 I'm Liselotte Ericsson and since 2022 I'm the new president of Miloma Patient Europe. We are a strong and very well-organized community and we are around in almost every corner where Miloma is discussed. We support members to raise the voice of the patients. We fight for a cure, better access to novel treatments and also a better care for Miloma patients. Together we can make a huge difference for the patients. Follow us on social media and hope to see you soon in any of our meetings.