There are over 6,000 genetic disorders that can be passed down through the generations, many of which are fatal or severely debilitating. Since 1997, the GDF has worked with Mount Sinai to help provide funding for research to improve early detection and treatment options for many of these disorders.
Being diagnosed with a genetic disease can be extremely difficult and confusing for you and your family. If you or a loved one has been diagnosed recently, the GDF may be able to help you navigate through this complicated time.
Through our affiliation with Mount Sinai School of Medicine’s Department of Genetics and Genomic Sciences, we can help connect you with world-class physicians and genetic counselors in specific disease groups.
The GDF has partnered with Mount Sinai School of Medicine’s Department of Genetics and Genomic Sciences in New York City, one of the largest and most productive genetics departments in the world. Recognized as a leader in its field, the 170-member department has made numerous contributions to the diagnosis, prevention and treatment of genetic diseases. Learn how advances at Mount Sinai have impacted the lives of thousands of people and provide hope for the future.
The GDF is proud to welcome Kelly Edwards, designer, lifestyle expert and co-host of the Style Network’s “Tacky House,” as Board member and spokesperson for the foundation. Kelly’s brother suffers from a rare genetic disorder and her desire to help him find information and support led her to the GDF and, ultimately, to join us in support of our mission.
Your support can lead to remarkable gene discoveries and treatments that fight against genetic diseases.
Newark Star Ledger article features the Trombino family and their new CD, “For the Children,” which benefits the GDF.
The community of Brighton, Michigan will come together for the Miles for Mia event this May 19th.
GDF supporters Emil and Sal Trombino will share proceeds from their new children’s CD, “For the Children.”



