Calling all federal employees or retirees—the Combined Federal Campaign (CFC) is now open! As the official workplace giving campaign for those employed by the federal government, the CFC has raised…
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If you haven't listened yet, Episode 25 of the Mogil's Mob podcast is out. It features host Ann Mogilevsky, who has scleroderma, in conversation with SRF Board Member Sharon Dobie....
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If you haven’t yet had the chance, we encourage you to check out Radio Rahim's moving podcast interview with SRF Board Member Bob Saget on Luminary’s Til This Day with Radio...
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Now available: the Scleroderma Research Foundation's latest Annual Report for FY 2021. You can read about the impact of donor support which allowed the SRF to invest $2.6 million in scleroderma research in the past...
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Today would have been Bob Saget's 66th birthday. It still seems unimaginable that we would lose him so soon, and all of us at the SRF miss him more than...
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SAN FRANCISCO (May 9, 2022) – The Scleroderma Research Foundation (SRF) will host its inaugural Virtual Patient Forum, Collaborating for a Cure, on Wednesday, June 1, 2022, to kick off...
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Today, we are deeply saddened to learn of the passing of Gilbert Gottfried. He was a good friend of late SRF Board Member Bob Saget, and so he also became…
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…
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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