PKAN fundraiser – Patient Worthy

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This Little Boy Won’t Let PKAN Be the Star of His Party!

Post author:Trudy Horsting
Post published:June 29, 2017
Post category:Pantothenate Kinase-associated Neurodegeneration Rare Disease

8-year-old Carter Anderson has PKAN. He’s only had his official diagnosis for about a year, as his parents were first told he had cerebral palsy. Since Pantothenate Kinase-Associated Neurodegeneration (PKAN)…

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