About
Empowerment for IgG4-rd Patients
Founded in September 2025, the European Federation of Patients with IgG4-RD based in Brussels, Belgium, aims to raise awareness about IgG4-rd, offer treatment options, and provide support to patients, caregivers, and families. Non-profit.
Initiatives
Empowering Patients
Advocacy Work
We lobby for better healthcare.
Support Groups
Providing comfort & understanding.
Awareness Campaigns
Educating the public on IgG4-rd.
Team
Meet Our Team
Tom O'Connor
Chairman
Leads organization's vision and strategy.
Elena Garcia
Community Liaison
Engages and supports patient community.
Anna Smith
Public Relations
Handles external communications and media relations.
Maxwell Lee
Finance Officer
Manages organization's financial resources.
Get involved
Empower Patients with IgG4-rd!
Join us in advocating for rare disease awareness, supporting research, and connecting with a community that values your unique perspective. Make a difference today!
Call to learn more