Katie Taylor, Certified Child Life Specialist

Inside the Children's Hospital

Kids EN ↓ 319 episodes

Inside the Children's Hospital shares real stories from parents, caregivers, and pediatric healthcare professionals navigating the emotional realities of caring for a hospitalized child with honesty, compassion, and hope.

Author

Katie Taylor, Certified Child Life Specialist

Category

Kids

Latest episode

Jul 8, 2026

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Episodes

212: CCLS Story: 18 Years of Supporting Kidney Families -Julie's Story 27.03.2024

"As a child life specialist, watching my tiniest patients grow and accomplish so many things is my favorite part of the job." - Julie, Certified Child Life Specialist Episode Summary: In this heartfelt episode of Child Life On Call, we celebrate Child Life Month by diving deep into the dedicated world of child life specialists and the resilient families they support. Host Katie Taylor talks to Jul...

211: A Son Born with End-Stage Kidney Disease (Part 1): Lyndsey's Story 20.03.2024

"Having a medically complex child, it's like everything's fine. And then, you know, we have a morning where we've thrown up a lot or our blood pressure is too low, and it just doesn't look good. You just never know what you're going to get." - Lyndsey, Episode 211 In this deeply moving episode, we are joined by Lyndsey, who shares the compelling journey of her son James's battle with post-urethral...

210: Connection, Healing, and Love: Insights from Patrice Karst, Author of The Invisible String 13.03.2024

"Love is the most powerful force in the universe, and the invisible string is a testament to the connections that bind us all." - Patrice Karst In this special Child Life Month episode, Katie Taylor sits down with Patrice Karst, the beloved author of "The Invisible String" and several other impactful books. They explore Patrice's journey from personal challenges to becoming a source of comfort and...

209: Research on Parent Caregivers of Children with Medical Complexities - Elise's Story 06.03.2024

Advocacy, Compassion, Innovation: Elise's Child Life Journey "Working with children with medical complexity and developmental differences isn't just a job; it's rooted in who I am." - Elise Cofer, CCLS Research Article: Fitting the Pieces Together  Lead Researcher: Elise Cofer In this captivating episode of Child Life On Call, Katie Taylor sits down with Elise, a Nashville-born child life speciali...

208: Military Life, Pediatric Complex Care Abroad & Resiliency: Kat's Story 28.02.2024

In this profound episode, we join Katie Taylor as she delves into the inspiring journey of a military family navigating pediatric healthcare for their two medically complex children. Through the voice of the remarkable mother, Kat, we explore the unique challenges and triumphs of securing continuous, specialized care amidst the frequent relocations and complexities inherent to military life. Kat s...

Healing Without Surgery: Umbilical Hernia Solutions from a Physical Therapist 21.02.2024

What if we could prevent more kids from having to have invasive surgery? During this episode, we are joined by Katie Corrado, who invented a product that works as an alternative to surgery for babies and children. Tune in to hear how her first-hand experience of watching her child struggle with an umbilical hernia led her to an innovative solution that she now offers to other families facing the s...

206: Founder's Vision: Katie's Journey, Child Life Tech, Future Insights 14.02.2024

In this special episode of Child Life On Call, we flip the script as Emily Martinec interviews our very own founder, Katie Taylor. Dive into Katie's journey from child life specialist to tech entrepreneur, exploring the roots of Child Life On Call, the challenges and triumphs of building a company, and how her upbringing shaped her mission to support families and healthcare professionals alike. "C...

205: How to Support Kids who are Grieving, Bittersweet Relationships & Personal Loss 07.02.2024

In this episode, we're honored to have Jessica Correnti, a certified child life specialist and a bereaved mother, share her profound insights on grief. Jessica's dual perspective offers a rich understanding of the multifaceted nature of grief beyond the loss of a loved one. She discusses her personal journey, the importance of recognizing and naming grief in children, and how this awareness can em...

204: Caregiver Isolation, Transitioning to Adult Special Needs, and Becoming CapeAble - Marna's Story 31.01.2024

"Millie's journey has taken me to the end of myself, but it's been the most beautiful beginning of understanding humanness and how to be compassionate and how to really be kind to other people and take notice that the story that is their life may not be what you see." How does trauma affect the whole family, and how can we show compassion to adults with special needs? One thing I have learned abou...

203: 12 Years to Diagnosis, Understanding Four Key Emotional Reactions, and Channeling Her Story into Positive Action - Jessica's Story 24.01.2024

"If you have a question, ask it. You are the parent, you need to know" -  Jessica Siddi-Sewart  How can medical parents use their experiences to promote action and advocacy? As a child life specialist, I know that there is not one "normal" or "best" reaction for a parent when their child receives a medical diagnosis. Today's guest, Jessica Siddi-Sewart and she helps us reflect on the different sta...

202: Infantile Spasms, Healing from Trauma and Emotional Resilience 17.01.2024

In this episode about parenting a child with infantile spasms, Katie Taylor, a certified child life specialist, has a profound conversation with Hailey, a resilient mother navigating the complexities of raising a child with a disability. Join us as we delve into Hailey's journey, exploring the challenges and triumphs of parenting under extraordinary circumstances. "It's not always about thriving i...

201: Personal Growth Theory, NEC in the NICU and Shielding Siblings - Kathryn's Story 10.01.2024

I'm his mom, and I carried him for almost nine months, and no one loved him more than me. I'm his expert, and I'm going to own that. - Kathryn Whitaker Have you ever found yourself amazed at the strength people find in the toughest of times?  Well, on today's podcast, we're talking about one of the common themes we've seen over the past 200 episodes of Child Life On Call and something I consistent...

200: Anonymous questions from Instagram, Katie's personal burn story, and reflecting on 2023 20.12.2023

In this milestone 200th episode, Katie delves into a unique mix of content, answering insightful questions from Instagram, sharing a personal story about her daughter Cameron's burn accident, and reflecting on the impactful moments of 2023. The episode features discussions on a variety of books Katie read throughout the year, the best toys of 2023, and tackles the challenging aspects of balancing...

Episode 199 | Kate's Story- A daughter with Infantile Spasms 13.12.2023

Join me for an emotional and insightful conversation as I sit down with Kate Kostolansky in this episode of Child Life On Call. Kate, a dedicated mother and advocate, shares her touching journey of raising her daughter, Charlotte, who battles infantile spasms. In this heartfelt discussion, Kate sheds light on the challenges faced by families dealing with rare medical conditions, emphasizing the im...

Episode 198 | Jennifer's Story- A son with necrotizing enterocolitis (NEC) 06.12.2023

In this episode of Child Life On Call, we are honored to host Jennifer Canvasser, the driving force behind the NEC Society, as she shares her poignant journey and advocacy for Necrotizing Enterocolitis (NEC) awareness in the NICU. Join us as Jennifer unveils her personal story and how she transformed her loss into a powerful force for supporting families grappling with NEC. Gain valuable insights...

Episode 197 | James' Story- A son with a congenital heart defect 29.11.2023

 In this episode, our guest James Robinson will share the keys to living life to its fullest, both inside and outside of the hospital, so that you can provide the result of bringing joy and happiness to your child's life, despite their medical condition.  James Robinson, the author of the book " More Than We Expected: 5 Years with A Remarkable Son."  On today's episode, he shares his personal expe...

Episode 196 | Hannah's Story-A son with VACTREL Association 15.11.2023

  In this episode, you will be able to: Discover the untold journey of NICU parents, gaining insights and understanding into their unique experiences. Uncover the challenges of medically complex pregnancies, and learn strategies for navigating this complex journey with support and resilience. Explore the support systems available for medical motherhood, and find out how to build a network of under...

Episode 195 | Mackenzie's Story- A daughter with Severe Tethered Cord and Caudal Regression Syndrome 08.11.2023

Join Katie Taylor in an emotional conversation with Mackenzie Carolin as they discuss the unexpected medical journey she faced with her daughter. Learn how Mackenzie navigated the complexities of her child's healthcare needs and discover the importance of trust and human connections during challenging times. This episode of Child Life On Call provides valuable insights and support for parents who...

Episode 194 | Keeley's Story- A daughter with hydrops fetalis 01.11.2023

Are you a parent of a child with a medical condition? Join me, Katie Taylor, as I chat with Keeley Machen Schares, a Child Life Specialist, in this special episode of Child Life On Call. Keeley takes us through her incredible journey as a mother to a premature baby with hydrops fetalis and profound hearing loss. From routine ultrasounds to a life-saving diagnosis, Keeley's story will captivate you...

Episode 193 | Katie's Takeaways from the American Academy of Pediatrics Conference 25.10.2023

It's a solo episode this week and our host, Katie Taylor, CCLS, dives in to what she experienced at the American Academy of Pediatrics Conference. Katie talks about her travels to Chicago to train a group of clinicians in Chicago, and then her trip to DC where she had hundreds of conversations with pediatricians from across the globe. What was the overwhelming takeaway? PEDIATRICIANS LOVE CHILD LI...

Episode 192 | [Repost] Teresa's Story- A daughter with Spina Bifida and a Tethered Cord 18.10.2023

This episode is a repost in honor of Spina Bifida awareness month.  Are you a parent of a child with spina bifida who is seeking support and guidance to navigate the challenges of raising your child? Are you looking for increased understanding, support, and strategies to help you and your child thrive? Join us as we welcome guest Teresa Crespo, who will be sharing the solution to help you achieve...

Episode 191 |[Repost] Shani's Story-A child with a learning difference #ADHD #Anxiety #Dyslexia #Dysmorphia 11.10.2023

We wanted to repost this epsidoe to highlight that October is Learning Disabilities / Dyslexia / Attention Deficit Hyperactivity Disorder Awareness Month.  In a world of unexpected twists, sometimes the greatest surprises lie within our own children. Child Life Specialist, Shani Thornton's journey with her son's learning differences took an unforeseen turn, unraveling a mystery that went beyond wh...

Episode 190 |Sara's Story- Telling your Child you have Cancer [Repost in honor of Breast Cancer Awareness Month] 04.10.2023

In honor of October being Breast Cancer Awareness month we wanted to repost this episode to provide awareness to our community.  Breast cancer survivor, Sara Olsher, battles the disease as a single parent, using her experience to empower others and create resources for families facing cancer, in a moving and inspiring episode of the Child Life On Call podcast. In this episode, you will be able to:...

Episode 189 | Ryan's Story - A son with Costello Syndrome 27.09.2023

  My special guest is Ryan Sheedy Meet Ryan Sheedy, an incredible father who, much to his own surprise, found himself immersed in the delightful chaos of caring for twin boys. His world drastically transformed ten years ago, when he moved from Pennsylvania to Bentonville, Arkansas. Not only has Ryan navigated the unexpected challenges of parenting twins, but he has also bravely navigated his son's...

Episode 188 | Rhandyl and Deonna's stories from Raising Disabled 20.09.2023

  My special guest is Rhandyl Vinyard, Deonna Wade Rhandyl Vinyard and Deonna Wade are two phenomenal mothers from Texas, each raising disabled children. Drawn together by shared circumstances, their friendship continues to strengthen others walking a similar path. Rhandyl, a physical therapist assistant, is the mother to Remy, who has required intensive medical care from an early age. Her backgro...

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