New Episodes Every Wednesday

Episodes

Episode 49 | Supporting families facing childhood medical experiences in the miltary
Nov. 3, 2020

Episode 49 | Supporting families facing childhood medical experiences…

Katie talks to two Certified Child Life Specialists and military spouses, Savannah Self and Lisa McWhorter about ways to support military families. From long waits in military hospitals to helping children navigate the deploy...

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Episode 48 | Meg's Story - A daughter with craniosynostosis
Oct. 13, 2020

Episode 48 | Meg's Story - A daughter with craniosynostosis

Meg, is mom to four children one of whom is living with syndromic craniosynostosis. Her daughter, Avery, who is now six-years-old is proof that children are resilient and capable of so much. She discusses the exhaustion that ...

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Episode 47 | Rosaria's Story - A son's legacy after passing from cancer
Oct. 6, 2020

Episode 47 | Rosaria's Story - A son's legacy after passing from canc…

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Episode 46 | Pediatric Pain with the Meg Foundation
Sept. 29, 2020

Episode 46 | Pediatric Pain with the Meg Foundation

Katie, Certified Child Life Specialist, talks with Jamie Gentille, Director of Child Life Services at Inova Children's Hospital and Dr. Jody Thomas, from the Meg Foundation for Pain , in this episode. Dr. Jody Thomas is a lic...

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Episode 45 | Amrita's Story - A son with GERD and feeding aversion
Sept. 22, 2020

Episode 45 | Amrita's Story - A son with GERD and feeding aversion

Spit up, and even reflux, can be a common problem for infants, but what happens when it's more than that? In this episode, Amrita shares with Katie, Certified Child Life Specialist, about what happens when a child's reflux be...

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Sickle Cell Anemia in Children: A Mother's Advocacy Journey
Sept. 15, 2020

Sickle Cell Anemia in Children: A Mother's Advocacy Journey

In this episode, Katie interviews Lisa, mom to Riley. Sweet Riley is a spunky and sweet two-year-old living with Sickle Cell Anemia. Lisa talks about how they knew it would be a possibility while she was pregnant due to the t...

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VACTERL Association: What Parents Need to Know About This Rare Diagnosis
Aug. 18, 2020

VACTERL Association: What Parents Need to Know About This Rare Diagno…

Meet Ashlyn, momma to her sweet and smiley boy, Myles. Myles was born with a rare disease that effects his limbs and other parts of his body. These symptoms are known as VACTERL association . As a self-proclaimed "planner," A...

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Down Syndrome: A Mother's Journey of Love and Advocacy
Aug. 11, 2020

Down Syndrome: A Mother's Journey of Love and Advocacy

Meet Maura Senneff, mom to sweet Ryan. Ryan is a thriving 8-year-old boy who has Down syndrome. The amazing advocate by his side, his momma Maura, describes that "zooming out" and looking at things from wide lens helped them ...

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Episode 41 | Dominique's Story - A daughter born three months premature
Aug. 4, 2020

Episode 41 | Dominique's Story - A daughter born three months prematu…

Katie talks to Dominique, mom to Mila, who shares her birth story and NICU experience. Born at just 1lb 11ounces at 26 weeks old, Mila has made tremendous progress thanks to proactive parents, therapies and her momma's un con...

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Anti-Racism and Diversity in Child Life: An Important Conversation
June 9, 2020

Anti-Racism and Diversity in Child Life: An Important Conversation

Katie interviews Meg and Jess, two certified child life specialists who also have dual certifications in rec therapy and nursing! These two ladies host a podcast called Don't Worry Bout My Hair and they are your @friendswithf...

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Autism Diagnosis: A Mother's Journey from Anxiety to Acceptance
May 25, 2020

Autism Diagnosis: A Mother's Journey from Anxiety to Acceptance

In this episode, Katie, Certified Child Life Specialist, interviews Jessica, mom to two special needs children and one of which who is on the Autism spectrum. Jessica is also an adult clinical neuropsychologist and also hosts...

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When Your Child is Diagnosed with Leukemia: What to Expect
April 26, 2020

When Your Child is Diagnosed with Leukemia: What to Expect

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 Eli...

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Episode 37 | Meg's Story - A daughter with Idiopathic Thrombocytopenic Purpura (ITP)
April 13, 2020

Episode 37 | Meg's Story - A daughter with Idiopathic Thrombocytopeni…

Katie, Certified Child Life Specialist, talks with Meg Casano, mother to Ella who has Idiopathic Thrombocytopenic Purpura (ITP) and also created the nonprofit Medi Teddy which is a stuffed animal cover for intravenous medicat...

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36. Delanie's story - An American in Quarantine in China
March 29, 2020

36. Delanie's story - An American in Quarantine in China

In this episode, Katie interviews Delanie, an American and child life student currently living in Beijing. She has been in quarantine since January 27. She shares what quarantine life has been like in China ... the center of...

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Episode 35 | Talking to kids about the Coronavirus
March 12, 2020

Episode 35 | Talking to kids about the Coronavirus

When it comes to the Coronavirus, how we inform our children is incredibly important. If you're wondering though, how can we talk to our kids when we as adults still don't know exactly what's happening, you're not alone. This...

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Episode 34 | Katie + Jamie's Top 10 - Heart Month
Feb. 26, 2020

Episode 34 | Katie + Jamie's Top 10 - Heart Month

Katie sits down (across the airwaves) with Jamie Gentille, Certified Child Life Specialist, Director of Child Life Services at Inova Children's Hospital, author and self-proclaimed animal themed yoga enthusiast to talk all th...

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Rare Childhood Cancer (atypical teratoid rhabdoid tumor): A Father's Perspective on His Daughter's Journey
Feb. 13, 2020

Rare Childhood Cancer (atypical teratoid rhabdoid tumor): A Father's …

This episode is not a cancer story. This is a story about a loving family, a precious child, and how to find miracles during the darkest parts of life. In this episode, Katie interviews Scott Kramer, father to Maddie. Maddie ...

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Neuroblastoma: Creating Joy During Childhood Cancer Treatment
Jan. 13, 2020

Neuroblastoma: Creating Joy During Childhood Cancer Treatment

In this episode Katie Taylor, Certified Child Life Specialist interviews Tara Geraghty, President and Founder of Making Cancer Fun . Tara is momma to Emily who was diagnosed with Stage 4 Neuroblastoma at just three years old....

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Child Life Specialists Share Their Expertise: A Roundtable Discussion
Nov. 25, 2019

Child Life Specialists Share Their Expertise: A Roundtable Discussion

This isn't your typical Child Life On Call episode! Katie sits down with two other child life specialists and each talks about their journey into child life, some "child life wins," and the hilarious things that kids have sai...

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Episode 29 | Tiger Livy's Story - An interview with Erin Garcia and Betsy Miller
Nov. 3, 2019

Episode 29 | Tiger Livy's Story - An interview with Erin Garcia and B…

This episode of the Child Life On Call podcast is different that what you're used to hearing, but I fell in LOVE with a book called Tiger Livy and I knew I had to interview the authors. Tiger Livy is the story of a brave six-...

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Episode 28 | Lauren's Story - A daughter with Congenital Heart Defects
Oct. 28, 2019

Episode 28 | Lauren's Story - A daughter with Congenital Heart Defects

This is Lauren's Story - A daughter with congenital heart defects on the Child Life On Call Podcast, hosted by Katie Taylor, Certified Child Life Specialist. Little Everly is just over two years and has more fight and life in...

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Birth Trauma and Prematurity: One Mother's Journey with Two Sons
May 7, 2019

Birth Trauma and Prematurity: One Mother's Journey with Two Sons

This episode features Alexandra Ortega, mom of three. She shares the stories of her two son's Theo and Noah. First, we talk about her second-born, Noah, who suffered a traumatic brain injury during his birth at 35 weeks. Next...

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Episode 26 | Gillian's Story - A daughter with Infant Leukemia
April 22, 2019

Episode 26 | Gillian's Story - A daughter with Infant Leukemia

In this episode you will hear from Gillian, cohost of the For Grits and Giggles podcast. Gillian describe her personal journey that includes a cancer diagnosis for her infant daughter and life altering accident that happened ...

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Episode 25 | Meredith Howell's Story - a daughter with a rare genetic condition (BBSOAS)
April 4, 2019

Episode 25 | Meredith Howell's Story - a daughter with a rare genetic…

Meredith, mom to now 8-year-old Lola, shares her experience with her daughter who was diagnosed with Bosch-Boonstra-Schaaf optic atrophy syndrome (BBSOAS) shortly after she was three-years-old. However, their story didn't beg...

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