August 6, 2019
When the World Gets Dark, Kristin Smedley Shines a Light
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June 3, 2019
Medical Students Learn About Zebras Through Patient Matching Program
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May 16, 2019
Peroxisomal Disorders Reach New Heights with Help from the RARE Patient Impact Grant
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April 24, 2019
Challenges Lead to Achievements
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December 28, 2018
Rare Leader: Christine Waggoner, President and Co-Founder, Cure GM1 Foundation
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December 20, 2018
Rare Leader: Brad Crittenden, Executive Director, Canadian Association of Pompe
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December 13, 2018
Gilbert Family Foundation Announces $12 Million Gene Therapy Initiative in NF1
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December 13, 2018
Rare Leader: Deanna Portero, Executive Director, Fibrous Dysplasia Foundation
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