BIO Patient & Health Advocacy Digital Summit
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BIO Patient & Health Advocacy Digital Summit
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In 2008, Melissa Bryce Gamble's daughter Ginny was born with a peroxisomal disorder. It took almost…
Diagnosed with ALS at the age of 37, Lorri Carey is the author of the podcast 'I'm Dying to Tell…
The EveryLife Foundation for Rare Diseases is a 501(c)(3) nonprofit, nonpartisan organization…
Melodie Narain-Blackwell is a serial entrepreneur and health advocate, who has always been…
The American Lung Association is the leading organization working to save lives by improving lung…
Sanath is a bold and visionary software leader, open source pioneer and a rare disease drug…
Tom has been part of Sepsis Alliance since 2007, serving as President and CEO since 2013. Tom has…
Vincenzo Piscopo began his tenure as United Spinal’s president and CEO on November 16, 2020…