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In the opening chapter, Tammet introduces himself and explains a bit about the way his mind works. He reveals right away that he has “a rare condition known as savant syndrome” that includes “an almost obsessive need for order and routine” (1). Part of the regular ordering of his world comes from the author’s ability to ground himself in numbers. Counting calms him down, and numbers help him be consistent with portions, routines, and seemingly every element of his life. His relationship to numbers, however, extends beyond their basic functionality. The author also reveals that he has particularly complex synesthesia, what he explains as “a neurological mixing of the senses” that allows him to “see numbers as shapes, colors, textures and motions” (2). He also identifies the “relatively mild and high-functioning form of autism” (7), called Asperger’s syndrome, that he has. He says that most people with savant syndrome are on the autistic spectrum.
Tammet provides some visual examples of what his imagining of numbers and larger life with synesthesia looks like. He illustrates certain numbers with curves and others with dots, for example. This holistic relationship with numbers is also emotional; Tammet likes certain numbers for the colors, shapes, and auras they embody in his mind and dislikes others whose sensory output is, for him, anxiety-inducing. He particularly enjoys power multiplication—“multiplying a number by itself a specified number of times” (4)—and prime numbers—the “building blocks of my numerical world” (9). He experiences words and language in a similarly complex and multisensory way. Different words have different colors and textures. These abilities aid memorization and foreign language learning.
The author provides some background on neurodiversity. He references the 1988 film Rain Man, which is one of the most famous popular depictions of savant syndrome, as well as books that document the abilities of people with synesthesia. The conditions vary from person to person, but themes of extraordinary memory and talent with mathematics and number memorization are common and apply in the author’s case. His objective in writing the book is to share his experiences in the hope that they can make other individuals on the autistic spectrum take comfort and “have confidence in the knowledge that it is ultimately possible to lead a happy and productive life” (12).
This chapter provides an account of what it was like to experience the developmental peculiarities of autism spectrum disorder (ASD), savant syndrome, and synesthesia as a young child growing up in East London. The author starts recounting the tale from the time of his mother’s late pregnancy. His parents were impoverished, patient, and lovingly devoted to their son (and eventually other children as well) according to his needs. They navigated his difficult behavior, defined largely in his earliest years by incessant crying, by calming him with soothing motions (like rocking and swinging) and enlisting the help of specialists early on.
A turning point in the author’s life came when his parents enrolled him in nursery school, where he experienced the many multisensory stimuli that it offered. He did not connect with the other children there (or his younger brother at home), but he explored the textures of the facility’s carpets, mats, and playgrounds with great interest and intensity. At home, he grew obsessed with numbers, collecting books that he couldn’t read just so that he could count the page numbers, his “numerical comfort blanket” (25).
Many of the activities the author enjoyed most as a child involved repetitive motion and silence. He would sit and immerse himself in silence in his bedroom or sit on swings or the merry-go-round in the early morning at a nearby park as his parents kept him swinging or spinning. Other stimuli he was likely to encounter around town, however—car horns, crowds—were frightening and painful.
The chapter traces the author’s life until around age five. In the final lines, he reflects that his parents’ recollections helped him write the account, and he calls them his heroes for the efforts they made and the love and patience they displayed (28).
Tammet opens with the story of a nearly fatal epileptic seizure he suffered at age four. His convulsions lasted nearly an hour, and he nearly suffocated and died before doctors stabilized his condition. Doctors diagnosed him with temporal lobe epilepsy, which Tammet says is not unusual among individuals on the autistic spectrum.
Though medication successfully prevented further seizures, the side effects included dizzy spells and drowsiness that severely impacted the author’s life and his ability to perform at school. For example, he would often fall asleep in class, and his teachers (informed and sympathetic) would make sure he was not alone as classrooms emptied and he slept on. While this condition isolated him from other students, he still did not particularly mind: “they just weren’t a part of my world” (38). Eventually, he was able to stop taking the medication, and his performance at school improved as he remained seizure-free and unmedicated.
Tammet discusses some brain science related to seizures, ASD, and savant abilities. For example, while people with typical brain and cognition functioning perceive certain things as a whole (like an image), a person on the autism spectrum might perceive it with more attention to its constituent parts and details. He illustrates this concept in the text itself. If the letter “H” is stamped several times and the group is arranged into a large letter “A,” people not on the spectrum are likely to immediately perceive the large “A,” but a brain like the author’s will likely first see the many “Hs” (40).
The author devotes space in the chapter to talking through a few theories that researchers have studied in relation to brains, epilepsy, creativity, and more. Researchers have suggested the possibility of “a link between epilepsy and creativity” (43), and indeed, the author developed a compulsion to write fiction stories when he was about eight years old. From then on, writing was an important and positive aspect of his life.
The book opens with the author’s positive outlook on living with the conditions he has. He explicitly says that he’s “living proof” that someone on the high-functioning end of the autism spectrum can live a happy and fulfilling life. From there, the author backtracks to describing the experiences of these conditions from the perspective of a young child. The reader learns about the lives of the author’s parents, who had to sooth a child who cried excessively through two years of infancy and continued to have tantrums, minimal verbal communication, and prolonged health issues thereafter. The author reflects on how difficult this must have been for his parents but notes the steps they took to keep him happy and encourage good behavior. He also notes that they refrained from labeling him, not wanting “to hold me back in any way” and probably fearing “the possible stigma attached to having a child with developmental problems” (19). Occasionally, the author speaks directly to parents who might be reading the book and be presented with similar challenges in their own families. Part of forming a strong support system and setting up a child for success involves educating oneself on neuroatypical conditions and encouraging a child’s “self-belief to hold on to their dreams” (45).
While we get a sense of the extreme difficulties that dealing with his conditions posed for a young child, the author maintains his positivity and hopefulness about life on the autistic spectrum or with epilepsy. Though conditions like epilepsy and ASD are often misunderstood in mainstream society, the author is hopeful that stigmas will disappear and that loved ones can provide productive support systems for individuals on the spectrum or with other atypical neurological functioning.
The author says several times throughout the section that especially during his youth but even as time went on, scientists understood very little about ASD. He participated in experiments to provide data for researchers, and he also discusses some of the most compelling research into brain science that relates to ASD, epilepsy, and savant syndrome. He talks, for example, about what different lobes and hemispheres in the brain do, and the possibility expressed by one researcher that “savant abilities may be in everyone, only most are unable to unlock them” (41). He also explains that while it’s possible that his seizures created a brain injury that influenced his cognition, it’s also possible that a brain injury produced his seizures (38). All of this conjecture reveals that brain science is elusive and poses interesting theories but has a long way to go before we can really understand how diverse brains and minds work.
Throughout this section, the young Tammet remains aloof from his peers, and the author often reveals that he did not mind that distance. He uses the imagery many times of living within his own world, full of his books, numbers, textures, silence, and compulsions. At various moments, however, he hints that the scope of his world would change after childhood. This section ends when the author is about eight years old, by which time his parents have discovered important resources and routines for their son and by which time the author himself had developed preferred habits and mechanisms for coping with stress. Some of his challenging experiences in early childhood were quite formative in terms of developing a sense of self and trajectory for his future. For example, intensive descriptive writing instilled “a permanent fascination for words and languages” (44), which the author says remained greatly beneficial for him.
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