Child Life On Call: Parents of children with an illness or medical condition share their stories wit

Child Life On Call: Parents of children with an illness or medical condition share their stories wit


Latest Episodes

Episode 85 | Lisa's Story - A daughter with Sickle Cell (Repost!)
September 15, 2021

It’s another day in September, which means we are going to be recognizing National Sickle Cell Awareness Month.  Sickle Cell Disease is an inherited blood disorder in which blood cells may become sick

Episode 84 | Parents of Kids with Cancer
September 08, 2021

September is Childhood Cancer Awareness Month.  Over the last four-and-a-half years, I have had the opportunity and honor to interview many parents who are a part of a club that they didn’t ask to be

Episode 83 | How to Talk to About a Friend or Classmate's Cancer
September 01, 2021

When it comes to talking about cancer with kids, there is no one that compares to Holly Senn (Certified Child Life Specialist at Inova L.J. Murphy Children’s Hospital). We’re going to share some tips

Episode 52 | Nichole's Story - A son fighting cancer with help from My Special Aflac Duck and Child Life
December 09, 2020

(This episode was developed in partnership with I was compensated for this episode, but all opinions are entirely my own. ) In this episode, Katie Taylor, Certified Child Life Specialist talks about the importance of a community for caregivers. She...

Episode 51 | Katie and Jamie's Top 5 of 2020
December 04, 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 some of the good parts....

Episode 50 | Eileen's Story - A son with Recessive Dystrophic Epidermolysis Bullosa
November 11, 2020

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 (RDEB). While he inspires...

Episode 49 | Supporting families facing childhood medical experiences in the miltary
November 04, 2020

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 deployment of parents, child...

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

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 comes from being the...

Episode 47 | Rosaria's Story - A son's legacy after passing from cancer
October 07, 2020

0000006D 0000006D 000032F8 00002EBB 00343E2F 0000CADB 00007EF8 00007E87 00343DFB 003438E0

Episode 46 | Pediatric Pain with the Meg Foundation
September 30, 2020

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 , in this episode. Dr. Jody Thomas is a licensed clinical psychologist, and specialist in...