Take Action

Donate

Every euro helps us advocate, connect, and grow — for every IgG4-RD patient in Europe.

Why it matters

A small federation.
A large mission.

The European Federation IgG4-RD is a non-profit run almost entirely by patients. We do not receive government funding. Everything we do — representing patients at European institutions, supporting new national associations, spreading awareness — is funded by generous donors and sponsors.

Every donation goes directly to our patient advocacy work. No admin fees. Non-profit.

Your donation enables

  • Representation at European Parliament and regulatory bodies
  • Start-up support for new national patient associations
  • Awareness campaigns to reach undiagnosed patients faster
  • Patient events where people living with IgG4-RD can meet

Make a donation

A fixed donation of € 50

We chose a single, fixed amount to keep things simple and to maximise impact per transaction.

€ 50,00

one-time

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Scan the QR-code with your phone to open the donation page directly.

Become a sponsor

Corporate or organisational support for the Federation’s work.

Learn more →

Share on social

Follow and share our channels to help reach patients who don’t know we exist.

Get socials →

Start an association

Become a national IgG4-RD association in your country, with our full support.

How it works →
Carsten Sørensen

Carsten Sørensen

Patient & Treasurer, Denmark

As a co-founder and chair of the federation, I am proud to lead a community advocating for better recognition and care for IgG4-RD.

About us
Uncovering a hidden disease

About the European Federation IgG4-RD

We are the bridge between you, the patient, be it as a direct member or through your own national association and  the medical world and wider community. We connect knowledge, compassion, and advocacy across Europe for those affected by IgG4-Related Disease.