Stacey Lintern

Contributor

Stacey Lintern is CEO, Muscular Dystrophy Canada

2 Contributions
by Homira Osman Stacey Lintern Danielle Campo McLeod

Fail-first drug rules defy logic, deny timely access for people with rare diseases

Despite the recent approval of targeted biologics that can significantly improve quality of life, Canadians living with Myasthenia Gravis continue to face unjust policy barriers.

by Homira Osman Stacey Lintern Danielle Campo McLeod

Approved but denied: Canadians with neuromuscular diseases face unequal access to treatment

We are told health care in Canada is equal for everyone. But it is not. Particularly for patients with neuromuscular diseases, what you get depends on where you live.

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