Jase and Missy Robertson, known from “Duck Dynasty,” express their hope that their daughter Mia’s recent surgery, the fourteenth procedure to correct her cleft lip and palate, will be the last. Mia, 18, underwent the surgery last month and is currently recovering at home.
The Robertsons have faced a prolonged and challenging journey since Mia’s birth in 2004, involving multiple trips to the hospital for various surgeries aimed at addressing her cleft lip and palate. The family is optimistic that Mia’s recent procedure will mark the end of this series of surgeries.
Jase and Missy Robertson, known for their appearances on “Duck Dynasty,” have been navigating a challenging journey with their daughter Mia, who was born with a cleft lip and palate. The family recently shared an update on Mia’s health as she underwent her fourteenth surgery to address her medical condition.
Mia’s surgery, which took place last month, marked another step in a lengthy process that began when she was born in 2004. The Robertson family has been steadfast in their support of Mia, accompanying her through numerous hospital visits and operations over the years.
The latest surgery prompted Jase Robertson to provide an update on Mia’s condition during a podcast episode of “Unashamed,” where he, along with his father Phil and brother Alan, shared the encouraging news. He expressed gratitude for the prayers and support received, noting that Mia had turned a corner and was doing well.
The surgery, while longer than expected, was deemed successful, and Mia is currently recuperating at home. Jase thanked those who had prayed for Mia and the family, describing her as a “champion” in facing the challenges associated with her cleft lip and palate.
Missy Robertson, Mia’s mother, had previously shared her anxiety about the surgery on social media. She addressed the uncertainty regarding the number of surgeries Mia might still need, emphasizing the family’s reliance on faith during such moments.
Mia herself took to social media to announce that she was at the “finish line,” expressing hope that it would be the last time she visited the doctors in that setting. The post reflected her positive outlook and determination to overcome the challenges she has faced.
Missy Robertson opened up about the evolving dynamic with Mia as she turned 18, highlighting Mia’s increased role in making decisions about her medical care. Missy emphasized the need to lean on the Lord and accept that she is not in control, acknowledging the unique journey they are on as a family.
Throughout Mia’s journey, the Robertsons believe there is a purpose in their family’s suffering and challenges. Missy expressed that looking back over the past few years, they see reasons for going through the difficulties, especially in Mia’s desire to help others.
Mia’s journey has not only showcased her strength but also provided an opportunity for her to positively influence others and bring them closer to God. Missy underscored the greatness of God’s plan and the humility to trust His purpose in Mia’s life.
As Mia continues to recover and the family remains optimistic, their story serves as an inspiration for many facing their own challenges, demonstrating the power of faith, resilience, and the support of a loving family.
In her commitment to ensure the well-being of children facing challenges like hers, Mia Robertson founded the Mia Moo Fund. This initiative aims to support families dealing with cleft lip and palate, congenital conditions that occur when the lips and roof of the mouth fail to fuse properly during pregnancy.
According to data from the Centers for Disease Control and Prevention, approximately one in every 1,600 babies in the United States is born with a cleft lip and palate. Additionally, about 1 in 2,800 pregnancies results in a baby born with both a cleft lip and palate. Moreover, one in 1,700 infants is born without a cleft lip but with a cleft palate.
The Mia Moo Fund serves dual purposes: raising awareness about the challenges associated with the cleft lip and palate journey and providing financial assistance to parents and families in the United States grappling with these medical conditions.
Missy Robertson, Mia’s mother, highlighted the fund’s objectives in an earlier interview, emphasizing the importance of both spreading awareness and offering practical support to families navigating the complexities of cleft lip and palate in their children. The Mia Moo Fund stands as a beacon of hope and assistance for families facing similar journeys, reflecting Mia’s desire to make a positive impact on others experiencing similar challenges.
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