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FARAFARA Cure FA

Dozens ride to raise awareness about rare neuro-muscular disease

PORTLAND, OR (KPTV) - There's no treatment and no cure, but a local man battling a rare, neuro-muscular disease called Friedreich's Ataxia hopes to change that.

Sam Bridgman, 22, was one of more than 150 people who participated in Ride Ataxia Portland on Saturday. Bridgman graduated from college in the spring and recently started a new job at Nike.

Bridgman's hope is that by raising awareness about Friedreich's Ataxia, it'll save lives and eventually lead to a cure.

During Saturday's ride around Sauvie Island, Bridgman was all smiles.

It hasn't always been that way. Especially when he was diagnosed with Friedreich's Ataxia at the age of 15, he said.

"When you get diagnosed with something like F.A., you No. 1 ... feel like you're all alone," Bridgman said. "And No. 2 ... you really don't want to realize what's going to happen with your body."

KPTV - FOX 12

Read More: Dozens ride to raise awareness about rare neuro-muscular disease

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