

HIE at Birth: A Dad’s Story of Brain Injury, NICU Trauma, and Finding Purpose
April 1, 2026
Diagnosis & Rare Disease, Our New Normal
297

Preparing Your Child for Surgery: A Pediatric ENT Surgeon’s Honest Advice
March 25, 2026
Surgery & Hospital Stays
296

Life After Pediatric Kidney Transplant: A Mom’s Journey Through Dialysis, Surgery, and Recovery
March 17, 2026
Surgery & Hospital Stays
295

Healing After the NICU: Processing Trauma, Loss, and Your Family's Story
March 10, 2026
NICU & Prematurity
294

Trust, Grief, and Loving Your Child Through Big Identity Changes
March 3, 2026
Our New Normal
293

Helping Kids Navigate Physical Differences: Child Life Strategies for Confidence, Curiosity & Resilience
February 25, 2026
Our New Normal
292

Tube Feeding Awareness: Lived Experience, Real Talk, and Hope for the Future
February 11, 2026
Our New Normal
290

How Camp Supports Healing, Play, and Belonging for Medically Complex Kids
February 4, 2026
Our New Normal
289

Rare Lung Disease, Epilepsy and the Diagnostic Journey
January 28, 2026
Diagnosis & Rare Disease
288

Severe Hemophilia: A Newborn, A Brain Bleed, and PICU Experience
January 21, 2026
Diagnosis & Rare Disease
287

When Insurance Isn't Enough: A Parent's Type 1 Diabetes Story
January 14, 2026
Our New Normal
286

Parent Guide: Your child is diagnosed, now what?
January 7, 2026
Diagnosis & Rare Disease
285

Launching Inside the Children's Hospital: What Listeners Can Expect
January 1, 2026
Our New Normal
284

3 Proven Strategies for Parents Navigating Pediatric Healthcare in 2025
December 18, 2025
Our New Normal
283

Pregnancy Loss, Healing, and Rainbow Baby: A Father's Journey
December 10, 2025
Our New Normal
282

Understanding Homocystinuria (HCU): How one Mother Uncovered her Son's Diagnosis
December 3, 2025
Diagnosis & Rare Disease
281

When Your Baby is Diagnosed with Type 1 Diabetes: Marlee's Story
November 12, 2025
Diagnosis & Rare Disease
279

Brain Surgery for Drug-Resistant Epilepsy: Managing Infantile Spasms
November 5, 2025
Surgery & Hospital Stays
278

Speech Therapy at Home: Expert Tips to Help Your Child Communicate
October 29, 2025
Our New Normal
277

Type 1 Diabetes: Finding Community and Humor After Diagnosis
October 22, 2025
Our New Normal
276

NICU Stay, Down Syndrome, and Infant Loss: A Grief Journey
October 15, 2025
NICU & Prematurity
275

Choosing the Best Children's Hospital: Why Rankings Matter (with Ben Harder)
October 7, 2025
Surgery & Hospital Stays
274

Heart Transplant for Children: A Mother and Son Face Danon Disease Together
October 1, 2025
Surgery & Hospital Stays
273

Bone Marrow Transplant for Sickle Cell: One Family's Cure Story
September 24, 2025
Cancer & Blood Disorders
272

Managing Severe Food Allergies in Children: A Parent's Guide
September 17, 2025
Our New Normal
271

Play-Based Physical Therapy at Home: How to Help Your Child Build Strength
September 10, 2025
Our New Normal
270

PANDAS (Pediatric Autoimmune Disorder): When Anxiety is Actually PANDAS
September 3, 2025
Diagnosis & Rare Disease
269

Down Syndrome with Heart Defects (AVSD): Managing Pulmonary Hypertension [Encore]
August 27, 2025
Diagnosis & Rare Disease
268

Tuberous Sclerosis Complex (TSC): Finding Strength Through Vulnerability
August 20, 2025
Diagnosis & Rare Disease
267

Prenatal Diagnosis of Achondroplasia (Dwarfism): A Nurse's Perspective
August 13, 2025
Diagnosis & Rare Disease
266

Crohn's Disease in Children: A Mother-Daughter Advocacy Journey
August 6, 2025
Our New Normal
265

Infantile Spasms Diagnosis at 22 Months: Early Recognition and Advocacy [Encore]
July 30, 2025
Diagnosis & Rare Disease
264

Reducing Pediatric Medical Trauma Through Play: The Butterfly Pig Mission
July 23, 2025
Surgery & Hospital Stays
263

A NICU Story: Healing, Advocacy, and Family-Centered Care [Encore]
July 16, 2025
NICU & Prematurity
262

Talking to Kids About Disasters and Illness: Child Life Expert Guidance
July 9, 2025
Our New Normal
261

When Your Child is Diagnosed with Leukemia: First Steps from a Cancer Parent
June 25, 2025
Cancer & Blood Disorders
260

Tetralogy of Fallot (TOF): A Nurse Practitioner's Journey Through Her Daughter's CHD
June 11, 2025
Diagnosis & Rare Disease
258

The NICU Dad Experience: A Father's Perspective on Prematurity [Encore]
June 4, 2025
NICU & Prematurity
257

Microtia Atresia: Hearing Aids, Surgery, and a Journey of Hope [REPOST]
May 21, 2025
Diagnosis & Rare Disease
255

Blended Tube Feeding for G-Tube Fed Kids & Adults: How a Dietitian Empowers Families Through Food
May 14, 2025
Our New Normal
254

Prader-Willi Syndrome: Motherhood & Finding Community Through Advocacy [REPOST]
May 7, 2025
Diagnosis & Rare Disease
253

Grief, Strength & Advocacy: A Nurse Practitioner's Story [REPOST]
April 23, 2025
Our New Normal
251

Collagenous Gastritis and IgG Deficiency: A Rare Diagnosis Journey
April 16, 2025
Diagnosis & Rare Disease
250

MERRF Syndrome: Raising and Remembering a Child with Mitochondrial Disease
April 2, 2025
Diagnosis & Rare Disease
248

Cerebral Palsy: Traumatic Birth, Micropreemie Twins & the Power of Hope [REPOST]
March 26, 2025
Diagnosis & Rare Disease
247

PYROXD1 Rare Disease: A Life-Saving Lesson & a Mission to Help Others
March 19, 2025
Diagnosis & Rare Disease
246

HIE (Hypoxic Ischemic Encephalopathy): Hope for Families and Life Beyond the NICU [REPOST]
March 12, 2025
NICU & Prematurity
245

NMOSD Diagnosis: A Mother and Physician Navigates Her Daughter's Journey
March 5, 2025
Diagnosis & Rare Disease
244

Long COVID in Children: A Child Life Specialist's Search for Answers
February 19, 2025
Diagnosis & Rare Disease
243

PCDH19 Epilepsy and Autism Diagnosis: The Motivation Behind The Connected Parent
February 5, 2025
Diagnosis & Rare Disease
242

Kidney Transplant in Children: How One Family Started a Mission to Help Transplant Families
January 22, 2025
Surgery & Hospital Stays
241

Near Drowning Accident: How Finding Grants Brought Hope to One Family
January 8, 2025
Surgery & Hospital Stays
239

Parents: How to Make the Most out of Rounds in the Hospital
January 6, 2025
Surgery & Hospital Stays
238

Lissencephaly, Lennox-Gastaut Syndrome, and Autism: Joy & Grief Through Medical Parenting
December 4, 2024
Diagnosis & Rare Disease
236

Crohn's Disease and Ulcerative Colitis: A Mother's Journey of Love, Loss, and Resilience
November 20, 2024
Our New Normal
235

Expert Child Life Tips for Supporting Children Through an Upper GI Procedure
November 13, 2024
Surgery & Hospital Stays
234

Premature Twins Born at 33 Weeks: From NICU Nurse to NICU Mom
October 30, 2024
NICU & Prematurity
233

Breath Holding Spells in Children: One Mother's Story of Preparation and Support
October 16, 2024
Diagnosis & Rare Disease
232

Child Life Specialist Secrets: Flu Shot Prep Strategies Every Parent Should Know
October 7, 2024
Our New Normal
231

Childhood Cancer: How One Mom Supports Other Families Through Her Own Experience
September 25, 2024
Cancer & Blood Disorders
230

Juvenile Arthritis: Trusting Your Parental Instincts About Chronic Pain
September 18, 2024
Our New Normal
229

Cystic Fibrosis: Early Diagnosis, Advocacy, and Equity
September 4, 2024
Diagnosis & Rare Disease
228

ADCY5 Rare Disease: A Mom and Advocate's Search for a Diagnosis
August 21, 2024
Diagnosis & Rare Disease
227

Moms on a Mission: Raising Pediatric Feeding Disorder Awareness with Jaclyn & Athena from Feeding Matters
August 7, 2024
Our New Normal
226

Alopecia in Children: A Mother's Journey of Advocacy, Instincts, and Resilience
July 24, 2024
Our New Normal
225

Burkitt Lymphoma at 8 Years Old: A Parent's Cancer Journey
July 10, 2024
Cancer & Blood Disorders
224

[6 minutes] Big News: The Child Life On Call App is Now SupportSpot!
July 1, 2024
Our New Normal
223

Premature Birth at 25 Weeks After Loss: A NICU NP Mom's Story
June 26, 2024
NICU & Prematurity
222

Collaborative Care Between Child Life Specialists and Social Workers at Hope for HIE
June 12, 2024
Our New Normal
221

Know EXACTLY When Rounds is Happening with Q-Rounds with Dr. Michael Pitt
May 29, 2024
Surgery & Hospital Stays
220

Ichthyosis: 60 Years of Reflection on a Daughter's Rare Skin Condition
May 22, 2024
Diagnosis & Rare Disease
219

CHARGE Syndrome: How NOT to Give Families Medical Information
May 15, 2024
Diagnosis & Rare Disease
218

STXBP1, Infantile Spasms, and NICU: Navigating IEPs and Advocacy
May 8, 2024
Diagnosis & Rare Disease
217

Ruptured Appendix in Children: Emergent Surgery, 6 Days in the Hospital & Struggles to Discharge
April 17, 2024
Surgery & Hospital Stays
215

End Stage Kidney Disease in Children: Sacrifice, Advocacy, and Joy
April 10, 2024
Diagnosis & Rare Disease
214

Kidney Disease in Children: 18 Years of Child Life Specialist Support
March 27, 2024
Our New Normal
212

End-Stage Kidney Disease at Birth: A Mother's NICU Journey (Part 1)
March 20, 2024
Diagnosis & Rare Disease
211

Connection, Healing, and Love: Insights from Patrice Karst, Author of The Invisible String
March 13, 2024
Our New Normal
210

Research on Parent Caregivers of Children with Medical Complexities
March 6, 2024
Our New Normal
209

Military Life and Pediatric Complex Care Abroad: One Family's Resilience
February 28, 2024
Our New Normal
208

Healing Without Surgery: Umbilical Hernia Solutions from a Physical Therapist
February 21, 2024
Surgery & Hospital Stays
207

Founder's Vision: Katie's Journey, Child Life Tech, Future Insights
February 14, 2024
Our New Normal
206

How to Support Kids who are Grieving, Bittersweet Relationships & Personal Loss
February 7, 2024
Our New Normal
205

Caregiver Isolation, Adult Special Needs Transition, and Becoming CapeAble
January 31, 2024
Our New Normal
204

Rare Disease: 12 Years to Diagnosis, Emotional Resilience, and Channeling Pain into Action
January 24, 2024
Diagnosis & Rare Disease
203

Infantile Spasms: Healing from Trauma and Building Emotional Resilience
January 17, 2024
Diagnosis & Rare Disease
202

NEC in the NICU: Personal Growth, Trauma, and Shielding Siblings
January 10, 2024
NICU & Prematurity
201

Anonymous questions from Instagram, Katie's personal burn story, and reflecting on 2023
December 20, 2023
Our New Normal
200

Infantile Spasms: One Mother's Diagnosis Story
December 13, 2023
Diagnosis & Rare Disease
199

Necrotizing Enterocolitis (NEC): A NICU Mother's Journey
December 6, 2023








