The International Scleroderma Network (ISN) is the nonprofit global leader for scleroderma and related illnesses. Our web site at sclero.org offers over 5,000 pages of quality medical and support information, in 23 languages.
We are a full-service nonprofit charitable foundation for scleroderma research, support, education and awareness for scleroderma and related illnesses, such as pulmonary hypertension.
We serve all types of scleroderma, including: systemic sclerosis (SSc), limited cutaneous systemic sclerosis (lSSc) or CREST Syndrome, diffuse systemic scleroderma (dSSc). We also serve localized forms such as morphea, linear scleroderma, en coup de sabre, morphea/linear, and childhood or juvenile scleroderma. (Also see Types of Scleroderma)
We publish the acclaimed Voices of Scleroderma book series. Our Sclero Forums Online Support Groups offer top notch support to our global audience.
SCLERO.ORG is the world's leading nonprofit for trustworthy research, support, education and awareness for scleroderma and related illnesses. We are a 501(c)(3) U.S.-based public charitable foundation, established in 2002. Meet Our Team. Donations may also be mailed to: