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Myeloma Patients Europe (MPE) is an umbrella organisation of myeloma and AL amyloidosis patient groups across Europe. We currently have 46 members in 30 different countries. 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 and equal access to treatment and care.

From time-to-time, we need to involve patients and carers in our work to ensure it represents the needs and wants of the patients we represent. To do this, we run surveys, research and activities with patients and carers to ensure we understand their preferences and that we advocate for treatments and standards of care they want.

If you are interested in participating in the patient focused research of MPE, please register your details in the form below.