Jase and Missy Robertson’s journey: Overcoming obstacles and finding strength

Mia Robertson, the youngest daughter of Duck Dynasty’s Jase & Missy Robertson, has been born with a condition known as cleft lip and palate, a gap in the upper lip that can involve the gum as well.

The U.S. Centers for Disease Control and Prevention shares that about one in every 1,600 babies is born with a cleft lip with a cleft palate in the U.S.

Because of her condition, sweet Mia, who is now 18 years old, has been forced to undergo 13 surgeries, with the 14th taking place just recently. The family truly hopes this would be Mia’s last procedure before her problem is finally solved.

Throughout every surgery, the young girl remains positive. What’s most, she hopes she serves as inspiration for other young children who are born with the same condition. On her own initiative and with the help of her family, Mia established the Mia Moo Fund in order to assist in making certain that each and every child wears a smile on their face.

“One of the functions of the Mia Moo Fund is to spread awareness of the cleft lip and palate journey,” Missy Robertson told Christian Post. “The other one is to help with medical funds for the parents and the families living right here in America.”

On his podcast Unashamed, Jase Robertson shared an update on Mia’s condition and said that his daughter is recovering well.

“She’s doing great. She’s turned a corner,” he said, and then added, “Everything seems great, seems to be fine.”

“Surgery went a little longer than expected, but she is home and recovering,” the loving father told his podcast listeners. “Thank you for praying for her and for our family. She is a champion!”

Before the surgery took place, Missy spoke of her daughter’s condition and explained that she had been constantly asked about the number of procedures Mia would need to undergo in the future. “There is never any other response than ‘We just don’t know,’” Missy said. She then added that they rely on God for assistance. “Since she is 18 now, she is taking the lead in all the discussions and medical forms. It’s been a little strange,” Missy wrote. “But it’s just another reminder to lean on the Lord and that I’m not in control.”

Mia also hopes that she’s at “the finish line.”

“Hopefully the last time I’ll see my doctors in this setting! It’s been a long road but we are at the finish line,” brave Mia said.

The Robertson’s have also been preparing for a new addition to the family as they open the doors to their hearts and home for a child whose mother was unfit to take care of.

We wish Mia speedy recovery.

This baby’s nickname was Pinocchio and check out what he looks like years later

From the moment little Olli Tresiz came into the world, it was clear he was unique, bearing the rare and intricate condition known as encephalocell. This distinctive trait marked the outset of a challenging journey toward finding medical solutions tailored to his needs.

As Olli’s journey progressed, his growing nose revealed a vulnerability: even minor injuries posed a grave threat, potentially triggering meningitis.

Realizing the seriousness of Olli’s situation, physicians strongly advised a crucial medical intervention to mitigate the risks associated with his condition.

Fortunately, the medical procedure proved effective, not only addressing the specific challenges of encephalocell but also significantly enhancing Olli’s respiratory capacity.

This pivotal moment marked a significant shift for the young lad, presenting him with an opportunity for a life marked by improved health and greater comfort.

In a bold act of both bravery and advocacy, Olli’s mother chose to unveil her son’s tale to the world. Taking to the vast expanse of the internet, she shared a heartfelt photo of Olli, shining a light on the rare medical circumstances that can find resolution through medical interventions.

The online community responded with an overwhelming display of solidarity, flooding the digital realm with well-wishes and hopes for Olli’s swift recovery.

This virtual embrace not only offered solace to the Tresiz family but also underscored the power of collective compassion and understanding in the face of exceptional medical trials.

Olli’s voyage, from the intricate labyrinth of encephalocell to the triumphant strides of medical intervention, stands as a testament to the strides made in medical science and the indomitable spirit of those confronting uncommon ailments.

Through the dissemination of awareness and shared narratives, Olli’s narrative has blossomed into a wellspring of inspiration, nurturing empathy and optimism within the online sphere and beyond.

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