Dear Member,
Welcome to IgAN Friends: A community of people who share the IgA Nephropathy (IgAN) journey. Together, we are creating a space of support, exchange, understanding, and empowerment, and with each new member, we’re excited to bring new perspectives to the table.
IgAN Friends, which started its journey in November 2024, is the fruit of a collaboration between the European Kidney Patients’ Federation (EKPF) and the European Reference Network for Rare Kidney Diseases (ERKNet).
Our mission is to build a strong community of voices and experiences to empower people living with IgAN throughout Europe.
Our members come from across Europe, fostering an exchange of diverse insights and experiences. Here, you’ll find a community of people who genuinely understand your experience and are ready to support each other every step of the way. A community that, thanks to you, is growing bigger and stronger.
IgAN Friends membership comes with the opportunity to access, share and exchange information and experiences and, soon, to engage directly with other community members, including in events across Europe.
In short, you now have access to:
We want to build a community that evolves and grows with its members. A community that truly meets your unique needs. This is why we kindly ask you to fill out a short survey. Your responses will help us refine priorities, understand challenges and strengthen the way in which we can support each other.
As the IgAN Friends Community Coordinator, I am always happy to hear from you and address any questions or feedback you may have about the community and our activities. Feel free to reach me using the contact details below.
Thank you for trusting us to be part of your journey. Together, we can make a meaningful impact for everyone living with IgAN.
Warm regards,
Mónica Suengas
IgAN Friends Community Coordinator
Manager, European Kidney Patients’ Federation
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