The SFDF is committed to both spreading awareness and directly helping the scleroderma and fibrotic diseases community. We further our mission through a variety of initiatives. Our Patient Advisory Board assists us in identifying problems in the community and determining how we can best solve them.
The SFDF’s quarterly publication, Scleroderma Stories, sheds light on the experience of living with scleroderma through a series of interviews with scleroderma warriors around the world.
Our website includes an extensive Learn Center as a resource that helps the broader community gain a more comprehensive understanding of scleroderma and other fibrotic diseases.
We host a variety of events such as benefit concerts and educational presentations to raise funds and awareness for our cause.