The Stevens Johnson Syndrome Foundation is a non-profit voluntary organization that works for people affected by Stevens Johnson Syndrome through programs of research, education, advocacy, and service. Established in 1995, the Foundation is located outside of Denver, Colorado and also support group serving over 700 patients and their families around the world. The SJS Foundation seeks to improve the quality of life for people affected by SJS, facilitate access to reliable information about Stevens Johnson Syndrome and act as a voice for people affected by this severe drug reaction. The Foundation supplies informational materials to the public and health care professionals. In addition, the Stevens Johnson Syndrome Foundation provides authoritative information to professionals and the public by means of computer access to major collections of medical information.
Stevens Johnson Syndrome Foundation has not yet started any petitions.