Ontario families are putting pressure on Health Minister Christine Elliott to fully fund life-altering drug for all people suffering from Spinal Muscular Atrophy or SMA. The drug, Spinraza, has been approved for everyone in Quebec and Saskatchewan but is limited for SMA patients in Ontario. Tom Hayes reports.
- Ontario patient with SMA reacts after government agrees to cover life-changing drug
- Families of patients with SMA meet with Ontario health minister, hope ‘miracle drug’ will get funded
- NDP MPP, patients with SMA call on Ontario to cover ‘miracle drug’ to treat rare disease