“Duck Dynasty” Stars Open Up about Family Medical Journey
Is Sugar Really That Bad for You?
Amy Robach and Andrew Shue Share Blended Family Challenges
2 Breathing Techniques to Start Your Day
The Cancer Diagnosis That Saved Amy Robach's Marriage
Amy Robach and Andrew Shue Share How They Learned to Parent Toge…
Tools to Help You Accomplish Anything!
How Breathing Can Help Your Mental and Physical Health!
New Mom Was Told She Couldn’t Have Kids Due to PCOS
New Hope in the Fight Against HIV
Woman Shares Her Story of Growing Up with Facial Hair!
Why Cheese Is a Great Snack for Your Oral Health!
Nutritionist Shares Her Favorite Healthy Cheeses!
The Stigma of HIV Still at Play in Blood Donation?
What Are the Signs and Symptoms of PCOS?
Concerned You Might Have Type 2 Diabetes?
Could an HIV Vaccine Be Available Soon?
How to Take Control of Your Diabetes Risk!
Would You Hire Someone to Test Your Partner’s Loyalty?
Do You Know How to Muscle Floss?
Missy and Jase Robertson, best known as stars of A&E’s hit reality show “Duck Dynasty,” join The Doctors to discuss a medical struggle the family has endured for the past 12 years.
Having always wanted a daughter, Missy explains how excited she was to learn she was pregnant with a baby girl. However, at a regular ultrasound appointment, she was given the devastating news that there was a problem. The couple’s daughter, Mia, was born with a bilateral cleft lip and palate. She was unable to eat without choking and needed numerous surgeries to correct the structural deformities in her face.
The family came together to support Mia as best they could, gaining strength through their religious faith and finding as much information about her condition as possible. They also reached out to the International Craniofacial Institute to begin repairs to her lip and nose.
Mia, now age 12, has since undergone eight separate surgeries and will require further operations as she continues to grow and develop to adulthood.
“We have been through the journey that we’re still on, but Mia has just become a phenomenal young lady – very confident and self-assured – and we wanted to share that story as hope for other people,” Missy says. Missy details the family’s journey in her new book, “Blessed, Blessed … Blessed.”
Listen as plastic surgeon Andrew Ordon explains how cleft palates develop, and meet Mia!
Since March 2014, the family has been running the Mia Moo Fund, a charitable organization that raises awareness and funds for research and treatments for cleft lips and palates. Jase and Missy add that when Mia was born, they felt confused and struggled to get information and assistance to help them navigate the course of treatment for their daughter. Jase says they began the Mia Moo Fund to help other families more easily find the information and financial assistance they need.