In a devastating moment from “I Am: Céline Dion,” the famous person battles through an unexpected and horrifying SPS episode.
Fans are getting an unheard-of glimpse inside Céline Dion’s tribulations during the last few years of her life.
After being diagnosed with stiff-person syndrome in August 2022, the 56-year-old superstar tentatively but proudly returns to the recording studio in a devastating sequence towards the end of her new documentary, I Am: Céline Dion (available for streaming globally on Prime Video).
Shortly after, as part of her continuous treatment regimen, she makes her way to physical therapy and her foot starts to hurt.
Dion’s body locks up, indicating that she is in severe agony while her care team gives her a diazepam nasal spray during the SPS crisis episode. One of her teammates says, “We’ll do a 9-1-1 if she goes back into a spasm.”
In the movie, Dion subsequently remarks, “Every time something like this happens, it makes you feel so embarrassed.” “I’m not sure how to say it. You know that you dislike losing control of yourself?
The five-time Grammy winner thought back on the horrifying moment that director Irene Taylor’s crew captured on camera during her PEOPLE cover interview.
“Overstimulation—whether it be happiness, sadness, sound, or a surprise—can put me into a crisis—that’s one part of the [SPS] condition,” Dion explains, adding that she “did not see” the crisis episode coming that day. “Before something triggered, I was fine.”
Taylor’s understanding of the condition deepened when she was “two feet away” from Dion during the crisis.
Taylor remarks, “That was really amazing, not just for Céline to go through it, but for me to see as well.” “I continued to film because that is how I work, and I thought we would decide later whether or not to incorporate that into the movie.”
Dion and Taylor had developed a close relationship by the time the movie was in post-production, and according to Taylor, “I knew that putting it in the film was really not a risk because she believed in me at that point.” “I really can only thank her for that because she is an open book, was there, and didn’t hold anything back.”
Dion is attempting to humanize the uncommon illness through the movie and contribute to fund-raising efforts for scientific studies in the pursuit of a solution.
Neuropathy has a very broad spectrum. For this reason, I’m making a lot of effort to raise money so that people can speak with their husbands, friends, or neighbors about it,” Dion explains.
Adds Dr. Amanda Piquet, the doctor who diagnosed Dion and director of the University of Colorado Anschutz Medical Campus’s program on autoimmune neurology: “There are many exciting things in store for SPS, and the future looks bright.”
Baby once labeled ‘hideous’ grows into a stunning little girl
Every individual is beautiful in their own way, including newborns with their unique features.
In 2018, Angelica entered the world, bringing immense joy to her family. Her delicate facial features and a heart-shaped port-wine stain made her even more special. While her family embraced her beauty, not everyone appreciated the uniqueness of her birthmark.
Angelica’s mother, Marianna Bowering, shared that while their family adored her daughter just as she was, some strangers online felt entitled to make cruel comments about Angelica’s appearance.
“The worst comment I’ve received online was from someone asking if her face had been pressed onto a skillet, essentially saying her face looked grilled,” Marianna told The Mirror.
Marianna also recalled times when Angelica was labeled “hideous” or described as a “defect.” These remarks were deeply hurtful and added to the challenges the family faced. Despite the negativity, they remained determined to shield Angelica from the impact of such cruelty and to help her embrace her unique beauty.
To instill confidence and self-love in her daughter, Marianna took an extraordinary step. Inspired by Vascular Birthmark Awareness Day, which encourages participants to paint a heart on their cheek, she decided to replicate Angelica’s birthmark on her own face using makeup.
“I initially painted a heart as part of my makeup look, but then I thought, why not go all out and recreate Angelica’s port-wine stain?” Marianna shared with The Epoch Times.
However, not all reactions were positive. Remarks suggesting the mark would fade over time or that Angelica could conceal it with makeup as she grew older left Marianna heartbroken. These comments reminded her of society’s rigid standards of beauty and the pressure to conform.
Determined to counter this, Marianna and her family encouraged Angelica to embrace her individuality. On occasion, Marianna would even decorate Angelica’s birthmark with glitter to celebrate its beauty.
“Thankfully, tests have shown Angelica is completely healthy,” Marianna said, acknowledging that children with similar birthmarks can sometimes face health concerns like glaucoma. “We just need regular check-ups to monitor her health, particularly her eyes.”
Angelica is now thriving, surrounded by love and support that teaches her to appreciate her uniqueness. Her story is a reminder that beauty comes in many forms and that self-love is a powerful gift.
Isn’t Angelica a stunning young girl with a story that inspires?
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