit in me. Sometimes I get too lazy, I think.

Last week my lovely grandmother was diagnosed with cancer. I found out a day after my graduation. In a way I knew it was serious because my mom and dad were visiting her often in the hospital. My uncle is a doctor and he came to town to see her, and my parents kept getting text messages all day. I never imagined cancer, though. We always thought about her heart, not her cells. She just had surgery and is trying to recover from it. I will be hoping and praying for her.

Since I behave so restlessly I don’t sit quietly easily in a hospital. It’s not a time for me to get restless. She needs quiet. So, my visits are really brief. I try to work on it because I need to. She needs moral support and I need more self control. It’s a thing of too much emotion for me. It’s hard for autistic people to control since we feel the emotions so strongly.

Wishing my grandmother comfort, strength and healing.

Father’s Day in a Wind Tunnel

It’s a lovely weekend and I enjoyed a camping trip with my dad and a friend. It was lovely in the high altitude and surrounded by pines. We had a roaring campfire and a tent for me and my dad, and a smaller one for our friend. We had the campground almost to ourselves. It was quiet and tranquil.

Then the wind woke up. Roaring through the canyons, howling and screaming it came in all directions, blasting us with cold air, battering the tents, and really making a sleep in peace impossible. Maybe we slept three hours, or maybe four, but we were truly sleep deprived. And still we enjoyed this beautiful area.

My dad was happy to pack us up this morning and have an early departure while the wind still roared.  We both fell asleep when we got home.

It is Father’s Day and it’s a great way to celebrate in a windy tent with my dad and me. This evening we enjoyed a delicious Father’s Day dinner at home. Best wishes to all the fathers reading this today.

The World of Autism

The truth is it must be awful to have autism in some parts of the world. I don’t forget my good luck in that if I had to have autism it was in the U.S. I am well aware how my life could have been in a lot of other lands. Since even here people confuse not speaking with retardation, I can only imagine how tough it would be to have no one have time, resources, or social support to help. Then I guess it’s a life of stagnation in an institution or worse. Now I see my blog gets world viewers which is pretty cool. I don’t know how autistic people are treated in these countries. I do hope that my words help in starting to make a new way to hear what autism is for many of us.

This Summer is Taking Too Long to Get Here

Whew. I need summer vacation SO much. This year has been hard. I sit in regular class from eight to three, except for P.E. Then homework. I blog. I write speeches. It’s been a challenge to work on my skills. I have more to accomplish but I am working hard.

I am ready to sit and relax. I count the days til I am free to watch cooking shows, eat a lot of watermelon, swim and ride my bike, see friends and family, and recover and be rejuvenated.

Two more weeks. Will they ever end?

Cooler Than Usual

The summer is not coming where I live. Today it rained. We were in long sleeves. This is odd because many times in May it is already like summer. I remember this because my birthday is in May and many times we are already swimming or at the beach. One year it was a huge heatwave. Now you couldn’t pay me to go in the ocean without a wetsuit.

I’m not complaining. Though I love swimming, I hate heat. This sort of prolonged spring is fine and great. The weather is unpredictable in its ways. I am enjoying the cooler end to spring.

Piano Lessons

I take piano lessons. When I started I was sure I could never do a thing with my clumsy hands. My hands don’t listen to me well. I fumble with buttons and shoelaces so I thought, “Right, I’ll play melodies. Ha ha.”

Cool in a way to remember that because I do play melodies now. Some are in two hands. My progress is slow but my skills improve steadily. Sometimes I get discouraged because I can’t control my hands better than I do, but I can control them better than I did. My teacher is patient and kind and I am so lucky to have her.

Nervous About Starting High School

In a few weeks I will graduate middle school and next year I will start a new school. It’s a big deal in my life.  My middle school was the first real opportunity I had to learn in school. I know 6th grade was like an experiment. They watched to see how I could cope in middle school. I went in to math and science only, and did regular work in the other subjects though I wasn’t mainstreamed in them then.  It was a very big adjustment to sit so long in self-control and quiet. The schoolwork was simple compared to sitting in a classroom all day. I was determined to get a decent education, so I tried. It was not always easy for me or my aide, but I got more capable each year. This year I am doing better.  I am mainstreamed practically from eight to three. I go to P.E. with autistic kids, but otherwise I am staying in a regular class all day. My school is big. I switch rooms.
Next year my high school will be bigger still. It has thousands of students, so many clubs I couldn’t believe it, and a track and football field. It is a real big school experience. It’s scary for new freshmen, I know. I’m really nervous. I worry that my sensory system will be overloaded. I worry that students will be mean to me. Then I tell myself, “OK, it’s just worries and I am going to be fine.” I will be with some kids I know. I can walk in the halls five minutes early to avoid the mob- but I can’t stop my worries.
My aide is the best. It’s wonderful to work with her. She is kind, smart, and good at working with me. I don’t know her plans next year. I hope she can stay to start me off, or even longer. Now I worry that getting a new aide and a new school will be too much. Some days I get overwhelmed by worry. I wish I didn’t, but I do.
I worry about the teachers. Will they accept me or think I am an odd nuisance to them? I worry about the students. Now I am in class with kids who are used to me. Next year there will be new kids. I always visit school before the year starts to meet all the teachers and tour the campus. That helps a lot. I also wrote a short speech that is read to the class on the first day of school to explain my behavior and communication style to the class. That helps put them at ease, but I am still so nervous inside.
I realize I am lucky. It’s a great high school. It’s a dream of mine to graduate and go to college. I will need to overcome my fears about high school. It’s a big shift in my life. It’s the third big change I’ve had in school. I went from remedial class in elementary school to a “high functioning” autism class in 5th grade. Then in 6th grade I went to my middle school. This time I really don’t need to prove I’m smart to a school of skeptics. I think I’ve done that, so that is one big relief to me. It’s wonderful that they believe in the need to educate me, so I no longer need to worry about that.
I feel next year could be good. Unfortunately it’s unknown, so I worry too much. I feel relieved to write this. If you have tips, once again, to help me relax about this- I’ll take them.
Ido

Autism and Shyness

In friendship, like many autistic people, I am sort of shy. I saw a friend the other day who was meeting some new people. He covered his face and hid in his jacket. I used to do that sometimes when I was small. Sometimes I even hid in my closet when a lot of company came over.

Though I don’t hide anymore, I’m still shy. I hide in myself. People hide in their stims too, or by leaving the room. It’s anxiety, I think, not stupidity or indifference to people. It’s sensory overwhelming sensations that  come in strong emotions.

My Speech at the Autism Society Conference

I am autistic, as you may have figured out by my restlessness and the obvious fact that someone else is reading my words. The question I have for you is if it surprises you that a non-verbal autistic person writes well?  This was mentioned a lot by professionals as I began communicating. People who thought of me as the “low-functioning” sort could not adapt to my intellectual abilities. This led to a rough time, to put it mildly. It’s a real problem. Truthfully, many theories made my early life challenging.
Theory One told my parents that I couldn’t understand speech, so I was talked to like this: “Go car”, “All  done”, “Hands quiet”, “Good job”, “no”, “Say hi”, “Go school”, and so on. I would have preferred if they had just spoken more normally.
Second Theory said that because I couldn’t understand speech, I needed super basic books. So, I was denied really interesting stories. Just last year an autism teacher I know gave me a cardboard toddler book as a gift. It is a comical notion because she was well aware that I was mainstreamed in my classes. Still, she thought, “Non-verbal autism/toddler”. I have to laugh it off, but what is she really implying? Is it this bias that really denies non-verbal people an exposure to interesting ideas? I read interesting, challenging books at home. This teacher thinks “Pokey the Lost Puppy” is better.
Theory Three was that because I didn’t show I understood, I didn’t. This meant that school was really a total bore. The teachers refused to teach interesting things because they knew we couldn’t understand. Like the teacher I just described, though well-meaning, they bored their students to a point of emotional withdrawal into stims or indifference. I think this is really sad.
 This leads me to Theory Four which says that there is an 80% chance that I am mentally retarded. In fact, a psychiatrist recently reminded me that most autistic people are mentally retarded. So I ask you this- is Stephen Hawking also mentally retarded? After all, he can’t speak, is locked internally, and needs constant support. Or is not speaking different than not thinking? 
There are a lot more theories, but I’ll stop here.
The problem was that these theories were not true for me at all, but when I was little I had no ability to show otherwise. My inability to get my body to do what I wanted was interpreted as a learning and thinking problem. Even as I emerged into communication, a majority of teachers and others I worked with were initially rigidly stuck in seeing my efforts as the imaginings of an over-zealous mom, rather than an intelligent, understanding non-verbal autistic boy finally finding a way to escape his prison.
So I was bitter for a long time. My journey was made harder by those who were in a position to help. They refused to see what was true. Good theories were better than reality. I felt really angry for several years because no one seemed even happy to help me grow. They were skeptical to the point of cruelty.
An example was when my first speech was published in a newsletter for The Friendship Circle three years ago. The only negative feedback came from a teacher of autistic kids who stated that in twenty-five years she had never met a non-verbal autistic person with such advanced thinking and writing skills, so therefore I couldn’t have such advanced thinking and writing skills. This way of thinking not only insulted me, but it meant that she was unable to see the potential in her own students. This needs to change, I think. 
Thanks to my persevering parents, we let go of the folks who thought like her because that was hindering my education. This led us to find people who were more open-minded. In the last four years I have had a much happier education. The School District has energetically supported me in mainstreaming since I began Middle School. They have provided me with my aide from an agency so that I can access my education.
The truth is, the changes set me free. Once people saw me in a new way, gave me opportunity and a chance to improve myself, and supported me- you can see what is possible. Next year I will go to a regular high school in all regular classes on a diploma track, and I will continue to do the same work as everyone else.
This is thanks first to Soma who taught me how to get my thoughts out in letters and typing, my physical fitness trainer who woke my sleeping body, and the many other professionals who help me achieve this.
Like all kids in middle school I have some great teachers and some lousy teachers. That’s OK. I’m not complaining. It’s a normal education, but only four years ago I was still in an autism class that showed me ABC movies every day, one plus one math, how to find stuff in play dough, and other thrilling lessons day after boring day.
To the credit of those who gave me the opportunity to learn at grade level, I am trying hard to do well. It can be lonely. Middle School is not a kind and compassionate age for any kid and I am the most different kid imaginable. I am far below the social pyramid. Still, I will be a successful man in my life. Disabled or not, I am determined to have a meaningful life.
The future is unknown to me like it is for everyone. I don’t know if I will have an improvement in my symptoms. I don’t know the path I will have in college or a career, but I know I will aim to achieve for myself some kind of job and intellectually stimulating work. I can’t stim my life away. Only I will need support to do this. I have a wonderful aide in school. She is helping me focus and communicate to the class. Without her I couldn’t access my education. She helps me function in society.
 
I will need smart, trained aides like her in college and after. The truth is I will always need someone, like Stephen Hawking does or Helen Keller did, but I will try to keep working on skills. I’m not sure where I will want to live. I see a lot of slackers still at home- ha ha, but I never, ever want to be in an institution or a place that patronizes me. I want to live as normally as I can.
Now, if my parents had not started to look at my illness in a new way, I might never have emerged from my prison. I would still be bored to death in a remedial autism class in high school, where my former classmates all are. I want to know if you think I am the only intact mind in all of them, or could it be that some of them are also intelligent and understand everything? I think the sad thing is, many will die and we will never know.
I used to come home from school in 6th grade, and I would weep so much for them. I was partially mainstreamed then and doing grade level work in the other subjects in the aut class as I adjusted to a longer and longer mainstreaming day. The other autistic students would watch me communicate and learn, though they were not doing either. 
Isn’t it possible to at least teach them some interesting lessons, even if the kid can’t communicate well yet, in the chance he is trapped internally, as I was? I wrote before that boring people to death is like denying them life, liberty, and the pursuit of happiness. 
I also think that autistic kids need more exercise than they get. Look at flabby, weak autistic kids who have poor body control. Don’t you think weights, coordination exercises, and cardio fitness would help? It did for me.
Communication is essential. To answer how,  will require a new way of working with autistic people. I feel non-verbal people will be heard from more and more. Will you be open to listening?

The Open-Minded Autism Researcher

I had a cool experience last night. It helped me think in a new way about my illness. I am still mulling it over. I will write some more ideas soon. The experience was a meeting at my home with a neuro-scientist who researches autism. He lives far from me so we have e-mailed but never met in person. He asks me a lot of hard questions about my thinking processing, my visual perceptions, my ability to control my body, and so on.

Overcoming autism means we people with the ability to describe it from the inside out to people doing important research is only right. It is sort of an intense experience to hear about new theories about what they think may be wrong in my brain, but I’m thrilled to meet an open-minded thinker.