For Researchers and Clinicians

Resources for Today’s MPN Researcher and Clinician

At the MPN Research Foundation, we’re different than other research funding organizations. As an organization that is founded by and funded by patients, we’re primarily influenced by the needs and concerns of MPN patients – the people who are most affected by myelofibrosis, essential thrombocythemia and polycythemia vera.

MPN Research Foundation resources for researchers include:

Stay informed and never miss a PFDD Meeting update!

Want to help MPN researchers find the best treatment options?

Take the steps you need to help change your prognosis.

x

NEVER MISS AN UPDATE

Get free, timely information on living with an MPN.

Subscribe