On Sept 4, 2000 our son Liam was born with Krabbe disease. When Liam was born we were unaware that he had this so called “rare” disease. We had no idea that he would not live to see his first birthday. After his death we formed a 501 ( c ) 3 organization called The Liam Hammonds Memorial Foundation in hopes of promoting awareness and offering financial assistance to families suffering with Krabbe disease and the other Leukodystrophies.

Until a cure is found, we are dedicated to supporting families suffering with these diseases and through your generosity, help supply the needs of these families.