loader from loading.io

When Your Child is Diagnosed with Leukemia: What to Expect

Inside the Children's Hospital

Release Date: 04/27/2020

ADNP Syndrome: A Child Life Specialist's Journey to Diagnosis, Advocacy & Hope show art ADNP Syndrome: A Child Life Specialist's Journey to Diagnosis, Advocacy & Hope

Inside the Children's Hospital

When Caitlin noticed that her daughter, Kennedy, wasn't meeting developmental milestones, she trusted her instincts—even when others reassured her that everything was fine. As both a former Child Life Specialist and mom of a child with ADNP syndrome, Caitlin shares her family's journey from early concerns and endless appointments to receiving a diagnosis for a condition so rare that only about 500 cases have been identified worldwide. In this conversation, Caitlin opens up about navigating uncertainty, advocating for her daughter in healthcare settings, finding support through rare disease...

info_outline
Growing Up with Chronic Intestinal Pseudo-Obstruction show art Growing Up with Chronic Intestinal Pseudo-Obstruction

Inside the Children's Hospital

For many families navigating chronic illness, it's hard to imagine what the future might look like for their child. This week on Inside the Children’s Hospital, Katie Taylor sits down with Vincent Rosche, a patient advocate, fitness enthusiast, and survivor who has spent most of his life navigating complex medical challenges. Diagnosed with chronic intestinal pseudo-obstruction (CIPO) at just 9 months old, Vincent grew up with feeding tubes, central lines, frequent hospitalizations, and even battled thyroid cancer as a teenager. Today, Vincent works as the Community Engagement Coordinator...

info_outline
Supporting Children Through Burn Injuries show art Supporting Children Through Burn Injuries

Inside the Children's Hospital

Has your child been burned? Whether it was hot water, ramen noodles, a stove, fireworks, or another accident, this episode guides parents through what to do next. In this episode, Katie sits down with Christella Almonacy, Certified Child Life Specialist at Wellstar's Burn Program, to discuss what families can expect after a child experiences a burn injury. Together, they explore the physical and emotional recovery process, how Child Life Specialists help children cope with painful procedures, and why giving kids choices can make all the difference. Christella also shares common causes of...

info_outline
What a NICU Nurse Wants Parents to Know show art What a NICU Nurse Wants Parents to Know

Inside the Children's Hospital

What is it really like to have a baby in the NICU?  Katie Taylor sits down with NICU nurse, educator, and content creator Alyssa Saldivar to discuss how families can find confidence, connection, and support during one of the most challenging experiences of parenthood. Alyssa shares her journey of becoming a nurse during the COVID-19 pandemic, her passion for supporting both families and fellow nurses, and the practical ways parents can become active participants in their baby's care. Together, Katie and Alyssa explore everything from skin-to-skin care and developmental support to...

info_outline
Recognizing Infantile Spasms: Navigating a Diagnosis as a Nurse Practitioner show art Recognizing Infantile Spasms: Navigating a Diagnosis as a Nurse Practitioner

Inside the Children's Hospital

What happens when a pediatric nurse practitioner suddenly finds herself on the other side of diagnosis? On this week's episode of Inside the Children's Hospital, Katie Taylor sits down with Laura Forcella, a developmental pediatric nurse practitioner and mom to a son with Dup15q syndrome and epilepsy. Laura shares the deeply personal journey of recognizing her son's infantile spasms, navigating a rare disease diagnosis, and balancing life as both a medical professional and a caregiver. Laura opens up about the unique challenges of being a "med mom," the emotional shift from provider to parent,...

info_outline
What Happens When Your Child Needs an Ambulance, Helicopter, or Medical Transport? show art What Happens When Your Child Needs an Ambulance, Helicopter, or Medical Transport?

Inside the Children's Hospital

When a child needs emergency transport to a children’s hospital, families are often facing one of the hardest moments of their lives. Behind every ambulance ride, helicopter flight, or plane transfer is a highly trained team working together to keep children safe, while also supporting parents through the unknown. In this episode of Inside the Children’s Hospital, Katie Taylor sits down with Kami Stone, Assistant Clinical Director at Texas Children’s Hospital Austin, and Jacob, a transport EMT with the Texas Children’s Kangaroo Crew, to talk about what pediatric transport really looks...

info_outline
When the Hospital Stay Ends: Understanding Pediatric Medical Traumatic Stress show art When the Hospital Stay Ends: Understanding Pediatric Medical Traumatic Stress

Inside the Children's Hospital

For many families, going home from the hospital feels like the finish line. But what happens when the emotional impact of a medical experience lingers long after discharge? On this episode of Inside the Children’s Hospital, Katie Taylor sits down with Jen Aspengren, founder of Alongside Network, to discuss pediatric medical traumatic stress (PMTS), a common yet often overlooked experience that affects children, parents, siblings, and caregivers following serious medical events. Jen shares her family's journey after her infant son underwent life-saving airway surgery at just seven months old....

info_outline
From Pharmacist to Mom: Navigating Type 1 Diabetes and Celiac Disease show art From Pharmacist to Mom: Navigating Type 1 Diabetes and Celiac Disease

Inside the Children's Hospital

What happens when the healthcare professional becomes the parent sitting on the other side of the diagnosis? In this episode, Katie Taylor sits down with Melissa Apa—a clinical pharmacist, diabetes educator, and mom—to share her family’s journey navigating both celiac disease and type 1 diabetes with her young son. Melissa opens up about the emotional overwhelm of receiving life-changing diagnoses, even with years of medical expertise behind her, and how her family learned to adapt, advocate, and find stability in the chaos. From replacing every pot and pan in her kitchen overnight to...

info_outline
A NICU Dad Story: Life After a 25 Week Premature Birth show art A NICU Dad Story: Life After a 25 Week Premature Birth

Inside the Children's Hospital

“I kept telling her, ‘We’ve got this.’ And inside, I had no clue what was coming next.” What does it look like to be “the strong one” when your world is falling apart? In this episode, Katie Taylor sits down with Jared Muscat—dad, surfer, and self-proclaimed “dad-vocate”—to share his family’s unexpected journey into the NICU after a high-risk pregnancy. From a routine 20-week appointment to welcoming his son Ollie at just 25 weeks, Jared opens up about fear, resilience, and what it means to show up as a partner and father in crisis. He shares the emotional weight of...

info_outline
Tay-Sachs Disease: A Father’s Story of Diagnosis, Parenting, and Purpose show art Tay-Sachs Disease: A Father’s Story of Diagnosis, Parenting, and Purpose

Inside the Children's Hospital

In this episode of Inside the Children’s Hospital, Katie Taylor sits down with Dr. Matt Goldstein—physician, biotech leader, and father—who shares the story of his daughter, Havi, and her diagnosis with Tay-Sachs disease. Despite both parents undergoing genetic screening before starting their family, a testing error led to a missed diagnosis. Javi appeared to develop typically at first, but over time, subtle changes led to a life-altering realization: she had a rare, fatal neurodegenerative condition. As a physician, Matt was trained to solve problems. As a parent, he was driven to...

info_outline
 
More Episodes

Elizabeth, mom to three girls, shares with us her experience of having a daughter with cancer. In just an hour and a half, her 9-year-old daughter went from a pediatricians office to a cancer ward. Elizabeth discusses her Elizabeth's "out of body" experience, how she was able to identify the "gifts" in each of her girls, and offers wisdom and compassion to others going through similar experiences.

We also talk about how the global pandemic of Covid19 and subsequent quarantine has impacted their family. Elizabeth is a writer by trade and published a book called The Puddle Jumper's Guide to Kicking Cancer 

which is available in both English and Spanish. You can listen to the book on YouTube. To get in touch or follow along with Elizabeth, you can email her at elizabethbillups@gmail.com or see her Instagram @teachingkidsaboutcancer.

When parents feel empowered, everyone wins – kids thrive and the care team excels!

Links and Resources:

  • 85% of users report high satisfaction, appreciating the SupportSpot app's comprehensive resources and user-friendly interface.
  • 92%  of parent users say the SupportSpot app's helped them understand medical procedures and treatment better.
  • 80% of parents believe the SupportSpot app's has contributed to better health outcomes for their child.
  • 73% of parent users believe the SupportSpot app's has made them feel more empowered to advocate for their child in healthcare

Learn more here.

Meet the host: 

Katie Taylor is the co-founder and CEO of Child Life On Call, a digital platform designed to provide parents, kids, and the care team with access to child life services tools and resources. She is a certified child life specialist with over 13 years of experience working in various pediatric healthcare settings. Katie is the author of the children's book, and has presented on the topics of child life and entrepreneurship, psychosocial care in the hospital, and supporting caregivers in the NICU setting both nationally and internationally. She is also the host of the Child Life On Call Podcast which features interviews with parents discussing their experiences throughout their child's medical journey. The podcast emphasizes the crucial role of child life services in enabling caregivers both at and beyond the bedside.

Instagram.com/childlifeoncall

 

The Child Life On Call Podcast is for informational and educational purposes only. The content shared in each episode, including stories, discussions, and interviews, is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified healthcare provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay seeking it because of something you heard on this podcast. The views and opinions expressed by guests on the Child Life On Call Podcast are their own and do not necessarily reflect those of Child Life On Call. Child Life On Call does not endorse any specific medical treatments, procedures, or opinions shared in the podcast. If you or your child are experiencing a medical emergency, call 911 or seek immediate medical attention. By listening to this podcast, you acknowledge that Child Life On Call and its affiliates are not responsible for any decisions made based on the information provided.

Facebook.com/childlifeoncall

linkedin.com/in/kfdonovan