Why Rare Disease Patient Advocacy Matters
Let’s talk about rare disease patient advocacy. We can use the word “advocacy” so much that it begins to lose...
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About Me
PKU, Newborn Screening, & Rare Disease Advocate
I produced my first PKU short documentary, "My PKU Life", in 2011. Since then I've been traveling the world speaking as a PKU & newborn screening advocate and producing videos about PKU.
