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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.
 
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