Advocate critical of B.C. government decision to end funding for girl with rare disease
On Friday, B.C. Health Minister Josie Osborne reiterated the province would end funding for the Brineura drug, a drug that cost $9 million a year and was only being used by one patient, nine-year-old Charleigh Pollock who suffers from the extremely rare Batten disease. Durhane Wong-Rieger, the CEO of the Canadian Organization for Rare Disorders, condemns the province for not using its federal money for rare disease sufferers to treat the child.