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Shani's Story - A child with a learning difference #ADHD #Anxiety #Dyslexia #Dysmorphia
Shani's Story - A child with a learning difference #ADHD #Anxiety #Dyslexia #Dysmorphia

Season 3 Episode 58

Katie, Certified Child Life Specialist welcomes back Shani (a.k.a. Child Life Mommy) to the podcast. 

Shani is a Certified Child Life Specialist who …

5 years, 4 months ago

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Amanda's Story - A NICU stay for micro preemie twins born at 23 weeks
Amanda's Story - A NICU stay for micro preemie twins born at 23 weeks

Season 3 Episode 57

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

Amanda and her husband met at Baylor Univ…

5 years, 4 months ago

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

Season 3 Episode 56

 

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 th…

5 years, 5 months ago

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Dana's Story - A Child Life Specialist in Schools
Dana's Story - A Child Life Specialist in Schools

Season 3 Episode 55

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

5 years, 5 months ago

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Danielle's Story - A daughter with Eosinophilic Gastroenteritis
Danielle's Story - A daughter with Eosinophilic Gastroenteritis

Season 3 Episode 54

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

You may know Danielle formally a…

5 years, 5 months ago

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Teresa's Story - A daughter with Spina Bifida and Tethered Cord
Teresa's Story - A daughter with Spina Bifida and Tethered Cord

Season 3 Episode 53

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

With no signs of abnormalities during her p…

5 years, 5 months ago

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Nichole's Story - A son with Langerhans Cell Histiocytosis
Nichole's Story - A son with Langerhans Cell Histiocytosis

Season 3 Episode 52

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

In this episod…

5 years, 6 months ago

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Katie and Jamie's Top 5 of 2020
Katie and Jamie's Top 5 of 2020

Season 3 Episode 51

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 th…

5 years, 6 months ago

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Kelsey's story - Searching for her son's diagnosis
Kelsey's story - Searching for her son's diagnosis

Season 3 Episode 51

Meet Kelsey, mom to Nolan, a happy, hilarious, smart little boy. She and her family of 5 live in a small town in Ontario. Nolan is the youngest of he…

5 years, 7 months ago

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

Season 3 Episode 50

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 …

5 years, 7 months ago

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