We are, and always have been, singularly focused on finding a cure for scleroderma.
Our Story
The Scleroderma Research Foundation (SRF) was founded in 1987 by Sharon Monsky, an entrepreneur, businesswoman, and person with scleroderma. Guided by Sharon’s passion for a cure, we have become the largest nonprofit investor in scleroderma research in the United States.
Annual Report
In our yearly publication, you can find financial highlights, read about research projects, learn about the impact of philanthropy, and more.
Board of Directors
The SRF is led by a dedicated and active Board of Directors. While the individual members come from many different professional backgrounds and bring diverse talents to the SRF, they are united by their passion to improve the lives of people living with scleroderma.
Staff
Our professional staff bring passion, expertise, and hard work to help accelerate the pace of medical discoveries and keep the scleroderma community informed.
Scientific Advisory Board
The SRF’s Scientific Advisory Board is comprised of some of the most highly-regarded scientists in the country. Their vision and dedication to the SRF and to scleroderma research ensures that our research program remains highly-focused, nimble, and impactful.
Our Donors
We are grateful for our community of donors who advance our scleroderma research. The SRF research program is 100% funded by philanthropy.
Frequently Asked Questions
We hope we can answer some of the more commonly asked questions.
