FCS Foundation hosts its first Patient and Caregiver Summit
The FCS Foundation hosted their first Patient and Caregiver Summit on April 27 and 28 in St. Louis, MO.
More than 20 participants connected with others living with familial chylomicronemia syndrome (FCS) and had an opportunity to meet with members of the Foundation’s Medical Advisory Board.
The weekend included an FCS Disease Q&A with Dr. Vikesh Singh, interactive nutrition demonstrations, and ended with a ‘Casino Night’ where patients and caregivers were able to unwind and share their own unique stories with others.
Learn more about the FCS Foundation and their mission at livingwithfcs.org.