We did It! Ten Ben’s Friends members traveled for more than 500 miles on foot and afloat to raise awareness
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Clasina Field, a rare disease patient herself believes that her true rehabilitation came in the form of an online support
Read MoreTen Ben’s Friends Members and Friends are traveling to Glacier National Park This August for five active days to prove
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Ben’s Friends, our network of patient communities and Rare Disease Review, a medical and health policy journal hosted a miniconference
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Your Ben’s Friends team (including TJ and Seenie) will be hosting a casual get together by the pool for members
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We launched our newest community – Living with Idiopathic Pulmonary Fibrosis ( livingwithidiopathicpulmonaryfibrosis.org ) Idiopathic pulmonary fibrosis (IPF) is a
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Ben’s Friends set up booth for the World Orphan Drug Congress in Washington D.C. the second week of April. Four
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