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.
myMPN is currently only available for MPN patients in the United States and is not yet mobile-friendly so please continue to use a laptop or desktop to access your myMPN account. Not located in the US? Keep checking back. We are working to expand the registry beyond the United States. If you need help, click on the Give Feedback link to be connected to registry customer support!