Over the past year, to raise awareness about PC Project and the patients who live with this rare and painful skin condition, PC Project’s Executive Director, Janice Schwartz, was interviewed by two different journals, the Dermatology Times and the Journal of Dermatology Nurses’ Association.
Click to read the article in The Dermatology Times called Living With Pachyonychia Congenita: Patient Perspectives and Activism.
Click to read the interview about the patient perspectives featured in the Journal of Dermatology Nurses’ Association.
The more we talk about PC and raise the profile of our work, the more progress we make and the more patients we help.
