Joining forces in Paris with researchers and physicians who care about rare
PC Project’s Executive Director, Janice Schwartz, participated with the Paris World Congress of Rare Skin Diseases on June 13-15, 2024 as physicians, scientists, and patient organization representatives gathered from around the world to network and present science regarding rare skin diseases.
PC Project featured three posters at the congress to raise awareness about PC and the work PC Project is doing, along with patient quality of life, and data from the other diseases in our registry.
Many thanks to Ashley Wittmer, Holly Evans, and Drs. Edel O’Toole and C. David Hansen for their work on these posters that highlight the excellent accomplishments and ongoing work of PC Project.
Patient representatives from various organizations around the world.
