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NGF Mourns the Loss of Dr. Roscoe Brady
Summary: The National Gaucher Foundation today mourns the passing of... Read more
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New Gaucher research protocol enrolling participants
Are you an adult 18 – 65 years of age... Read more
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Helping kids battle a rare disease
In the blink of an eye, life completely changed for... Read more
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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
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Was your child recently diagnosed with Gaucher Disease?
Find out about a research study for children with Gaucher... Read more
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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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Gaucher Stories
Fairleigh Dickinson University graduate student, Lauren Edwards, has Gaucher disease.... Read more
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Lindsay Zuckerman Dance-A-Thon Fundraiser
Twelve-year-old Lindsay Zuckerman was determined to raise awareness of Gaucher... Read more
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Gaucher Disease Study
Palo Alto University graduate student Andrea Alioto, M.S., is directing... Read more
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Lindsay Zuckerman Dance-A-Thon
Twelve year old Lindsay Zuckerman, who has Gaucher disease, was... Read more