In this lighthearted episode, we’re talking all things summer—favorite foods, travel plans, bucket-list adventures, beach days, concerts, festivals, and the vacations we still can’t stop thinking about.

We share some of our best summer memories, talk about the sensory chaos that can come with a day at the beach, and dream about future adventures—including whether we could actually survive something like Coachella. We also check in on what summer really looks like for families, especially caregivers and anyone living somewhere that feels approximately seven inches from the sun.

It’s a fun, nostalgic, very real conversation about making the most of summer, staying connected, and finding joy wherever we can.

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In this episode, Jean and Tash sit down with Kendra Davenport, President and CEO of Easterseals, to talk about the work the organization is doing to support individuals with disabilities and their families. Kendra shares how she found her way into the nonprofit world, why advocacy and collaboration matter so much, and the personal stories that continue to drive her work. It’s a hopeful and heartfelt conversation about creating stronger support systems—and the real difference they can make for families.

IG: eastersealshq 

Linkedin: Easterseals, Kendra Davenport

https://drive.google.com/open?id=1UUHOmhQ7JclckXif11pwRTtWO60_yYSS

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In this episode, Shannon and Brittney talk about one of those feelings no one really wants to admit out loud: jealousy.

After reading a listener email about feeling jealous of families with neurotypical kids, they unpack what is often underneath it all—grief. Grief for the conversations you wish you could have, the experiences you pictured, and the version of parenting you thought you were going to get.

They also share their own experiences with acceptance, mental health, supportive friendships, and the way grief can sneak back in when you least expect it. This is an honest conversation about giving yourself grace, finding people who truly get it, and knowing that having hard feelings does not make you a bad parent.

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 In this episode, we’re joined by Erin Clarelli, a neurodiversity-affirming occupational therapist, to rethink the way we understand behavior, communication, and motor challenges in autistic and disabled children.

Erin explains why behavior is often a form of communication—especially for nonspeaking individuals—and why interpreting that behavior can feel so complicated for parents. We discuss the power of connection, narration, and slowing down long enough to understand what a child may be communicating through their body.

We also explore apraxia and the misconception that it only affects speech. Erin explains how motor-planning differences can impact the entire body, including a child’s ability to begin, stop, or complete an action—even when they understand exactly what is being asked of them.

The conversation also takes an honest look at the limitations of the insurance-driven therapy model and why progress cannot always be measured through checkboxes, compliance, or isolated skills. Erin shares how scaffolding, individualized support, parent coaching, and a more holistic approach can help children participate without placing unnecessary pressure on them.

Most importantly, we talk about empowering parents to trust what they see, ask better questions, and become active partners in their child’s care. Therapy should not be about fixing a child. It should be about understanding their needs, supporting their autonomy, and helping them feel safe and successful in their own body.

Find Erin at:

Website: https://www.sunrisetherapiesinc.com/

Instagram: https://www.instagram.com/sunrise.therapies

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In this episode of Moms Talk Autism, we’re talking about the kind of friendship that can make a hard day feel a little less impossible. After receiving a listener email from someone who wants to better support her friend raising an autistic child, we dive into what helpful support can actually look like—and why simply showing up without judgment can mean more than people realize.

We talk about navigating outings, communicating needs, building trust, and how friends can offer help without making a parent feel like a burden. We also get honest about the mental load that comes with autism parenting, from therapy decisions and packed schedules to the constant pressure to make the “right” choices for your child.

Plus, we discuss trusting your gut, finding consistency without burning everyone out, and remembering that parents deserve care too. Because supporting your child matters—but so does supporting yourself.

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Today Brittney and Tash welcome Sara Intonato, a passionate advocate for autism awareness and a mother of two. Sara shares her unique parenting journey, focusing on her experiences with her non-speaking son, Rocco, and the importance of self-care for parents. The conversation delves into the significance of community support, the impact of yoga on mental health, and the discovery of spelling as a communication method for non-speakers.

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No interviews. No heavy topics. Just moms sharing the funny, chaotic, and surprisingly relatable moments that come with raising autistic kids. From food battles to sensory adventures and everything in between, this episode is full of laughs, real-life parenting stories, and the reminder that you're never alone in this journey.

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This week, Tash is joined by special needs mom and advocate Julie Hillyard for a heartfelt conversation about parenting, perspective, and finding joy in the hard. Julie shares her family's journey raising a son with autism and Phelan-McDermid syndrome, along with the lessons she's learned about advocacy, comparison, kindness, and giving both yourself and others a little more grace. Whether you're navigating school challenges, public misunderstandings, or just a difficult season of parenting, this episode is packed with encouragement and hope.

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Have you ever felt stuck asking "Why us?" In this episode, we're having an honest conversation about victim mentality, acceptance, and the mindset shifts that have helped us navigate autism parenting. We share personal stories, talk about finding joy in the middle of hard seasons, and discuss how taking back control of the things we can control can change everything. It's real, it's relatable, and it's a conversation every autism parent needs to hear.

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Understanding autism isn't a one-size-fits-all journey. While many are exploring the spectrum, it's crucial to recognize that every child is unique. Rebecca Fontanetta, a neuropsychologist and a mom navigating the world of neurodivergence, shares her insights on the importance of individualized care. From her early experiences working with children with autism to her evolving views on interventions, her story emphasizes the need for tailored approaches in supporting families.

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In this episode, we’re getting real about boundaries (the kind we know we need but don’t always set ). We talk through our own experiences with grief, support, and how community has shifted—from in-person friendships to more online connections.

We also dive into balancing advocacy, friendships, and actually having time for ourselves. Friendships look different in every season, and finding your people—whatever that looks like—matters more than ever. Consider this your reminder that taking care of yourself isn’t optional.

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