Neuroinflammation and Autism: What Every Parent Needs to Know (Part 1) (S8E18)

Could neuroinflammation be driving your child’s symptoms? This episode will change how you think about autism and health. In this two-part series of The Autism Dad Podcast, I sit down with Dr. Theoharis Theoharides, one of the world’s leading experts in neuroimmune medicine and mast cell research. We dig deep into how inflammation in the brain—driven by overactive mast cells—can contribute to the struggles many autistic and neurodivergent kids face, including sensory issues, eczema, gut problems, chronic sinus issues, and even regression. Dr. Theo doesn’t just talk theory—he shares actionable steps and science-backed insights that have the potential to improve quality of life for families like ours. I even share some personal stories about my sons, and how this research explains things we’ve experienced for years. Whether your child is…

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Real Talk: Parenting a Child with Down Syndrome (S8E17)

Episode Summary: In this powerful and deeply human episode of The Autism Dad Podcast, I sit down with husband-and-wife team Jeremy Dyen and Dr. Mika Gupta, co-founders of Mama Bird, to explore the emotional and transformative journey of parenting a child with Down syndrome. We talk about: Navigating a life-changing diagnosis Finding purpose in unexpected places Supporting your child’s unique needs without losing yourself in the process How their personal journey led to creating brain-focused supplements for kids and families Whether you’re parenting a child with a disability or looking for inspiration from parents who truly get it, this is an episode you don’t want to miss. Topics Covered: Birth and diagnosis stories NICU experiences and emotional aftermath Early intervention and the Family Hope Center How Down syndrome changed their…

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Special Needs Financial Planning (Part 3) (S8E16)

In this powerful conclusion to our three-part Special Needs Financial Planning series, I’m joined once again by Katy Bryan, a Special Needs Financial Planner with Skylight Financial Group. In this episode, we tackle the toughest part of the journey—planning for our child’s future after we’re gone. This isn’t easy to talk about, but having a plan in place can ease a lot of the anxiety many of us carry every day. Katy and I dive into what end-of-life planning looks like for special needs families, including estate planning, guardianship, housing options, and how to prepare siblings or support systems for what’s ahead. What You’ll Learn in This Episode: Why end-of-life planning is one of the most important steps for special needs families What a Special Needs Trust is and how…

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Special Needs Financial Planning (Part 2) (S8E15)

Show Notes: Special Needs Financial Planning (Part 2) — The Autism Dad Podcast In this episode of The Autism Dad Podcast, Rob Gorski continues the special needs financial planning series with guest Katy Bryan from Skylight Financial Group. Katy specializes in helping families of children with disabilities plan for the future and shares key steps to prepare for your child’s transition to adulthood. Rob and Katy discuss why everything changes at age 18: managing assets under $2,000, understanding Social Security benefits (SSI/SSDI), and navigating Medicaid. They explore common questions around special needs trusts, guardianship, and power of attorney, and offer tips for finding a financial or estate planner with real disability expertise. Rob shares his own family’s journey—the struggles, learning curves, and how resources like vocational programs made a difference…

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Understanding Non-Speaking Autism and Apraxia (S8E14)

While my production computer is down, I’m re-releasing this powerful episode that so many parents found helpful the first time around. If you’re raising a non-speaking or minimally speaking child, or if you're trying to better understand apraxia and communication differences in autism—this conversation is for you. I’m joined again by Samantha Fox, M.A., CCC-SLP—an incredible speech-language pathologist and founder of Beyond Speech Therapy Center. Samantha specializes in working with non-speaking autistic individuals and is a certified Spelling to Communicate (S2C) practitioner. We talk openly about: What apraxia really is—and how it’s often misunderstood Why some autistic kids can understand language but still can’t speak The difference between language delays and motor-based speech challenges Why “presume competence” isn’t just a buzzword—it’s essential My son Emmett’s experience being non-speaking and how…

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Navigating Puberty With Autistic Kids (w/ Dr. Whitney Casares) (S8E13)

This episode is being re-released for Autism Awareness Month. In this powerful and important conversation, I’m joined by returning guest Dr. Whitney Casares. She’s not only a Stanford-trained pediatrician and public health expert, but she’s also an autism mom raising two differently wired kids. Together, we tackle a topic many of us try to avoid—puberty. This episode is packed with practical advice, validation, and real talk for parents raising autistic and neurodivergent children. We explore how puberty may present differently, how to support our kids through emotional and physical changes, and how to have open, shame-free conversations about boundaries, hygiene, sex, and self-care. Whether your child is verbal, non-speaking, cognitively delayed, or anywhere in between—this episode is for you. Key Topics Covered: Puberty differences in neurodivergent vs. neurotypical kids Hygiene…

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Understanding Autism in Girls with Dr. Taylor Day (S8E12)

April is Autism Awareness Month, and this episode with Dr. Tay is one of the most important conversations I’ve had. We dive into how autism shows up differently in girls—and why so many are missed or misdiagnosed. If you’re a parent, educator, or just want to better understand the nuances of autism, this one’s a must-listen. In this episode, I’m joined by Dr. Taylor Day (aka Dr. Tay), a licensed psychologist who specializes in neuroaffirming care for autistic kids—especially girls. We talk about how autism can look very different in girls compared to boys, why so many girls are misdiagnosed or missed altogether, and what parents can do to make sure their daughters get the support they need. Dr. Tay breaks down the most common signs of autism in girls,…

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Aria’s Kid-Friendly Minecraft Movie Review (S8E11)

Today’s episode is full of joy and Minecraft magic! Rob is joined by a very special guest, Aria. Aria is Kelly's 8 year old daughter with autism. Fresh off seeing the new Minecraft Movie, Aria shares her thoughts, favorite moments, and tips for parents wondering if it’s a good pick for their kids. They also dive deep into the game itself—breaking down game modes, favorite mobs, plushies, add-ons, and the endless creativity that makes Minecraft such a hit for kids and grownups alike. Whether you're a longtime Minecraft fan or just curious what the hype is about, this lighthearted conversation is guaranteed to make you smile. Aria, you're amazing, and we’re all so proud of you! 🎮 Topics Covered: Aria’s honest review of the Minecraft Movie (spoiler-light) Game modes in…

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Gavin’s Journey to Independence (S8E10)

In this special Autism Acceptance Month episode, I’m re-sharing an important and personal conversation with my oldest son, Gavin. Gavin is 25 years old, autistic, and immunocompromised. In this episode, we talk about his journey toward independent living and why he’s choosing to move into a group home. Gavin shares his thoughts, hopes, fears, and goals—including launching his own YouTube channel and building a sustainable future for himself. We discuss: What Gavin is looking for in a group home Health and hygiene concerns due to his compromised immune system The emotional challenges of touring potential homes Gavin’s budgeting process and side-hustle plans His passion for gaming and creating a relaxed, inclusive online space This is a real, unfiltered conversation about growing up, letting go, and navigating life with autism. Whether…

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Special Needs Financial Planning (Part 1) – Building the Foundation (S8E09)

Welcome to Part 1 of a powerful three-part series focused on special needs financial planning. In this episode, I’m joined by the amazing Katy Bryan, a Chartered Special Needs Consultant from Skylight Financial Group. Katy brings over 14 years of experience helping more than 250 families plan for their future. We’re breaking things down into real, understandable steps—starting with the basics. This episode focuses on the early stages of the journey—from diagnosis (or even before) to preparing for the unexpected. We talk about what parents should start thinking about when they first realize their child may need lifelong support, and how to start planning financially without being overwhelmed. What We Cover: Why financial planning matters early in the special needs journey Common challenges families face right after diagnosis How and…

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