Moms Like Me Podcast by SupportNow
We dive into the messy middle of life's major moments and learn how everyday people make it through. Jordan Arogeti unpacks the struggles and successes during parenthood, hospitalizations, major diagnosis, loss, and more.
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The Weight No One Sees: Vanessa Weilnhammer on Medical Motherhood, Marriage, and the Unknown
04/23/2026
The Weight No One Sees: Vanessa Weilnhammer on Medical Motherhood, Marriage, and the Unknown
What happens when your child is medically complex, deeply loved, and still undiagnosed? In this raw and deeply moving episode of Moms Like Me, Vanessa Weilnhammer shares the reality of raising her daughter Camila through hospital stays, constant caregiving, unanswered medical questions, and the emotional weight that never fully turns off. Vanessa opens up about grief, isolation, marriage under pressure, the myth of “self-care” in survival mode, and the tension of holding both joy and heartbreak at the same time. Her powerful “island and waves” analogy gives voice to what so many medical moms feel but rarely say out loud. This is an honest, validating conversation for parents, caregivers, and anyone wanting to better understand the hidden weight families like Vanessa’s carry every day.
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She Thought It Was “Just Sleep Issues” — Then 3 Kids and Mom Were Diagnosed With Autism
04/21/2026
She Thought It Was “Just Sleep Issues” — Then 3 Kids and Mom Were Diagnosed With Autism
What happens when years of unanswered questions finally turn into life-changing clarity? In this powerful episode, Alicia Trautwein shares her family’s journey through autism diagnosis — from early warning signs that were missed, to raising three neurodivergent children, to eventually realizing she was autistic too. Her story is honest, emotional, and incredibly encouraging for parents who may be wondering if something deeper is going on with their child. Alicia opens up about the grief, relief, and hard-won perspective that came with finally getting answers. She talks about how delayed diagnoses affected her older children, why early intervention can make such a difference, what autism can look like in girls and women, and how her nonprofit, The Mom Kind, now helps other families feel less alone. This is a must-listen conversation for parents navigating autism, advocating in schools, or trying to replace fear with understanding.
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Still in the PICU: Austyn Morrin on Covey’s Fight, Mom Guilt, and Finding Strength
04/16/2026
Still in the PICU: Austyn Morrin on Covey’s Fight, Mom Guilt, and Finding Strength
What does it look like to keep going when your baby has spent months in the hospital and your family is living between the PICU and home? In this powerful episode of Moms Like Me, Austyn Morrin shares her son Covey’s journey through a prenatal Down syndrome diagnosis, heart complications, cardiac arrest, ECMO, a trach, open-heart surgery, and the long road of recovery that still is not over. With incredible honesty, Austyn opens up about balancing life between a critically ill baby and her older daughter, the reality of mom guilt, and the simple survival habits that help her keep moving forward. This is a deeply moving conversation about resilience, love, and what support really looks like in the hardest seasons of motherhood.
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Her Daughter’s Life Depends on a Trach: Adrianna Stallard on Faith, Fear & Fighting for Abigail
04/14/2026
Her Daughter’s Life Depends on a Trach: Adrianna Stallard on Faith, Fear & Fighting for Abigail
What do you do when your child’s life depends on a single medical device? In this deeply moving episode of Moms Like Me, Adrianna Stallard shares the raw, real story of her daughter Abigail’s medically complex journey — from a long NICU stay and multiple diagnoses to the terrifying reality that Abigail’s airway is now fully collapsed and major reconstruction surgery lies ahead. Adrianna opens up about the trauma of watching her daughter code, the emotional toll this journey has taken on her family, how writing became a lifeline, and why faith and community have carried them through the darkest moments. She also shares what it means to fight for a “normal” childhood for Abigail in the middle of extraordinary medical challenges. This episode is a powerful reminder that even in fear, uncertainty, and exhaustion, hope can still take root. In this episode, you’ll hear: Abigail’s diagnosis and complex medical journey What life looks like caring for a child with a trach and feeding tube The trauma, grief, and mental load of medically complex parenting How Adrianna and her husband support both Abigail and her older brother Why faith, writing, and community have become anchors in the storm The urgent road ahead as their family prepares for high-risk surgery in Boston If this story moves you, be sure to like, comment, and subscribe — and share this episode with someone who needs encouragement today.
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Her Son Lived 16 Days in the NICU—Now She’s Helping Other Families Stay Together | Jenna Laws
03/31/2026
Her Son Lived 16 Days in the NICU—Now She’s Helping Other Families Stay Together | Jenna Laws
What happens when the worst day of your life becomes the beginning of someone else’s hope? In this powerful episode of Moms Like Me, Jenna Laws shares the story of her son Benny, whose unexpected diagnosis led to a 16-day NICU journey that changed her family forever. Jenna opens up about the shock of late-pregnancy complications, the heartbreak of difficult medical decisions, and the sacred memories they made with Benny during his short but deeply meaningful life. Out of that pain, Jenna and her husband created 16 Days, a nonprofit that helps NICU families stay close to their babies when financial barriers would otherwise keep them apart. This is a moving conversation about grief, motherhood, advocacy, and turning unimaginable loss into lasting purpose. If you’ve ever experienced the NICU, loved someone who has, or want to hear a story of heartbreak transformed into hope, this episode is for you.
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Her Dad Went From Ironman Athlete to Needing a Lung Transplant in 2 Years | Megan Holmes
03/24/2026
Her Dad Went From Ironman Athlete to Needing a Lung Transplant in 2 Years | Megan Holmes
His lungs went from 85% capacity to 16%. He was walking 4-6 miles a day, running Ironman triathlons — and then he couldn't breathe. In this episode, Megan Holmes shares the deeply personal story of supporting her parents through her father's sudden pulmonary fibrosis diagnosis and eventual double lung transplant. From the 8-hour overnight surgery to sitting under fluorescent lights in the waiting room at 1 AM with her mom, Megan opens up about what it really looks like when the sandwich generation steps into the caregiving role. What you'll learn in this episode: Why you should TELL your parents how you'll help instead of asking permission How to prevent caregiver burnout by being the "second shift" for the primary caregiver The emotional weight of watching your invincible parent become vulnerable Practical ways to support aging parents through major medical events (managing communication, attending medication meetings, giving your parent permission to rest) How generational patterns of caregiving get passed down — and why that's a gift Megan's powerful reminder: caring for your parents isn't a burden. It's a privilege. And if you wait for them to ask for help, you'll be waiting forever.
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From Caregiver Burnout to Hope: Jess Ronne’s Powerful Story of Grief, Disability & Healing
03/19/2026
From Caregiver Burnout to Hope: Jess Ronne’s Powerful Story of Grief, Disability & Healing
What happens when life asks more of you than you ever thought you could carry? In this powerful episode of The Moms Like Me Podcast, Jess Ronne shares her extraordinary journey through special needs parenting, widowhood, caregiving burnout, trauma, and healing. From learning her son Lucas had suffered a stroke in utero, to losing her first husband to brain cancer, to raising eight children and eventually creating a better long-term future for her son, Jess offers a raw, honest, and deeply hopeful look at what life can really feel like behind the scenes for caregiving families. This conversation dives into the realities many families live every day but few people truly understand: profound disability, aggression, exhaustion, grief that layers over decades, the lack of practical support for caregivers, and the courage it takes to rethink what “loving your child well” can look like. Jess also shares how The Lucas Project was born, why she helped create new resources when none existed, and what healing has looked like for her in this new season of life. If you’re a parent, caregiver, medical mom, or someone who wants to better understand the hidden weight families carry, this episode is full of truth, compassion, and hard-won wisdom.
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They Said Her Son Would Never Walk or Talk...Now He’s Earning His PhD | Laura Joslin
03/17/2026
They Said Her Son Would Never Walk or Talk...Now He’s Earning His PhD | Laura Joslin
What do you do when doctors tell you your child may never walk, talk, or live beyond the limits they’ve predicted? In this deeply inspiring episode of Moms Like Me, Laura Joslin shares her extraordinary journey as a medical mom raising two sons with spastic quadriplegic cerebral palsy. From the fear and heartbreak of a devastating early diagnosis to watching one son prepare for his PhD and the other pursue his own meaningful path, Laura’s story is a powerful reminder that a diagnosis does not define a child’s future. Laura opens up about the faith that carried her, the fight it took to advocate for her children, and why parents must never let others under-potentialize what their child can become. She also shares how her family’s journey led her to create Ability Plus Therapy and No Limits Academy—resources designed to help other families access the tools, education, and support she wishes she’d had from the beginning. This conversation is full of hope, hard-earned wisdom, and practical encouragement for any parent navigating disability, special needs, or the overwhelming early days of a medical journey.
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How One Mom Helped Change Cancer Treatment for Kids | Diana Jenner’s Story
03/10/2026
How One Mom Helped Change Cancer Treatment for Kids | Diana Jenner’s Story
What happens when a mother’s instincts, relentless advocacy, and a breakthrough in precision medicine collide? In this powerful episode of Moms Like Me, Jordan Arogeti sits down with Diana Jenner... patient advocate at First Ascent Biomedical and mom to Logan, a little boy who battled leukemia not once, but twice. Diana shares the emotional reality of hearing her son’s cancer had returned, the fear of relapse, and the moment an innovative test helped doctors identify a better treatment path. The result was remarkable: Logan went into remission in just 33 days instead of 150.   This conversation is full of hope, hard-won wisdom, and practical encouragement for families walking through unimaginable medical battles. Diana opens up about trusting your gut, asking hard questions, finding strength in community, and turning pain into purpose as she now helps other families navigate cancer care.   If you care about stories of resilience, motherhood, advocacy, and life-changing medical innovation, this is an episode you won’t want to miss.
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Life After a Near-Drowning: Meagan Chisholm's Story
03/05/2026
Life After a Near-Drowning: Meagan Chisholm's Story
Support Registry for Levi - What began as a simple family evening during the COVID lockdown turned into every parent’s worst nightmare. In this powerful episode of the Moms Like Me Podcast, Meagan Chisholm shares the unimaginable moment when her 22-month-old twins were found under a pool cover—and how that single night changed her family forever. One twin, Lainey, made a miraculous recovery. Her brother Levi survived but now lives with severe medical needs that have reshaped their entire world. Meagan opens up about the trauma of that night, the emotional toll of becoming a full-time caregiver, and the hidden mental load carried by medical moms. She speaks honestly about grief, faith, community support, and the ongoing fight to give her children the best life possible.  Through heartbreak and hope, Meagan also reveals how her family turned pain into purpose by creating the Light for Levi Foundation, helping other children with brain injuries receive life-changing therapies. This episode is a raw and inspiring look at motherhood, resilience, and the incredible power of community when life takes an unexpected turn. In this episode you’ll hear: • The terrifying accident that changed Meagan’s family forever • What it’s really like to be a “medical mom” caring for multiple children with complex needs • The emotional impact of grief when a healthy child suddenly loses abilities • How community support helped carry her family through the darkest moments • Why asking for help can be one of the hardest things for parents • How the Light for Levi Foundation is now helping other families facing similar battles If this story moves you, consider sharing it—because someone else might need to hear that they’re not alone.
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From “Perfect Pregnancy” to 12 Surgeries: Bethany Gurbal’s Fight for Her Son’s Life
03/03/2026
From “Perfect Pregnancy” to 12 Surgeries: Bethany Gurbal’s Fight for Her Son’s Life
What happens when a healthy pregnancy suddenly turns into a medical nightmare no one saw coming? In this powerful episode of the Moms Like Me podcast, host Jordan Arogeti sits down with Bethany Gurbal to share the emotional, raw, and ultimately hope-filled story of her son John. After a routine pregnancy filled with reassuring weekly ultrasounds, Bethany and her husband were blindsided. Born at 35½ weeks, John initially seemed small but stable—until doctors discovered a rare condition called piriform aperture stenosis, a severe nasal obstruction that made it nearly impossible for him to breathe. What followed was months in and out of the NICU and PICU, feeding tubes, life-threatening respiratory distress, and more than a dozen surgeries in his first year of life . Bethany shares what it was like to go from hearing “everything looks perfect” at every appointment  to facing the possibility of devastating brain complications and even losing her newborn.. She opens up about the financial stress of losing health insurance late in pregnancy, the trauma of watching her baby struggle to breathe, and the emotional toll of balancing hospital life with caring for a toddler at home. But this episode isn’t only about medical crisis. It’s about marriage strengthened under pressure. It’s about community showing up in extraordinary ways. And it’s about the courage it takes to ask for help—especially when you’re used to doing it all yourself. Bethany also shares how documenting John’s journey became both a lifeline and a legacy—helping her process the trauma, align with her husband, and allow others to step in and support their family. If you’re a parent navigating uncertainty, a mom who feels like she has to hold everything together, or someone walking through a hard season you never planned for—this conversation will remind you that you are not alone. This is a story of fear, faith, resilience, and the quiet strength it takes to say: “I can’t do this alone.” Subscribe for more honest conversations with moms facing life’s unexpected chapters.
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You Don’t Choose to Be a Medical Mom… But You Can Choose How You Rise
02/26/2026
You Don’t Choose to Be a Medical Mom… But You Can Choose How You Rise
In this powerful episode of Moms Like Me, Jordan sits down with entrepreneur, podcast host, and mom of four, Alana Kayfetz, for a raw and unforgettable conversation about identity, grief, ambition, and resilience. Alana shares the life-altering moment when her son Henry was diagnosed with an ultra-rare genetic condition, Myhre Syndrome, after undergoing open-heart surgery as a baby during the height of COVID. What began as a routine checkup quickly spiraled into hospital stays, surgeries, and a diagnosis that would permanently change their family’s trajectory. But this story isn’t just about survival. - It’s about becoming an “alpha mom” when life demands it. - It’s about saying “I feel unsafe” and advocating without apology. - It’s about turning unimaginable pain into purpose—raising over $265,000 for a hospital caregiver lounge while still sitting bedside. Alana opens up about the moment her son flatlined. The PTSD that followed. The six months she disappeared from social media. And how rebuilding her life meant redefining success, motherhood, and ambition. If you’re a medical mom, a caregiver, an entrepreneur, or anyone navigating the unpredictable reality of life, this episode will meet you exactly where you are: and remind you that you are stronger than you know. ✨ Topics We Cover: • What it really means to become a “medical mom” • Grief responses: shutting down vs. over-functioning • The power of community in crisis • The “Dinner Table Test” and redefining priorities • Building a business while living in uncertainty • Finding joy again after trauma This is an honest, hopeful conversation about living boldly...even when nothing feels certain. Subscribe for more real conversations with women who are doing hard things with heart.
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She Dropped Him at Daycare...10 Days Later Shelby Cannon's Son Was Fighting for His Life
02/11/2026
She Dropped Him at Daycare...10 Days Later Shelby Cannon's Son Was Fighting for His Life
What happens when a routine daycare drop-off turns into every parent’s worst nightmare? In this powerful episode of Moms Like Me Podcast, host Jordan Arogeti sits down with Shelby Cannon, a mom of three whose world changed forever after her infant son, Benny, suffered a devastating hypoxic brain injury while in daycare. Shelby walks us through the moment she received the call, the frantic race to the hospital, and the days doctors warned her family that Benny might not survive—or might never breathe on his own again. She shares what it’s like to grieve the life you thought your child would have while learning how to care for a child with cerebral palsy, dystonia, cortical visual impairment, and complex medical needs. This conversation goes far beyond tragedy. Shelby opens up about: • Navigating marriage under unimaginable pressure • Parenting siblings through trauma and uncertainty • Facing a legal system that didn’t feel like justice • Finding purpose in advocacy, including the push for “Benny’s Law” • Learning how to keep going when “strong” feels like the only option If you’re a parent, caregiver, or someone walking through an unexpected life detour, this episode is raw, honest, and deeply human—and a reminder that resilience doesn’t mean pretending it doesn’t hurt.
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My Husband Suffered a Traumatic Brain Injury: Here’s How Our Family Survived
02/04/2026
My Husband Suffered a Traumatic Brain Injury: Here’s How Our Family Survived
What happens when an ordinary Friday morning turns into every parent’s worst nightmare? In this deeply moving episode of the Moms Like Me podcast, host Jordan Arogeti sits down with Ashley Hughey to share the raw, unfiltered story behind a life-altering accident that nearly took her husband’s life—and forever changed how she views faith, family, and support. Ashley recounts the moment she received a call no spouse ever expects, the terrifying hours of uncertainty, and the long road of recovery that followed her husband’s traumatic brain injury. Along the way, she opens up about anger, guilt, parenting through crisis, and the unexpected power of community showing up in practical, tangible ways. This episode isn’t just about survival—it’s about what happens after: how trauma reshapes perspective, how asking for help becomes an act of strength, and why meaningful support goes far beyond meals and money. If you’re a parent, caregiver, or someone who wants to show up better for people in hard seasons, this conversation will stay with you long after it ends. 🎧 In this episode, you’ll hear about: • A near-fatal accident and the moments that followed • Navigating fear, anger, and uncertainty as a parent • How community support can change recovery outcomes • Why accepting help isn’t weakness—it’s necessary • A powerful reminder about life, gratitude, and wearing a helmet 👉 Don’t forget to like, subscribe, and share this episode with someone who needs encouragement today.
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Raising Hope Through the Hardest Days: A Rare Diagnosis, Resilience, and a Service Dog
12/23/2025
Raising Hope Through the Hardest Days: A Rare Diagnosis, Resilience, and a Service Dog
What happens when motherhood doesn’t look the way you imagined...but love, grit, and hope lead the way anyway? In this powerful episode of the Moms Like Me podcast, host Jordan Arogeti sits down with Brenda Marra, a mom whose life was transformed when her daughter Renna was diagnosed with the rare genetic condition Pitt Hopkins Syndrome. Brenda shares her deeply honest journey through delayed milestones, uncertainty, grief, and ultimately, profound resilience. From Renna’s first independent steps at four and a half years old, to building community through other moms, Instagram, and disability advocacy groups, Brenda offers encouragement to parents navigating unfamiliar and challenging paths. She opens up about comparison, inclusion, and the courage it takes to show up in public spaces when your child’s needs are different. The conversation also explores Brenda’s mission to bring more joy, safety, and independence into Renna’s life—including their inspiring journey to raise funds for a specially trained service dog through Four Paws for Ability. Along the way, Brenda introduces Renna’s Corner, her growing platform dedicated to sharing adaptive resources, partnerships, and hope with other families. This episode is a reminder that progress doesn’t always look typical—and that community, creativity, and compassion can change everything. ✨ In this episode, you’ll hear about: • Life with Pitt Hopkins Syndrome • Finding support beyond Google searches • Navigating comparison and public spaces as a mom • The emotional impact of developmental milestones • Why service dogs can be life-changing for children with disabilities • Building community through Renna’s Corner Whether you’re parenting a child with a disability, supporting someone who is, or simply looking for a story grounded in perseverance and love—this episode offers perspective, encouragement, and hope. https://www.instagram.com/rennascorner/ https://www.supportnow.org/renna-marra
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A Statistic of One: How Elise Tedeschi Beat Stage IV Pancreatic Cancer as a Mom of Two
12/16/2025
A Statistic of One: How Elise Tedeschi Beat Stage IV Pancreatic Cancer as a Mom of Two
What do you do when doctors tell you that you have Stage IV pancreatic cancer and young children who still need you? In this deeply moving episode of The Moms Like Me Podcast, host Jordan Arogeti sits down with Elise Tedeschi, a mom of two who defied the odds and became a 13-year survivor of one of the deadliest cancer diagnoses. Elise shares her journey from months of unexplained pain, to a life-stopping diagnosis, to becoming what her doctor called “a statistic of one.” This conversation goes far beyond cancer treatment. Elise opens up about motherhood, faith, mindset, community support, advocating for yourself in the medical system, and choosing hope when the statistics say otherwise. From raising young boys while undergoing aggressive treatment, to finding the right doctor willing to fight with her, Elise’s story is a powerful reminder that survival is not just physical: it’s emotional, spiritual, and deeply human. Whether you’re facing a serious diagnosis, supporting someone you love, or simply searching for perspective and courage, this episode offers wisdom, honesty, and real hope. ✨ In this episode, you’ll hear about: • Living with a Stage IV pancreatic cancer diagnosis • Motherhood as a driving force for survival • The power of mindset and choosing your attitude • Why finding the right doctor can change everything • Advocating for yourself through second and third opinions • How community support makes survival possible • Life, fear, and purpose after cancer 📲 Follow Elise for advocacy, encouragement, and real talk: Instagram: @stagefoursurvivor TikTok: @stagefoursurvivor Coming soon: survivorsguidetocancer.com
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Shanna Jenkins on Raising a Child With Epilepsy & Finding Strength as a Mom
12/09/2025
Shanna Jenkins on Raising a Child With Epilepsy & Finding Strength as a Mom
When Shanna Jenkins buckled her toddler into the car for a normal morning in 2011, everything changed in seconds. A sudden seizure, an emergency ambulance, and a diagnosis of epilepsy reshaped her world overnight. In this moving and deeply human episode of Moms Like Me, Shanna opens up about the early fear, the sleepless nights, the medical maze, and the constant question every parent asks: Will my child be okay? But this isn’t a story of fear, it’s a story of resilience. Today, her son Malachi is a thriving 17-year-old: marching band member, soccer player, self-taught PC builder, world traveler, and budding adult ready to take on the world. Shanna walks us through the journey from helplessness to empowerment, and how honesty, community, and faith helped her release control and raise an independent, confident young man. You’ll hear: - What those first terrifying moments felt like and how the diagnosis unfolded - How Shanna learned to balance safety with giving her son independence - The emotional weight of raising a child whose health requires constant vigilance - Why teaching kids about their diagnosis is essential for long-term confidence - How she’s preparing her graduating senior for life beyond home - Her powerful message of hope for any parent walking a similar road This episode is equal parts heart, wisdom, and inspiration: a tribute to strong kids and even stronger moms.
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Paralyzed at 23, Twin Mom at 30: Daniela Izzie on Redefining Independence & Motherhood
11/19/2025
Paralyzed at 23, Twin Mom at 30: Daniela Izzie on Redefining Independence & Motherhood
What happens when your entire life changes overnight… and you still decide to pursue the dream of motherhood? In this powerful conversation, Jordan Arogeti sits down with quadriplegic mom of twins and business owner Daniela Izzie to talk about courage, identity, and the real logistics of raising kids with a profound disability. Daniela shares how a freak spinal cord injury at 23 left her paralyzed, the years-long journey of relearning independence, and the moment she decided she did deserve to be a mom. She opens up about navigating a high-risk twin pregnancy, giving birth during the early days of COVID, and building a life where caregiving support and independence can coexist. Daniela also talks honestly about divorce, rebuilding her “infrastructure” as a solo mom, and why she teaches her daughters that disability is neutral, not something to be pitied. In this episode, you’ll hear: - How Daniela moved from “Why me?” to “I can figure this out” after her injury - The mindset shift that helped her see independence as a state of mind, not doing everything alone - What it was really like to have a high-risk twin pregnancy as a quadriplegic during the COVID shutdown - The creative division of labor she and her partner used in the baby “bootcamp” years - How she talks to her 5-year-old twins about disability, grief, and difference - What it took to rebuild her life after divorce, emotionally and practically, as a disabled mom - Why community, especially among women, is her greatest source of strength If you’ve ever questioned whether you’re “allowed” to want more for your life because of your circumstances, Daniela’s story will challenge and inspire you.
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Heartbreak to Hope: The Sigmons’ Journey Through Their Son’s Heart Transplant and Legacy of Love
10/28/2025
Heartbreak to Hope: The Sigmons’ Journey Through Their Son’s Heart Transplant and Legacy of Love
When Lyndsi and Wesley Sigmon welcomed their first child, Luke, they never imagined their world would change forever. Diagnosed with a congenital heart defect at just nine days old, Luke’s fight for life took their family from Charlotte to Boston Children’s Hospital and back again: through surgeries, setbacks, and moments of unimaginable courage. In this powerful episode of The Moms Like Me Podcast, host Jordan Arogeti sits down with the Sigmons to share their extraordinary story: a journey of faith, resilience, and the boundless power of community. They open up about the highs and lows of Luke’s six precious years, how they turned grief into purpose through the Hearts and Hope Foundation, and how their family continues to honor his joyful spirit every day. ✨ In this episode: • Luke’s miraculous early days and life-saving surgeries • How a supportive community carried them through crisis • The founding of Hearts and Hope Foundation to help other families in need • Finding purpose and healing after unimaginable loss • The beauty of remembering and speaking your child’s name If you’ve ever wondered how love can transform tragedy into hope, this episode will stay with you long after you listen. 🔗 Learn more about the Sigmons’ work at Hearts and Hope Foundation 🎧 Listen now to discover how one family’s “mess became their message” and how Luke’s light continues to shine through every act of kindness.
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Living on the Brink: Ellen Wingate on Epilepsy, Caregiving, and Empowering ‘Team Logan'
10/21/2025
Living on the Brink: Ellen Wingate on Epilepsy, Caregiving, and Empowering ‘Team Logan'
When Ellen Wingate’s son, Logan, was diagnosed at 3½ months with polymicrogyria and later Lennox-Gastaut syndrome, everything changed—jobs, routines, expectations, and definitions of success. In this powerful Moms Like Me episode, Ellen shares how her family built “Team Logan,” why seizure logging and clear data transformed doctor visits, and how faith, marriage, and community support sustain them through daily, uncontrolled epilepsy. What you’ll learn • The early signs that led to Logan’s diagnosis, and what those moments feel like for parents • How to “be the expert on your child” while partnering with medical specialists • Practical tracking tips (what to log, how often, and why details matter) • Why epilepsy is often misunderstood, and how it shapes daily life even when you can’t see it • Guardrails for caregivers: accepting help, communicating with family, and staying grounded in faith • The mission of the Logan Jet Research Foundation and ways to help families who fall through the cracks
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Turning Love Into Action: How Brittany Anderson Built Hope for Families Like Hers
10/14/2025
Turning Love Into Action: How Brittany Anderson Built Hope for Families Like Hers
When nurse and mom Brittany Anderson learned her son Bennett had cerebral palsy, her world changed overnight. What began as a journey through fear and resilience turned into a powerful mission to help other families through her nonprofit, Wolf Pups on Wheels. In this heartfelt episode, Brittany shares how her experience transformed the way she sees healthcare, motherhood, and community, and how one family’s fight can inspire a movement. 💛 Brittany Anderson’s story is one of strength, empathy, and relentless love. As a nurse and mother navigating her son’s cerebral palsy diagnosis, Brittany saw firsthand how challenging it can be to access care, resources, and equipment, even for medical professionals. Her journey led to the creation of Wolf Pups on Wheels, a nonprofit providing small grants to families for adaptive bikes, mobility tools, and therapy resources often not covered by insurance. 🌐 Learn more: https://wolfpupsonwheels.org
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Andria Parks - A Mother’s Battle, A Daughter’s Resilience, and a New Dawn in Cancer Treatment
10/08/2025
Andria Parks - A Mother’s Battle, A Daughter’s Resilience, and a New Dawn in Cancer Treatment
When Andria Parks heard the words no parent ever wants to hear: “There’s a mass” ...her world stopped. What followed was an extraordinary two-part journey of courage, faith, and science as her teenage daughter fought through not one, but two bouts of advanced cancer. In this heartfelt conversation, Andria shares how her family faced 54 weeks of chemotherapy, moments of near loss, and the miracle of recovery: twice. But her story doesn’t end there. Inspired by her daughter’s resilience and driven by a calling to make a difference, Andria joined First Ascent Biomedical, a company using AI to personalize cancer treatment and give families new hope. This episode is a moving blend of love, science, and the human spirit: a must-watch for anyone who believes in miracles powered by medicine. In this episode: • The emotional journey of a mom navigating childhood cancer — twice • How faith, family, and community carried them through • The founding story of First Ascent Biomedical and how AI is revolutionizing cancer care • A daughter’s decision to become a nurse — and the nurses who inspired her • The life-changing moment of hearing, “It’s back,” and finding strength again
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From Heartbreak to Hope: Katie Talman’s Journey Through Loss & Legacy
10/02/2025
From Heartbreak to Hope: Katie Talman’s Journey Through Loss & Legacy
What happens when the unimaginable becomes your reality? In this powerful episode of The Moms Like Me Podcast, Katie Talman opens up about her deeply personal journey through infertility, twin loss, and the devastating diagnosis of Turner Syndrome. With courage and honesty, Katie shares how she navigated grief, isolation, and the silence that so many families face when experiencing pregnancy and infant loss. But Katie’s story doesn’t end in heartbreak...she transformed her pain into purpose. Through her advocacy, the groundbreaking Everly’s Law was passed in Texas, making it the first state to require every hospital to provide Cuddle Cots, giving grieving families the priceless gift of more time with their babies. ✨ In this episode you’ll hear: - Katie’s raw story of loss and resilience. - How she found ways to honor her daughter, Everly, while holding onto hope. - The role of faith, community, and inner strength in surviving grief. - Her journey from personal tragedy to public advocacy...and creating lasting change for families nationwide. - This is a conversation about love, loss, and the incredible strength of a mother’s heart. Whether you’ve walked this road or want to better support those who have, Katie’s story will inspire and move you.
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From Pediatric Nurse to Mom on a Mission: Molly Trexler’s Story of Healing & Hope
09/25/2025
From Pediatric Nurse to Mom on a Mission: Molly Trexler’s Story of Healing & Hope
In this powerful episode of The Moms Like Me Podcast, Jordan Arogeti sits down with Molly Trexler: a pediatric nurse practitioner who has walked both sides of the hospital bed. With years of experience helping families navigate congenital heart disease, Molly’s world shifted when her own daughter faced brain surgery at just three years old. Molly opens up about: The unique role of nurse practitioners as translators and advocates for families in crisis Her daughter’s diagnosis with Chiari malformation and the life-changing lessons that came with it Why parents must trust their gut when seeking answers for their children’s health The emotional intelligence it takes to guide families through fear, grief, and hope How her personal story inspired her to create Heartstrings, a coaching program designed to help families thrive through life’s hardest chapters This episode is about resilience, faith, and the courage to let go of control while finding peace in the process. Whether you’re a parent, a caregiver, or simply someone who wants to hear a story of strength and heart, Molly’s wisdom will leave you inspired. 👉 Learn more about Molly’s work at mollytrexler.com and follow her @MollyTrexlerCoaching
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How Ivelisse Page Beat Stage 4 Cancer and Founded Believe Big
09/04/2025
How Ivelisse Page Beat Stage 4 Cancer and Founded Believe Big
When Ivelisse Page was diagnosed with stage 4 colon cancer, the very disease that claimed her father and grandmother, she faced an impossible decision. Instead of following the conventional path, she and her husband turned to prayer, research, and integrative therapies, including mistletoe treatment. Against all odds, she overcame the disease, founded Believe Big, and has since impacted nearly 2 million people worldwide with resources, hope, and groundbreaking clinical trials at Johns Hopkins. In this inspiring conversation, Ivelisse shares: Her genetic battle with Lynch syndrome and colon cancer The pivotal choice to forgo chemotherapy in favor of integrative therapies How mistletoe therapy and faith became central to her healing The creation and growth of Believe Big: helping patients and families find hope Practical advice for anyone supporting a loved one through cancer This is a story of courage, conviction, and unwavering faith: one you won’t want to miss. 👉 Learn more at believebig.org
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A Mother’s Strength: Dina Besic on Childhood Cancer, Hope & Maxwell’s Toy Box
08/28/2025
A Mother’s Strength: Dina Besic on Childhood Cancer, Hope & Maxwell’s Toy Box
When Dina Besic’s two-year-old son Max was suddenly diagnosed with leukemia, her world turned upside down. In this emotional and inspiring episode of Moms Like Me, Dina opens up about the shock, anger, and resilience it took to face the unthinkable. She shares how she and her husband leaned on each other, the power of community support, and why small gestures—from coffee drop-offs to simple texts—made all the difference. Dina also talks about founding Maxwell’s Toy Box, a nonprofit bringing comfort, toys, and joy to children battling cancer—and hope to their families. Her story is a reminder of the strength of love, the importance of support systems, and the resilience of both parents and children in the hardest of times. ✨ Don’t miss this moving conversation—you’ll come away with new insight into how to truly show up for families facing childhood cancer. 🔗 Learn more or support Maxwell’s Toy Box: maxwellstoybox.com
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From Friday Night Lights to Game Plan for Hope | Melissa Bass’s Story
08/19/2025
From Friday Night Lights to Game Plan for Hope | Melissa Bass’s Story
One Friday night changed everything for Melissa Bass and her family. When her son Trenton suffered a life-altering spinal cord injury during a high school football game, their world was turned upside down. In this heartfelt conversation, Melissa shares: The moments leading up to Trenton’s injury and the immediate aftermath How her family and community rallied in prayer and support Trenton’s incredible resilience, graduating with a mechanical engineering degree and becoming a speaker and advocate The birth of Game Plan for Hope, the nonprofit she founded to walk alongside families facing sudden, life-changing hardships Practical advice for supporters who want to help but don’t know how Melissa’s story is one of faith, resilience, and choosing hope—reminding us all that while we can’t control what happens, we can choose how we respond. 👉 Learn more about Game Plan for Hope: gameplan4hope.org
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From Corporate Climb to Purpose-Driven Living | Molly Asplin on Redefining Success
08/14/2025
From Corporate Climb to Purpose-Driven Living | Molly Asplin on Redefining Success
What happens when you spend years climbing the corporate ladder—only to realize you’re on the wrong one? In this heartfelt and energizing conversation, entrepreneur and mom of three Molly Asplin shares her journey from a high-achieving finance career to creating a life and business centered on fulfillment, intention, and personal growth. Molly opens up about: - The “nudges” that told her corporate life wasn’t her calling - Overcoming guilt and fear to pivot into entrepreneurship - Redefining success in different seasons of life, especially as a mom - The inner work required to align your strengths with your daily work - Balancing ambition with being present for her children Whether you’re a parent, a professional feeling stuck, or someone seeking a more intentional life, Molly’s story will inspire you to give yourself permission to evolve. 🎙 Listen now and start designing a life that feels as good on the inside as it looks on the outside. #MomsLikeMe #MollyAsplin #RedefiningSuccess #CareerPivot #EntrepreneurLife #WorkingMoms #IntentionalLiving #PersonalGrowth
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Love, Loss, and Fierce Resilience: Parker Wilson’s Story of Fighting for Her Family
08/12/2025
Love, Loss, and Fierce Resilience: Parker Wilson’s Story of Fighting for Her Family
When Parker Wilson’s husband Thomas was diagnosed with an ultra-rare cancer, their world turned upside down. What followed was a two-and-a-half-year journey of relentless research, late-night phone calls with doctors, and a united “Team Thomas” determined to fight for every moment. In this raw and moving conversation, Parker shares: How she and Thomas first met in a scene straight out of a movie The winding path to a diagnosis, and why second opinions matter Navigating parenthood, marriage, and caregiving in the midst of cancer treatment Honest reflections on grief just 48 days after losing her husband Why she’s determined to help other families facing rare cancers This episode is about more than loss, it’s about love that shows up, communities that hold you together, and finding purpose in the middle of unimaginable pain.
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From Perfectionist to Purposeful: Danielle Ireland’s Journey to Fulfillment and Self-Compassion
07/31/2025
From Perfectionist to Purposeful: Danielle Ireland’s Journey to Fulfillment and Self-Compassion
Danielle Ireland wears many hats—therapist, author, mom, podcaster, and former ballroom dancer—but her most transformative role has been rebuilding her relationship with herself. In this powerful episode of the Moms Like Me podcast, Danielle joins host Jordan Arogeti to unpack her journey from people-pleasing perfectionism to living with clarity, courage, and emotional awareness. 💡 What you'll take away: Why chasing external validation never fills the internal void How perfectionism is really just shame in disguise The unexpected moment that changed Danielle’s life course A simple mirror practice that can radically increase self-love Why emotional regulation in moms is just as critical as it is for kids 🎧 Whether you're in the thick of motherhood or reevaluating your own identity, this episode is full of compassionate wisdom, accessible tools, and a refreshing reminder that you don’t need to be perfect to be powerful. IG: https://www.instagram.com/dontcutyourownbangs/ Website: https://danielleireland.com/ Book: https://www.amazon.com/dp/1735155810?ref=cm_sw_r_ffobk_cso_cp_apin_dp_8Z6614TVV8SGYMW5ZX3Y_1&ref_=cm_sw_r_ffobk_cso_cp_apin_dp_8Z6614TVV8SGYMW5ZX3Y_1&social_share=cm_sw_r_ffobk_cso_cp_apin_dp_8Z6614TVV8SGYMW5ZX3Y_1&bestFormat=true&previewDoh=1
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