Myeloma Patients Europe (MPE)

EMPOWERING MYELOMA ADVOCACY ACROSS EUROPE

The MPE Navigator is an online search tool to learn about and find clinical trials for myeloma, monoclonal gammopathy of undetermined significance (MGUS), smouldering myeloma and AL amyloidosis in Europe.

Have you explored the MPE Navigator?

Join the MPE European Young Myeloma Patients Group! Click here to learn more

Click Here Explore the latest AL amyloidosis
report about quality of life
and treatment experiences

Report “Health-related quality of life, diagnosis and treatment experiences of AL amyloidosis patients”

SHARED DECISION MAKING IN MYELOMA

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Fill in this survey to help MPE understand your experience making decisions with healthcare professionals

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The perspectives of myeloma patients and health care professionals on Minimal Residual Disease (MRD) section

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Check out all the MRD resources!

Explore the new myeloma and AL amyloidosis patient's guides available for download!

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Check out the MPE patient guide section!

Read MPE's report Access barriers to myeloma clinical trials in Central and Eastern Europe

What is AL amyloidosis?

Learn about the condition

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Myeloma Access Atlas

Find out more!

Education

Access

Research

Myeloma Access Atlas →

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. Visit the Myeloma Access Atlas here.

Myeloma is a rare, incurable disease of the bone marrow and accounts for approximately one per cent of cancers. In this animated video, we explain what myeloma is, how it is diagnosed, its symptoms and its treatments.

MPE Advocate Development Programme→

The ADP is a 12-month training programme designed to develop participants’ advocacy knowledge and skills to better serve patients locally, nationally and across Europe. Through the course, participants improve their understanding of clinical research and development, mechanisms of accessing diagnostics and drugs, interaction with stakeholders, including clinicians and industry, and the basics of evidence-based advocacy. Read more information here.