MPNRF's Executive Director speaks about myMPN and plans for the research
December 22, 2016
MPNRF's Executive Director Michelle Woehrle discusses research plan, their take on ASH16 and the launch of myMPN - the patient registry the Foundation is kicking off for people with PV, ET and MF. To learn more about the registry or to be part of the beta test, reach out to firstname.lastname@example.org
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Check back regularly for updates about what’s happening in the MPN community, from advocacy to research..