I Am: Céline Dion offers an unflinching look at the Canadian singer's life with stiff person syndrome

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Céline Dion kept her diagnosis with stiff person syndrome a secret from her fans for years. This new documentary offers an unfiltered glimpse at what her life is like now.

— a rare autoimmune neurological disorder that causes muscles to stiffen and spasm — as a seizure contorts the French Canadian superstar's body, leaving her twitching, moaning in pain and totally incapacitated."She's in a crisis," says Terrill Lobo, her sports medicine therapist, who, along with another team member, calmly and gently rides out the 40-minute spasm with Dion, monitoring vital signs and giving medication as the cameras roll.

"And I thought, Oh my God, this is what she's been talking to me about for eight months. This is it." "It is very ironic that a one-in-a-million performer would get this statistically one-in-a-million disease," Taylor says. As I Am: Céline Dion takes fans behind the scenes of the superstar's life, here are some key takeaways from the film and reflections from its director.

I Am: Céline Dion shares details of what it took for her to continue recording and performing until her final concert in early 2020, including taking up to 80-90 milligrams of valium a day — more than double the safe daily dosage for adults. Dion has performed with the best singers in the world, including Luciano Pavarotti, with whom she performed 'I Hate You Then I Love You' in 1998."It was not a business decision. It was a passion decision … She wanted to keep going. So I think that's what surprised me the most — for 17 years that she could hold up that front."Come on, this is Céline "Where Does My Heart Beat Now" Dion we're talking about. Of course there is.

Source: Entertainment Trends (entertainmenttrends.net)

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