I’m Lauren. This is my story.
My name is Lauren Edwards and I was diagnosed with Type 1 Gaucher Disease when I was 18 years old. This information came as a shock to me because I was just …
Trip to NY for the NGF Patient Conference
October is Gaucher Awareness month and I was honored to be selected as a member of the National Gaucher Foundation’s (NGF) first-ever ambassador program. As ambassadors, our first task was …
Lauren’s Interview with Rare Disease Report
It was an amazing opportunity to be able to sit down with Rare Disease Report to talk about my experience with Gaucher Disease, as well as to be recognized as …