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

1 May 2012
Tickets on sale for Bay Area MPN symposium
Patients and caregivers are welcome to attend and hear from specialists in the field

13 April 2012
Video from Dr. Ruben Mesa of Mayo Clinic
Dr. Mesa gives his update on PV for 2012

5 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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