The following programmes aim to build and empower a network of effective patient advocates and organisations across Europe, and provide a strong platform for the voice of myeloma and AL amyloidosis patients to be heard.
What we do
- Member and patient community programmes
- MPE Masterclass
- Scholarship programme
- Myeloma CABs
- MPE Myeloma and AL amyloidosis Community Taskforce
- Advocate Development Programme
- European Young Myeloma Patients Group
- Reasonable Agreements between Patient Advocates and Pharmaceutical Companies (RAPP)
- Research
- Access and Policy
- Educational Resources