June 22, 2015
Hannah’s Story: National Gaucher Foundation Gears Up for Conference
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July 24, 2012
Little Miss Hannah Foundation To Host First Annual “Rainbows to the Sky” Rare Disease Event in Henderson, Nevada
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August 23, 2010
Thank you Frances Perraudin – YES, It Is Time The World Pays Attention To Rare Disease!
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April 29, 2009
A Fine Line Between Research and Parenting – Living With Neuronopathic Gaucher's Disease
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