Rare Disease Report

Origins of NOTA

JANUARY 11, 2016
Jon Miller

We spoke with Jon Miller, president and founder of the Network of Tyrosinemia Advocates (NOTA) about his son, how the non-profit got its start and the accomplishments NOTA has done.
For more information, please visit www.notacares.org.

Copyright © RareDR 2013-2018 Rare Disease Communications. All Rights Reserved.