Celine Dion puts on impromptu performance backstage at the Grammys amid battle with stiff person syndrome

Celine Dion not only shocked everyone by performing unexpectedly backstage at the Grammy Awards, but she also made a surprise appearance to present Album of the Year.

Dion, 55, has maintained a low profile since disclosing her condition in December 2022 in order to combat stiff person syndrome.

In the video, Sonyaé—who is up for a Grammy—and Dion dance to the beautiful harmony of their voices.

The singer of “My Heart Will Go On” made her first appearance in public since November, when she attended an NHL game with her kids. She also made a surprise appearance at the Grammy Awards.

Although there are rumors that Dion’s voice isn’t getting better in a way that would allow her to perform or record again, it appears that she can still hit the notes that we are all familiar with.

LONDON, ENGLAND – JULY 05: On July 5, 2019 in London, England, Celine Dion will give a live performance at Barclaycard Presents British Summer Time Hyde Park at Hyde Park. Redferns/Samir Hussein photo

After disclosing her illness, she postponed the remainder of her tour dates, raising doubts about her ability to give a complete performance.

Celine, you have our undying love and support.

“She’s a real Thumbelina” – Meet the girl who’s only 99cm tall and defied all the odds

Kenadie Jourdin-Bromley, a Canadian child from Ontario, seemed ordinary at first glance.

She had high hopes for the future, loved sports and drawing, and went to school.

Nonetheless, one characteristic set Kenadie apart from her peers: her diminutive height of 99 centimeters.

Reports state that when Kenadie was born in February 2023, she weighed a mere 2.5 pounds. Her condition was quickly diagnosed by doctors as an uncommon form of cardiovascular disease, thought to affect only 100 people globally. The nurses dubbed her “Thumbelina,” quite fittingly.

Regretfully, Kenadie had slim chances of surviving.

According to reports, the girl’s condition can lead to complications like delayed mental development, respiratory issues, and digestive issues. Doctors at the hospital where the girl was born were concerned that she wouldn’t have much time to live due to her brain injuries.

Understandably, her parents were devastated. In order to give their little girl a name in case she passed away, they chose to christen her on the day of her birth.

“We thought we were going to take her home to die, because that’s what the doctors told us,” mom Brianne explained to Barcroft TV back in 2016.

Still, as the days went by, Kenadie steadfastly refused to give up. After she triumphed over all the challenges and hardships, her parents were able to dream again that she would survive. It was nothing less than a miracle for them.

Many years later, Kenadie still astounds everyone she encounters. She is only 99 centimeters tall, her arms and legs are still immature, and she struggles to learn new things, but she is a content young girl who enjoys life to the fullest.

Kenadie reportedly enjoys bowling and ice skating. Above all, she makes people happy that she meets.

“Kenadie makes me laugh. She’s very empathetic – if you hurt your finger she comes and gives you a hug. She’s got an infectious laugh that makes you want to laugh along with her,” Kenadie’s assistant Jessica Putnam mentioned to Barcroft TV in 2016.

Naturally, Kenadie and her family face many new challenges in their lives. Despite her loved ones’ best efforts to take each day as it comes, the young girl is continuously dealing with medical issues.

“My hope for Kenadie’s future– my biggest hope for her– is I want her to be happy. I want her to smile and be successful. If we can get through today, then we’ll see about tomorrow,” her mom said.

We are happy to share Kenadie’s inspiring story!

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