May 24, 2017
Shire’s Swelling Disorder Drug Moves Closer to U.S. Approval
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April 24, 2017
Colorado Sisters to Present Science Project On Their Own Rare Disease
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May 16, 2015
HAE Day :) One Woman Shares Her Story for Hereditary Angioedema Awareness
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April 7, 2015
Unexplained and Reoccurring Swellings Lead to Hereditary Angioedema Diagnosis
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September 25, 2014
Teen Swims for His Family’s Battle with Hereditary Angioedema
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July 30, 2014
Drug Derived From Milk of Genetically Modified Rabbits to Treat Rare Swelling Disorder
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November 14, 2013
Shire to Pay $4.2 Billion for Rare Disease Firm ViroPharma
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March 19, 2013
When is it Time to Reveal a Rare Disease: 25-Year-Old Woman with Hereditary Angiodema Speaks Out
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September 16, 2012
HAE Canada – Patient Organization for Hereditary Angioedema Hosting 2012 Patient Summit in Toronto
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June 1, 2011
NEW DOCUMENTARY: RARE DISEASE THE FOCUS – BE INFORMED AND INSPIRED
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