Celine Dion lives a key day in the midst of her fight against her illness


has reappeared

The singer has reappeared on the occasion of the premiere of her documentary

In the audiovisual piece, the artist explains how she has had to adapt her life after learning about the disease she suffers from.


  • Sheila González Oliva
  • Journalist specialized in heart, fashion, beauty and lifestyle.

    • 06/18/2024 16:46
    • Updated: 06/18/2024 16:46

Celine Dion has reappeared on a key date in her professional career. And since she announced the neurological disease that she suffers from, rigid person syndrome, there are few occasions in which she attends a public event. However, the occasion deserved it and the singer presented, very excited, her own documentary, which she called I’m Celine Dion (I am Celine Dion).

The actress has arrived at the presentation of said audiovisual piece, which was held in NY (United States) wearing a total white consisting of a satin blouse pussy bow and a straight skirt with a belt with black details. As for the hairstyle, the interpreter of My Heart Will Go On She has worn wavy hair parted on one side and, as makeup, she has opted for earth tones.

Celine Dion posing. (Photo: Gtres)

In a recent interview, Celine Dion opened up about her illness and how it affects her environment. «My children are afraid because they lost their father, and they wonder if I’m going to die. I don’t want to die, I don’t want to lie… I panic. It can be life-threatening. What is going to happen? », He expressed in Sunrise.

This is how he communicated his illness

In December 2022the singer made use of social networks to address her more than 5.2 million followers. fans around the world and break news that he would never have liked. It was then when he said that they had detected a rare neurological disease. Reason why he had to cancel his 2023 European tour.

Celine Dion
Celine Dion at the presentation of her documentary. (Photo: Gtres)

“I was recently diagnosed with a very rare neurological condition called stiff person syndrome, which affects one in a million people. “While we are still learning about this rare disease, we now know that this is what has been causing all the spasms I have been having,” he said. «The spasms affect all aspects of my life“Sometimes they even make it difficult for me to walk and they don’t allow me to use my vocal cords like I did before,” she added, visibly moved.

Likewise, he also said that he had a “great medical team working alongside me to help me get well, and they also give me hope and I support my children». «Everything I know how to do, what I have done in my life and what I love most is singing (…) I am working hard with my sports medicine therapist every day to regain my strength and my ability to perform again, But I have to admit that it has been a struggle,” he continued.

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