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Celine Dion hopes for a miracle in her battle against her auto immune disorder

Dion is suffering from a rare auto-immune disorder, but is hopeful about her full recovery



Canadian singer Celine Dion
Image Credit: AFP

Renowned singer Celine Dion has opened up about her ongoing battle with Stiff Person Syndrome (SPS) and her relentless pursuit of a cure.

In an interview with The Hollywood Reporter, Dion expressed her optimism for a breakthrough while acknowledging the challenges posed by the rare autoimmune disorder.

“I haven’t beat the disease, as it’s still within me and always will be. I hope that we’ll find a miracle, a way to cure it with scientific research, but for now I have to learn to live with it,” Dion revealed.

Stiff Person Syndrome, characterised by severe muscle stiffness and spasms, presents a formidable challenge for Dion. Despite the absence of a cure, she remains steadfast in her commitment to managing the condition. Dion detailed her rigorous regimen of “athletic, physical, and vocal therapy” conducted five days a week, emphasising her holistic approach to treatment.

Reflecting on her journey, Dion acknowledged the initial struggle to accept her diagnosis. “At the beginning I would ask myself: why me? How did this happen? What have I done? Is this my fault?”

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However, her perspective has since evolved, with Dion adopting a more proactive mindset. “Life doesn’t give you any answers. You just have to live it!” she asserted.

“I’ve chosen to work with all my body and soul, from head to toe, with a medical team. I want to be the best I can be,” she said.

Her unwavering resolve extends to her aspirations, including the dream of revisiting the Eiffel Tower which itself is a symbol of hope and resilience.

Amid the uncertainty surrounding her future touring plans, Dion remains pragmatic. “I can’t stand here and say to you: ‘Yes, in four months.’ I don’t know ... My body will tell me,” she confessed in the interview.

Dion also acknowledged the privilege of access to quality health care and expressed solidarity with those less fortunate.

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“People who suffer from SPS may not be lucky enough or have the means to have good doctors and good treatments, I have those means, and this is a gift. What’s more, I have this strength within me,” she noted.

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