22 episodes listed below
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Parents share their unique experiences of raising kids with special needs, disabilities, developmental delays, diseases and other challenges.
When a grocery cart needs an accessibility plan, you'll want Sarah Evans in your headphones.
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Short reviews from the PlayNext desk, based on the episodes we processed.
A grocery cart problem leads into disability, public cruelty, and the work of helping strangers see Matthew's abilities.
Donna Kirk's account of disability and parenting starts with a grocery cart that cannot keep Betty upright, then opens into a broader reflection on where access helps and where it falls short.
A candid, thoughtful conversation about disability, kindness, and the tiring complexity of being seen.
Mary Evelyn Smith brings the episode to its most useful point: kind attention can still wear on a family living with disability. In conversation with Sarah, she moves through the difficulty of choosing language around disability and the everyday reality of how adults and…
Mary Evelyn Smith's story shows how Franny's arrival reshaped her understanding of Simeon's disability and family life.
The episode centers on a family shift that unsettles what Mary Evelyn Smith thought she had learned. After preparing intensely for her son Simeon's spina bifida, she found that the birth of her daughter Franny changed her sense of what difficulty could mean.
A season finale where practical help, playdates, and an accessible home define kindness.
Kindness lands here as something concrete. Friends turn child care into a playdate for Henry, a pediatrician treats Cooper as a child before anything else, and a husband's office helps send the family toward a specialty-clinic trip with an envelope of cash.
A practical episode on feeding difficulties, picky eating, and easing mealtime stress for families.
Mealtimes sit at the center of this episode, where feeding difficulties, swallowing concerns, and everyday picky eating are treated as overlapping pressures rather than separate problems.
A warm look at a cape company turning purchases and sponsorships into support for children facing illness or disability.
Sarah Evans's conversation with Robin Rosenberger follows Tiny Superheroes, a cape company shaped around a simple act of encouragement. Rosenberger describes a model in which each purchased superhero cape funds a donated one, while families can nominate children facing illness…
A candid, practical look at keeping family adventures possible when disability reshapes everyday fun.
Families trying to keep ordinary pleasures ordinary will recognize the tension here: a hike in the Wasatch Range can mean carrying Betty, managing bright sunlight, and balancing one child's limits against everyone else's wish to stay together.
Parenthood and bodies, told one honest story at a time.
Sarah Evans introduces Bringing Up Betty as a show about special needs parenting and frames Donna Kirk's story around her son Matthew, born in 1970 with severe brain damage after an oxygen loss at birth.
Sarah Evans opens Bringing Up Betty episode 19 with uncut audio from her earlier conversation with Mary Evelyn Smith, who returns after episode 17 and talks about parenting a child with a disability.
Mary Evelyn Smith describes learning at a 20-week ultrasound that her son Simeon had spina bifida, then being sent straight to a high-risk OB and a genetic counselor.
Sarah Evans opens "The Kindest Thing...
Sarah Evans hosts Bringing Up Betty episode 14 as a rebroadcast of her Blab conversation with Don Winkleman, a speech-language pathologist and feeding therapist with 20 years of experience.
Sarah Evans interviews Robin Rosenberger on Bringing Up Betty #13, where a sewing project for Brenna and her mom's blog "Blessed by Brenna" led to Tiny Superheroes.
Bringing Up Betty #12 features Sarah Evans talking with Courtney Westlake about parenting Brenna, who was diagnosed with harlequin ichthyosis, a condition estimated at around 100 people.
A mother reflects on the unexpected journey of raising a child with special needs and introduces a story about a parent who chose to adopt a child with disabilities.
A parent reflects on how much information to share when explaining her child's disabilities to others.
A mother shares how her daughter with special needs has positively impacted her community and peers.
A mother shares how she found support through Facebook groups after her daughter's rare syndrome diagnosis.
A mother discusses an article about the positive effects of having a sibling with special needs and interviews the author about sibling relationships and parenting challenges.