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Child Life On Call |  Medical, Parenting, Healthcare, Grief, Trauma, Pediatrics, Coping Skills, Community & Support - Podcast

Child Life On Call | Medical, Parenting, Healthcare, Grief, Trauma, Pediatrics, Coping Skills, Community & Support

Stories, Hope, Healing and Help for Parents Navigating Illness and Healthcare with Their Children
*Top 15% Globally Ranked Podcast*

Katie Taylor has been a child life specialist for almost 15 years and has one mission: to ensure that any parent who has a child with medical needs has access to other parents who have walked through the path before.

With over 200+ diagnoses covered in this podcast, Katie interviews parents of children with an illness or medical condition share their stories in safe, supportive discussions with a child life specialist.

Navigating life with a child who is sick can feel isolating, and this podcast offers parents a sense of connection.

Hosted by Katie Taylor, a Certified Child Life Specialist who provides evidence-based, developmentally appropriate interventions to help promote positive coping with hospitalization and illness.

Family Kids Medicine Parenting Kids & Family Health & Fitness
Update frequency
every 7 days
Average duration
37 minutes
Episodes
277
Years Active
2017 - 2025
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Episode 57 | A NICU stay for micro preemie twins born at 23 weeks

Episode 57 | A NICU stay for micro preemie twins born at 23 weeks

Katie, Certified Child Life Specialist interviews Amanda, mom to two micro preemie twins born at 23 weeks. 

Amanda and her husband met at Baylor University and had a normal pregnancy and delivery wit…

01:05:42  |   Wed 03 Feb 2021
Episode 56 | Effie's Story - A son with a Rare Disease , CTNNB1

Episode 56 | Effie's Story - A son with a Rare Disease , CTNNB1

 

Katie, Certified Child Life Specialist interviews Effie Parks, mom to Ford who was born with a rare disease called CTNNB1.

Effie is the host of the Once Upon a Gene podcast and in this episode she…

00:48:39  |   Wed 27 Jan 2021
Episode 55 | Dana's Story - Child Life Speialists in Schools - 12:14:20, 8.23 PM

Episode 55 | Dana's Story - Child Life Speialists in Schools - 12:14:20, 8.23 PM

Katie Taylor, Certified Child Life Specialist interviews Dana Burnett, Certified Child Life Specialist for the Bougier City, Louisiana school district. 

Dana talks about her child life journey up unt…

00:29:35  |   Wed 20 Jan 2021
Episode 54 | Danielle's Story - A daughter with Eosinophilic Gastroenteritis

Episode 54 | Danielle's Story - A daughter with Eosinophilic Gastroenteritis

Katie, Certified Child Life Specialist talks to Danielle, mom to Della a daughter with Eosinophilic Gastroenteritis.

You may know Danielle formally as Danni Starr, the media personality, but she is a…

00:43:11  |   Wed 13 Jan 2021
Episode 53 | Teresa's Story - A daugther with Spina Bifida and Tethered Cord

Episode 53 | Teresa's Story - A daugther with Spina Bifida and Tethered Cord

Katie, Certified Child Life Specialist interviews Teresa, a mom of a teenage daughter with Spina Bifida. 

With no signs of abnormalities during her pregnancy, Teresa was shocked to learn that a fatty…

00:44:46  |   Wed 06 Jan 2021
Episode 52 | Nichole's Story - A son fighting cancer with help from My Special Aflac Duck and Child Life

Episode 52 | Nichole's Story - A son fighting cancer with help from My Special Aflac Duck and Child Life

(This episode was developed in partnership with Aflac. I was compensated for this episode, but all opinions are entirely my own. #ad)

In this episode, Katie Taylor, Certified Child Life Specialist t…

00:36:21  |   Wed 09 Dec 2020
Episode 51 | Katie and Jamie's Top 5 of 2020

Episode 51 | Katie and Jamie's Top 5 of 2020

In another version of "Katie and Jamie's Top 5" these two friends and child life specialists try to lighten the mood by talking about our favorite things of 2020. We can all admit the year was...meh.…

00:39:34  |   Fri 04 Dec 2020
Episode 50 | Eileen's Story - A son with Recessive Dystrophic Epidermolysis Bullosa

Episode 50 | Eileen's Story - A son with Recessive Dystrophic Epidermolysis Bullosa

In this episode, Annie, Certified Child Life Specialist, talks to Eilieen. She is the amazing mom of a determined, fun loving, 4-year-old hero named Brady. Brady was diagnosed with Recessive Dystroph…

00:53:42  |   Wed 11 Nov 2020
Episode 49 | Supporting families facing childhood medical experiences in the miltary

Episode 49 | Supporting families facing childhood medical experiences in the miltary

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 ch…

00:44:25  |   Wed 04 Nov 2020
Episode 48 | Meg's Story - A daughter with craniosynostosis

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 disc…

00:53:35  |   Wed 14 Oct 2020
Episode 47 | Rosaria's Story - A son's legacy after passing from cancer

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

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00:57:06  |   Wed 07 Oct 2020
Episode 46 | Pediatric Pain with the Meg Foundation

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.

00:49:10  |   Wed 30 Sep 2020
Episode 45 | Amrita's Story - A son with GERD and feeding aversion

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 happen…

00:53:25  |   Wed 23 Sep 2020
Episode 44 | Lisa's Story - A daughter with Sickle Cell Anemia

Episode 44 | Lisa's Story - A daughter with Sickle Cell Anemia

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 sh…

00:47:41  |   Wed 16 Sep 2020
Episode 43 | Ashlyn's Story - A son with VACTERL association

Episode 43 | Ashlyn's Story - A son with VACTERL association

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 s…

01:04:39  |   Wed 19 Aug 2020
Episode 42 | Maura Senneff's Story - A son with Down syndrome

Episode 42 | Maura Senneff's Story - A son with Down syndrome

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 f…

01:11:47  |   Wed 12 Aug 2020
Episode 41 | Dominique's Story - A daughter born three months premature

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

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, therap…

00:35:45  |   Wed 05 Aug 2020
Episode 40 | A conversation about anti-racism and diversity in the field of Child Life

Episode 40 | A conversation about anti-racism and diversity in the field of Child Life

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 …

00:39:26  |   Wed 10 Jun 2020
Episode 39 | Jessica's Story - A son with Autism

Episode 39 | Jessica's Story - A son with Autism

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 neurop…

00:46:06  |   Tue 26 May 2020
Episode 38 | Elizabeth's Story - A daughter with Leukemia

Episode 38 | Elizabeth's Story - A daughter with Leukemia

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. E…

00:50:38  |   Mon 27 Apr 2020
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