As a dedicated follower and admirer of the Robertson family, I have been deeply moved by Mia Robertson’s courage and resilience throughout her health journey. Having followed her story since its beginning, I can truly appreciate the strength that this young woman possesses.
The Robertsons are continuing to share insight into Mia Robertson‘s health journey.
The stars of Duck Dynasty, Missy Robertson and Jase Robertson, have requested prayers from their followers as their 20-year-old daughter prepares for her sixteenth operation to correct a cleft palate.
Missy posted on Instagram on July 28th, “Another night in a familiar hotel room,” accompanied by a picture of herself and Mia. She no longer uses words like ‘last’ or ‘minor’, but she still requests prayers. Tomorrow is Mia Robertson’s 16th surgery. (Instagram handle: @miarobertson1)
Undoubtedly, the reality TV personality’s followers were eager to express their backing. One fan even wrote, “Sending prayers for Mia, may she be blessed!!”.
A supporter reminisced about the surgical procedures experienced by their “cleft-affected darling,” and remarked, “I simply chose to stop tallying the number.”
Regarding Mia, she approached her upcoming surgery with optimism, sharing a photo on Instagram Stories from the hospital with her mom and the caption, “Sixteen surgeries and still going strong with my incredible mom!” She also included a prayer hands symbol in her post, indicating this was her final operation.
For quite a while now, I’ve been open about my surgical journey, regularly updating fans along the way. After my 13th surgery in 2021, which I had hoped would mark the end of this chapter, I couldn’t help but express how profound it was to have my loved ones by my side during this time.
She expressed on Instagram, “Surgery wasn’t my idea of fun, but with this incredible family and friends, it was tough not to feel showered with love 😊. I can hardly believe the surgeries are done, but I am incredibly thankful for this journey. Thanks for your prayers!!!”
Mia, who had a birth defect affecting both her upper lip and palate (cleft lip and palate), was the inspiration for the Mia Moo Fund, an organization that was established by her family in the year 2014, as they shared their experiences with the public.
At just three months old, Mia had her initial operation, followed by multiple surgeries over time, including those for lip reshaping, nasal passages, and a bone transplant, among others.
Consequently, Mia, along with her relatives, namely Reed and Cole, have committed their efforts to the Mia Moo Fund, with the aim of assisting those who encounter circumstances akin to their own.
As a lifestyle advocate, I’m passionate about sharing knowledge, sparking inspiration, and enhancing the lives of children born with cleft lips or palates. At Mia Moo Fund, our heartfelt aim is to ensure every child in this situation receives superior medical attention, regardless of their financial background.
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2024-07-31 00:47