National Minority Health Month is here. April is an opportunity to raise awareness and encourage advocacy about how health disparities can affect people from racial and ethnic minority groups, including…
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We remain overwhelmed by the outpouring of involvement and support from people across the world who are putting their talent and treasure towards the SRF, finding their own personal ways…
Saget’s commitment to building awareness of the disease will continue through support of family, friends, and fans San Francisco, CA (January 13, 2022) – The Scleroderma Research Foundation (SRF)—the country’s...
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It is with a very heavy heart that we mourn the loss of our dear friend and Board member, Bob Saget. Bob was a champion for scleroderma patients everywhere dating...
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As we start 2022, thank you for inspiring all of us at the SRF to remain laser-focused on our mission—finding a cure for scleroderma. And thanks to the support of our…
SRF researchers Michael Longaker, MD, MBA, and Howard Chang, MD, PhD, both of Stanford University, recently published a paper in PNAS on their newly-developed integrated spatial multi-omic analysis platform, which they used to understand...
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This holiday season, we're reflecting with gratitude on the many ways we’ve been able to accelerate the pace of scleroderma research. This is all because of people like YOU. Thanks...
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25 years ago today, “For Hope”—a movie Directed and Executive Produced by Scleroderma Research Foundation board member @BobSaget—aired on ABC, gaining critical acclaim and changing how the world sees scleroderma....
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"I learned about scleroderma when my mom had a mild case...Many people are misdiagnosed for years and there is not a lot of awareness or research funding." SRF Board Member...
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The Scleroderma Research Foundation’s 2020 Annual Report is now available online. This report demonstrates the many ways in which we drove our mission forward during a global pandemic, thanks to dedicated...
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