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'Is this the best we can do?': B.C. mom of boy with muscular dystrophy calls for rare disease strategy

Kasha Mitton says kids with rare degenerative diseases shouldn't have to wait for drugs that have already been approved by Health Canada and other countries

We haven't written up this one. Vancouver Sun has the full story — the link below goes straight to it.

Read the original at vancouversun.com →

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