Smiles and Sunshine for the 2018 Miles for Mia Memorial 5K Walk/Run

This year’s Miles for Mia Memorial 5K Walk/Run was another big success in support of genetic disease research and education.

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Miles for Mia 2018

Miles for Mia, a benefit dedicated to the life of Mia Jeanette Walts, will be held on Saturday, June 2, 2018 in Brighton, MI.

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Beautiful new book, “An Ordinary Day,” documents families living with rare genetic diseases

Sunday, December 3rd, 2017

Acclaimed portrait photographer Karen Haberberg recently turned her lens on families raising children with rare genetic conditions in a stunning new book.

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Elisa and Jim Ross and the GDF Breast Health Fellowship

Wednesday, September 6th, 2017

The Ross Family and the GDF support breast cancer education and management at the University of Michigan.

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Dr. Robert J. Desnick Honored with NORD Rare Impact Award

Tuesday, July 25th, 2017

NORD honors Dr. Robert Desnick with 2017 Rare Impact Award.

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GDF Grant Supports the Launch of the Mount Sinai Pediatric Precision Medicine Initiative

Sunday, May 7th, 2017

A recent grant by the GDF supports the launch of the Mount Sinai Pediatric Precision Medicine Initiative led by Dr. Bruce Gelb at the Mindich Child Health and Development Institute.

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Genetic Disease Foundation 2013 Benefit Gala

See photos from this year’s GDF Gala at Gotham Hall in New York City.

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Genzyme’s Head of Rare Diseases Honored by the GDF

Tuesday, March 5th, 2013

Dr. Rogerio Vivaldi, MD, was presented with the GDF’s Industry Person of the Year award.

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Protected: Genetic Disease Foundation 2013 Gala

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A family’s quest to raise awareness about Gaucher’s disease

Tuesday, May 15th, 2012

Newark Star Ledger article features the Trombino family and their new CD, “For the Children,” which benefits the GDF.

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