Neurodegenerative
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‘Uncharted territory’: Toronto family of child with rare disease raises $3M for therapy'This could change his life,' said Terry Pirovolakis of a gene therapy clinical trial to treat son Michael's ultra-rare condition, SPG50.HealthAug 15, 2022
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London man with lifelong illness sues government after being denied self-directed homecare funding"The service is being provided, [but it is not being] provided in a way that relieves Mr. Foley's substantial suffering," said Ken Berger, Foley's lawyer.HealthMar 17, 2018
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