Taylor Swift made history at the 2024 Grammys, becoming the first person ever to win “Album of the Year” four times. That came when her album Midnights, reIeased to much fanfare in 2023, took the top award. Not everyone was fawning over Taylor, however, with some on social media expressing their displeasure with how, in their view, rudely she acted when she accepted their award.
Essentially, they argued that Ms. Swift should have done more to show her gratitude to Celine Dion, who presented the award to Taylor despite having been diagnosed with an incurable neurologicaI disease called stiff man syn drome. To many viewers, it appeared that Taylor ignored Dion when accepting the award despite Dion’s difficulty in being on stage.
For example, one commenter on Fox News’ post on Facebook about Taylor’s Grammys win wrote, “Good for her but she should absolutely be ashamed of herself! She walked on stage, took the Grammy from Celine & dismissed her like she was no one! Celine Dion is battling a disease & I’m sure struggIed to even show up! I felt so sorry for her & the way she was treated! Somebody, please teach Ms. Taylor some manners!”
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.
Leave a Reply