Recent News
- PAN Foundation Has Expanded Insurance Eligibility for Philadelphia Chromosome Negative Myeloproliferative Neoplasms
- Ajax Therapeutics Announces FDA Clearance of IND Application for AJ1-11095, a First-in-Class Type II JAK2 inhibitor, for the Treatment of Myelofibrosis
- Novel Targets Beyond the JAK-STAT Pathway Aim to Push Myelofibrosis Treatment Forward
Upcoming Events
- Monday, May 20th 8:00-9:00pm EST - MPN Patient Support Group Virtual Meeting
- Tuesday, May 21, 2024 12:00-1:00pm EST - A Conversation with an MPN Specialist: Blood Cell Count Targets in Polycythemia Vera: What Are They and What Do They Mean
- Wednesday, May 22nd 8:00-9:00pm EST - Caregiver Support Group Virtual Meeting
- Thursday, May 23, 2024 11:00am-12:00pm EST - MPN Patient Resources
MPN Advocacy & Education International provides educational programs, materials and resources for patients, caregivers, physicians and entire healthcare teams to improve their understanding of myelofibrosis, polycythemia vera, and essential thrombocythemia. We are dedicated to making a difference in the lives of those affected by MPNs and strive to grow awareness and advocate on behalf of the MPN community. Our advocacy efforts extend beyond responding to the unmet needs of the MPN community. MPN Education Programs are held across the country and internationally each year. Our speakers are MPN specialists who share updated information on research, clinical trials, treatment options, and comprehensive quality of life direction.