http://www.raredr.com/news/the-story-of-the-rare-disease-family-who-needed-a-car
The Story of the Rare Disease Family Who Needed a Car

Jon Miller



We spoke with Jon Miller, president and founder of the Network of Tyrosinemia Advocates (NOTA) about what he did to help a family suffering from tyrosinemia. 
 
For more information, please visit http://notacares.org
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