NGF Blog

Blog / Living With Gaucher Disease

Meet Lauren: Gaucher Disease Patient Journey

This month we are introducing you to several faces of... Read more


Sanofi Genzyme announces “Seven Tests for Managing Gaucher”

It’s important to monitor Gaucher disease with regular assessments. For... Read more

Blog / About Gaucher Disease

Can Gaucher Disease Carriers Have Symptoms?

The National Gaucher Foundation has received several inquiries from people... Read more

Blog / Gaucher Disease Research

The 25th Anniversary of FDA Approval of ERT

In 1991, the U.S. Food and Drug Administration (FDA) approved... Read more


NGF Mourns the Loss of Dr. Roscoe Brady

Summary: The National Gaucher Foundation today mourns the passing of... Read more


New Gaucher research protocol enrolling participants

Are you an adult 18 – 65 years of age... Read more


Helping kids battle a rare disease

In the blink of an eye, life completely changed for... Read more


Chart Your Own Course 2016 – A Scholarship Program for the Lysosomal Storage Disorder Community

Sanofi Genzyme established the Chart Your Own Course program four... Read more


Was your child recently diagnosed with Gaucher Disease?

Find out about a research study for children with Gaucher... Read more


RARE Patient Advocacy Symposium May 6, 2016 in Philadelphia

Join rare disease patient advocates and caregivers to learn and... Read more

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