SCLERODERMA STORIES

The Scleroderma and Fibrotic Diseases Foundation’s “Scleroderma Stories” initiative began in January of 2020. Featuring the journeys of people living with scleroderma in states from the east to west coast as well as in countries such as South Africa and Canada, the first issue of Scleroderma Stories was published on June 6, 2020. 

In these interviews, scleroderma warriors share their hardships, triumphs, passions, and more. Scleroderma Stories aims to raise awareness about this rare disease and to inspire those affected by scleroderma and help them understand that they are not alone. 

Click on each issue’s cover below to read!