Written by Valaree DonFrancesco on December 6, 2019
Tell us a little bit about yourself! Where are you from?
My name is Viridiana Murillo, and I am from Pomona, California. I am a first-generation Mexican-American scientist and the first in my family to explore the field of genomics and data science. With six years of combined… Read More
Written by Lisa Sencen on May 20, 2019
Debra Regier, M.D., Ph.D. is the Director of Genetic and Genomic Education at Washington, DC’s Children’s National Medical Center, attending physician in genetics and metabolism and Primary Investigator (PI) for the Rare Disease Clinical Research Scholars Program. A graduate of the University of Utah School of… Read More
Written by Jennifer Huron on August 26, 2015
“I really appreciate all that NORD does for those living and managing their lives with rare disorders.” -Paula Mann
Paula Mann is a mother of a boy, Garrett, born in 2008 with Mitochondrial Disease, a rare disease that can be present at birth or come on later in life…. Read More