A single sentence from a teacher can echo for decades: “He just doesn’t get it.” We decided to go backwards today and share a raw piece of childhood memoir about what it feels like to be the kid who can laugh on the playground but falls apart in the classroom, where the rules seem written in a language you never learned.

We talk through the slow build of shame in fourth and fifth grade, including public progress reports, old school discipline, and how humiliation spreads when other kids laugh just to survive the moment. From there, the story turns inward to the private battles families rarely say out loud: bedwetting, doctor visits, the exhausting mental math of sleepovers, and the constant fear of being exposed. When sleepaway camp forces that fear into the open, the coping gets strange and honest fast, right down to the summer Matt decided he was going to be a dog because dogs don’t get judged.

The shift happens when someone finally chooses understanding over punishment: a new school built for learning differences, a teacher who sees a person instead of a problem, and a friendship grounded in plain truth about Tourette’s syndrome. Everything connects back to what we’re building at the Ed Asner Family Center and why we keep saying it: understanding changes everything for autistic kids, neurodivergent kids, and the families raising them.

If this hits home for your child or for the kid you used to be, subscribe, share this with someone who needs it, and leave a review so more families can find the show.

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Silence can sound like “I’m fine,” but for many autism parents and special needs caregivers, it’s actually anxiety, depression, grief, and burnout stacking up day after day. We sit down for a Mental Health Awareness Month Ed Talk to say the quiet part out loud: mental health deserves the same urgency and compassion as physical health, and getting support is not a weakness.

We’re joined by Ed Asner Family Center clinicians Chrisa Sadd, LMFT and Michelle Tapia, LMFT, plus autism moms and advocates Shannon Penrod (Autism Live) and Nancy Alspaugh-Jackson. Nancy shares a raw, hopeful recovery story, from overwhelming grief and overmedication to detox, treatment, counseling, and the tools that help her stay present for her son. Shannon adds what it’s like to love someone through that fire and why the bravest move is often simply asking for help again and again.

We also get practical about what blocks families from care: insurance hoops, referrals, long waitlists, and the stress of trying to find the right therapist fit. We talk about how telehealth expanded access, why group therapy can be powerful, how small acts of kindness like meal trains can keep a caregiver afloat, and what to watch for if you’re worried about a depressed teen or a partner who shuts down emotionally. If you’re planning for your child’s future and the fear feels relentless, you’re not alone, and you don’t have to carry it in secret.

Subscribe for more family-centered autism conversations, share this with a parent who needs it, and leave a review to help more caregivers find mental health support when it matters most.

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Valerie Gilpeer and Emily Grodin share their remarkable journey from autism diagnosis to breakthrough communication, chronicling how facilitated communication unlocked Emily's voice after 25 years of limited verbal expression.

• Valerie describes Emily's autism diagnosis at age two and years of traditional therapies that yielded limited verbal communication
• Emily was frequently underestimated intellectually because she couldn't speak conversationally
• Introduction to facilitated communication (FC) as an alternative communication method that involves typing with support
• FC revealed Emily's rich inner thoughts, intelligence, and poetry that had been trapped inside for years
• Emily now attends college with a 4.0 GPA and aspires to be a journalist who covers "things that don't get covered"
• Emily explains that behavior issues often stem from communication frustration
• The breakthrough improved their relationship and gave Emily agency in her own life
• Valerie emphasizes there is no age cutoff for development—parents should never stop seeking solutions
• Emily's powerful message: "People have many thoughts, even if they can't get them out"

The book "I Have Been Buried Under Years of Dust" by Valerie Gilpeer and Emily Grodin is available on Amazon, iBooks, and local bookstores like BookSoup, published by HarperCollins.

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Step into the fascinating world of voice acting and discover how the industry is evolving to embrace performers on the autism spectrum. In this illuminating conversation, veteran voice actor Phil LaMarr (known for roles in Rick and Morty, Star Wars: The Clone Wars, and countless other beloved animated series) joins Disney casting directors Jennifer Trujillo and Colleen O'Donnell to share insider perspectives on landing voiceover work and thriving in this unique corner of entertainment.

The panel, which includes talented autistic actors Spencer Hart and Dominique Brown, explores how Disney is actively working to create inclusive casting processes. "We've been working very hard specifically with actors with autism and all neurodiversity to make sure that's specifically represented in our cast," explains Jennifer, highlighting their commitment to reading actors with autism for all roles—not just characters explicitly written as autistic.

For aspiring voice actors, the discussion offers practical guidance on getting started without breaking the bank. Phil reveals that voice acting is fundamentally about acting skills rather than just vocal talents: "Voice acting—the term is kind of backwards, because the acting comes first, the voice comes second." The panel demystifies the auditioning process, equipment needs (a decent microphone and clothes closet can be enough to start), and how pandemic-era changes have actually made the industry more accessible by normalizing remote recording.

Perhaps most profound is the discussion around why animated characters might hold special appeal for the autism community. As Phil thoughtfully observes, "If you spend the whole rest of your day trying to read code and all of this intricate stuff and then you get a half an hour where things are clear and fun and simple, like, how welcoming must that feel?" This insight resonates deeply with parents and autistic viewers alike, highlighting animation's unique power to create clear emotional experiences.

Whether you're an aspiring voice actor, a parent supporting a child's creative interests, or simply curious about how the entertainment industry is evolving to be more inclusive, this conversation offers valuable insights into a world where imagination knows no boundaries. Ready to discover how your unique voice might find its place in animation?

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What happens when authentic voices tell their own stories? Magic—the kind that changes how we see the world.

Amazon's groundbreaking series "As We See It" breaks new territory in autism representation by casting actually autistic actors in autistic roles. In this powerful conversation, the cast and creators open up about the challenges, triumphs, and revolutionary approach that makes this show unlike anything we've seen before.

Creator Jason Katims (known for his work on "Parenthood") reveals how his experience as a parent of an autistic son informed his storytelling, while going further by ensuring neurodivergent voices were present at every level of production—from the writer's room to behind the camera. "Authenticity in every aspect was the goal from the very beginning," Katims explains, describing how the trust between neurotypical and neurodivergent team members created a unique creative environment.

The heart of this discussion lies with the three lead actors—Sue Ann Pien, Albert Rutecki, and Rick Glassman—who share remarkably candid insights about portraying characters whose autism presentations sometimes differ from their own experiences. Sue Ann describes finding safety in the structured environment of filming, while Rick opens up about the challenge of playing a character hiding his autism when his own late-in-life diagnosis brought such relief.

Joe Mantegna brings powerful perspective as both an actor playing a father to an autistic son and as the real-life father of an autistic daughter. His emotional reflection on his character's cancer diagnosis—"What's going to happen when I'm no longer here?"—resonates deeply with special needs parents everywhere.

What emerges from this conversation isn't just talk about representation—it's a blueprint for how meaningful inclusion can transform storytelling. As Sue Ann beautifully puts it, the set itself became "a microcosm of what life could be like" when environments are thoughtfully designed for neurodivergent individuals.

Whether you're part of the autism community, a fan of groundbreaking television, or simply interested in authentic storytelling, this discussion will transform how you think about representation in media. Watch "As We See It" on Amazon now, and join the conversation about this show that's changing hearts and minds through honest, unflinching storytelling.

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When Connor Tomlinson's mother Lise Smith joins Matt and Navah Asner on The Brady Bunch of Autism, what unfolds is a masterclass in authentic parenting, neurodivergent relationships, and the unexpected journey of sharing your family's story with millions.

The conversation flows naturally between two families who immediately recognize their shared experiences. As blended families raising children across the neurodivergent spectrum, their connection is palpable. Lise offers a behind-the-scenes glimpse into their Love on the Spectrum journey, from Connor's initial panic attacks during speed dating to the breathless moment of his first kiss – a transformation that has inspired countless viewers.

What makes this episode particularly valuable is Lise's candid discussion of her parenting philosophy. She describes finding the "optimal anxiety zone" – that delicate balance where growth happens when we're slightly uncomfortable but still supported. "I don't want to throw them in the deep end," she explains, "but I'm going to push them a little because that's where the confidence comes from." Her approach resonates deeply with parents navigating similar paths.

The conversation takes a poignant turn when discussing divisions within the autism community. Lise makes an impassioned plea for unity: "The division is how they weaken us. We need to stop and say: I want to understand where you are, what your day-to-day looks like, and how I can support you." This call for empathy across the spectrum offers a refreshing perspective in a community sometimes fractured by different experiences.

Perhaps the most profound moment comes when Matt shares his son's description of autism as "all the apps running at once" – a metaphor that instantly illuminates the neurodivergent experience. These moments of clarity, along with updates on the Ed Asner Family Center's groundbreaking programs like Camp Ed and their adult day program, make this episode essential listening for anyone touched by autism.

Join the conversation and discover how authenticity, gentle boundary-pushing, and a willingness to embrace optimal anxiety can transform lives. Then check out Lise's podcast "Talk To Me Sis" for more insight from autism parents across the spectrum.

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Ever felt trapped in a crowded space with your heart racing and nowhere to escape? In our most vulnerable episode yet, Navah opens up about her struggle with anxiety disorders and shares a harrowing panic attack experience at Dodger Stadium. What began as a family night out quickly spiraled when a crowded stairwell became an anxiety trigger, highlighting the real challenges many neurodivergent people face in everyday situations.

The conversation takes an important turn as we discuss how one security guard's compassionate response made all the difference. This moment perfectly captures what we advocate for at the Ed Asner Family Center – understanding, accommodation, and human kindness toward those with visible and invisible disabilities. For anyone navigating anxiety alongside neurodivergence, Navah's willingness to share her experience offers both validation and community.

We're also thrilled to spotlight our Academy's media program through a special segment featuring participant Maggie interviewing our Disney artist teacher Jackie. Their conversation about creativity, learning processes, and artistic expression showcases the incredible talents being developed in our adult job training program. Watching our participants grow from hesitant beginners to confident communicators has been one of our greatest joys.

Looking ahead, we touch briefly on concerning Medicaid budget cuts affecting special needs services (a topic we'll dive deeper into next episode) and promote our upcoming Poker for Ed fundraiser on June 14th at Radford Studios. This annual event helps fund crucial programs like our Academy and social clubs for neurodivergent individuals of all ages.

Whether you're a parent, caregiver, or someone navigating neurodivergence yourself, this episode reminds us that behind every diagnosis are real human experiences – challenges and triumphs alike. Connect with us at teafc.org to learn more about our programs or reach out directly to Nava at navah@teafc.org.

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Step into the chaotic, loving world of Matt Asner and Navah Paskowitz-Asner as they bring you the sixth episode of The Brady Bunch of Autism from their home base at the Ed Asner Family Center. The couple brims with excitement, sharing that their academy for adults with autism has reached full capacity for the first time – a milestone achievement in their mission to provide meaningful support beyond high school years.

Television takes center stage as Matt and Navah offer thoughtful commentary on recent shows featuring authentic neurodivergent representation. They dissect HBO's "The Pit," praising its nuanced portrayal of a character who, while never explicitly labeled autistic, displays genuine neurodivergent traits that resonate with real-life experiences. Their discussion of "Love on the Spectrum" becomes particularly moving when they reflect on Connor and Georgie's relationship, describing one interaction as "one of the most pure and beautiful moments I think I've ever seen on TV" – a connection they hope their own children might experience someday.

The conversation shifts to their upcoming poker tournament fundraiser on June 14th, where they've thoughtfully reduced ticket prices while still offering an outstanding experience with celebrity guests and cuisine from Ma's Italian Kitchen. Listeners get a special treat as the hosts introduce Asher from their academy's podcasting class, showcasing his "Music Junkies" podcast and demonstrating the real-world skills their participants develop. The episode closes with a heartwarming introduction to Gizmo, the Pekingese who serves as both Matt's emotional support companion and the Center's unofficial mascot – a small dog who knows he's "working" when at the Center but can let loose at home.

Whether you're a family touched by autism, an advocate, or someone seeking connection through shared experiences, this episode offers the perfect blend of practical information, authentic representation, and heartfelt storytelling. Subscribe to join this extraordinary Brady Bunch on their continuing journey of education, advocacy, and community.

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What makes an autism portrayal authentic and meaningful? Matt and Navah Asner dive into this compelling question while highlighting their favorite performances that got it right. From the groundbreaking ensemble cast of "As We See It" to Diane Kruger's nuanced character in "The Bridge," we explore what makes these portrayals resonate with both autistic and neurotypical viewers.

The conversation tackles the ongoing debate about whether autistic characters should exclusively be played by autistic actors. While recognizing the importance of opportunity for autistic performers, Matt and Navah offer thoughtful perspectives on the nature of acting and representation in entertainment. This discussion reveals how complex the question of authentic portrayal truly is in an industry built on imagination.

A highlight of this episode is the debut of "Target Talk," a podcast created by Ed Asner Family Center Academy participant Zoey Frankel. This charming conversation between Zoey and her friend Peter about shopping preferences at Target showcases the incredible talent and personality of our Academy participants. It's a testament to how the Center's Podcasting 101 program helps build confidence and communication skills.

With World Autism Acceptance Month underway, Matt and Navah also reflect on the sometimes divisive nature of autism advocacy. They make a heartfelt plea for unity, encouraging everyone to "listen more and judge less" while appreciating each person's unique journey. This message of compassion extends beyond April, reinforcing their belief that "every day is Autism Acceptance Day."

Don't miss our upcoming events! Join our Funko auction on May 8th featuring items signed by celebrities like Ben Stiller and Keanu Reeves, then mark your calendar for the 13th annual Ed Asner Celebrity Poker Tournament on June 14th. With tickets starting at just $100, it's your chance to play alongside celebrities while supporting our mission.

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Autism has transformed from a diagnosis that affected 1 in 10,000 people to today's prevalence of 1 in 36. What does this dramatic shift mean for families, individuals, and our society? Hosts Matt and Navah Asner tackle this question head-on as they commemorate World Autism Acceptance Day with candid conversation about where we stand in 2025.

The episode explores the complex divide within the autism community itself – between parents of children with profound autism requiring higher support needs and autistic self-advocates. "Each person's own story is righteous," Navah emphasizes, pointing out that these different experiences are equally valid yet often at odds. This tension creates challenges precisely when the community needs unity most, especially regarding funding and support services.

Media representation remains problematic, with both hosts expressing frustration about harmful stereotypes. "No one commits a crime because they're autistic," Matt firmly states, addressing recent cases where autism has been inappropriately cited in criminal behavior. While awareness has grown, many people remain woefully uninformed about what autism actually means for those living with it daily.

The conversation highlights progress through initiatives like the Ed Asner Family Center's "Dating Spectrum" program, which focuses on building confidence for social interactions. This commitment to incorporating autistic voices extends throughout their programming, showcased through a special segment featuring Academy participant Maggie and instructor Max discussing their podcasting class.

Whether you're new to learning about autism or deeply familiar with the spectrum, this episode offers valuable perspective on how far we've come and the significant work still ahead. Listen now to join this important conversation about moving beyond mere awareness to genuine acceptance for autistic individuals of all support needs.

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Matt and Navah Asner sound the alarm on a critical issue that could devastate autism families nationwide. The hosts of "The Brady Bunch of Autism" break down how proposed cuts to Medicaid and the Department of Education would directly impact essential services for the autism community – from regional centers and special education to in-home support services and self-determination funding.

"If it doesn't affect the people who are making these slashes, they don't really understand the magnitude of the community that we're in," Navah explains, highlighting the disconnect between policy decisions and their real-world consequences for vulnerable populations. The discussion goes beyond simple political talking points to examine the concrete ways these cuts would harm families already struggling to access necessary support.

The Asners don't just raise concerns – they offer solutions, directing listeners to advocacy organizations like Disability Voices United (DVunited.org) where families can join forces to fight these proposed cuts. This blend of passionate advocacy with practical action steps demonstrates why the couple has become such trusted voices in the autism community.

Between these serious discussions, the episode lightens with exciting news about the Ed Asner Family Center's innovative "Podcasting 101" class for adults with autism, and Navah's endearingly honest account of her fear of flying as the couple prepares to attend a major autism benefit in New York.

Whether you're directly connected to the autism community or simply care about disability rights, this episode provides both urgent information and heartfelt storytelling from two advocates who understand these challenges on both professional and deeply personal levels. Subscribe now to join the conversation and be part of this vital community.

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Parenting autistic children comes with unexpected twists and turns, especially when appearances don't match reality. In this deeply personal episode, we share the story of our son Wolfie, whose journey through the prestigious Berklee School of Music ended in crisis but ultimately led to profound growth and understanding.

Wolfie always seemed to be our "easy" child with autism. Academically successful and apparently needing minimal support, we celebrated when he was accepted to his dream school. Despite setting up therapy and support systems, what we couldn't anticipate was the emotional toll that sudden independence would take. Behind our regular check-ins, Wolfie was struggling silently - doctoring grades, withdrawing from classes, and maintaining a façade that grew increasingly unsustainable.

When the truth finally emerged, our initial shock and anger quickly gave way to heartbreak over the profound isolation our son had experienced. This powerful lesson reshaped our understanding of autism parenting: sometimes the children who appear to need the least support actually require the most. We realized no prestigious degree is worth sacrificing mental health, and our dreams for our children must sometimes step aside so they can create their own paths.

We also discuss exciting developments at the Ed Asner Family Center, including our groundbreaking partnership with Funko that's creating meaningful employment opportunities for autistic adults. Three program participants have already become regular employees, demonstrating what's possible when companies commit to authentic inclusion.

Whether you're parenting autistic children or simply interested in better understanding autism, this episode offers honest insights into balancing expectations with reality, recognizing hidden struggles, and creating environments where neurodivergent individuals can truly thrive. Visit teafc.org to connect with our community and explore our programs designed by and for neurodivergent people.

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Get ready for an inspiring ride with Navah and Matt Asner in this new episode of "The Brady Bunch of Autism." After a hiatus, the hosts are thrilled to reconnect with their audience and share their powerful experiences navigating the world of autism. Drawing from their journey of being parents of six children in a blended family, they talk about the chaos, the laughter, and the unbreakable bonds that tie them to their community.

As they reflect on their own lives, the Asners provide insights into the growth of the Ed Asner Family Center, a sanctuary for families dealing with autism and special needs. They share the pivotal moves they've made as a family, discussing the importance of community support and the value of mental health resources. If you've ever felt overwhelmed, this episode is a heartfelt reminder that you’re not alone and that reaching out to others can create light in dark times.

Stay tuned for future discussions on current affairs, personal stories, and all the topics that matter to families navigating the complexities of autism. We invite you to join the conversation, share your challenges, and find inspiration within the community we’re building together. Don't forget to subscribe to catch all future episodes!

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