MYELOMA PATIENTS EUROPE

Our mission is to provide education, information and support to member groups, and to advocate at European, national and local levels for the best possible research as well as equal access to the best possible treatment and care... The Myeloma Access Atlas is an online platform designed to provide myeloma and AL amyloidosis patient advocates with the information they need to work effectively on access issues. It provides country-specific and comparative information on European health systems, including data on system performance and on access to treatment and care. Through the Atlas Coaching Programme, MPE provides advocacy tools and one-to-one support designed to help patient organisations develop and implement effective strategies to address identified access issues... Myeloma Patients Europe (MPE) unites 49 local and national patient myeloma and AL amyloidosis organisations in 31 countries. We aim to advocate at a European level for the best possible research and equal access to..

Also known as: MPE

Primary location: Brussels Belgium