The diagnosis journey for those with rare disease can be a long and isolating experience. Join Mike Porath, CEO & Founder of The Mighty, Skye Gailing, patient advocate & Mighty editor of 'Rare Weekly,' Greg, LEMS patient advocate, and Debbie Drell, Director of Membership at NORD, for a live discussion covering their perspectives across the diagnosis process, community support, and mental health impact of rare disease.

This event was made possible by an unrestricted educational grant from Catalyst Pharmaceuticals.