As the sun sets behind the mountains in an exclusive neighborhood 30 minutes from the Las Vegas Strip, I can hear a recognizable voice singing behind a closed door.
“Is that Celine?” I ask.
The security man guarding the hotel suite nods.
I am about to interview a musical megastar, and it sounds like she is in a cheerful mood.
But the iconic voice I can hear casually singing away is one that fans feared they might never hear again.
“I’ve been dealing with health problems for a long time,” she shared in an Instagram video in December 2022.
“I have been diagnosed with a very rare neurological disorder.”
After that devastating announcement, Celine Dion canceled the remainder of her world tour and has rarely been seen in public since.
Signs of trouble
The medical name for her little-known illness is Stiff Person Syndrome (SPS), a neurological condition that causes muscles to spasm.
As we sit down to talk, Celine says it went undiagnosed for years.
The 56-year-old artist describes the distress she felt as a performer when she began to notice changes in her voice on tour.
“It just felt a little strange, like a little spasm,” says the Canadian star.
“My voice was struggling, I was starting to push a little bit.”
She demonstrates the subtle difference by singing the first few bars of her 1993 hit The Power of Love, showing how she had to force her voice to hold the notes that once came more easily.
Occasionally, she would ask the conductor of her backing musicians to bring certain songs down a key for a few performances.
“I needed to find a way to be on stage,” she explains.
She hoped singing slightly lower might give her voice a chance to recover.
Audiences would never have known the struggle she was facing behind the scenes.
But Celine says at the time it felt impossible to take time off.
“These shows were sold out for a year and a half, going around the globe.
“And I’m going to say to people, ‘Excuse me about my spasm? Excuse me about my je ne sais quoi?'”
She put huge pressure on herself to keep the show on the road, not understanding what was causing the symptoms she was experiencing.
But it all became too much.
Her eventual diagnosis brought the realization that this was not tour fatigue. It was permanent.
SPS is an autoimmune disease that can be debilitating. There is no known cure.
It is caused by the signals from the nerves to muscles not working properly.
During a particularly severe episode, the spasms can be so bad that she can barely move.
But having been properly diagnosed, she now understands much more about the condition, which can be managed.
“My goal is to be part of the funds and raising money for awareness and to find a cure. That would be amazing,” she says.
During her time away from performing, Celine has been learning to adapt with medication, physical therapy, and the help of experts like Dr. Amanda Piquet.z z z z z z z z z z z z z
“Now this disease is gaining public awareness, it’s in the public eye,” says Dr. Piquet.
Dr. Piquet has treated a number of patients who had also gone undiagnosed for years.
The publicity gained by Celine speaking out about her battle with the illness is something she hopes will help others.
“We need to diagnose this disease better,” Dr. Piquet says. “When we do, that’s going to lead to more clinical trials, and more treatments that are approved.”
She says that although Celine will live with this condition for the rest of her life, the therapy she is undergoing to lessen the muscle spasms will help her to sing on stage again.
“My voice will be rebuilt,” says Celine. “I mean, it started a while ago already. My voice is being rebuilt as we speak, right now.”
