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.
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.
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.
