Two Types of Autism

 

Ten years ago, I knew very little about a developmental disability called Autism. In fact, my primary source of knowledge about the subject was a 1980’s film, entitled Rainman, starring Dustin Hoffman and Tom Cruise. Dustin Hoffman played a character that was based on Kim Peek, a young adult from Utah who occasionally appeared on talk shows and showed an uncanny ability to instantly count hundreds of matches that fell on the floor, or could recall what the weather was like in North Adams, Massachusetts on May 5, 1889. Dustin’s character in the movie exposed more of the difficulties of the affliction, including screaming tantrums, a strong attraction to watching Judge Wapner at 7 pm and going to Kmart.

        As a young teacher, my exposure to autism remained limited. I do not recall any of my educational courses ever addressing the topic, and only once did I come in contact with someone who had the affliction. I was substitute teaching, and I noticed a boy in the class who had an adult aide with him. Somehow I found out that he had autism, and I wondered if he could do that match counting trick. However, I never talked to him, as the aide seemed to protect his boundaries from any intrusion. He seemed like a nice enough boy, though, with no obvious difficulties.

        My first son, Gabriel, had some difficulties as his life was beginning. When he was born, the midwife needed to give him mouth-to-mouth resuscitation to help him begin breathing. His Apgar score after one minute was 4/10, but soon went up to 9/10. His placenta was noticeably gray in one area. He started “dusking” when he was two days old. When he was 4 days old, he turned unmistakably blue. The La Leche League person there who was helping with nursing thought she had just watched him die. We took him to immediate care where we discovered his temperature to be 96 degrees Fahrenheit. The doctor checked him into the infant intensive care unit where he stayed for a week, as he struggled to thrive against some unexplained difficulties. He was not strong enough to even suck from a bottle.  After he’d been warmed and tube fed for a week and potential causes were gradually ruled out, he’d gained a pound and the blue episodes stopped. They trained us in CPR and sent him home with all of us scratching our heads.

        Within a few years, we noticed several strange mannerisms. He loved ceiling fans. In fact, “ceiling fan” was one of his first words, if not the first. It was pronounced “ng-ahh,” but we knew what he meant. A spinning ceiling fan really visually stimulated him. He would get so excited that he would open his mouth wide and flap his hands. We also noticed that he had a relatively low vocabulary. That can be hard to discern for a two year old, but when I called Early Intervention to let them know my son had a vocabulary of about fifty words, they wanted to come over.

        Autism may have been suspected at that point, but Gabriel had very good eye contact with us, and did not seem to be in his own little world like the classic symptoms would warrant. However, the people at Early Intervention did see enough that they diagnosed him with something called PDD-NOS. That is “pervasive developmental disorder, not otherwise specified.” That is basically when a person has some, but not all of the symptoms in order to be called true autism. It is a term from the DSM-IV manual of psychological disorders. However, it is not a very accurate term, as autism is a spectrum disorder, with mild and severe cases and with many and diverse symptoms, as we were to find out later. PDD-NOS seemed to a way for doctors not to have to use the “A” word, possibly in an effort to let parents down easy.

        Gabriel had about two years of speech therapy, occupational therapy, and schooling before he ever set foot in a kindergarten class. We were amazed and delighted with the progress he made. Geri Aman, his occupational therapist, showed us something that I think is called brush therapy. In it, we used a surgical brush and stroked his arms and legs, and then provided ten counts of pressure against his arm and leg joints. That did seem to help calm him down, as it took away some of the hypersensitivity of his skin and also provided some vestibular feedback. Camille, his speech therapist, used a little vibrating thing in his mouth that helped strengthen up his mouth muscles and ended his drooling. Geri and Camille were part of an extraordinary team of Early Intervention teachers, as Gabriel learned to place the green triangle at his next workstation in the Early Intervention program. We were lucky to get them while we could, as Corvallis School District budget cuts soon had them looking for jobs elsewhere, mostly in private practice. But anyway, Gabriel made remarkable progress thanks to all of these wonderful professionals and measures.

        Gabriel had a wonderful kindergarten teacher, Clare Staton, and life skills teacher, Mo Ruzek, who performed a miracle and helped Gabriel learn how to read. I was astounded when I saw that happening. Gabriel’s math skills also proved to be strong at an early age

        We met other families in the area affected by autism, and one of them gave us a bottle of Super Nu-Thera vitamins, made by the Kirkman Company. That had been ineffective with their child, but for Gabriel, it instantly calmed him from some terrible tantrums, although he hated the taste. Super Nu-Thera was formulated especially for autism, and featured a mega dose of Vitamin B-6 along with other vitamins. It really seems to do the trick for Gabriel, although it may not be as effective for all.

        Our second child, Silas, was born 2 ½ years after Gabriel. His early life could not have been much more different from Gabriel’s. Whereas Gabriel was too weak to even suck from a bottle, Silas was strikingly strong and robust, even as a newborn. Whereas Gabriel would shriek and cry from hunger or pain, Silas was remarkably calm as a baby, content with life.

        A new phase of Silas’s personality began to emerge as he obtained mobility. He began to become rather destructive, as he was curious about a lot of things. In his life, Silas has toasted audiotapes in the toaster oven, broken the handle to the car door, broken the rear view mirror and the radio antenna on the car, pushed the button on the television into an irretrievable spot, and other such things. Many of these seem related to his curiosity of how things work and also his physical strength.

        Silas began preschool early in life, since we were happy with Gabriel’s progress in preschool. Also he adored and emulated Gabriel and it seemed like early typical peer exposure might be a good idea. Silas seemed to really enjoy school, enthusiastically wishing all his new school friends a hearty “Good Morning,” out his bedroom window when he would wake up. However, about the time Silas turned three, his enjoyment of schooling started to go downhill, as did teachers’ enjoyment of him. He began to hit or push other kids for no apparent reason. He was never angry with them; it was sort of like he just wanted to see what would happen, similar to his audiotape toasting experiment. It happened in all three of his different settings with other small kids—preschool, nursery at church, and at the day care center at the fitness center where Sandy and I exercised. Our sweet Silas was spending a lot of time in time out chairs, seemingly without remorse or even recognition that he had done something wrong. He also was having a lot of trouble staying still in circle time, as longer books were being read. His preschool ended up asking us not to return with him, and we soon got a refund check for our summer tuition.

        As this was happening, we were rather aware of the benefits of Early Intervention, and we had Silas screened several times. However, each of these screenings turned back negative, as Silas was charming with the adult test takers and effortlessly completed some complicated jigsaw puzzles. Finally, one of the preschool teachers wrote a report on him, and he was screened again.

        Our own theories revolved around the fact that Silas’s behavior started to go downhill about the time of the birth of his younger sister. Silas loved his little sister, Eve, in fact he couldn’t hold her enough when she was born. However, he was now a middle child, with siblings on either side of him being rather needy, and the formerly content little child now maybe felt a little squeezed.

So while we suspected maybe something like Attention Deficit Disorder, or even depression, we were astounded when the diagnosis came back as autism. Silas was nothing like Gabriel with his symptoms. There was no flapping at ceiling fans (except in imitation of his brother’s modeled behavior), there were no screaming fits, no drooling. There was not the same hypersensitivity; in fact, if anything, it was hyposensitivity. Silas could get stung by a bee; but if you didn’t see it happen, you wouldn’t know it.

        Silas’s autism was termed Asperger’s Syndrome, which can often have superior intelligence (or at least vocabulary) with diminished social skills. It’s known as sort of the nutty professor’s disease. But Silas did not speak in the monotone that is characteristic of the disorder, nor did his vocabulary seem all that superior. But again, we have accepted the fact that autism is a spectrum disorder, with many varieties of symptoms and severities.

        Silas loves finding out how things work, and seems to appeal to the young child in many people who are otherwise trying to do their job. He has pushed the buttons on recycling trucks to watch the trash compactor, he has operated a dentist chair and dentist drill, and has sat in a Boeing 737 pilot’s lap as he found out what all the buttons of the cockpit do. He also enjoys being helpful, which is not especially characteristic of his older sibling. He especially loves washing people’s windows with a squeegee, whether they need it or not.

        Silas has especially benefited from our move to Virginia. Here, he attends the Shenandoah Autism Center, and finally gets the one on one attention from teaching staff that he so desperately has needed. He has really blossomed in that environment, and the staff is looking at placing him in kindergarten several months early, as he has topped out in all of the academic things they have to offer, while he has grown well with his behavior.

        Gabriel is also continuing to do well in school. He now reads fluently, with expression. He continues to be notably strong in math, and no longer needs an aide to assist him in the classroom. He has come a long way from the little boy with the echolalia speech pattern who would stand stiffly in a classroom not knowing what to do. His current second grade teacher is not experienced in dealing with the needs of autism, in fact, Gabriel is her first student with autism, but his skills are more sufficient and he seems to be doing as well as his more typical peers. Plus, he has a very skilled resource teacher and he spends some time in his classroom as well.

 

 

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