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All Blogs & News
Advocating for SDS Research at Rare Drug Development Symposium
This week, I had the great honor to present at the 2021 Rare Drug Development Symposium, hosted by Global Genes and the UPenn ODC.
A Cure for SDS: Our Mission
From the Founder, Dr. Eszter Hars “Mom, why do I have SDS? Why can’t I be like everyone else?” my daughter asks me… Imagine a world...
Bone marrow-on-a-chip provides new research directions for Shwachman-Diamond syndrome
Boston Children's Hospital's Discoveries Blog features this exciting story about SDS research. Read the full story, here. In a research...
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