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Stevens Johnson Syndrome Foundation


PO Box 350333
Westminster, CO 80035-0333





Email Address

[email protected]


The Stevens Johnson Syndrome (SJS) Foundation and Support Group is a national, non-profit support group organization providing emotional support to individuals affected by SJS and their families. Stevens-Johnson syndrome is a severe form of erythema multiforme characterized by blistery lesions on the mucous membranes of the mouth, throat, anogenital region, eyelids and corneal lining. Established in 1995, the group provides current information on SJS, its causes and treatments, and distributes this information through a nationwide networking system. Educational materials include reprints of current medical information on SJS.

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