Céline Dion’s children have largely stayed out of the public eye, maintaining a low profile. However, as they grow older, their resemblance to their late father, René Angélil, becomes more apparent. Now 56, Céline is raising her three sons — René-Charles, 24, and twins Eddy and Nelson, 14 — on her own. Recently, fans have been amazed by how much they’ve grown. Let’s take a closer look.
Céline Dion is courageously fighting Stiff-Person Syndrome, a rare neurological disorder, yet she continues to show remarkable strength and resilience.
Céline Dion recently attended the TGL match between the Atlanta Drive GC and the Jupiter Links Club at SoFi Center in Palm Beach Gardens, Florida, on March 4. While there, she reunited with an old friend, Tiger Woods, who plays for Jupiter Links, and brought her three sons along for the event. Céline later shared some fun photos on social media.
Her team posted the images that included a shot of Céline being interviewed and another one where she posed with Tiger and her sons. Eddy and Nelson, especially, looked grown-up in white tees and chinos, perfectly matching the golf vibe, with René-Charles on his mom’s other side.
Céline Dion dazzled in a white button-up blouse knotted at the waist, accessorized with chains, skinny jeans, and crisp white sneakers. Her glowing look was especially striking, considering her ongoing fight against Stiff-Person Syndrome.
Céline is deeply loved by her fans.
Fans were quick to praise her appearance, with one person saying, “Always happy to see your beautiful face.” Another commented, “She’s looking so good,” while a third wrote, “So wonderful to see you out and about!” One fan even expressed their admiration, sharing, “She’s my hero!!”
Social media users were clearly taken aback by the teenage twins, Eddy and Nelson, particularly due to how mature they appear for their age. Many were surprised by their full beards, with some even questioning how they could possibly be just 14. However, others pointed out that it’s not uncommon for some teens to develop facial hair early, with some even noting that the twins seem to resemble their late father, who shared similar traits.
Despite the initial surprise, many people recognized that it’s simply a natural part of growing up.
On the anniversary of René’s passing, Céline shared a touching new photo with her sons and wrote a heartfelt message: “René, we can’t believe you’ve been gone nine years already. Not a day goes by that we don’t feel your presence, RC, Eddy, Nelson, and I. You were my greatest champion, my partner, and the one who always saw the best in me. I honor you, and you are forever missed mon amour… We love you.”
Before you leave, be sure to check out another article where we dive into Céline Dion’s heartbreaking journey with illness. It offers a poignant and personal look at the challenges she’s enduring while remaining strong for her family.
7 Biggest Reveals From the New Celine Dion Documentary
Celine Dion, also known as the “Queen of the Power Ballad,” has captivated audiences for decades with her dynamic performances and incredible vocal range.
Born in Quebec, Canada, the youngest of 14 children, Dion got her big break when she won the 1988 Eurovision Song Contest at age 20. She became a global superstar in the 1990s with the release of numerous international chart-topping songs, including the theme from the movie Titanic, “My Heart Will Go On.”
In December 2022 Dion made news for a different reason: After postponing and canceling a number of concerts on her worldwide tour, she revealed that she had been diagnosed with a rare and disabling disorder called stiff person syndrome (SPS) that had affected her ability to sing and walk.
The new documentary I Am: Celine Dion, directed by Irene Taylor, and currently streaming on Amazon Prime, offers an intimate and at times shocking look at Dion’s life with this debilitating condition.
Here are seven of the biggest revelations from the film.
1. It Took 17 Years for Dion to Get the Right Diagnosis
The 56-year-old’s first signs of stiff person syndrome appeared 17 years before her July 2022 diagnosis, when she first began experiencing unexplained muscle spasms that affected her vocal cords and overall well-being.
Identifying stiff person syndrome can be very challenging, and that often means people aren’t diagnosed early and may even be misdiagnosed, says Sarah Wesley, MD, MPH, a neurologist who specializes in inflammatory disorders at Columbia University in New York City. (Dr. Wesley isn’t involved in Dion’s treatment.)
The syndrome most commonly develops in women (by a ratio of 2 to 1 over men) and in people between 40 and 50 years old, though in very unusual cases, it can occur in children and older adults. It’s estimated that only about 1 or 2 people in one million have the condition.
Physicians often misidentify stiff person syndrome as Parkinson’s disease, multiple sclerosis, fibromyalgia, or anxiety. A test that measures levels of glutamic acid decarboxylase (GAD) antibodies in the blood can lead to a definitive diagnosis. People with stiff person syndrome can have GAD levels that are 100 times higher than normal.
2. Dion and Her Team Came Up With Fake Excuses for Her Canceled Tour Dates
The documentary details how symptoms of stiff person syndrome caused Dion to cancel shows or leave the stage mid-show when spasms caused her voice to fail.
In the film, the singer breaks down in tears as she reveals that she and her team lied about the reasons for the cancellations, giving fake excuses like ear or sinus infections.
In the spring of 2023, she says she made the agonizing decision to cancel the remainder of her Courage World tour, knowing how disappointed her fans would be.
The singer largely stayed out of the public eye after that, in part out of concern that people would see her having excursions with her family on a night when she was supposed to be on stage.
3. Stiff Person Syndrome Makes Dion’s Everyday Life Difficult
“I was losing my balance a lot. It was hard to walk. A lot of pain,” Dion recounts in the documentary.
People with stiff person syndrome can have episodes where they’ll be walking and just freeze; that stiffness poses a high risk of falls and subsequent fractures or head injuries, says Wesley.
With stiff person syndrome, the body’s own immune system goes awry and attacks an important enzyme in the nervous system that “turns off” muscles when a person is not using them. As a result muscles are constantly stimulated, which can lead to extreme stiffness and spasms, Wesley explains.
The pain of those spasms is not to be underestimated, says Wesley.
“It’s really severe — 10 out of 10 pain. Spasms are often prolonged and that can lead to people’s heart rates going up, sweating, and almost feeling like they are going to faint from the pain,” she says.
4. Dion Was Using Life-Threatening Amounts of Valium Before Her Diagnosis
Pre-diagnosis, the singer tried numerous remedies to keep performing, including steam showers and over-the-counter medications. As her symptoms worsened, her doctors prescribed different drugs, including Valium (diazepam) as a muscle relaxant.
Dion began with a standard dose of the medication, typically 2 to 10 milligrams.
But it began wearing off quickly. At one point, she took 90 milligrams of Valium to get through a performance.
“It could have been fatal. I did not question the level because I don’t know medicine,” Dion says in the film, adding, “I did not understand that I could have gone to bed and stopped breathing. And you learn. You learn through your mistakes.”
Currently there are no approved drugs specifically for stiff person syndrome. Treatments include drugs to relieve symptoms — things like anti-anxiety medications and muscle relaxants — and immunotherapy, which doctors hope can manage symptoms and slow disease progression.
5. Progress on Her Journey Back to Performing Led to a Frightening Disease Flare
Near the end of the documentary, the singer returns to the studio and nails a recording. After that exultant moment, Dion fist-bumps members of her team.
But soon after she is in a physical therapy appointment (part of her ongoing treatment) and begins to feel spasms in her foot. Her whole body locks up and it’s clear she’s in excruciating pain. Her team gives her diazepam nasal spray, which provides some relief.
With stiff person syndrome, moments of excitement or stress can trigger a flare. “One part of the condition is that overstimulation — whether it’s happiness, whether it’s sadness, whether there’s a sound, a surprise — can put me into a crisis,” says Dion.
Although flares can be agonizing, they aren’t typically life-threatening, though in extreme cases, spasms of the chest muscles can affect a person’s ability to breathe.
6. The Documentary Includes Intimate Moments From the Star’s Home Life
Although the film includes clips of the singer on stage, it mostly shows her in everyday life, makeup-free, her hair pulled back in a simple bun.
Dion shares home video footage from the birth of her eldest son, René-Charles, and her current home life as the mother of 13-year-old twins, her children from the singer’s marriage to her longtime husband and manager René Angélil. Angélil died in 2016 at the age of 73 from throat cancer.
7. Celine Dion Isn’t Giving Up
The flare at the end of the movie is harrowing, and it’s hard not to wonder if Dion will ever realize her dream of recording and performing again.
But her will is strong. “If I can’t run, I’ll walk. If I can’t walk, I’ll crawl. But I won’t stop,” she says.
