January 30, 2017
Alagille Syndrome Alliance Accepting Applications for Alaina Kaitlyn Hahn Celebratory Scholarship
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December 12, 2016
Eighth Annual SBP Rare Disease Day Symposium Alagille Syndrome
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January 21, 2015
Rare Community Mourns Loss of Daughter of Founders of The Alagille Syndrome Alliance
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September 6, 2014
Mom Creates “Remarkably Rare” Apparel for Daughter with Alagille Syndrome
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April 8, 2013
Two Talented Scientists Nominated for Time’s Top 100 Most Influential People List
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August 7, 2012
Mom From Cuba Describes Daughter’s Battle Against Alagille Syndrome
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