New Episodes Every Wednesday

Episodes

Episode 73 | Should Kids Go To Funerals?
June 22, 2021

Episode 73 | Should Kids Go To Funerals?

Katie, Certified Child Life Specialist talks with Lauren Holley, CCLS and Professor answers the question and discusses the topic: Should Young Kids Go To Funerals? We talk about: +How to assess whether or not your child is re...

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Episode 72 | Laurie's Story - A son with Fanconi Anemia and Tetralogy of Fallot
June 15, 2021

Episode 72 | Laurie's Story - A son with Fanconi Anemia and Tetralogy…

"It was a life or death... that was our life and we rose to the occasion." Katie, Certified Child Life Specialist talks with Laurie Strongin from Hope for Henry. We talk about: +How parenthood started out with hearing the new...

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Episode 71 | How To Tell Your Kids That Mom Has Cancer
June 8, 2021

Episode 71 | How To Tell Your Kids That Mom Has Cancer

Answering Parent Questions: How Do I Tell My Kids that I Have Cancer? Katie, Certified Child Life Specialist gives you tips, language and things to consider when you're telling children about a cancer diagnosis in the family....

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Episode 70 | Sara's Story - Telling Your Child You Have Cancer
June 1, 2021

Episode 70 | Sara's Story - Telling Your Child You Have Cancer

Katie, Certified Child Life Specialist talks with Sara Olsher, mom, cancer survivor, and owner of Mighty and Bright. Not only does Sara talk with us about getting diagnosed with breast cancer at the age of 34, but she also ta...

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Episode 69 | Liza's Story - A daugther with Lyme Disease
May 18, 2021

Episode 69 | Liza's Story - A daugther with Lyme Disease

Episode 69 | Liza's Story - A daugther with Lyme Disease "I don't think I would have ever done the work on myself had it not been for my daughter's struggle." Katie, Certified Child Life Specialist talks with Liza Blas from V...

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Episode 68 | Child Life Specialists Talk About How They Support Transplant Families
May 11, 2021

Episode 68 | Child Life Specialists Talk About How They Support Trans…

"Being a child life specialist with this population is not just about supporting them through their hospital experience, its about preparing them for the rest of their life." Katie, Certified Child Life Specialist talks with ...

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Episode 67  | Todd and Morgan's Story - A son with Biliary Atresia and a liver transplant
May 4, 2021

Episode 67 | Todd and Morgan's Story - A son with Biliary Atresia an…

"We had to learn everything we could because our son's life was literally on the line." Katie, Certified Child Life Specialist talks with Todd and Morgan who just a few weeks after the birth of their first child were faced wi...

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Episode 66 | How to Support Siblings of Children with Medical or Special Needs
April 20, 2021

Episode 66 | How to Support Siblings of Children with Medical or Spec…

Katie, Certified Child Life Specialist is interviewed and asked about ways to support children of chronically ill or medically complex children. Questions that Katie discusses include: +How to have hard conversations with chi...

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Episode 65 | Holly's Story - A son with Hereditary Spastic Paraparesis (HSP)
April 13, 2021

Episode 65 | Holly's Story - A son with Hereditary Spastic Paraparesi…

"I think this may be a parent's worst nightmare." Katie, Certified Child Life Specialist interviews Holly, mom to three children living in Northern California. Holly's son, Austin, was typical until just after his 1st birthda...

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Episode 64 | Mijha's Story - A daughter with Triplication of Gends on Chromosome 15q
April 6, 2021

Episode 64 | Mijha's Story - A daughter with Triplication of Gends on…

Mijha and her husband live in Atlanta with their three daughters—ages 9, 5, and 8 months at the time of this conversation with Child Life On Call. Her middle daughter, Violet, was born with challenges that became evident only...

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Episode 62 | Madeline's Story - The sibling of a child with a rare genetic condition
March 23, 2021

Episode 62 | Madeline's Story - The sibling of a child with a rare ge…

"It's been rough. It's like your heart is in two different places." Katie, Certified Child Life Specialist interviews Madeline, a mom from Utah that shares her son's experience with having a rare form of skeletal dysplasia an...

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Episode 61 | Lindsey's Story - A son with Infant Botulism
March 9, 2021

Episode 61 | Lindsey's Story - A son with Infant Botulism

Annie, Certified Child Life Specialist interviews Lindsey, mom to Memphis a son who suffered from Infant Botulism. Lindsey is an experienced mother of three when her son, Memphis, came into the world. She breastfed him like s...

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Episode 60 | Dafne's Story - Children with Chronic Illness: Juvenile Type 1 Diabetes, Psoriatic Arthritis and Ankylosing Spondylitis
March 2, 2021

Episode 60 | Dafne's Story - Children with Chronic Illness: Juvenile …

Katie, Certified Child Life Specialist interviews Dafne, The Chronic Illness Coach. Dafne is mom to three college-age kids and she and her husband live in Houston, Texas. In this episode, we talk about how her children all su...

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Klippel-Trenaunay Syndrome (KTS): One Family's Rare Disease Journey
Feb. 23, 2021

Klippel-Trenaunay Syndrome (KTS): One Family's Rare Disease Journey

Katie, Certified Child Life Specialist interviews Shay Shull from Mix & Match Mama. Shay is a cookbook author, lifestyle blogger, travel agency owner, wife and mama who loves making every day special for my family. Shay is mo...

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Episode 58 | Shani's Story - A child with a learning difference #ADHD #Anxiety #Dyslexia #Dysmorphia
Feb. 9, 2021

Episode 58 | Shani's Story - A child with a learning difference #ADHD…

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 has a private practice in Northern California and you can learn more about ...

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Episode 57 | A NICU stay for micro preemie twins born at 23 weeks
Feb. 2, 2021

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 with their first son. Their se...

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Episode 56 | Effie's Story - A son with a Rare Disease , CTNNB1
Jan. 26, 2021

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 shares about her journey int...

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Episode 55 | Dana's Story - Child Life Speialists in Schools - 12:14:20, 8.23 PM
Jan. 19, 2021

Episode 55 | Dana's Story - Child Life Speialists in Schools - 12:14:…

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 until this point and how she h...

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Episode 54 | Danielle's Story - A daughter with Eosinophilic Gastroenteritis
Jan. 12, 2021

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

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 also momma of two girls, on...

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Episode 53 | Teresa's Story - A daugther with Spina Bifida and Tethered Cord
Jan. 5, 2021

Episode 53 | Teresa's Story - A daugther with Spina Bifida and Tether…

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 lump on her daughter's ski...

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Episode 52 | Nichole's Story - A son fighting cancer with help from My Special Aflac Duck and Child Life
Dec. 8, 2020

Episode 52 | Nichole's Story - A son fighting cancer with help from M…

(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 talks about the importance ...

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Episode 51 | Katie and Jamie's Top 5 of 2020
Dec. 3, 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... so why not chat about s...

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Episode 50 | Eileen's Story - A son with Recessive Dystrophic Epidermolysis Bullosa
Nov. 10, 2020

Episode 50 | Eileen's Story - A son with Recessive Dystrophic Epiderm…

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 Dystrophic Epidermolysis Bullosa (...

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