It's time for the annual Research Challenge, where we celebrate and support the hard work of the SRF-funded investigators. This year, we are pleased to highlight the work of Dr....
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"I never imagined I would be grateful for my diagnosis, but it has helped me understand myself better and given new meaning to my life,” says Nafisa Z. (dx 2020)....
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Introduction time—please join us in welcoming the SRF’s new Senior Staff Accountant, Neha Pamboo! She is a seasoned finance and accounting professional with experience managing financial operations, reporting, and analysis…
Throughout June, we invited you to join us in the #SayScleroderma campaign by sharing your own stories and pictures on social media. The response has been incredible. Your posts, photos,...
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In this edition of eNews, help us kick off our Annual Research Challenge, learn about the recent NIH workshop co-sponsored by the SRF, discover how members of the scleroderma community...
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"I have scleroderma, so I'm asking you to say it." —Cynthia, dx 2021 Why #SayScleroderma? Many people are unaware of what scleroderma is and the impact it has on those...
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Governors Brad Little (ID) and Jay Inslee (WA) have signed scleroderma awareness proclamations and have been very supportive of Scleroderma Outreach Northwest and the Scleroderma Research Foundation. These proclamations have provided the…
This year, the SRF was proud to be represented by our Chief Medical Officer, Dr. Gregory Gordon, at the EULAR Congress 2024 in Vienna, Austria. Held from June 12-15, the…
San Francisco, CA (June 25, 2024)—CONQUEST, a highly innovative platform clinical trial conceived of and led by the Scleroderma Research Foundation (SRF) and designed to rapidly advance promising treatments for...
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This month, members of the scleroderma community joined us to #SayScleroderma by sharing their valuable lifehacks, which are practical tips and strategies for navigating life with scleroderma. These lifehacks are...
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