admin | March 24, 2021
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 lwhyte@mpnresearchfoundation.org