myMPN: a tool for people with PV, ET and MF

On December 31, 2020, the myMPN Patient Registry will be taking a pause from collecting patient-reported data to reflect on our progress and evaluate how to grow the program further. We appreciate your understanding, and we look forward to seeing you back soon! Please direct any questions, comments, or concerns to mympn@mpnrf.org.

 
 
 
 
 

 

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