Memory of late son inspires Tigard family's search for SMA cure

Four years after Shawna and Dave Randall lost their infant son, Cole Parker Randall, to spinal muscular atrophy, they continue to raise money for a cure.

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Infant's life, smile brings awareness to rare disease

Tigard family started Cole Parker Randall Foundation in their son's memory

Not many people have heard of spinal muscular atrophy type 1, a rare disease that affects infants. But the Randalls want to change that.

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Tigard family fighting to find cure for SMA in son's honor

TIGARD, OR (KPTV) -Three years ago, a Tigard couple lost their newborn son to a devastating neuromuscular disease.

But instead of dwelling on their grief, they started a foundation in his honor. Now, they’re making history with awareness and the money they’re raising to find a cure.

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