The Hannah Mollie Foundation
This website is dedicated to helping people learn more about Niemann Pick Type A and to educate everyone about genetic diseases and lysosomal storage diseases. Through raising awareness and money for research along with encouraging women to donate their umbilical cord blood, our family strives to give hope to other children that have been diagnosed with these terrible diseases.

We welcome you to the site and please revisit us soon!
Contact Information
Email :
jands44@aol.com
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