WHERE DO YOU GET YOUR MPN CARE?
Doctors drive our treatment options. We’ve got a rare disease. MPN specialists are even more rare. So who do we see to check our blood counts, monitor our condition, plan our therapy?
Please take this 2 minute survey. It’s part of the work being done by the MS3T Taskforce exploring timing of therapeutic options, a project sponsored by the MPN Research Foundation. Full results published July 19. https://goo.gl/forms/UzuS2n2cWYk5KEEP2
And thank you,