Join Us for the 2019 RARE Patient Advocacy Summit

Registration for the 8th annual RARE Patient Advocacy Summit is now open! Join us in San Diego, California for the RARE Patient Advocacy Summit, the largest gathering of rare disease patients, caregivers, thought leaders and other rare disease stakeholders in the world. The Summit is an unparalleled opportunity to forge meaningful connections with other rare advocates and take home actionable strategies and tools to accelerate change. Find your path to success with four tracks, spread throughout two days and designed for different stages of advocacy. Day One:  Track 1: Caring for Yourself and Others While Rare Track 2: Building and Activating Your Community Track 3: Patients as Drivers in Drug Development Track 4: What’s Now: Innovations in Rare Disease Day Two: Track 1: Owning Your Future with a Rare Disease Track 2: Becoming a Stronger Advocate Track 3: The Drug Development Future: Science, Policy, Partnerships and Economics Track 4: What’s Next: Advances in Science and Treatment for Rare Disease View the Agenda Join hundreds of rare disease thought leaders, advocates and patients as we help you find solutions for your evolving needs in rare disease. Take advantage of early-bird rates and register now for the 2019 RARE Patient Advocacy Summit. Register

Global Genes is a non-profit 501(c)(3) organization working to connect, empower and inspire the rare disease community. Global Genes ® | 28 Argonaut, Suite 150, Aliso Viejo, CA 92656 | globalgenes.org Tax ID: 26-3331487 | © Global Genes 2019