The Pachyonychia Congenita Project is supported by the Pachyonychia Congenita Fund, a charitable foundation established by the Schwartz family of Salt Lake City. Their website serves as an information and communication tool for doctors, clinical researchers and PC patients. Be sure to check out the International Pachyonychia Congenita Consortium, scheduled for May 2005 in St. Louis, and their patient support meeting, schedule for August in Niagara Falls. Click here to access the website.