The Patient Experience Project (PEP), a patient-centered communications agency, will host its third annual “Rare Disease Day at the Movies” on , in Saratoga Springs, New York. The event raises awareness and funds for people living with rare conditions. This year, inspired by Megan Cronin and her family, PEP will feature a special screening of the movie Wonder, based on R.J. Palacio’s book of the same name. Additionally, hundreds of students in several school districts in New York’s Capital Region have participated in a poster contest for the event, depicting the themes of kindness and acceptance in their artwork. All proceeds will benefit the Children’s Craniofacial Association (CCA).