Welcome

Thank you for visiting. We have built this website to be informative, accessible and of value to MPN patients everywhere. We hope this site will be a source of information and a connector between MPN patients, the medical community, patient groups and other constituents.

The primary mission of MPN Research Foundation is to promote, fund and support the most innovative and effective research into the causes, treatments, and potentially the cure for ET, PV, and MF. Read about how we execute our mission.

Latest News


3 February 2012
Watch MPN Research Foundation's Robert Rosen discuss the Foundation
The video was filmed at the American Society of Hematology's Annual Meeting

27 January 2012
Cigna approves Pegasys for use by MPN patients
Insurance company responds to MPN Research Foundation request to approve it for use in PV and ET patients

23 January 2012
New grant opportunity for myelofibrosis
MPN Research Foundation and The Leukemia Lymphoma Society partner to fund concept grants aimed at reversing fibrosis


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Our Stories

 
"My name is JoAnn Mason and I am the parent of an MPN patient. Our daughter Jaclyn was diagnosed with polycythemia vera at age 17. Hematological malignancy? Blood cancer? Incurable? What would that mean for her future?"
~JoAnn

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