Rare disease affects 350 million people worldwide. Read about the connections that bond us, the moments that challenge us and the accomplishments that help us persevere.

July 9, 2021
RARE Foundation Alliance Member Spotlight: Ashley Point
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June 24, 2021
RARE Foundation Alliance Member Spotlight: Matt Larsen
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May 10, 2021
RARE Foundation Alliance Member Spotlight: Sharon Rose Nissley
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April 5, 2021
RARE Foundation Alliance Member Spotlight: Allison Kaczenski
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March 8, 2021
RARE Foundation Alliance Member Spotlight: Stephanie Fischer
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February 9, 2021
Solving Barriers to Financial Wellness for Rare Disease Patients
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December 2, 2020
Fenrici Backpacks: Lessons in Resilience
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November 24, 2020
SIGNAL Coffee Roasters: A Rare Profile
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November 10, 2020
RARE Patient Advocacy: Forging Connections for Change
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October 8, 2020
Growing Up Rare: The Young Adult Experience with Rare Disease
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October 5, 2020
It’s Never Too Late to Find your Community
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September 22, 2020
Turning my secret into my passion: Jeune Syndrome
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