Autism

Wrong

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I have found myself talking a lot lately about what my childhood was like in some aspects. Parents of my students, My teaching team, students in my Newspaper club, all seem to want to know about my past. I have been upfront with my teaching team about my autism. To my students I just admit to being different. My own daughter told them about my balance issues, and me falling down the stairs often.

Coloring in Black

When I was a child, I would be given a coloring page by a teacher and given the instructions to “Color it.” While my classmates would share and trade the colored crayons with each other, all trying to make the most beautiful piece of art they could, I would take 1.

Usually Black.

Then I would get lost in the action of filling in all the spaces of the page. It did not occur to me that each of the spaces might require a different color. I would just zone out, forget about the world, and be focused, hyperfocused if you will, on the act of filling in these spaces.

My teachers used to report that there was something wrong with me. My picture that had started with a building, or a pretty pony, was now pitch black, with no traces of the original picture. It was all clearly colored, not scribbled on, but they didn’t seem to understand. There must be something wrong.

I was just happy I had colored it. I followed the instructions. I did not understand why this caused such commotion. The other children couldn’t even color in the lines, and were haphazardly colored with a lot of white space shown. But their pictures were considered beautiful. Mine was clearly colored in the lines, and no white spaces left. It just cost the whole black crayon, or most of it.

Nobody explained this to me. Not even as I grew up. I was an adult when I figured this out on my own.

Coloring still soothes me to this day.

Living with Dad

When I was quite young, I moved in with my father and stepmother. It was a new town and a new school. It was a small town, with a small town school. Differences are not understood, or appreciated in small towns. I used to get off the school bus so overwhelmed by the other kids, that I would have shut downs.

Once I apparently got off the bus and smacked another kid in the head with my metal lunch box. I don’t remember doing this, but I remember getting off the bus, and then I was suddenly in the principal’s office, not knowing what had happened. I was of course lectured about this. To this day, I don’t know who I hit, or if they were the cause of the shut down, or if they just happen to be too close, when I lashed out.

I had been told, of course that when I was really young I would lash out at my brothers, like an animal. I don’t have memories of this either. But I do remember promising to never let the monster out again. I hated myself for many years, and would come home from school and lock myself away just so that I could calm down and make sure nobody else got hurt.

My dad, and stepmom were unprepared for this, and they began looking for solutions. My condition was not well known back then. They believed something was wrong with me, and looked for ways to ‘cure’ me. I remember hearing something about electric shock therapy being considered. My mother took me back to her house before they decided.

Recess

Elementary was not an easy time. While other children would run and play with their friends, I would purposely walk laps around the school, or the school yard, depending on which school I was at. I would mostly look at the ground and focus on the walk. This was another method I had devised to keep the monster from escaping. But even when I was not overwhelmed, I kept it up. Routine is very important, and it would seem strange not to walk around in loops.

I made friends with the parent volunteers that would walk around the school for student safety. Teachers in those days did not monitor the playground. Parents did. Teachers stayed indoors, and I believe, enjoyed the little time they had without the children.

The Skateboard Incident

I had a skateboard. I liked it, and would ride on it around my house. One time I had to go to the corner store to get something for my stepdad. I rode my skateboard. I ran into some of my classmates, who had never seen me on my board. They asked me, in a very rude way, if I was a skater.

I have a skateboard, I ride my skateboard, thus by my logic, I am a skater. I was completely oblivious to the fact that there was, and still is, a whole subculture of people called “skaters.” So I said yes. They then began demanding that I do some tricks for them to prove it. I had never heard of these terms. One was called an “Ollie.” When I didn’t know what they were talking about they called me a “poser.” I did not know this term either, but the way they said it hurt. That was the last time I rode my skateboard. It sat in the corner of my room for years.

I didn’t know what I had done to make them angry or upset with me. All I knew was something about that board made people dislike me. So I stopped.

There were other things I stopped for the same reason. I stopped admitting I liked wrestling, but didn’t want to wrestle, that made people angry. I stopped bringing toys to school for show and tell, because I had the wrong toys. I stopped talking about books because I took twice as long as everyone else to read, and apparently that is bad. I even tried my hand at poetry once, but that almost got me beat up.

I was told by my mother that I would be a smart child, but that also seemed to make people upset with me, so I settled for the average grades. Not too high, people didn’t like that. Not too low, Mom wouldn’t like that. So I would just do enough, then doodle in my book. Which I could then fill in the doodles to calm myself.led an “Ollie.” When I didn’t know what they were talking about they called me a “poser.” I did not know this term either, but the way they said it hurt. That was the last time I rode my skateboard. It sat in the corner of my room for years.

I didn’t know what I had done to make them angry or upset with me. All I knew was something about that board made people dislike me. So I stopped.

There were other things I stopped for the same reason. I stopped admitting I liked wrestling, but didn’t want to wrestle, that made people angry. I stopped bringing toys to school for show and tell, because I had the wrong toys. I stopped talking about books because I took twice as long as everyone else to read, and apparently that is bad. I even tried my hand at poetry once, but that almost got me beat up.

I was told by my mother that I would be a smart child, but that also seemed to make people upset with me, so I settled for the average grades. Not too high, people didn’t like that. Not too low, Mom wouldn’t like that. So I would just do enough, then doodle in my book. Which I could then fill in the doodles to calm myself.

Now

If someone had told me back then that filling a page in black crayon wasn’t wrong, just different, I think I would have believed in myself a little more. That’s what I hope to give my students. I have been at schools that ignore the odd kids. I have been at schools that outright ostracize them. I have been at school where they want to help the “spectrum kids,” but the leadership doesn’t understand them, and doesn’t accept advice from teachers that do.

When parents or colleagues ask me what my childhood was like, I often hesitate. Do I tell them the truth; that difference was treated as wrong? Or do I tell them what I wish had been true?

It’s even more heartbreaking when the parents, also ignore, refuse to acknowledge, or help their kids. I have met parents who want others to “fix their kid” and won’t hear that they, as adults, need to learn how to work with their child. How dare someone tell them that their kid needs them to step up and learn something new. Shame on us for wanting to help the child survive their family.

I still try to have difficult conversations with families and school leadership about these things. And I know we all can make a difference. I know we can make the world a place where a little boy or girl is not afraid to be themselves, and enjoy the things they do. Where they will never feel like what they are is wrong.

Hong Kong

Earlier this week, my family and I took the fabled train to Hong Kong. It was one of the things everyone tells your about ShenZhen. It’s so easy to go to Hong Kong. It is made to sound like a weekend trip. We took 2 nights and 3 days.

To begin with, yes, the train to Hong Kong is very short. I have been on subway rides longer. It is a 15 minute train ride from downtown Shen Zhen. We sat in a nice, comfortable train, but there is no time to relax. By time you get comfortable in your chair, you have arrived.

Immigration takes about an hour, just like in an airport. Possibly longer than an hour. I know Hong Kong belongs to China, but you still have to go through Customs and Immigration.

There are lots of arguments about Hong Kong and China. From my observations, it is not treated as a part of China, but is treated as a colony of China. You have to go through Immigration between the two, even if you are Chinese. Hong Kong has it’s own Money. Chinese Drivers drive like Americans, on the right, Hong Kongers (Hong Kongnese?) drive on the left. The have different flags. You get the idea. Hong Kong is a country, but it belongs to the Chinese Government.

It’s similar to Canada still being part of the Commonwealth of the UK.

My family made the mistake of getting a hotel room in Kowloon.Yes, that Kowloon. It is no longer a Walled city, but the building we stayed in at least still felt like the mega structure of the past. It was however, mostly Indian and Filipino residents running everything in the building.

Our hotel was a “Guest House” on the 15th floor of a building. This guest house had 18 rooms. There were 5 guest houses on each floor of the building. There was also inside the building: streets and alleys, that led to shops, restaurants, money exchanges, and more on each floor.It felt like a mini city inside this building.

The region around our building was similarly cramped outside in the street. The buildings were uncomfortably close, and the alleys on the ground level were filled with shops. Even the local Mall (Across from the building we were staying in) had everything uncomfortably close.

I know this is not how most of the city of Hong Kong is, we did visit a couple other areas. We went to Victoria Park, and relaxed there for a few hours. And we took a 45 minute yacht ride around the bay.

We will not stay in Kowloon again and I will explain why below.

As you may all know by know, My family is a Spectrum Family. We are all on the Autistic Spectrum at some spot. One of the disadvantages of this, is the emotional weight. Some of us, are empathic. The emotions of others nearby can be felt by us. More people, more weight.

On our second day there, everyone was on edge. We ended up spending half the day locked in our tiny guest room. There were 5 of us in an 11m square room.

We had tried the Mall nearby earlier, but it was too much, and we had shaky hands, as we tried to regulate. We had tempers flaring at each other, we had lots of stimming. We all needed to escape.

Honestly, the best part of the trip for my family was the yacht ride. My Sister in Law set it up for us. Yes it was a full boat. But everyone’s emotions on the boat were positive. We got to see the beautiful night sky line of Hong Kong. We got to talk, take pictures, and the yacht supplied free drinks and snacks.

It was so relaxing, I was disappointed it wasn’t a longer trip. But good things must come to an end.

My family learned some important things on this trip:

  • It’s okay to take time to yourself, and go slow, even when time is limited.
  • You can find good places in anywhere you go, if you look.
  • Be patient with those you love, when they are overwhelmed.
  • Bring your noise canceling ear plugs when traveling.
  • Indian food is the Mexican food of Asia: Tastes good going in, but hurts coming out.
  • Bring cash. Chinese Payment Apps do not work in Hong Kong.

The Healing School.

Today was a busy day for me.

One of the things that happened today was the student council lunch. I have done my best to support our student council for the past 4 years. Today was their end of year lunch. One of my students who is in the council invited me to join the lunch. I have never been to one of their lunches before, and so was very honored.

I got to eat and mingle with the student council members. I was joined by Ms Albor, our Council head teacher and head of our school spirit. Ms Jessie, our Assistant principal of student well-being, and Mr Brown, our Principal, also participated.

The table I was sitting with, noticed my lanyard, and one of the girls asked about my autism. I told her a bit about how masking works. It makes it hard for me to eat certain foods. One of the foods that was on today’s special menu was chicken legs. I love chicken. Fried. I explained that I can’t eat the chicken they provided. It had sauce all over it, and I would get sticky fingers. I explained that sticky fingers is a sensation that I cannot handle well.

When she complimented me by saying I don’t act like the autistic people she had to research. I bit my tongue first. She is a student who is honestly trying to learn more. I did not tell her that the expression of not looking or acting autistic is hurtful. Instead, I told her that I spend a lot of my mental energy masking all day. I do this so I appear like everyone else. This was not the answer she was expecting, but was polite about it.

Mr Brown made an amazing speech about leadership. I was so happy to hear it, but to also see the children listening to it. You see my special requirements precluded my ability to be part of Student Council or other similar clubs and activities as a child. That’s one reason I support them every time I can.

All in all, I think I handled this well, and helped someone understand a part of my experience.

Today was also, the day that my school said farewell to leaving teachers. My good friend James (Mr. K) made a speech for me. It was heartfelt. He told me later about his thoughts of “Roasting” me. Every other speech maker had done this to their chosen leaving teacher. However, he decided against it. I’m glad he did.

But after I was expected to say something, and up in front of everyone, my mind went blank. I at first could only say something along the lines of “I have nothing.” Then I realized that it would be considered rude. I didn’t want to be seen as rude, not as I am leaving the school. So My mind scrambled for something to say, but I couldn’t think.

Eventually it settled upon how the past four years have had ups and downs. There have been mostly positives. I would miss everyone.

Like many things in my life: Hours later, when I can think straight, I know what should have been said.


BIBA has been a place of healing. I came in immediately from a school I had been at for a very long time. Near the end of my time there, someone had used the knowledge of my autism as a political weapon. When I arrived here, I had nightmares for months about this happening again.

BIBA, and Dennis, our empathetic leader, has helped me recover from that. You all helped me, whether you knew it or not, deal with almost losing my mother twice. Once from a near fatal car accident, in 2021. Once from cancer. In 2023, My mother was given 3 months to live. She is still fighting the good fight. This school was there to help me figure out my head when I lost aunts and uncles. You where hereto help me deal with many other family catastrophes in just 4 years. My team, James and Kai both helped me when I had shut downs, and meltdowns. When I finally felt I had to reveal my autism here, I was welcomed with open arms.

The Student Support Team welcomed my ideas for Pink Shirt day, and consulted me on ideas for well-being month.

I created a support group for Dads at BIBA, and found an emotional support group in my Trauma Bonded friends.

I met wonderful friends here. My Dungeons & Dragons Team: Including Jeff & Pablo from KG. Friends who have left, or are leaving for other pasture: David Boddington, Richard, Frank, Dr Raven, Mark Nicholson, David Richards, Mark Markham, James Helbringer, Ed,

So many of you made working here special. Was it easy? No. It was exhausting. I would come home from work almost daily and pass out on the sofa. Waking later to play with my daughter or help her with homework.

But it also re-sparked my desire to write, and to help.

We are told everywhere, that if a company says that they are like a family, to run. run away as fast as you can. We are told this is a sign of overworking, and under paying for the illusion of family.

However, despite what we are always told, BIBA became like family to me, and my actual family.

I will miss you all. We will miss you all. Including your insane desire for loud music and seizure inducing light shows.


Pictures supplied by Dr. K.C. Pang. The heart and Soul of BIBA.