Because every child deserves the chance to fight no matter how rare the disease
In 2010 two year old Chloe Barnes lost her battle with metachromatic leukodystrophy (MLD), a rare degenerative neural disease. Like 95% of the other 7,000 rare diseases that disproportionately affect children there is no cure. But Chloe's journey inspired her friends and family to support research in Minnesota to change that and now world renown researchers at the University of Minnesota have set their sites on finding a cure for MLD and other lysosomal storage diseases. Through partnering with one of the most innovative research institutions in the world, Chloe's Fight Rare Disease Foundation has a vision for a world where every rare disease has a treatment option. Please donate today and fund life changing research and help us raise awareness.. Because every child deserves the chance to fight.
Help us find cures for the over 7,000 rare diseases that affect 1 in 10 Americans