Rare Trait Hope Society was established to fund research and human clinical trials to cure childhood rare diseases. Our current project is to fund a gene replacement therapy to cure Aspartylglucosaminuria (AGU), a fatal neurodegenerative disease that impacts children.
Barbara Insley, Executive Director of Rare Trait Hope Society, and the Board of Directors invite you to take part in the 2nd annual Red Diamond Gala, benefitting children with the rare disease AGU. You can order tickets, sponsor the event or donate to the cause. This year the money raised through the gala event will have real impact in a number of areas.
For questions about the Red Diamond Gala or our Charity you can contact us at:
