Moms Like Me Podcast by SupportNow

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.

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.

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

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 

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.

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.

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.

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

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

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

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.

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

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

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

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

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 childrenWhether 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

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.

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

When Natalie Proshek’s son Jace went into cardiac arrest for a full hour at just two months old, her world turned upside down. In this powerful episode, Natalie shares the raw story of her son’s traumatic brain injury, how their family endured over 300 days in the hospital, and what it really means to support someone going through the unimaginable. Natalie brings a unique perspective as a mom, a clinical social worker, and now an advocate through Team Luke—an organization supporting brain injury survivors and their families. She opens up about ambiguous grief, over-functioning in trauma, and the small ways her community showed up when words and fixes weren’t enough. If you’ve ever wanted to know how to truly help a family in crisis—or if you are that family—this conversation will move you, equip you, and remind you that showing up matters. 🔗 Learn more about Team Luke and support groups Natalie leads: teamlukehopeforminds.org 📲 Follow Jace’s journey: @jacethebrave on Instagram #GriefSupport #BrainInjuryAwareness #CaregiverLife #TeamLuke #SupportNow

Why are so many women struggling to get pregnant, and what if there’s another way? In this empowering episode of the Moms Like Me podcast, holistic fertility expert and acupuncturist Katherine Rohland shares her deeply personal journey from misdiagnosis and medical gaslighting to healing through Chinese medicine. Katherine opens up about: - How a sports injury led her to acupuncture - Her 13-year journey with birth control masking deeper issues - Why your mindset might be your biggest fertility tool - How stress, cortisol, and “modern womanhood” impact our ability to conceive - The quiet power of tuning out social media and tuning in to your intuition - Whether you're trying to conceive or simply curious about alternative paths to wellness, Katherine’s insights will inspire you to rethink your relationship with your body, and your timeline. ✨ Connect with Katherine on Instagram: https://www.instagram.com/manhattan_medicine_woman/✨ Connect on TikTok: https://www.tiktok.com/@manhattanmedicinewoman🎧 Her podcast: https://www.youtube.com/@ThereQiGoes🌿 Upcoming fertility course: Launching August!

Katie's SupportNow Registry:https://www.supportnow.org/lewis-laczko-familyWhen Katie Lewis’s son Leo began having seizures at just six months old, her world changed overnight. In this heartfelt episode of Moms Like Me, host Jordan Arogeti talks with Katie about navigating Leo’s rare brain disorder (PMG – polymicrogyria), the decision to travel cross-country for a life-changing brain surgery, and how their family stayed connected through it all. 🎧 Katie opens up about: – Receiving a rare disease diagnosis – Leo’s seizure treatment and UCLA frontal lobectomy – The emotional toll and hidden grief of parenting a medically complex child – How she and her husband stayed strong as a team – Helping her daughters process uncertainty and fear – Reclaiming her identity after years of survival mode This episode is a raw, inspiring reminder of the strength found in motherhood, marriage, and community support. 📌 Don't forget to like, subscribe, and share this episode to support more moms navigating medical challenges. #RareDisease #MedicalMom #SeizureAwareness #MotherhoodJourney #Polymicrogyria #FamilyResilience #ParentingThroughCrisis #SupportNow #MomLifePodcast

What happens when life prepares you for something you never expected? Monica Gellinas—mom of quadruplets, caregiver, life coach, and now Executive Director of CC4C—opens up about her family’s journey through rare disease, personal transformation, and the power of listening and showing up. In this heartfelt conversation, Monica shares: 💡 What it was like to walk with her niece through a mysterious and painful illness 🌱 How she cultivated emotional resilience while raising four children as a single mom 🧡 Why listening, not fixing, is the most powerful act of support 🌳 Her practical “gratitude hacks” that help shift from anxiety to peace 👨‍👩‍👧‍👦 And how CC4C is wrapping arms around the entire family, not just the child Whether you’re supporting a loved one through crisis or navigating your own uncertainty, Monica’s story will leave you with perspective, peace, and purpose.

What happens when one child life specialist decides families deserve more than overstretched hospital staff can offer? Meet Katie Taylor (IG - https://www.instagram.com/childlifeoncall/) —CEO of Support Spot and host of Child Life On Call—who’s reimagining how hospitals and parents care for children through trauma, diagnosis, and recovery. In this powerful conversation, Katie shares: - What a child life specialist actually does (it’s not what most people think) - The real reason she started Support Spot—with her dad as co-founder! - Why redefining success as a mompreneur matters more than metrics - What hospitals and caregivers alike can learn from empowered parents - Whether you’re a caregiver, medical professional, or entrepreneur, this episode is packed with heart, wisdom, and a bold vision for what pediatric support could—and should—look like in today’s world. 👉 Watch now to hear how Katie is building tech-enabled, trauma-informed care for families—one app and one story at a time.

When Paige Bautz’s daughter Presley was diagnosed with cerebral palsy, autism, ADHD, and anxiety, life took a turn she never expected. In this raw and uplifting episode, Paige—author, empowerment coach, and mom—shares how she transformed fear into fierce advocacy. From NICU to spinal surgery, from ableism to empowerment, Paige opens up about what it really means to parent a child with disabilities. Host Jordan Arogeti sits down with Paige for a conversation about grief, grit, and growth—including the surprising power of social media, the challenges of caregiving, and the hidden ways communities can truly show up. 👣 Topics include: The moment Paige learned about cerebral palsy Processing complex diagnoses as a parent Ableism, advocacy, and finding hope in unexpected places How caregivers can ask for and receive support Building true community through SupportNow 🎧 Listen in and be reminded: everyone’s carrying something—and with the right circle, we don’t have to carry it alone. 🔗 Learn more about Paige: https://paigebautz.com📷 Follow Paige on Instagram: @paigebautz #CerebralPalsy #DisabilityAwareness #CaregiverSupport #SupportNow #MomsLikeMe

Sara Valenzula’s journey to motherhood started with heartbreak: multiple battles with cancer and a devastating NICU loss. But her story didn’t stop there. In this episode of Moms Like Me, Sara shares how she became a fierce advocate for her son Kenny — born at 25 weeks and later diagnosed with cerebral palsy and epilepsy — and how discovering the Trexo robotic gait trainer changed everything. 🎙️ You’ll hear: - How Sara defied the odds to become a mom - What it’s like parenting a child with profound disabilities - The moment she first saw her son walk using the Trexo - Real talk about the guilt, grief, and courage behind asking for help - Practical advice on funding life-changing equipment through platforms like SupportNow - If you’ve ever wondered how far a mother’s love can go — this is it. 🔗 Learn more about Trexo: https://trexorobotics.com 🔗 Explore medical grants and fundraising support: https://supportnow.org

In this episode of The Moms Like Me podcast, Jordan interviews the inspiring Katherine Wolf, who shares her powerful story of resilience, faith, and advocacy. Katherine suffered a near-fatal brainstem stroke at 26, which dramatically changed her life, leading her to become a prominent advocate for the disabilities community. She co-founded Hope Heals, a nonprofit focused on supporting families with disabilities, and discusses the importance of radically accepting life's challenges to move forward. Katherine also shares personal insights into how her marriage and family life have adapted and thrived despite her disabilities. Learn about her upcoming projects, the role of community in her journey, and the importance of dreaming new dreams despite life's setbacks. Katherine's insta: https://www.instagram.com/hopeheals/ 00:00 Introduction and Guest Overview 01:26 Katherine Wolf's Life-Altering Stroke 04:12 Journey to Acceptance and Advocacy 09:03 The Role of Community and Caregivers 18:17 Parenting and Family Dynamics 21:52 Finding Joy and Purpose in Disability 23:49 Exciting Future Endeavors 27:40 Closing Remarks and Gratitude

In this powerful episode of Moms Like Me, host Jordan Arogeti sits down with Scarlett Lewis, whose 6-year-old son Jesse was tragically killed in the Sandy Hook Elementary School shooting. But rather than spiral into despair, Scarlett made a bold decision—to lead with love. Scarlett shares: - The story of Jesse’s heroic final moments - How she found strength in his message: "Nurturing, Healing, Love" - Why focusing on prevention, not just protection, is the real answer to school safety - The incredible work of her nonprofit: The Choose Love Movement This is a story about resilience, purpose, and the power of emotional intelligence in healing communities. 👉 Learn more and support the movement: https://chooselovemovement.org #ChooseLove #ScarlettLewis #SandyHook #MomsLikeMe #SchoolSafety #EmotionalIntelligence

In this heartfelt episode of Moms Like Me, host Jordan Arogeti sits down with Ashlyn Burger—wife of MLB player Jake Burger and mom to two beautiful children, including baby Penelope, who was born with Down Syndrome. Ashlyn shares the emotional story of receiving Penelope’s diagnosis, navigating uncertainty during pregnancy, and embracing the unexpected with grace, courage, and joy. She opens up about: - The moment they found out via email - Jake’s calm and grounding reaction - Advocating for Penelope amid medical bias - Launching the Burger Family Foundation & Lucky Ranch - The power of representation in the Down Syndrome community This episode is a must-watch for parents, advocates, and anyone who believes in the beauty of every life and the strength of family. 📍 Learn more or donate: https://burgerfamilyfoundation.org

When Kristin Johnston saw a Facebook post about an old high school friend battling stage 4 colon cancer, she did something extraordinary—she volunteered to be his liver donor. Despite not speaking in over 20 years, Kristin followed a series of small nudges that led to a life-altering decision. In this deeply moving conversation, she shares how her faith, family, and fierce sense of purpose guided her through the process. 🎙️ Hosted by Jordan Arogeti on The Moms Like Me Podcast, this episode explores the power of community, faith, and what it means to show up in someone else’s darkest hour. 👩‍👧‍👦 Kristin is also a mom of three, making her decision even more remarkable. Read more at https://www.supportnow.org/the-register-family

⚠️ Trigger warning: child loss / SIDS When Martha dropped 16-week-old Everly at daycare, she never imagined the phone call that would shatter her world. In this powerful conversation, Martha shares how she and her family moved from unimaginable grief to founding Just Enduring, a nonprofit that now walks with other parents through their darkest days. 👇 Keep watching if you need: • Real-life insight on surviving the loss of a child • Practical ways to support grieving families • Inspiration to turn pain into purpose ⏱️ Chapters 00:00 Welcome & show intro 01:05 Meet Martha — mom of three from St Louis 03:12 The day everything changed (Everly’s story) 05:26 Hospital nightmare & unanswered questions 07:20 SIDS vs. suffocation ― understanding the diagnosis 09:18 What actually helps a grieving family 12:35 Telling a 3-year-old her sister died 15:48 Children’s grief: honesty, language & healing 17:55 Choosing to try again — pregnancy after loss 20:21 NICU scare & postpartum reflections 23:18 Birth of Just Enduring — mission & resources 25:10 Where to find help + closing thoughts 🔗 Links & resources 🌐 Just Enduring – immediate support & resources for bereaved parents https://www.justenduring.org 👍 Support the show • Subscribe for new episodes

CEO-mom Nicole Connell shares how battling perinatal and postpartum depression inspired her to launch a virtual maternal-care startup that’s changing the way modern moms get help. ​ Jordan welcomes entrepreneur and mother Nicole Connell—founder of Meré (“mother” in French)—for a frank conversation about mental-health gaps in pregnancy, loss, and early motherhood. Nicole recounts experiencing severe prenatal insomnia and depression, a heartbreaking miscarriage, and year-long postpartum depression while juggling work and two young daughters. Discover how those struggles sparked her mission to deliver virtual, whole-person care from pre-conception through perimenopause. They unpack: - What constitutes a perinatal mood & anxiety disorder (PMAD) and how to spot it early - The added pressure working moms face—and why accessible tele-health matters - Building a preventative “village”: pelvic-floor therapy, hormone panels, mental-health check-ins, and practical support from friends - Simple, game-changing ways loved ones can help (hint: let mom sleep!) If you’re a mom-to-be, already parenting, or supporting someone who is, this episode will leave you better equipped—and less alone—on every chapter of the journey. 👉 Subscribe for more real-life mom stories and expert insights. 👉 Explore Mere’s resources: https://www.mere-foreverychapter.com https://www.instagram.com/mere_foreverychapter/👉 Need immediate help? Call or text 988 (USA) for the Suicide & Crisis Lifeline. Chapters / Timestamps 00:00 Intro & why this episode matters 00:34 Meet Nicole Connell & maire’s “why” 02:50 First pregnancy: severe prenatal depression 04:30 Miscarriage, fear, and pregnancy after loss 06:05 Postpartum depression meets no maternity leave 08:00 PMAD red-flags & clinical definition 10:50 Are depression rates rising—or just recognized? 12:00 Working-mom realities & the case for virtual care 14:30 Preventative care: pelvic floor, labs, mental health 18:00 Building your baseline before baby arrives 21:30 How friends/family can really help 23:20 Tech-enabled villages & cultural shifts 25:14 Where to find Nicole & maire 26:10 Wrap-up & next steps

In this episode of Moms Like Me, host Jordan Arogeti sits down with writer, teacher, and mother Amy Julia Becker to explore the deeply personal journey of raising a daughter with Down Syndrome. From the moment of Penny’s birth to navigating teenage years, Amy Julia shares the grief, joy, and unexpected gifts that come with parenting a child with disabilities. She opens up about identity, community, comparison, and the life-changing power of presence. Whether you're a parent of a child with special needs, a friend walking alongside someone who is, or just looking for a raw and inspiring story of resilience and hope—this conversation is for you. 🔗 Learn more about Amy Julia Becker and her work: 🌐 https://amyjuliabecker.com 📚 A Good and Perfect Gift and To Be Made Well available now 🎧 Podcast: Reimagining the Good Life 👉 Don’t forget to subscribe for more inspiring stories from moms like you.

In this heartfelt episode, we sit down with the incredible Abigail Johnston as she shares her inspiring journey of living with stage four metastatic breast cancer. Diagnosed while tandem breastfeeding her children, Abigail details her proactive approach to her diagnosis, highlighting the importance of self-advocacy, and the power of a support network. From catching medical mistakes to creating her own 'tumor board,' Abigail’s story is one of resilience, determination, and maintaining quality of life. We delve into the emotional aspects of discussing her condition with her children and her fears and hopes moving forward. Perfect for anyone seeking inspiration, understanding, and practical advice on navigating life with a chronic illness. Don’t miss this remarkable conversation! 00:00 Introduction and Guest Welcome 00:19 Abigail's Breast Cancer Diagnosis 02:36 Navigating the Healthcare System 05:44 Living with Stage Four Cancer 15:40 Advocacy and Longevity 24:53 Communicating with Family 28:06 Finding Purpose and Fulfillment 32:16 Conclusion and Contact Information ✨ Learn more about Abigail’s work: https://projectlifembc.com 📖 Her blog: No Half Measures - https://nohalfmeasures.blog

Tara Accardo lost both of her parents in her late twenties—and then her childhood dog, her last living connection to them. What could have been the end of her story became the beginning of her mission: helping others navigate grief with honesty, hope, and healing. 💛 In this heartfelt episode of the Moms Like Me podcast, Tara shares her story, how grief shaped her journey into motherhood, and how she's keeping her parents' legacy alive through her work at Losses Become Gains and the Life With Grief podcast. 🎧 Whether you’ve experienced loss or want to support someone who has, this episode is a must-listen. ⏰ Timestamps: 00:00 – Welcome & Guest Intro 01:24 – Tara’s story: Losing both parents to cancer 05:45 – How her father’s health declined after losing her mom 08:00 – Losing her childhood dog & hitting rock bottom 09:40 – Where "Losses Become Gains" began 11:00 – Why talking about grief helps her heal 14:35 – Grief & hope can coexist 15:54 – Did grief affect her view of motherhood? 18:10 – What it’s like parenting without your parents 22:00 – Passing down memories to her daughter 25:40 – The double-edged sword of watching in-laws become grandparents 30:00 – Shifting from “what if” to “what is” 34:14 – Finding balance in grief, gratitude, and motherhood 36:53 – Where to find Tara online

In this episode of the Moms Like Me Podcast, we welcome grief specialist, TEDx speaker, keynote speaker, and author Ashley Jones. Ashley shares her poignant journey through anticipatory grief and the heartbreaking reality of losing her daughter Skyler to spinal muscular atrophy (SMA). She discusses her path from personal grief to founding Memento Foundation, which offers free professional portrait sessions to families facing terminal diagnoses and provides grief support through various programs. Ashley also talks about her forthcoming book, 'When You Can't See the Light,' a trauma-informed survival guide to loss, designed to help people navigate raw grief. Tune in for an inspiring conversation about resilience, advocacy, and the power of turning pain into purpose. 00:00 Welcome and Introduction 00:59 Ashley Jones' Story: Skyler's Diagnosis 02:51 The Journey of Anticipatory Grief 05:24 Becoming an Advocate for Your Child 07:47 Ashley's Background and Early Experiences 11:22 Coping with Grief and Loss 19:05 Founding Memento Foundation 22:54 The Power of Photography in Grief 26:04 Upcoming Projects and Resources 32:09 Conclusion and Contact Information

Welcome back to The Moms Like Me podcast! In this heartfelt episode, host Jordan is joined by Ashlyn Thompson, a mom and community leader who is making a tremendous impact. Ashlyn is one of the co-founders of the Parent Empowerment Network, an organization dedicated to supporting families with children who have medical needs. Ashlyn delves into her compelling personal journey, from her childhood experiences to becoming a third-generation parent advocate. She shares the profound challenges and inspiring moments that led her to create an impactful nonprofit. Listen as Ashlyn discusses the importance of providing emotional triage and building a supportive community for parents navigating difficult medical landscapes. Discover how Parent Empowerment Network and their podcast, Empowered by Hope, are changing lives by offering hope and connection. Don’t miss this powerful episode filled with valuable insights and actionable takeaways for parents, caregivers, and supporters alike. 00:00 Introduction and Guest Welcome 01:21 Ashlyn's Background and Family Story 06:28 Challenges and Advocacy 11:17 The Birth of Parent Empowerment Network 16:38 The Power of Community and Support 32:54 Conclusion and Contact Information

Join us on The Moms Like Me podcast, powered by Support, as we delve into the heart-wrenching yet inspiring story of Lisa Ward and her son Jace. Diagnosed with a universally terminal brain cancer called DIPG, Jace's courageous battle transformed him into an advocate for others afflicted by this devastating disease. Lisa shares how this journey led to the founding of an impactful advocacy group aimed at improving awareness, research, and support for families dealing with brain cancer. Despite the harrowing diagnosis, Jace's unwavering spirit and mission to make a difference continue to inspire through the incredible work of Tough Together and other initiatives. Don't miss this powerful episode that highlights the importance of hope, advocacy, and community in the face of unimaginable challenges. 00:00 Introduction and Guest Welcome 00:47 Lisa Ward's Heartbreaking Story Begins 01:15 Jace's Diagnosis and Response 03:38 Understanding DIPG 04:57 Jace's Strength and Advocacy 07:57 Balancing Family and Advocacy 11:16 Navigating Treatment and Trials 13:47 Jace's Final Days and Legacy 21:47 Continuing the Fight Against DIPG 25:40 Resources and Final Thoughts

In this episode of the Moms Like Me Podcast, host Jordan welcomes the iconic Natalie Grant, a nine-time Grammy nominee and celebrated vocalist in the Christian and gospel music sphere. Natalie shares her journey from childhood to motherhood, including her struggles with infertility, IVF, and the joy and challenges of raising her three children. She opens up about the pressures moms face, her battle with postpartum depression, and the importance of community and support. Natalie also discusses her passion for philanthropy, including her work with the non-profit Hope for Justice. Join us for an inspiring and heartfelt conversation. 00:00 Introduction and Special Guest Announcement 01:39 Natalie Grant's Early Life and Family Background 04:03 Breaking Off the Engagement and Pursuing Music 07:46 Struggles with Infertility and IVF Journey 20:11 Unexpected Pregnancy and Postpartum Depression 29:48 The Importance of Community and Support 33:21 Conclusion and Final Thoughts

In this heartwarming episode of Moms Like Me, host Jordan Arogeti sits down with Jamie O’Neal, CEO of The Mom Walk Collective, to uncover how a simple social media post turned into a thriving global movement spanning 300+ cities. Jamie shares her personal journey—from navigating single motherhood and mental health challenges to creating an inclusive, judgment-free space where moms can find support, friendship, and empowerment. 🚶‍♀️ Why do so many moms feel isolated today? 💡 How can a simple walk change your entire motherhood experience? 🌍 How The Mom Walk Collective is redefining community for modern moms Whether you're a new mom looking for connection or an entrepreneur inspired by purpose-driven leadership, this conversation is packed with real talk, laughs, and encouragement. Don’t miss it! 📍 Find a walk near you or start your own: themomwalkcollective.com 📲 Follow on Instagram: @themomwalkco #MomWalk #MotherhoodCommunity #SupportForMoms #MomLife #Entrepreneurship

In this deeply moving episode of Moms Like Me, host Jordan Arogeti sits down with Martha Sharkey, founder of Today is a Good Day, to discuss the raw and emotional realities of the NICU experience. Martha shares her personal journey of giving birth to identical twin daughters at just 23 weeks, navigating the heartbreaking loss of her daughter Mary, and later, the challenges of carrying a child diagnosed with Trisomy 18. Through her family's trials, Martha has turned pain into purpose, founding a nonprofit that has supported thousands of NICU families with vital resources, advocacy, and community. Join us as we explore: ✅ The emotional rollercoaster of premature birth and NICU life ✅ How faith and community helped Martha's family through loss ✅ The power of connection and shared experiences in times of hardship ✅ How Today is a Good Day is changing lives for families with NICU babies If you or someone you love has experienced the NICU, this conversation is a must-watch. Share this video to spread awareness and support for families navigating similar journeys. 🔔 Subscribe for more powerful stories from moms supporting moms! #NICU #MomsLikeMe #ParentingJourney

In this powerful episode of Moms Like Me, host Jordan Arogeti sits down with Samantha Brinson, founder of Hugs for Harrison, to discuss her journey through loss, grief, and healing. After losing her son Harrison at 20 weeks, Samantha turned her pain into a mission—creating a nonprofit that supports families experiencing pregnancy and infant loss.   🔹 Samantha’s personal story of love, loss, and resilience 🔹 How grief changes over time and the importance of support 🔹 The inspiration behind Hugs for Harrison and how it helps grieving families 🔹 Practical advice for supporting a loved one through child loss  If you or someone you know is walking through grief, this conversation is a must-watch. Join us as we explore the power of presence, patience, and community in the healing journey.  🌐 Learn more: www.hugs4harrison.com 📲 Follow Hugs for Harrison on Instagram: @hugs4_harrison  #ChildLoss #PregnancyLoss #HugsForHarrison #GriefSupport #HealingJourney

In this powerful episode of Moms Like Me, host Jordan Arogeti sits down with Emily Bingham, a widow, mom, and spiritual life coach, to discuss her journey through grief, resilience, and transformation. Emily opens up about losing her husband, Ian, to uveal melanoma, how she navigated life as a solo parent to two young children, and how she turned her pain into purpose. She shares insights on embracing mortality, finding support, and living with intention. If you're looking for inspiration, healing, or guidance on grief and personal growth, this conversation is a must-watch. Emily’s wisdom on balancing emotions, seeking help, and redefining life after loss is both moving and transformational. 🔗 Watch now and be inspired by Emily's story of strength and purpose! #GriefHealing #MomLife #SelfGrowth #Podcast

When Heidi Feyerherm-Smith’s daughter, Chloe, was diagnosed with DIPG, a rare and aggressive pediatric brain cancer, she faced an unimaginable journey. Despite the heartbreaking loss, Heidi turned her grief into action, founding the Love Chloe Foundation and Monkey In My Chair to support children battling cancer and their families. In this emotional and inspiring conversation, Heidi shares: ✅ Chloe’s story and the challenges of DIPG ✅ The resilience of children facing illness ✅ How Monkey In My Chair helps kids stay connected to school ✅ The impact of community support on families in crisis ✅ Practical ways you can help families facing childhood cancer 💛 Learn more about Love Chloe Foundation: lovechloe.org 🐵 Support Monkey In My Chair: monkeyinmychair.org If you or someone you know is facing a cancer diagnosis, check out SupportNow, a platform helping families coordinate meals, fundraisers, and volunteer efforts. 🔔 Subscribe for more powerful stories of resilience and hope! #ChildhoodCancer #DIPG #LoveChloeFoundation #MonkeyInMyChair #CancerSupport #MomsLikeMe #SupportNow

In this powerful episode of Moms Like Me, host Jordan Arogeti sits down with Maria Fernandez, a devoted wife, mother, and caregiver, to discuss the life-changing impact of ALS. Maria shares the emotional and physical journey of supporting her husband, Jules, through his diagnosis while raising their young son. With raw honesty, she opens up about grief, resilience, and the unexpected lessons of joy, humor, and hope in the face of hardship. This conversation is a must-watch for caregivers, families facing chronic illness, and anyone seeking inspiration in the midst of life's toughest challenges. Discover how Maria has learned to advocate for herself, embrace support, and redefine what it means to be a caregiver. 🔹 Key Takeaways: The reality of an ALS diagnosis and its impact on the entire family. The emotional and physical toll of caregiving—and how to find balance. The importance of community, advocacy, and self-care for caregivers. A powerful perspective on embracing life’s challenges with grace and humor. 🔗 Resources & Support: Follow Maria and her journey: @TeamHighOctaneJules & @WalkingInMagic Listen to The Couple Shift and The Caregiver Spirit podcasts Learn how SupportNow is helping caregivers lighten their load. 💙 Like, share, and subscribe to support caregivers everywhere. Let’s spread awareness and hope together! #ALS #Caregiving #SupportNow #MomsLikeMe

In this inspiring episode of Moms Like Me, host Jordan Arogeti welcomes Suzy Griswold, founder of Healing Strong, to discuss her powerful journey of overcoming cancer through a holistic approach. Suzy shares how a surprising book recommendation transformed her perspective on healing, leading her to explore integrative methods that rebuild the body, renew the soul, and refresh the spirit. Discover how Healing Strong has grown into a global network of support groups helping cancer thrivers take control of their health and wellness. Suzy breaks down the role of nutrition, emotional healing, and faith in the recovery process and shares why community support is crucial for anyone facing a cancer diagnosis. 🔹 Key Topics Covered: ✔️ Suzy’s personal cancer journey & alternative healing methods ✔️ The power of emotional and spiritual healing in recovery ✔️ Why Healing Strong is changing the way people approach cancer ✔️ How to find or start a Healing Strong support group ✔️ Practical tips to begin a holistic healing journey If you or someone you love is navigating cancer, this episode is a must-listen! Learn more about Healing Strong at healingstrong.org. #HolisticHealing #CancerRecovery #HealingStrong #WellnessJourney #AlternativeMedicine

Why is the funeral industry still stuck in the past? 💭 Caroline Schrank, founder of Ripple, joins Moms Like Me to reveal the hidden truths behind funeral planning and why families deserve a better way to honor their loved ones. 💜 🚨 Key Topics Covered: ✅ The emotional and financial burden of traditional funeral homes ✅ How small conversations can make a huge impact on end-of-life planning ✅ Why modern technology is reshaping the way we support grieving families ✅ The surprising history of funeral flowers (hint: it’s not what you think!) ✅ How Ripple is changing the game with transparency, support, and real solutions Don't let outdated traditions make a tough time even harder. Tune in and learn how to prepare, plan, and support loved ones in a way that truly matters. 🙌 🔗 Watch now & rethink how we honor life’s most difficult moments. #FuneralPlanning #GriefSupport #DeathCare #MomsLikeMe

In this episode of Moms Like Me, host Jordan Arogeti sits down with Dr. Morgan Cutlip, a renowned author and relationship expert, to dive deep into the unspoken burden of the mental load—the invisible, exhausting to-do list that many women carry in their relationships and motherhood. Dr. Cutlip shares her personal journey, growing up immersed in relationship psychology, and how becoming a mom reshaped her understanding of marriage and self-care. They tackle key questions like: Why does motherhood often feel overwhelming, even for the most prepared moms? How does the mental load impact relationships, and why do women carry the bulk of it? What strategies can couples use to balance responsibilities and reduce resentment? How does redefining partnership and support lead to stronger marriages and even better intimacy? Dr. Cutlip introduces her new book, A Better Share, which provides practical tools for couples to tackle the mental load together—leading to less stress, fewer arguments, and even a better sex life. If you’ve ever felt buried under the weight of parenting and household responsibilities, this conversation is packed with real-life strategies to help you reclaim balance. 🔹 Perfect for: Moms, couples, and anyone struggling with burnout and mental load in relationships. 🔹 Watch now to learn: How to shift from frustration to teamwork and lighten the load together! #Motherhood #Marriage #MentalLoad #MomLife #Relationships #Parenting #MomSupport

In this deeply personal and inspiring episode of Moms Like Me, host Jordan Arogeti sits down with Sarah Kernion, founder of Saturday Story, to discuss her journey as a mother navigating neurodiversity. Sarah shares the emotional rollercoaster of receiving autism diagnoses for two of her children, her battle with postpartum anxiety, and how she redefined success through the concept of inchstones—celebrating small but meaningful victories rather than traditional developmental milestones. This episode is a must-watch for parents seeking encouragement, whether navigating special needs parenting or simply looking for ways to embrace the present moment. Learn how Sarah’s mindset shift transformed her life, why community support is crucial, and how Support Now provides resources for families in need. 🔹 Key Topics: - The emotional impact of an autism diagnosis Reframing success with inchstones instead of milestones - - The importance of self-care for special needs parents - How community support can make all the difference Subscribe for more real and empowering conversations! 💙 #Neurodiversity #Parenting #MomsLikeMe

In this powerful episode of Moms Like Me, host Jordan Arogeti sits down with Lindsey Garcia, a mother, advocate, and nonprofit leader, to discuss her journey with 22Q11.2 Deletion Syndrome. From the shock of diagnosis to becoming a fierce advocate, Lindsey shares how she navigated medical challenges, found community, and launched the 22Q Family Foundation to support other families. 👉 Learn about 22Q symptoms, diagnosis, and the importance of advocacy 👉 Discover how Lindsey turned her family's journey into a mission to help others 👉 Gain insights into balancing caregiving, family dynamics, and self-care 🔹 Support & Resources: 22Q Family Foundation 🔹 Support Now: Your fundraising & volunteer coordination tool 🎧 Don’t forget to LIKE, SUBSCRIBE, and SHARE this episode to spread awareness! #22Q #MedicalParenting #MomsLikeMe #RareDiseases

Becoming a mom is life-changing—and overwhelming! In this episode of Moms Like Me, host Jordan Arogeti sits down with renowned postpartum doula Penny Gilchrist to discuss the vital role doulas play in supporting new moms. Penny shares insights from her 26 years of experience, including: ✅ How a postpartum doula provides emotional and practical support ✅ The biggest struggles new moms face (and how to overcome them) ✅ Why Instagram might be hurting your confidence as a parent ✅ How partners can get involved and feel empowered ✅ The importance of community and finding your support system Whether you're a new mom, expecting, or supporting someone in postpartum, this episode is packed with wisdom to help you navigate this beautiful but challenging season. 🔗 Learn more about Penny Gilchrist: www.2heartsdoula.com 🔗 Support Now: www.supportnow.org 🎧 Listen now and discover how to bring calm and confidence into postpartum life! #Postpartum #NewMom #Doula #Motherhood