Patient Story: Lotta’s Journey with Relapsing Polychondritis

As part of Rare Disease Month, ERN ReCONNET and the JARDIN Joint Action are sharing real patient experiences from across Europe.

We are pleased to highlight Lotta, a member of the Relapsing Polychondritis community, who shares her journey to diagnosis and what daily life with RP can look like.

Her story highlights the challenges of rare disease diagnosis and the importance of specialist care and international collaboration.

You can read Lotta’s story here.

By sharing experiences like these, we hope to improve understanding, awareness and support for people living with Relapsing Polychondritis.