amyloidosis: what it feels like
when anne marie carr was diagnosed in 2015, she was told most patients only survive three years. six years later, she's the founder and executive director of hereditary amyloidosis canada.
the vancouver canucks also paid tribute on their social media channels. “gino was a fan favourite from the moment he joined the organization, putting his heart and soul into every shift on and off the ice,” francesco aquilini, the team’s chairman and governor, said in a statement posted to twitter.
odjick had a rare disease called amyloidosis, which involves an abnormal protein, called amyloid, that accumulates in the tissue and organs. it impacts organ function, and can lead to organ failure and deaeth. he was diagnosed in 2014, and was told he likely had only weeks to live.
he explained his diagnosis in an open letter to his fans in 2014. “my spirit is strong even if my body isn’t,” he wrote. “i’m going to use all of my time to be with my kids and everyone i love.”
he received experimental treatments for his amyloidosis in ottawa, and also underwent chemotherapy. chemo is a common treatment for the condition: it interferes with fast-dividing cells in the body, columbia medicine explains. in patients with amyloidosis, chemotherapy can destroy abnormal plasma that results in amyloid deposits.
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“i was shocked,” former canucks teammate geoff courtnall told the province. “i knew that he obviously had health issues, but he looked so good at the rink when i saw him last month. he wasn’t moving well with the issues he had with his leg (infection), but he had good energy and was positive.”