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Parenting

Parenting

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Parenting

Parenting

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4d ago

Level One Does Not Mean Easy | Stephanie Kerns

Stephanie Kerns was a teacher before she was an autism mom, and the only autism she had seen up close was in boys. So when her daughter started putting sponges in her mouth and echoing every question back in the exact tone it was asked, the first read was a speech delay. Her daughter is 14 now, verbal, and diagnosed Level 1, the level everybody hears as easy. Stephanie talks about the hour-long meltdowns before school, the routine that starts at five every morning, and three straight weeks of spirit week that took nightly planning to survive. She talks about the stutter that showed up out of nowhere at 13, and the win when it stopped. And she talks about a creative, funny kid who writes songs with her dad, acts in the school drama program, and does accents her mom can't. Then there is the part aimed at the rest of us. To the outside world, Stephanie says, autism families can feel like a secret society. Nobody sees the therapy, the paraprofessional, the hunt for friends, the phasing in and phasing out. Inside the community, her message is about finding your people, and what happens to the parents who never do. And if anyone tells you their kid doesn't look autistic, she has an answer for that. Hang out with her for a day. Level one does not mean easy. It never has. CHAPTERS 00:00 Welcome to Seen and Heard 00:25 Meet Stephanie, a teacher before she was an autism mom 01:44 Sponges, echolalia, and hour-long meltdowns 02:53 The IEP at three, and the level that came years later 04:14 Five a.m., routine, and three weeks of spirit week 06:03 Rob on uniforms, and why level one does not mean easy 07:27 The win: a stutter at 13, and phasing out of speech 08:55 Who she is: creative, a writer, a memorizer, an actor 10:03 She doesn't look autistic. Hang out with her for a day 10:57 Rob on his oldest son's regression 12:15 What she wishes the outside world understood 13:41 Does the world see and hear her family 14:29 Finding your people 16:04 Both sides of the IEP table 16:38 Rob on 30 pairs of shoes, and staying curious 19:30 The book, and where to find everything SPONSOR #ad This episode is presented by Mightier. Thanks to Mightier for presenting this episode. Mightier is a biofeedback video game program developed and tested at Boston Children's Hospital. Your kid wears a heart rate monitor and plays games that get harder when they get dysregulated and easier when they calm down. So instead of being told to take a deep breath in the middle of a meltdown, they practice regulation in their own body, at a moment when they can actually feel it working. It is one of the very few things I have stood behind for years, because it helped my own kids connect the dots when nothing else did. Visit https://www.mightier.com and use code theautismdad22 for 10% off. ABOUT SEEN AND HEARD Seen and Heard is a short series from The Autism Dad Podcast. Real families get about fifteen minutes to describe their actual lives, in their own words, without anyone smoothing it out for them. MY BOOK So Your Child Was Just Diagnosed with Autism: Real Talk, Support, and Next Steps from a Dad Who's Been There is out December 29, 2026 from Fair Winds Press. If your child has just been diagnosed with autism, this is your compassionate first step guide from someone who has lived it. Preorder: https://theautismdad.com/book/?utm_source=youtube&utm_medium=social&utm_campaign=book-preorder&utm_content=text-post MORE FROM ME Everything I do lives here: https://theautismdad.com/?utm_source=youtube&utm_medium=social&utm_campaign=ep-s9e19-stephanie-kerns&utm_content=text-post Listen to the podcast on Apple, Spotify, or wherever you get your shows. QUESTIONS FOR YOU What do people get wrong about your kid because of how they look? If your child is diagnosed Level 1, what is the part nobody outside your house sees? When did you finally find your people, and what took so long?
Sep 9

Autism Doesn't End With Your Military Service | Jaime Parent

This episode is presented by Mightier. In 1988, Jaime and Tracy Parent were stationed in England when their son Bryan was diagnosed with autism. There was nothing out there. No resources, no roadmap, no Rain Man yet. What they found instead was other families, and Jaime says that has been their best resource ever since. Jaime is a retired Air Force lieutenant colonel with twenty years of service, and a family that moved every three years. Every move meant starting over. New doctors, new teachers, new school district, and a lot of guesswork about which house to buy so they landed in the county with the services Bryan needed. In this Seen and Heard conversation, he talks about the day clinicians at a UCLA residency program asked what their goals for Bryan were. A job, drive a car, balance a checkbook. He says the looks on their faces were pure pity. You poor delusional people. Bryan is an adult now. He works at Publix, he lives at home, and he competes in Special Olympics bowling, soccer, and basketball. He also tells the wrestling story. Bryan made the team at Oakland Mills High School in Maryland with no shortcuts, wrestled heavyweight, won matches, and went to regionals, states, and nationals. The first time Jaime watched him wrestle, Bryan got pinned in about thirty seconds. His dad calls it one of the biggest wins of their lives. Then there is the part aimed at the rest of us. Jaime's advice to other autism families is four words: don't become a wallflower. His message about bureaucracy is that there are big boulders everywhere, but get past them and you will find angels. And his message to military families is one you need before you separate. Autism does not end with your military service. Jaime B. Parent and Elizabeth Tracy Parent are the authors of The Mission at Home: Navigating Military Assignments, TRICARE, Education, Benefits, and Everyday Life with Your Child on the Autism Spectrum. Available on Amazon and Barnes and Noble. SPONSOR This episode is presented by Mightier. Mightier is a biofeedback video game program developed and tested at Boston Children's Hospital. Your kid wears a heart rate monitor and plays games that get harder when they get dysregulated and easier when they calm down, so they practice regulation in their own body at a moment when they can feel it working. Visit mightier.com and use code theautismdad22 for 10% off. Rob's book, So Your Child Was Just Diagnosed with Autism, comes out December 29, 2026. Preorder at theautismdad.com/book.
Aug 20

The Brain Isn't Broken, It's Inflamed | Dr. Theoharides

Dr. Theoharis Theoharides is back, and this time we got into the stuff that has been all over the news. Leucovorin. Tylenol. Benadryl. Underneath the headlines there is actual science, and Dr. Theo walks through what inflammation, mast cells, and folate really have to do with our kids. The throughline is simple. A diagnosis is a label, not a treatment plan, and there is measurable biology underneath that label that most workups never look at. Dr. Theo holds five degrees from Yale, spent 37 years at Tufts, has published more than 500 peer reviewed papers, and was the first researcher to connect mast cells to autism. He now runs the Center of Excellence for Neuroinflammation Research in Florida. In this episode: - What a mast cell actually is, and why the ones in the brain matter- Propionic acid, and why it is sitting in most kids' cereal- The four things he wants every autism workup to cover- The folate test most kids never get, and why normal bloodwork can still be wrong- A 30-second test you can run at your kitchen table tonight- Why constipation changes behavior more than almost anything he has seen- What to do when your pediatrician refuses to order a test- How to tell a real supplement from an expensive one- Twenty years of autism fads, and why stem cells do not work- When to stop something that is not working His most honest moment: "I hate the term therapeutic because I don't know what I'm treating." His best one: "The brain is working. The fact that they don't speak doesn't mean anything." RESOURCESFRAT, the Folate Receptor Autoantibody Test. Must be ordered by a physician.MTHFR gene analysis.RBC folate and RBC B12, to see what is getting inside the cells.Flat abdominal X-ray, when behavior spikes and nobody can explain it. FIND DR. THEOdrtheoharides.com, which has an intake form.Instagram: @drtheoharidesHe sees patients in Fort Lauderdale the third week of each month, adolescents and adults only. FIND ROBtheautismdad.comThe book, So Your Child Was Just Diagnosed with Autism, is out December 29. Preorder at theautismdad.com/book/ DISCLAIMERDr. Theoharides is a physician and PhD pharmacologist with five degrees from Yale and more than 500 peer reviewed publications. This conversation is education, not personalized medical advice. He names specific tests, supplements, medications, and doses, and he gives them as clinical context. The right number for any individual child depends on age, weight, and labs. Do not start, stop, or change anything based on a podcast. Talk to your child's doctor.
Sep 3

Does He Ever Shut That Motor Off? | Nicole Carbone (S9E17)

This episode is sponsored by PESI. Nicole Carbone's son Luca is almost four, nonspeaking, and diagnosed with Level 2 autism. When he can't tell her what he needs, he bangs his head on whatever is closest. His pain tolerance is high enough that the thing strangers always say, that he'll stop before he really hurts himself, is just not true. In this Seen and Heard conversation, Nicole talks about the communication barrier underneath the self injury, the AAC device she hopes will ease it, and what it was like to separate her twins into different preschools so Luca could get what he needed. She also talks about the best 40 seconds of her life so far, the day he looked right at her and said "hi mommy" for the first time, and she got it on video. Then there's the part aimed at the rest of us. A stranger at the park watched Luca hum and asked her if he ever shuts that motor off. And inside the autism community, Nicole says the hardest thing about a Level 2 diagnosis is not the diagnosis. It's the comparing. Her advice is blunt and it applies to every level: don't compare your kid to any other kid. Nicole is the founder and president of The NEST Project, a nonprofit serving families in Pennsylvania and Ohio that buys what insurance won't cover for kids with special needs. Find them at nestcares.org. SPONSORThis episode is sponsored by PESI. Their 2026 Kids and Teens Autism Symposium runs November 18 and 19, online, and it is neuro-affirming the whole way through. There is a full session on demand avoidance, for every kid who got called defiant when it was really their nervous system, and another on kids who mask so well they get treated for anxiety instead of what is actually going on. Two hundred dollars for both days, up to 18 CE hours, and a 30 day replay if you cannot be there live. Built for clinicians, and parents can register too. pesi.com/theautismdad Rob's book, So Your Child Was Just Diagnosed with Autism, comes out December 29, 2026. Preorder at theautismdad.com/book.
Jul 15

What Level 2 Autism Can Look Like | Lauren Murray (S9E12)

“Most people don’t even tag her with autism, because she’s smart, she’s so articulate.” Lauren Murray Lauren Murray is a New Jersey mom of two, and her daughters are almost twenty years apart. Her oldest is about to turn 21, a UCF graduate thriving in Florida. Her youngest is four, level two autistic, with sensory processing disorder and a short list of safe foods. She is also, in Lauren’s words, doing fantastic. In this Seen and Heard episode, Lauren gives Rob an honest look at a day that starts at six in the morning and does not end until nine at night. Her husband works long days, so most of the week she is her daughter’s sole care provider. Lauren is a former teacher who kept a tight schedule at home, and school does it even better, down to the minute, and her daughter loves it. Then there is the part so many parents will feel in their chest. Lauren’s daughter is bright and verbal, she speaks better than most of her peers, and that is exactly why people do not believe she is autistic. At the park, one mom packs up her kids and leaves every time she sees them coming, because Lauren’s daughter does not understand personal space and just wants to play. In public, a meltdown gets read as a bratty toddler, when the truth is they have done everything from A to Z to get ahead of it. And the win. Flying home from a day trip to visit her oldest in Florida, their flight got canceled. They spent the night in the airport, then got emergency landed at an airport none of them had ever seen. Her four-year-old took the whole thing in stride, iPad, comfort snacks, a blanket Lauren packed just in case, a bench, and a kid who just went with the flow. Lauren also names something a lot of families hit. In New Jersey, the services show up the moment you are diagnosed, but if you do not use them inside six months, they close your file. Not because you will never need help, just because you did not need it that week. What you’ll hear: “She took it better than I did.” Lauren Murray This episode is sponsored by Mightier, a biofeedback emotional-regulation gaming program for kids, developed and tested at Boston Children’s Hospital. Kids play games that get harder when they get dysregulated and easier as they calm down, so they practice regulating themselves in the moment. Read Rob’s full review at theautismdad.com/mightier-review and use code theautismdad22 for 10% off. #ad About Rob: Rob Gorski is the founder of The Autism Dad, a blog and podcast dedicated to supporting parents raising kids on the autism spectrum. As a dad of three autistic sons with over 25 years of experience, Rob brings lived experience, honesty, and heart to every conversation. Rob’s book, So Your Child Was Just Diagnosed with Autism, lands December 29, 2026 from Fair Winds Press. Updates and preorder: theautismdad.com/book Where to find Rob: You can find me at theautismdad.com, on Facebook, Instagram, and TikTok at The Autism Dad, and on YouTube at The Autism Dad. New episodes drop every week at listen.theautismdad.com.
Apr 15

This Is What Level 1 Autism Parenting Can Look Like

What does autism level one actually look like inside a real family's home? That is exactly what Justin Bowman, autism dad and founder of VizyPlan, is here to share. In this episode of Seen and Heard, Justin gives us a 15-minute glimpse into life with his son Sawyer, who is turning six and diagnosed autism level one. Sawyer is the kid they call the mayor at school because he just wants to say hi to everyone. He is also a kid who went from completely nonverbal to holding full conversations in under three years, carries a full alphabet soup of providers, and battles a deep self-awareness that sometimes makes him avoid the very things he wants to do most. Justin also makes a point in this episode that stopped me cold: being seen and heard in the autism community is not a level playing field. Zip code matters. Access matters. And until we recognize that, we are missing something important. What you will hear in this episode: • Sawyer's journey from nonverbal to conversational in under three years • Why his follower mentality is both his biggest strength and his parents' biggest worry • The full support team keeping Sawyer thriving inside and outside of school • Why self-awareness in an autistic child can be both remarkable and heartbreaking • What autism level one really looks like when the diagnosis label does not tell the whole story • Why comparison is the thief of joy in the autism community • Why being seen and heard is not equal for every autism family regardless of diagnosis level ABOUT THE GUEST Justin Bowman is the founder and CEO of VizyPlan, a visual routine and planning app built for the neurodivergent community, and Associate Director of Product Management at Chewy. He is an autism dad based in central Massachusetts with his wife Danielle, a speech-language pathologist, and their two children, Sawyer, who is turning six and diagnosed autism level one, and Peyton, who is four. ABOUT YOUR HOST Rob Gorski is the founder of The Autism Dad, a blog and podcast dedicated to supporting parents raising kids on the autism spectrum. As a dad of three autistic sons with over 25 years of experience, Rob brings lived experience, honesty, and heart to every conversation. THIS EPISODE IS BROUGHT TO YOU BY Mightier is a clinically proven app that helps kids build emotional regulation skills through biofeedback-based video games. It meets kids where they are and gives parents real tools to support them at home. Visit mightier.com and use code theautismdad22 for 10% off. If you found this episode helpful, please follow The Autism Dad Podcast on Apple Podcasts, Spotify, or wherever you listen. Visit listen.theautismdad.com for past episodes, resources, and ways to support the show.
May 13

This Is What Level 1 Autism Parenting Can Look Like | Liz Covington (S9E07)

Liz Covington's son Bennett was diagnosed with ADHD and ODD at age four. The autism diagnosis didn't come until he was ten. Now he's 18, in college, and just spent two hours shoveling the driveway in a snowstorm without being asked twice. That's the kind of win that doesn't make the highlight reels but means everything to families like hers. In this Seen and Heard episode, Rob sits down with Liz, a Utah mom of four, for a 15-minute glimpse into what level 1 autism parenting can actually look like. They cover late diagnosis, the daughter who has friends at school but can't handle anything else after, and why some autism families feel like they don't belong inside their own community. What you'll hear in this episode: Why ADHD and ODD diagnoses came years before autism for Bennett What the win looks like at 18: independence, problem-solving, and no resistance The ten-year-old daughter who masks at school and crashes at home Why "high functioning" families can feel invisible inside the autism community The school principal who misread Bennett's nervous laugh as disrespect The phrase Liz heard too many times: "autistic kids don't do that" Why every kid wants to be connected, appreciated, and seen "Every kid is good. They all want to be connected. They all want to be appreciated. And they're all trying their best." — Liz Covington ABOUT THE GUEST Liz Covington is a mom of four based in Utah. Her oldest son Bennett, 18, was diagnosed with ADHD and ODD at age four and with autism at age ten. He is now in college. Liz's ten-year-old daughter is believed to be on the spectrum and is awaiting formal evaluation. Liz advocates for autism families whose kids' challenges aren't visible on the surface. ABOUT YOUR HOST Rob Gorski is the founder of The Autism Dad, a blog and podcast dedicated to supporting parents raising kids on the autism spectrum. As a dad of three autistic sons with over 25 years of experience, Rob brings lived experience, honesty, and heart to every conversation. Rob's first book lands early 2027 from Quarto. Updates and preorder: theautismdad.com/book THIS EPISODE IS PRESENTED BY ALGONOT This episode is presented by Algonot. Algonot makes science-backed supplements developed by Dr. Theoharis Theoharides, a Yale-trained researcher who has spent decades studying neuroinflammation, mast cells, and the brain. Every product is third-party tested for purity and free of common irritants. Visit algonot.com and use code ROB5 to save on your order. RESOURCES MENTIONED More Seen and Heard episodes: listen.theautismdad.com Algonot supplements (use code ROB5): algonot.com Preorder Rob's book: theautismdad.com/book If you found this episode helpful, please follow The Autism Dad Podcast on Apple Podcasts, Spotify, or wherever you listen. Visit listen.theautismdad.com for past episodes, resources, and ways to support the show. You can find Rob at theautismdad.com, on Facebook, Instagram, and TikTok at The Autism Dad, and on YouTube at The Autism Dad. New episodes drop every week at listen.theautismdad.com.
Apr 8

This Is What Level 1 Autism Parenting Can Look Like | Brandon Shaw (S9E02)

What does it really feel like to fight for your child's autism diagnosis, navigate school battles, and find joy in a glove and a game of catch? In this episode of Seen and Heard, I'm joined by Brandon Shaw, an autism dad from Orlando, Florida, who shares a candid, unfiltered look at life with his seven-year-old son Mason, who is diagnosed level one but often teeters between one and two. Brandon opens up about the moment everything changed, the silence that followed diagnosis, and the small victories that keep his family moving forward. What you will hear in this episode: How Brandon and his wife Alyssa fought for Mason's autism diagnosis after being turned away by two pediatricians Why there was no roadmap after diagnosis and how the family built one on their own The everyday reality of raising two brothers, one neurotypical and one autistic, under the same roof How Mason went from an autism-specific pre-K unit to a mainstream first-grade classroom with an IEP Why small wins, like answering how his school day went or grabbing a baseball glove, mean everything What Brandon wishes the outside world understood about Mason and the autism community Why Brandon believes advocacy is a team sport and how community support changes everything ABOUT THE GUEST Brandon Shaw is an autism dad living in Orlando, Florida with his wife Alyssa and their two sons, Mason, age seven, and Hunter, who is nearly three. Mason was diagnosed as autistic around age three and a half after his family fought to be heard by multiple doctors. Since diagnosis, Brandon and Alyssa have dedicated themselves to learning, advocating, and celebrating every step of Mason's journey. Brandon is passionate about breaking autism stigmas, building community, and reminding other parents that they are not alone. ABOUT YOUR HOST Rob Gorski is the founder of The Autism Dad, a blog and podcast dedicated to supporting parents raising kids on the autism spectrum. As a dad of three autistic sons with over 25 years of experience, Rob brings lived experience, honesty, and heart to every conversation. THIS EPISODE IS BROUGHT TO YOU BY VizyPlan — If your mornings feel like a battle before the day even starts, check out VizyPlan. Built by a dad who gets it, VizyPlan uses AI to create visual routines with photos of your actual child. Visit VizyPlan.com/app and use code theautismdad to get your first month free. If you found this episode helpful, please follow The Autism Dad Podcast on Apple Podcasts, Spotify, or wherever you listen. Visit listen.theautismdad.com for past episodes, resources, and ways to support the show.
Aug 12

The Day He Called Her Mom | Deena Nathan (S9E14)

Deena Nathan's five year old son Hayden is autistic and non-speaking, and he's fluent on his AAC device. In this episode she walks through a day that starts with therapy at 8am, the win she's still not over, and the one thing she wants people to understand about a kid who doesn't talk. She's also honest about something most people won't say out loud. She has real support, good family, friends who get it, and it's still lonely. Both of those things are true at once, and that might be the most useful thing in this conversation. What you'll hear 00:00 Welcome 00:43 Meet Deena, Hayden, and the family 01:43 A day built around therapy, and being the chauffeur 04:42 The hardest part is time, and the guilt that comes with it 06:16 The win, the day he called out for Mom 08:02 Who Hayden is, hyperlexic, happy, and fluent on his AAC device 10:28 What she wishes people outside the community understood 12:00 Supported and still lonely 13:22 What she wishes autism families understood, no one's future is predicted 14:57 Feeling seen and heard inside the community 15:58 Why families at different levels end up disconnected 17:48 Deena's coaching work with special needs parents 18:21 Why Rob started sharing in the first place 21:33 Closing About the guest Deena Fierstein Nathan is a Certified Life Coach at DFN Connected Growth Coaching, where she works with parents of kids with unique needs. She lives in the North Shore suburbs of Chicago with her husband Kevin and their two kids. She stopped working when Hayden was diagnosed and went all in, including taking classes with his AAC device company so she could use it with him. Website: dfnconnectedgrowth.com Instagram: @connectedgrowthwithdeena Sponsors This episode is sponsored. Mightier is a biofeedback emotional regulation program for kids developed at Boston Children's Hospital. Use code theautismdad22 for 10% off at theautismdad.com/mightier-review. Best Part Kids is a sensory-friendly multivitamin for selective eaters created by dietitian Brittyn Coleman. Use code THEAUTISMDAD for 10% off at BestPartKids.com. About your host Rob Gorski is the founder of The Autism Dad. His book, So Your Child Was Just Diagnosed with Autism, is out December 29 2026. theautismdad.com/book
Jul 22

Outsourcing the Panic | Erin Lamb

Erin Lamb has been a speech language pathologist for 26 years. She runs a Baltimore nonprofit with its own school for autistic kids. She has a Ph.D. She still missed her own daughter's autism. Why does autism get missed in girls? Most of the foundational autism research was done on boys. As Erin puts it, everything she knew about autism she learned from boys in the 90s, because that's what the research was done on. That research shaped the training, and the training shaped what people picture when they hear the word autism. Girls who talk early, who mask well, or whose struggles get read as anxiety often reach their teens before anyone says it out loud. This is a Seen and Heard episode, so Erin gets the floor. She walks Rob through what a day actually looks like in a house with a kid in autistic burnout, with a PDA profile and ARFID, where separation anxiety is the most clinically significant thing in the room. She's honest about what it costs her. "People are like, what are you doing this weekend? And my answer is always caregiving. Because I do not know. I cannot plan." Then she tells us what changed. She calls it outsourcing the panic. If the school professional isn't panicking, why is she? She handed the worry to the people whose job it is to worry, and her daughter started coming back to her within weeks. She also gives the best description of an autistic kid this show has had. In the wrong environment it's like parenting all the kids from Willy Wonka at once. In the right one, with the right accommodations and supports, her kid is Charlie. WHAT YOU'LL HEAR Why a speech language pathologist with 26 years of practice missed autism in her own daughter What a day really looks like with a kid in autistic burnout, a PDA profile, and ARFID What outsourcing the panic means, and how she started doing it Who her daughter actually is: the Lorax, Willy Wonka, and Charlie What she wishes the outside world, and the autism community, understood TERMS FROM THIS EPISODE Autism in girls: autism is underdiagnosed in girls largely because the foundational research was conducted on boys, so the diagnostic picture most clinicians trained on describes boys. Girls who mask well or present as anxious are routinely missed. PDA, pathological demand avoidance: a profile in which an autistic person's nervous system treats demands as threats, even small or pleasant ones. Approaches that add pressure usually make it worse. ARFID, avoidant restrictive food intake disorder: more than picky eating. A child avoids whole categories of food by texture, smell, or fear, to the point that nutrition and growth are affected. Autistic burnout: exhaustion and loss of previously held skills following a long stretch of masking, sensory overload, and unmet needs. Recovery takes fewer demands and real rest, not more pushing. Outsourcing the panic: Erin's strategy of handing specific worries to the professionals whose job it is to hold them, instead of carrying every worry herself. ABOUT ERIN LAMB Erin Lamb is the President and CEO of Gateway Maryland, the Baltimore nonprofit formerly known as HASA, which has served Maryland families for nearly 100 years. She's a licensed speech language pathologist, holds a Ph.D. in public policy, and is the mom of two neurodivergent teenage daughters. SPONSOR This episode is sponsored by Mightier, a biofeedback emotional-regulation gaming program for kids, developed and tested at Boston Children's Hospital. Kids wear a heart-rate monitor and play games that get harder when they get dysregulated and easier as they calm down, so they practice regulating themselves in the moment. Read Rob's full review at theautismdad.com/mightier-review and use code theautismdad22 for 10% off. #ad RESOURCES Gateway Maryland: gatewaymaryland.org Rob's full Mightier review: theautismdad.com/mightier-review More Seen and Heard episodes: listen.theautismdad.com Find Rob at theautismdad.com, and on Facebook, Instagram, TikTok, and YouTube at The Autism Dad.

Welcome to The Autism Dad Podcast Network, your one-stop destination for invaluable insights into autism and special needs parenting. Our network features two dedicated podcasts: The Autism Dad Podcast and The Autism Dad Ohio Podcast. Each podcast aims to provide a candid, informative, and supportive space for parents, caregivers, and anyone interested in understanding the complexities and joys of raising children with special needs. Whether you're searching for actionable advice, expert interviews, or simply a community that gets it, The Autism Dad Podcast Network is here to support your journey. Tune in for an authentic look into the challenges and triumphs faced by families like yours. Don't navigate this path alone; join us and become part of a network focused on hope, education, and perseverance.

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