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Faultlines Canon Wiki: Greg Matsuda and Cody Matsuda — Relationship


Overview

The relationship between Dr. Gregory "Greg" Matsuda and his son Cody Michael Matsuda, born February 15, 1979, is fundamentally about recognition without language, two autistic people seeing themselves reflected in each other for decades before either had diagnostic vocabulary. From early childhood, Cody resembled Greg strongly—people often commented that he looked just like his father. But the resemblance went deeper than physical appearance, extending to patterns of thinking, communication style, social vulnerability, and the particular way their brains processed the world.

Greg, undiagnosed autistic until the late 1990s, saw himself reflected in Cody even before understanding why they shared such similar patterns of thinking and being. Watching Cody struggle socially, seeing his literal thinking and special interests and gullibility, Greg recognized patterns across decades without having framework to name what he was observing. The connection was profound but largely unspoken, characterized by shared companionable silence, intellectual engagement, and mutual understanding that transcended neurotypical emotional scripts.

When Cody attempted suicide in spring 1995 and survived with profound changes including loss of speech from anoxic brain injury, Greg threw himself into learning ASL and researching autism to support his son's recovery. That research led ultimately to recognizing his own autism, seeing his traits described in clinical literature as he tried to understand Cody better. The father-son relationship transformed from unspoken recognition to explicit understanding, from parallel neurology to shared diagnostic identity.

Greg and Cody eventually co-authored academic work about autism, their collaboration informed by lived experience across two generations and professional expertise in educational psychology and disability rights. Their relationship models what autistic connection looks like when it spans decades before diagnosis, when recognition precedes vocabulary, when love is expressed through intellectual partnership rather than neurotypical emotional performance.


Origins

Cody was born February 15, 1979, Greg's second child and first son after Susie (born 1977). Greg was in his late twenties or early thirties, establishing his career as an educational psychology professor while navigating the demands of fatherhood as an undiagnosed autistic man. The early father-son bond was shaped by Greg's neurology—his capacity for intellectual engagement and practical care, his difficulty with emotional expressiveness and neurotypical parenting scripts.

From infancy and early childhood, Cody resembled Greg strongly. People commented constantly that Cody looked just like his father, but the resemblance extended far beyond physical appearance. Cody showed early signs of high intelligence and curiosity, with specific interests that suggested autistic traits similar to Greg's childhood fascination with trains. He was quiet, observant, intellectually focused—patterns Greg recognized intuitively even without understanding why his son felt so familiar.

Greg was "distant" during Cody's childhood, as Susie would later describe it. This wasn't rejection or disinterest but rather autistic self-protection—Greg managing his own sensory and social overwhelm by withdrawing when the household became too loud or chaotic. He couldn't intuitively read Cody's needs the way neurotypical parents might, couldn't parse cries or facial expressions without conscious analysis. But he could provide predictable structure, could maintain household routines, could engage intellectually when Cody had questions about systems or patterns.

The father-son relationship during Cody's childhood was characterized by parallel play and companionable silence rather than constant interaction. They could exist in the same space for hours without speaking, both absorbed in their own focused activities, finding comfort in shared quiet rather than demanding conversation. When they did engage, it was often intellectual—Greg explaining concepts, Cody asking detailed questions, both appreciating precision and accuracy.

Greg saw patterns in Cody that he recognized from his own experience without having language for the connection. The gullibility that made Cody socially vulnerable, the literal thinking that caused confusion when people didn't mean what they said, the special interests that absorbed complete attention—all of it resonated with Greg's own neurology. But in the 1980s and early 1990s, neither father nor son had diagnostic framework for understanding why they shared these traits.

As Cody entered adolescence and the chronic fatigue began around 1993-1995, Greg witnessed his son's deterioration with methodical concern. He took Cody to doctors seeking explanations, supported Ellen's advocacy for proper diagnosis, helped with homework when Cody had energy for it. His response was characteristically practical rather than emotionally demonstrative, but the concern was genuine even if unexpressed in neurotypical ways.


Dynamics and Communication

The communication dynamic between Greg and Cody reflects their shared autistic neurology, though neither had language for that commonality during most of Cody's childhood. Greg speaks with formal precision, using complete sentences and exact vocabulary. His tone remains flat, lacking dramatic inflection. He pauses deliberately before responding, processing thoroughly before speaking. He means exactly what he says and expects others to do the same.

Before the suicide attempt in spring 1995, Cody's communication mirrored Greg's patterns almost exactly. He spoke with quiet, measured tone, choosing words carefully, speaking with minimal vocal inflection. Everything he said was thoughtful and deliberate. He took people at their word and expected directness in return. The literal thinking, the difficulty detecting sarcasm, the preference for clear communication without subtext—these were traits father and son shared completely.

The communication match between Greg and Cody worked beautifully when they interacted. Neither demanded neurotypical emotional performance from the other. Neither required constant verbal reassurance or emotional processing. They could work in parallel for hours, share companionable silence without awkwardness, have substantive conversations about topics that interested them without wasting time on social preamble. Greg's relationship with Cody was easier in many ways than his relationships with his neurotypical or differently neurodivergent children, because Cody naturally communicated in ways that aligned with Greg's processing style.

When Cody became exhausted from chronic fatigue in the 1993-1995 period, he became even quieter—a pattern Greg understood viscerally from his own experience with autistic burnout after social interaction. Greg didn't demand that Cody "cheer up" or "try harder" to engage. He simply allowed the quiet, maintained routines, provided stability without emotional demands.

After Cody's suicide attempt in spring 1995 and the loss of speech from anoxic brain injury, the communication dynamic transformed completely. Cody could no longer speak, could no longer use the verbal communication that had matched Greg's style so perfectly. But Greg threw himself into learning ASL alongside the rest of the family, and something unexpected happened: sign language felt more natural in some ways than spoken language had.

For Greg, ASL's visual-spatial nature, its directness, the reduced demand for prosody and vocal inflection—all of it aligned well with his cognitive style. He could communicate with Cody through signs without needing to manage tone or facial expression in the same ways spoken language required. The physicality of signing, the clear visual signals, the elimination of auditory processing demands—all of it created a communication modality that worked beautifully for Greg's autistic neurology.

Greg and Cody developed rich communication through ASL, AAC devices, and Cody's full-body communication (stomping, clapping, dramatic gestures). Greg learned to read Cody's nuanced vocalizations—the difference between excited stomping and angry stomping, the meaning of various hums and whines, the emotional content of sounds without words. The communication became more explicit in some ways after Cody lost speech, because everything had to be intentional rather than automatic.


Cultural Architecture

Greg and Cody's relationship is the purest expression of the Matsuda family's cultural architecture: two autistic people recognizing each other across decades without language, their connection shaped by the intersection of Japanese-American post-internment identity, Sansei generational silence, and the specific invisibility of autism in men whose cultural background already provides a framework for the very behaviors that would otherwise prompt clinical attention.

Greg's recognition of himself in Cody—the gullibility, the literal thinking, the quiet intensity, the special interests—operated within a Japanese-American cultural context where such recognition had no diagnostic vocabulary available. The Sansei generation inherited ''gaman'' (endurance, bearing difficulty with dignity) and ''enryo'' (restraint, deference) as cultural values that mapped almost perfectly onto autistic behavioral patterns. A Japanese-American father seeing his quiet, studious, socially vulnerable son and thinking "he's like me" didn't trigger clinical concern in the 1980s—it triggered cultural recognition. Father and son were both quiet. Both were precise. Both preferred structured environments and intellectual engagement over social performance. In a Japanese-American family, this read as cultural continuity, not shared neurology.

The medical system's dismissal of Cody's chronic fatigue sits at the intersection of racial and disability invisibility. A mixed-race boy—white mother, Japanese-American father—in 1990s Pasadena occupied a diagnostic no-man's-land. The "model minority" framework that shaped how Asian-American students were perceived in schools (hardworking, compliant, high-achieving) made Cody's declining performance legible only as personal failure, not as illness. His fatigue was read through the same cultural lens that had made Greg's autism invisible for decades: quiet Asian-American boys who stop performing are seen as lacking effort, not as suffering from conditions the system isn't designed to recognize.

Greg's response to Cody's crisis—methodical, practical, internally devastating but externally controlled—was simultaneously autistic processing and Japanese-American ''gaman'' in action. He didn't sob at Cody's bedside the way Ellen did, not because he felt less but because neither his neurology nor his cultural inheritance provided channels for that expression. The four days in the ICU were processed the way Greg processed everything: internally, at full depth, without the expressive output that neurotypical and Western-cultural frameworks expect from a father watching his son almost die.

The ASL discovery—that sign language felt more natural than spoken language for Greg's autistic neurology—carries cultural resonance beyond the personal. Japanese-American communication has always valued non-verbal channels: the significance of physical presence, the meaning carried by gesture and spatial arrangement, the cultural weight of what is shown rather than said. Greg's comfort with ASL's visual-spatial grammar reflects not just autistic preference for visual processing but a cultural inheritance where communication through the body has always been legitimate. The Matsuda household's absorption of ASL into its communication landscape was less jarring than it might have been in a family whose cultural DNA demanded verbal expression as the primary carrier of meaning.

Greg's late-life autism diagnosis—arrived at through researching his son—inverts the typical diagnostic trajectory in Japanese-American families, where generational silence about difference means conditions go unnamed indefinitely. The Sansei inheritance says: you endure, you don't name, you don't draw attention to what makes you different. Greg broke that inheritance by pursuing diagnosis, by claiming language for his experience, by eventually going public academically. The break was enabled by Cody's crisis—it took nearly losing his son to make Greg look closely enough at the clinical literature to see himself in it. And the co-authoring partnership that followed—father and son publishing together about autism, presenting different generational presentations of the same neurology—represents a new cultural practice for the Matsuda line: naming what the previous generations endured in silence, making visible what Japanese-American ''gaman'' had made invisible.

Shared History and Milestones

February 15, 1979: Cody's Birth Cody was born Greg's first son, arriving when Greg was in his late twenties or early thirties. From the beginning, people commented on how much Cody looked like Greg, but the resemblance went deeper than physical appearance—into patterns of neurology neither would understand for decades.

Early Childhood: Recognition Without Language Throughout Cody's early childhood, Greg recognized himself reflected in his son. The quiet intensity, the intellectual curiosity, the literal thinking, the gullibility that made social situations confusing and sometimes painful—all of it resonated with Greg's own experience. But without diagnostic vocabulary, Greg couldn't name what he was observing. He simply knew that Cody made sense to him in ways his other children sometimes didn't.

~1993: Onset of Chronic Fatigue (Cody Age 14) When Cody's chronic fatigue began around 1993, Greg supported Ellen's advocacy for proper diagnosis while maintaining household routines and helping with homework when Cody had energy. His response was characteristically practical—problem-solving focused rather than emotionally demonstrative—but the concern was genuine.

Spring 1995: The Suicide Attempt and ICU Stay When Cody overdosed on Fluoxetine in spring 1995 after years of medical dismissal, Greg spent four days in the ICU alongside Ellen watching machines breathe for their son. Greg's processing of the crisis was methodical and internal—he didn't break down crying the way Ellen did, didn't express emotion through typical channels. But the fear and devastation were real even if unexpressed in neurotypical ways.

When Cody woke up unable to speak due to anoxic brain injury from cardiac arrest, Greg faced the reality that his son was fundamentally changed. The voice that had sounded like Greg's own communication style—quiet, measured, precise—was gone.

1995 Onwards: Learning ASL Together Greg threw himself into learning ASL with intensity and focus characteristic of his autistic hyperfocus. Ellen made the decision that the whole family would learn, but Greg's particular investment in mastering sign language reflected both his love for Cody and his discovery that this communication modality worked beautifully for his own neurology.

Learning ASL together became a shared project that deepened the father-son bond. Greg's methodical approach to language acquisition, his appreciation for visual-spatial communication, his relief at reduced demand for vocal prosody—all of it meant that ASL felt natural in ways spoken language sometimes didn't. He and Cody could sign to each other with precision and clarity, their communication perhaps even more aligned than it had been before Cody lost speech.

Late 1990s: Greg's Autism Research and Self-Recognition As Greg researched autism to support Cody's recovery and eventual diagnosis (ages 20-22), he began recognizing himself in the clinical literature. Reading descriptions of autistic traits—gullibility, literal thinking, social confusion, special interests, need for routine and predictability—Greg saw himself reflected across decades. The recognition was both revelation and confirmation.

The moment Greg tentatively approached Ellen with his hypothesis that he might be autistic encapsulated their relationship dynamic. Ellen responded simply that she'd known for years but didn't think he needed a label to be himself. Greg appreciated having language for his experience—relief at knowing he wasn't just "weird." The diagnosis helped him support Cody more effectively, providing framework for understanding their shared neurology.

Late 1990s - Early 2000s: Cody's Autism Diagnosis (Ages 20-22) When Cody was diagnosed autistic between approximately 1999 and 2001, it confirmed what Greg had already recognized through his research. Father and son were not just similar—they shared fundamental neurological patterns. The gullibility, the literal thinking, the communication style, the need for routine, the special interests—all of it had neurological explanation.

Having diagnosis for both father and son transformed their relationship from implicit understanding to explicit shared identity. They were both autistic, both navigating a neurotypical world, both using academic expertise and lived experience to advocate for disability rights.

2000s Onwards: Co-Authoring Academic Work Greg and adult Cody eventually co-authored academic publications about autism, educational psychology, and family systems. Their collaboration brought together Greg's decades of professional expertise in educational psychology with Cody's lived experience as nonspeaking autistic advocate. The intellectual partnership that characterized their relationship from Cody's childhood evolved into professional collaboration, their shared neurology informing research that would influence disability rights policy and educational practice.


Public vs. Private Life

In public spaces before spring 1995, Greg and Cody's relationship appeared as distant professor father and quiet gifted son. Greg rarely attended school events or public gatherings where emotional performance would be expected. When he did appear in public family contexts, he was formal, seemingly aloof, communicating minimally. Cody mirrored this presentation—quiet, formal, intellectually focused when he had energy.

Observers might have interpreted their relationship as cold or disconnected, missing entirely the deep recognition and understanding underneath. The companionable silence, the intellectual engagement, the shared preference for routine and predictability—none of this read as connection to neurotypical observers expecting constant verbal interaction and emotional demonstration.

After Cody's suicide attempt and loss of speech, the public dynamic shifted. Greg was father of nonspeaking son, learning ASL alongside his family, adapting household systems to support nonverbal communication. The Matsuda-Davis Homeschool Cooperative that Ellen established included Greg teaching math and science, bringing his professional expertise directly into Cody's education. Greg's teaching style—structured, logical, precise—worked beautifully for Cody's learning needs.

In private, the relationship revealed different depths. Greg and Cody could exist together in comfortable silence for hours, both absorbed in focused activities, finding regulation in shared quiet. When they communicated—first through speech, later through ASL and AAC—it was direct and substantive, without neurotypical social scripts complicating the message.

Greg's response to Cody's crisis was characteristically practical. He learned ASL methodically, researched autism obsessively, adapted his communication and household routines to support Cody's recovery. He couldn't provide emotional comfort through typical channels—hugs, reassuring words, emotional demonstrations—but he could provide what Cody actually needed: structured support, intellectual engagement, acceptance without demands for neurotypical performance.

Greg and Cody's later public work together—co-authoring academic publications, presenting at conferences—made their private connection visible in professional contexts. Their collaboration demonstrated what autistic intellectual partnership looks like, how shared neurology can inform research and advocacy.


Emotional Landscape

Greg's love for Cody is profound and expressed through practical actions rather than emotional demonstration. He loved Cody before the suicide attempt—his first son, brilliant and gentle and recognizably similar to himself in ways Greg couldn't articulate. He loved Cody after—changed, nonspeaking, rebuilding life and communication through AAC and ASL.

Greg's emotional experience during Cody's four-day ICU stay in spring 1995 was intense but largely internal. He didn't sob beside Cody's hospital bed the way Ellen did. He didn't express fear or devastation through typical emotional channels. But the terror of losing his son, the relief when Cody woke up, the grief at seeing him changed—all of it existed as profound internal experience without obvious external expression.

Greg's guilt about the suicide attempt was different from Ellen's. He hadn't been the one to bring Cody home from the psychiatry appointment, hadn't been the one making medical decisions. But he'd been "distant" throughout Cody's childhood, managing his own autistic overwhelm by withdrawing, unable to provide emotional support in ways neurotypical fathers might. He wondered if that distance had contributed to Cody's isolation, if more engaged parenting might have prevented the crisis.

But Greg's greatest emotional experience regarding Cody was recognition—the profound sense of seeing himself reflected across generations. Watching Cody struggle with gullibility, literal thinking, social confusion, Greg saw his own childhood and adolescence. When he began researching autism to support Cody's recovery and recognized himself in the literature, the recognition was both painful and validating. He'd spent fifty years not understanding why so much of the world felt inexplicably difficult. Cody gave him framework for understanding his own neurology.

For Cody, the emotional landscape regarding Greg is characterized by understanding and acceptance. Even when Greg was "distant" during childhood, even when he couldn't provide emotional comfort in neurotypical ways, Cody knew his father loved him. The practical care, the intellectual engagement, the companionable silence—these communicated love in vocabulary both father and son understood.

After losing speech, Cody experienced Greg's methodical support—learning ASL, adapting household systems, teaching in the homeschool cooperative. Greg's communication through sign language worked beautifully for Cody because it was direct and visual, without the prosodic demands of spoken language. Their signing conversations had clarity and precision that honored both their neurologies.

As adults, the emotional connection between Greg and Cody evolved into professional respect and intellectual partnership. Co-authoring academic work, presenting together, collaborating on disability rights advocacy—all of it demonstrated mutual recognition and appreciation. They were both autistic, both navigating neurotypical academia, both using their expertise to create systemic change.


Intersection with Health and Access

Greg's professional expertise in educational psychology meant he understood learning differences and neurodiversity better than most parents, though he didn't yet have framework for understanding his own autism or Cody's during most of Cody's childhood. His research focused on why traditional education fails certain learners, how to support "difficult" students, what accommodation means in practice. He was researching his own experience and Cody's without recognizing that connection until the late 1990s.

When Cody developed chronic fatigue around 1993-1995, Greg supported Ellen's advocacy for proper diagnosis while recognizing patterns he understood from his own experience with autistic burnout. The exhaustion after social interaction, the need for recovery time, the physical limits that seemed invisible to others—Greg knew what that felt like even if he couldn't name it as autistic experience.

After Cody's suicide attempt and loss of speech from anoxic brain injury, Greg's response was informed by his understanding of accommodation and access. Learning ASL wasn't reluctant adaptation but enthusiastic engagement—Greg discovered that sign language worked beautifully for his own neurology, that visual-spatial communication aligned with his cognitive strengths.

The Matsuda-Davis Homeschool Cooperative that Ellen established included Greg teaching math and science with accommodations built into the structure. Cody could be tired without shame, could communicate through AAC and ASL, could learn lying down if needed. Greg's teaching style—structured, logical, precise—worked perfectly for Cody's learning needs. The cooperative demonstrated what education could look like when systems adapted to disabled students rather than forcing disabled students to adapt to inflexible systems.

Greg's autism research starting in the late 1990s was initially about supporting Cody, but it became about understanding himself. Reading clinical descriptions of autistic traits, seeing himself reflected in literature meant to describe his son, Greg finally had vocabulary for lifelong experiences. The diagnosis he pursued around age fifty provided legitimacy in academic contexts and helped him support Cody more effectively.

When Cody was diagnosed autistic ages 20-22, Greg had framework for understanding their shared neurology. The gullibility, the literal thinking, the communication patterns, the need for routine—all of it had neurological explanation. Father and son could discuss autism from inside the experience, could collaborate on research informed by lived expertise rather than observing from outside.


Crises and Transformations

Spring 1995: The Suicide Attempt and ICU Stay Cody's suicide attempt in spring 1995 was the crisis that shattered the Matsuda family and transformed all relationships within it. For Greg, the four days watching machines breathe for Cody while Ellen sobbed and Cody remained unconscious were processed internally and methodically. Greg's fear didn't manifest in typical emotional expressions, but it was real and devastating.

When Cody woke up unable to speak due to anoxic brain injury, Greg faced the reality that his son was fundamentally changed. The voice that had mirrored Greg's own communication style—quiet, measured, precise—was gone. But Cody's intelligence was intact, his personality fundamentally preserved even if communication required new modalities.

1995 Onwards: Learning ASL and Discovering Natural Communication Greg threw himself into learning ASL with characteristic intensity, and discovered something unexpected: sign language felt more natural than spoken language in some ways. The visual-spatial nature, the directness, the reduced demand for prosody and vocal inflection—all of it aligned beautifully with Greg's autistic neurology.

This crisis transformation meant that losing spoken communication with Cody actually created a communication modality that worked better for both of them. Their ASL conversations had clarity and precision, their signing partnership honored their shared neurology in ways spoken language sometimes complicated with neurotypical expectations around tone and emotional expression.

Late 1990s: Greg's Autism Diagnosis The crisis of Cody's suicide attempt led Greg to research autism to support his son's recovery. That research led to recognizing himself in clinical literature, seeing his traits described as autistic rather than simply "weird" or "difficult." The diagnosis Greg pursued around age fifty was transformative—suddenly lifelong experiences had language, validation that he wasn't failing at being neurotypical but succeeding at being autistic.

This transformation deepened Greg's relationship with Cody. They weren't just father and son who happened to share traits—they were both autistic, both navigating a neurotypical world, both using their experiences to inform advocacy and research. The recognition that had characterized their relationship from Cody's birth finally had diagnostic vocabulary.

Late 1990s - Early 2000s: Cody's Autism Diagnosis When Cody was diagnosed autistic ages 20-22, it confirmed what Greg had already recognized. The diagnosis transformation meant father and son could discuss their shared neurology explicitly, could collaborate on research from inside autistic experience, could use their combined expertise to advocate for systemic change.

2000s Onwards: Co-Authoring and Professional Partnership Greg and Cody's evolution from father-son to professional collaborators transformed their relationship into intellectual partnership. Co-authoring academic work, presenting at conferences, contributing to disability rights policy—all of it demonstrated that their relationship had become collaborative rather than hierarchical, that Cody's expertise mattered equally to Greg's professional credentials.


Legacy and Lasting Impact

Greg's legacy in Cody's life is recognition and acceptance—the profound gift of being seen clearly by someone who shares your neurology even before either of you had language for it. Greg modeled that autistic adults can have successful careers, long marriages, intellectual engagement, meaningful lives. He demonstrated that difficulty with emotional expressiveness doesn't mean absence of love, that practical care is valid demonstration of commitment, that autistic communication is legitimate and valuable.

Greg's research into autism to support Cody led to his own diagnosis, which led to their collaborative work that influenced disability rights policy and educational practice. The legacy extends beyond their personal relationship into systemic advocacy that benefits autistic people across generations.

For Greg, Cody represents both mirror and teacher. Cody reflected back Greg's own neurology before Greg had framework to understand it. Cody's suicide attempt and recovery taught Greg about medical dismissal, about the cost of invisible disability, about what accommodation and access actually mean in practice. Cody's eventual professional work as disability rights advocate demonstrated that autistic people can thrive, can build meaningful lives, can contribute expertise that transforms systems.

The lasting impact is Greg and Cody's collaborative work becoming foundational in autism studies and disability rights. Their publications demonstrate what happens when autistic people research autism from inside the experience, when professional expertise combines with lived knowledge, when father and son recognize each other across decades and use that recognition to create systemic change.

For the Matsuda family, Greg's relationship with Cody models what autistic connection looks like—companionable silence, intellectual partnership, practical care, recognition without demands for neurotypical emotional performance. Pattie and Joey, both eventually diagnosed autistic themselves, learned from watching Greg and Cody that autistic adults can parent, can build relationships, can live full meaningful lives.

Greg and Cody's story demonstrates that recognition can precede vocabulary, that shared neurology creates connection even without diagnostic framework, that crisis can transform relationships in ways that deepen rather than destroy them. Their father-son bond—built on parallel neurology, sustained through catastrophic medical failure, transformed into professional partnership—shows what autistic family relationships can be when acceptance and understanding replace demands for neurotypical performance.


Canonical Cross-References

Related Entries: [Greg Matsuda – Biography]; [Greg Matsuda – Career and Legacy]; [Cody Matsuda – Biography]; [Cody Matsuda – Career and Legacy]; [Ellen Matsuda – Biography]; [Andy Davis – Biography]; [Matsuda Family – Family Tree]; [Autism Reference]; [Chronic Fatigue Syndrome/ME Reference]; [Motor Apraxia – Medical Reference]; [AAC – Technology Reference]; [American Sign Language – Communication Reference]


Revision History

Entry created 10/24/2025 following Relationship Template. All details drawn from character biography files for Greg Matsuda and Cody Matsuda, documenting recognition without language across decades, Greg's autism research after Cody's suicide attempt leading to own diagnosis late 1990s, ASL learning as natural communication modality, collaborative academic work on autism and disability rights, shared autistic neurology transforming father-son relationship into intellectual partnership.