Join the GFPD on November 13th – 15th for our West Coast (Los Angeles) Regional Meetup, a three-day, in-person gathering designed to connect families, caregivers, researchers, and medical experts impacted by peroxisomal disorders.
These meetups reduce isolation, provide education, and create meaningful opportunities to build community — because no family should navigate a rare disease alone.
Location and Hotel Information
Information coming soon
Travel Stipends & Accessibility Support
To help reduce financial barriers, GFPD offers limited travel stipends for families who need assistance attending.
What To Expect
Detailed agenda coming soon!
Who Should Attend?
- GFPD Warriors
- Families and Caregivers
- GFPD Medical & Scientific Advisors
- Advocates and Professionals
Whether you’re newly diagnosed or a longtime community member, this event is designed to support connection, education, and shared experience.
Questions?
For any questions about the meetup, registration, or travel stipends, please reach out to:
Katie Sacra, Director of Family and Community Engagement at katie@thegfpd.org
Ryan Maple, Executive Director at ryan@thegfpd.org
Sponsorship or donation inquiries to support meetups should be directed to:
Kevin Johnson, Partnership Advisor kevin@thegfpd.org