Partner Spotlight: Updates From the MPN Research Foundation at ASH 2016

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At ASH 2016, Patient Power's Mary Windishar caught up with Michelle Woehrle, Executive Director of the MPN Research Foundation, on a new patient registry system called myMPN that will help patients with polycythemia vera (PV), essential thrombocythemia (ET) and myelofibrosis (MF) to share information about their condition to share with the research community. Michelle also shared her perspective on the latest news coming from ASH related to interferon therapy and results from clinical trials.

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Page last updated on December 21, 2016