EPP Patient Day

The American Porphyria Foundation and the Canadian Association for Porphyria Present - EPP Patient Day - featuring Porphyria Expert Dr. Karl Saardi with Q&A Session, Youngster and Adult Patient Presentations, and a VERY SPECIAL ANNOUNCEMENT for ALL EPP Patients!!

You will not want to miss this important event. Please feel free to invite family and friends to this event as they can better understand what EPP is, and possibly learn how better to support you.

We look forward to seeing you on EPP Patient Day! If you have any questions for the Q&A Session, please send them to deborah@porphyriafoundation.org so we can prepare Dr. Saardi for you!”