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  • CVI, Motherhood, and the Power of Story: A Conversation with Rachel Worden
    11/21/25

    CVI, Motherhood, and the Power of Story: A Conversation with Rachel Worden

    In this episode, Sarah talks with Rachel Worden, founder of Little Dandelion Press and mom to Moira, about the journey that reshaped the way she sees childhood, vision, and learning. Rachel shares how her daughter’s CVI and rare genetic condition set her on a path she never expected, from searching for answers to creating books that finally made sense for her child. Rachel opens up about the early days of Moira’s diagnosis, the fear of the unknown, and the moment she realized that most children’s books were not designed with kids like her daughter in mind. That realization pushed her to create her own CVI friendly materials, which later grew into Little Dandelion Press, a publishing imprint dedicated to accessibility, inclusion, and joyful literacy for all learners. Her perspective as a writer, designer, and advocate gives families a grounded, real world look at what CVI can feel like at home and how small changes in design can open the door to connection and learning. She talks about the emotional weight parents carry during diagnosis, the hope that comes with understanding, and the joy she finds in creating stories that meet children where they are. If you want to explore CVI supportive books and resources, visit littledandelionpress.com. Whether you are a caregiver, educator, or parent beginning your own CVI journey, Rachel’s story offers comfort, clarity, and a reminder that every child deserves to be included in the magic of story.

  • Caregiver Connection with Paige Siemers
    11/14/25

    Caregiver Connection with Paige Siemers

    In this episode, Sarah sits down with her mentor of more than ten years, Paige Siemers. Their conversation is honest, emotional, and full of the moments that only two moms raising children with disabilities can understand. They talk about how their mentorship began, what it has grown into, and why this kind of support matters so much. Paige opens up about her own journey as a mom, the grief and growth she has walked through, and the beauty she has found along the way. Sarah shares how Paige helped her move from surviving to actually liking her life again, and how their friendship shaped the way she now supports other caregivers. They cover the early years, the medical chaos, the guilt, the humor that keeps you going, and the deep connection that forms when two people walk a similar path. They also talk about the heart behind the new Caregiver Connection program and what makes this kind of one-on-one support different from what families get online. If you are a caregiver, a mentor, or someone who loves a family in the disability community, this conversation will meet you right where you are.

  • What is the Anat Baniel Method?! With Carol Keefe
    10/23/25

    What is the Anat Baniel Method?! With Carol Keefe

    In this episode, we dive into the Anat Baniel Method® with Carol Keefe, a certified NeuroMovement® practitioner who helps children and adults tap into the brain’s ability to change through gentle, science-backed movement.

    Carol shares how she discovered this powerful method, the incredible progress she’s seen in children with special needs, and how parents can start applying neuroplasticity exercises at home to help their kids thrive.

    💡 Learn how the brain can rewire itself, how small movements can lead to big transformations, and why awareness is key to lasting change.

    👉 Explore the Parent Child 5-Day Workshop for Children with Special Needs mentioned in this episode:
    https://www.anatbanielmethod.com/parents-childrens-5-day-workshop

    🔗 Learn more about the Anat Baniel Method:
    https://www.anatbanielmethod.com

    #NeuroMovement #AnatBanielMethod #Neuroplasticity #Parenting #SpecialNeeds #BrainHealth #LiveWellLoveStrongPodcast

  • Food is first! With Julie Bombacino
    • 10/17/25

    Food is first! With Julie Bombacino

    The full episode is here! 🎧

    When her son AJ was placed on a feeding tube, Julie Bombacino refused to settle for formula alone. Her search for a better way to nourish her child led to Real Food Blends, a company that changed feeding tube care for families everywhere.

    In this episode of Live Well, Love Strong, Sarah and Julie talk about motherhood, perseverance, and why food should always come first.

    Listen now on Spotify, Apple Podcasts, or YouTube.

    #LiveWellLoveStrong #FoodIsFirst #RealFoodBlends #FeedingTubeAwareness #SpecialNeedsParenting #MomStrong #ParentingJourney #NutritionMatters

  • Healthy Habits for the WIN! With Allie Mazzapica and Catherine Slaydon
    • 10/10/25

    Healthy Habits for the WIN! With Allie Mazzapica and Catherine Slaydon

    In this inspiring episode, Sarah sits down with health coaches and wellness leaders Allie Mazzapica and Catherine Slaydon to talk about what it really takes to create lasting healthy habits. From losing over 40 to 50 pounds to keeping the weight off for years, these women share their stories of transformation, discipline, and grace.

    Allie reveals the simple systems that keep her consistent, from planning workouts ahead of time to building accountability into her daily routine, while Catherine opens up about starting her journey during the holidays and proving that there is never a wrong time to make a change. Together, they unpack the mindset, structure, and self-compassion that make healthy living sustainable long term.

    Tune in to learn practical strategies for staying on track when life gets chaotic, how to rebuild momentum after setbacks, and how to create habits that truly stick.

  • Embodiment, Yoga, and Thriving Beyond Survival
    10/3/25

    Embodiment, Yoga, and Thriving Beyond Survival

    In this episode of Live Well, Love Strong, Sarah sits down with friend and fellow mama Kendall Knight, for a heartfelt conversation about embodiment, yoga, and creating space to truly come home to yourself. Kendall shares her journey into yoga, why she founded Home Yoga, and how slowing down allowed her to reconnect with her body and spirit. Together, Sarah and Kendall reflect on motherhood, shifting goals over the years, and the importance of building supportive communities for women and families.

    This conversation is filled with wisdom on thriving rather than just surviving, and practical encouragement to listen to what your body is really asking for.

    Connect with Kendall on Facebook:
    https://www.facebook.com/profile.php?id=100049127598007&mibextid=wwXIfr&rdid=lFuMad2BZBl1smm7&share_url=https%3A%2F%2Fwww.facebook.com%2Fshare%2F19XykCYoHE%2F%3Fmibextid%3DwwXIfr

  • Welcome to Holland
    • 9/26/25

    Welcome to Holland

    In this episode, Sarah is joined by her friend Candace to reflect on the poem Welcome to Holland and the ways it speaks to the journey of parenting children with disabilities. Together, they share personal insights, moments of honesty, and encouragement for families learning to embrace a path that looks different than expected. Through their conversation, Sarah and Candace show how this poem continues to bring perspective, comfort, and hope to those navigating their own version of “Holland.”

  • A Big Deep Breath with Dr. Sarat Susarla
    9/19/25

    A Big Deep Breath with Dr. Sarat Susarla

    In this episode of Live Well. Love Strong., Sarah sits down with Dr. Sarat Susarla, a pediatric pulmonologist and sleep medicine specialist at Houston Specialty Clinic. For more than a decade, Dr. Susarla has cared for children like Sarah’s daughter, Mary Elizabeth, with both medical expertise and uncommon compassion.

    They talk about his journey into pediatric pulmonology, the importance of communication and trust between doctors and families, and how a physician’s presence can feel like “a big, deep breath” during stressful moments. Dr. Susarla also shares insights into caring for children with disabilities and medical complexities, offering encouragement and practical wisdom for parents navigating these challenges.

    If you’re a parent, caregiver, or advocate looking for support, this conversation is both educational and uplifting.

    👉 Learn more about Dr. Susarla and his work:
    🌐 www.houstonspecialtyclinic.com
    📘 facebook.com/houston.pediatric.neurology.pulmonary.sleep

  • Everything No One Tells You with Kelley Coleman
    9/12/25

    Everything No One Tells You with Kelley Coleman

    In this episode of the Live Well, Love Strong podcast, Sarah welcomes back Kelley Coleman, author of Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Essential Systems, Services, and Supports. Kelley shares her journey from working in Hollywood to navigating life as a mom raising children, including a son with disabilities. Together, Sarah and Kelley explore the challenges of caregiving, the moments of humor and resilience that carry families forward, and the power of creating the “manual” so many parents wish they had.

    📖 Learn more about Kelley and her book: https://www.kelleycoleman.com/books

    📲 Follow on Instagram: https://instagram.com/livewelllovestrong

  • Running for Inclusion: The Rossiter Family & Ainsley’s Angels
    • 9/5/25

    Running for Inclusion: The Rossiter Family & Ainsley’s Angels

    In this week’s episode of the Live Well, Love Strong podcast, Sarah welcomes Lori and Rooster Rossiter, proud parents and leaders with Ainsley’s Angels of America. Together, they share the powerful story of their daughter Ainsley, how her life and joy inspired a nationwide movement, and the ways families and communities can experience true inclusion through running.

    The Rossiters open up about Ainsley’s journey, the challenges and triumphs along the way, and how Ainsley’s Angels continues to impact lives across the country. From the first 5K to full marathons, they reveal how running became a pathway to belonging and how inclusion transforms both riders and runners alike.

    👟 Learn more about Ainsley’s Angels: ainsleysangels.org
    ✨ Sign up for the Twilight 5K: runsignup.com/Race/TX/Tomball/AinsleysAngelsTwilight5K

  • Mixing Things Up | with Kelley Coleman
    • 8/28/25

    Mixing Things Up | with Kelley Coleman

    Kelley Coleman brings humor, honesty, and hard-won wisdom to the conversation. A former feature film development executive, Kelley is now an author and advocate for parent caregivers and individuals with disabilities. Her book Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Essential Systems, Services, and Supports draws on over a decade of parenting experience and advocacy.

    In this episode, Kelley opens up about her journey, why she believes parents deserve more support from the very beginning, and how “mixing things up” can make the caregiving path clearer and more empowering.

    📌 Connect with Kelley:
    Instagram: @hellokellycoleman
    Facebook: Kelley Coleman
    Website: kellycoleman.com

  • Better at Belonging with Paige Siemers
    • 8/22/25

    Better at Belonging with Paige Siemers

    In this episode of Live Well, Love Strong, Sarah welcomes Paige Siemers, a wife, mom, counselor in training, and former teacher with a heart for serving the disability community. As the parent of a child with a disability, Paige shares openly about both the overwhelming challenges and the beauty of the caregiving journey. After 27 years in education, she now focuses on helping families build emotional resilience, break cycles of burnout, and rediscover joy. Rooted in her faith, Paige believes that spiritual hope is just as vital as practical support. Together, Sarah and Paige dive into belonging, community, and what it means to walk faithfully in the sacred work of caregiving.

  • Special Needs Divorce: Advocacy, Strategy, and Hope with Mary Ann Hughes
    • 8/15/25

    Special Needs Divorce: Advocacy, Strategy, and Hope with Mary Ann Hughes

    In this episode of Live Well Love Strong, Sarah Washington sits down with Mary Ann Hughes, certified special needs divorce coach, mediator, parenting coordinator, and founder of Special Family Transitions. Drawing from her own experience as a mother to two sons on the autism spectrum, Mary Ann shares how an unexpected divorce led her to create a service dedicated to helping parents navigate the overwhelming complexities of divorce involving children with disabilities.

    With divorce rates reported as high as 80–87% among families raising a child with special needs, Mary Ann’s mission is to help parents move from the emotion of divorce to the business of divorce, while ensuring their child’s unique needs remain at the forefront. She offers practical strategies on where to start, how to prepare before seeing an attorney, and why organized advocacy is key for both legal and emotional success.

    About Mary Ann Hughes:
    Mary Ann is a Certified Divorce Coach, Certified Special Needs Divorce Coach, Certified Divorce Specialist, Pre-Mediation Divorce Coach, Mosten-Guthrie Disability-Informed Professional, and graduate of the LoneStar LEND Leadership Education in Autism & Neurodevelopmental Disabilities program. She is also trained in Family and Divorce Mediation, Parenting Coordination, Arbitration, and Neurolinguistic Programming.

    She serves in leadership roles in the Special Needs Chapter of the National Association of Divorce Professionals, Texas Association of Mediators, and Association for Conflict Resolution Houston Chapter, and is a trainer in Divorce Coach and Mediation programs. Mary Ann is also a contributing author to the bestselling book The Other Side of Divorce: Breakups That Lead to Breakthroughs.

    💻 Learn more at: specialfamilytransitions.com
    📌 Follow on Facebook: Special Family Transitions
    📷 Instagram: @specialfamilytransitions

  • Hyperbaric Oxygen Therapy (HBOT) and Idling Neurons with Dr. Paul Harch
    • 8/8/25

    Hyperbaric Oxygen Therapy (HBOT) and Idling Neurons with Dr. Paul Harch

    In this episode of Live Well Love Strong, we sit down with Dr. Paul Harch, a leading expert in Hyperbaric Oxygen Therapy (HBOT), to explore how this life-changing treatment is giving hope to families facing neurological disorders, traumatic brain injuries, autism, and more.

    Dr. Harch explains the concept of idling neurons, which are brain cells that are alive but not functioning, and how HBOT can help bring them back online, leading to remarkable improvements in cognition, vision, and quality of life. You will also hear my personal story of watching joy and life return to my daughter, Mary Elizabeth, through this therapy, one day at a time.

    We talk about the emotional side of seeking treatment, the perseverance it takes to advocate for our loved ones, and why raising awareness about HBOT matters so much.

    If you are a parent, caregiver, or advocate, this episode is here to offer information, encouragement, and community.

    🔗 Learn more about Dr. Paul Harch: https://hbot.com/dr-paul-harch/
    🔗 Explore HBOT treatment resources: https://treatnow.org
    🔗 Read the research on HBOT in neurological disorders:
    https://www.frontiersin.org/research-topics/41116/review-of-hyperbaric-therapy-hyperbaric-oxygen-therapy-in-the-treatment-of-neurological-disorders-according-to-dose-of-pressure-and-hyperoxia/magazine

  • Services dogs, safety, elopement, and Taylor Swift
    • 8/1/25

    Services dogs, safety, elopement, and Taylor Swift

    Allison Hill is a disability advocate, writer, and founder of Harvesting Hope Acres, a nonprofit farm-in-the-making dedicated to creating meaningful employment and community for individuals with disabilities. She holds a master’s degree in special education and elementary education and has served for years in both volunteer and professional roles in disability ministry. Allison published a book called Jacob's Special Power and has contributed to Autism Speaks, Autism Parenting Magazine, and her blog Jacob’s Journey Through Autism, sharing stories from her family’s journey with autism. She’s been married for 17 years to her best friend, Charles, and together they’re raising three wonderful kids. Their oldest just graduated from Texas A&M, their middle son keeps everyone laughing with his smarts and wit, and their youngest, Jacob, is a joy-filled teen with level 3 autism who continues to inspire their mission every day.

    Website for finding a service dog is assistancedogsinternational.org

    Her farm is harvestinghopeacres.com

    Blog: jacobsjourneythroughautism.blogspot.com

  • Lisa Graham-Garza
    • 7/29/25

    Lisa Graham-Garza

    I had the privilege of speaking with Dr. Lisa Graham-Garza, a remarkable mother and advocate, for my podcast recently. Lisa's journey as a mother to Tyler, an adult son with autism, is nothing short of inspiring. We delved into the complexities of special needs parenting, particularly the constant demands of therapies and the relentless race to “heal.” But, perhaps what struck me most during our conversation was Lisa's perspective on the importance of community. She shared her belief that every parent, especially those raising children with extra needs, needs a village—a network of support, education, and understanding. Reflecting on her own experience, she spoke about how fortunate she was to have had a strong community around her when Tyler was younger. This support was instrumental in her ability to keep going, and it made all the difference in their lives. Lisa stressed that everyone deserves that same level of community and access to resources. It was clear to me that her advocacy work comes from a place of deep empathy, as she genuinely wants every family to have the same opportunities for connection and support. DR. Graham-Garza also shared the story of how she founded Autism Rescue Angels, an organization dedicated to helping families navigate the often overwhelming world of autism. Her tireless effort to support others while maintaining a healthy mindset was awe-inspiring. What stood out even more was her belief that if we want community, we have to build it ourselves. Lisa emphasized that we can't wait for someone else to provide the solutions we need; we have to take action and create the change we seek. Her words resonated deeply with me, and I left the conversation feeling more motivated than ever to contribute to creating stronger, more inclusive communities for families like hers. Her resilience and unwavering commitment to both her family and the broader autism community were truly humbling.

    Autismrescueangels.org

  • A Straight Path is an Accessible Path with Cindy Mood
    • 7/29/25

    A Straight Path is an Accessible Path with Cindy Mood

    Speaking with the wonderful Cindy Mood, a Pastor and fellow Mama of a disabled kiddo as we dive into God and all the things.