What if every milestone your child was supposed to reach came with countless curve balls? For Alexis Kaplan, motherhood quickly turned into a journey of advocacy, strength, and unwavering love as she navigated her daughter Gabby’s complex and rare health conditions....
Episode 67 | Todd and Morgan’s Story – A son with Biliary Atresia and a liver transplant
Podcast Show Notes
“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 with the truth that he had a life threatening condition called Biliary Atresia. The cure? A liver transplant.
Despite the many challenges they faced, Todd and Morgan talk about:
+How they used family to be their “google doctors”
+How to find your voice during bedside rounds
+Why started a business called Child Life Coffee
*Sponsor: Jambo Books
A Jambo Books subscription is like hitting the easy button for great diverse literature for your children. Every month, Jambo Books sends you 2 or 3 age-appropriate fiction books that star children of color. Jambo Books is a great gift for baby showers, birthdays, holidays or just because. Jambo serves children from birth to age 13.
Have you heard? The Child Life On Call mobile app for parents, kids
and their care team will be available in 2022. Sign up to stay informed here.
Child Life On Call is a community of parents and professionals that share ideas, stories and resources to help YOU navigate your child’s unique experiences. We give you strategies to support yourself and your family through life’s challenges. We are so glad you are here.
You Might Also Like…
249:How to Talk With Children About Child Abuse [REPOST]- Jane’s Story
Knowing how to talk to kids about child abuse can feel overwhelming—but it doesn’t have to be. In this impactful episode of Child Life On Call, host Katie Taylor interviews child abuse prevention advocate Jane Donovan—who also happens to be her mom. Jane shares her...
248: MERRF Syndrome and Motherhood: Raising and Remembering Dahlia-Jessica’s Story
"We followed Dahlia’s lead—and Dahlia was not going to let this stop her.” — Jessica Fein What happens when your child’s diagnosis is so rare that no one—including your doctors—knows how to help? For Jessica Fein, navigating life with her daughter Dahlia’s MERRF...