For years, the MPN Research Foundation has delivered on a bold commitment to fund global pioneers studying innovative approaches to prevention, new therapies and improved quality of life for people living with essential thrombocythemia, polycythemia vera and myelofibrosis. We could not do this without your support.
Learn more about MPN Research Foundation's impact for more than two decades.
Patient Stories
Essential Thrombocythemia (ET)
Polycythemia Vera (PV)
Vivienne
Throughout the ten years that Vivienne had PV, she has been very fortunate to see great strides in knowledge about MPNs.
Read Vivienne's story
Myelofibrosis (MF)
Julie
Julie felt compelled to do something to help find better treatments and eventually a cure.
Read Julie's story
Don
Don’s story of his MPN diagnosis began roughly twenty years ago in the spring of 2001 when he was hospitalized for stroke-like symptoms.
Read Don's story
