Founder with a vision
Each May, we celebrate the life and legacy of our founder, Bob Rosen, and 25 years of research driven by his vision: to find answers and – eventually cures- for those living with essential thrombocythemia (ET), polycythemia vera (PV), and myelofibrosis (MF), together known as myeloproliferative neoplasms (MPNs).
This May, Bob’s family and friends are honoring his commitment to MPN research with a special challenge:
Every dollar raised will be matched, up to $25,000!
That means your donation goes twice as far – fueling research, supporting innovation, and bringing new possibilities to MPN patients.
Bob’s journey began with a shocking PV diagnosis in 1997. At the time, MPN research was nearly non-existent, and answers were hard to find. But Bob didn’t accept the unknown – he took action. He founded MPN Research Foundation to drive scientific discovery, accelerate treatments, and bring hope to countless others like him.
Today, you have the power to continue his vision. Become a monthly donor today and be part of the grassroots movement Bob started that is changing lives.
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Plus, you will receive the latest NCCN guidelines and resources to support your journey when you join our community.
Plus, you will receive the latest NCCN guidelines and resources to support your journey when you join our community.
Register for MPN Pathways training series
Do you want to make a real difference
in MPN Research?
Become a MPNRF certified research advocate by joining our MPN Pathways: Empowered Voices in Research training series, a comprehensive program designed to educate, engage, and empower patients and caregivers
in MPN Research?
Become a MPNRF certified research advocate by joining our MPN Pathways: Empowered Voices in Research training series, a comprehensive program designed to educate, engage, and empower patients and caregivers
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