I've Just Seen A Face - Toolkit for Caregivers with Amy Mendillo

On this month’s myFace, myStory podcast, host Dina Zuckerberg is joined by Amy Mendillo – author, advocate, and parent of a child born with a cleft lip and palate. Amy discusses themes from her new parent guidebook, I’ve Just Seen a Face: A Practical and Emotional Guide for Parents of Children Born with Cleft Lip and Palate, including the roles of caregivers as key advocates in their child’s journey, both in and out of health settings. She also touches on the emotional issues that can arise for cleft parents before and during their baby’s first year of life, such as fears related to bonding, sadness and loss when a baby is unable to breast-feed, and the complex feelings caregivers experience when a baby’s face changes through surgery.

Learn more about the book, I’ve Just Seen a Face, at: www.amymendillo.com. To explore more parent guides and family resources, check out www.myface.org/parent-guides.

 

[FULL EPISODE TRANSCRIPT]

- [Announcer] Welcome to "myFace, myStory: Voices from the Craniofacial Community", with your host, Dina Zuckerberg.

 

- Hello and welcome to "myFace, myStory: Voices from the Craniofacial Community". Whether you're watching on YouTube or listening on Apple Podcast, click subscribe now, so you don't never miss a future episode. And if you're a fan of "myFace, myStory", rate and review the program on Apple Podcast, so we can get on messages of inclusivity and empowerment to more people. I'm your host, Dina Zuckerberg, the Director of Family Programs at myFace. I was born with a clef lip, a hearing loss, and no vision in my left eye. "myFace, myStory" is about people like us being seen and heard, about sharing stories within the craniofacial community and with others. Today, I will be joined by Amy Mendillo. Amy Mendillo is a writer, author, and advocate. Her book, "I've Just Seen a Face" is a practical and emotional guide for parents of children born with cleft lip and/or palate. Amy holds a master's in public policy from Brown University and master's in bachelor's degrees in music from Northwestern University and the Oberlin Conservatory of Music. She has consulted on state level health issues, advocated for local and city level policy, and worked as a writer-editor for the American Cleft Palate Craniofacial Association, where she currently serves on this family resources committee and board of directors. A proud cleft parent and adoptive parent, Amy lives with her family in Providence, Rhode Island. Welcome, Amy. I look forward to our conversation.

 

- Me too, Dina. Thank you so much for having me. It really is a pleasure to be here. I am a big fan of this show.

 

- Oh, thank you. So, can you share when you first learned that your daughter would be born with a cleft lip and palate? And take us back to that day?

 

- Yes. My husband and I learned about our daughter's diagnosis at a prenatal ultrasound at around 20 weeks gestation. And we had come into that experience with a long history of infertility. We tried for years to conceive and carry a pregnancy, and we ultimately adopted our first child joyfully, and then subsequently returned to the fertility clinic and were able to become pregnant and carry this pregnancy. And we ultimately learned of our daughter's diagnosis at around week 20. And so, at every turn, our history involved bad news. We would, at every ultrasound, at every test, every measure of progress, we were accustomed to hitting roadblocks. And so, when we came into this 20-week ultrasound, we were in a kind of position where we were braced. That said, I was totally taken aback by the news. I remember when the doctor was clicking and blinking and the tones were so soft and everyone was trying to stay, all the professionals were try