Welcome, MPN Advocacy & Education International works with the Patient Access Network (PAN) Foundation to provide resources to the patients, caregivers, physicians and healthcare teams to improve their understanding of essential thrombocythemia (ET), polycythemia vera (PV)and myelofibrosis (MF) known as myeloproliferative neoplasms (MPN).
We host patient educational programs across the country, with MPN specialists presenting on a wide range of topics impacting the MPN community, including treatments, clinical trials, and emerging research. Our advocacy efforts focus on identifying the unmet needs of the MPN community, as well as creating initiatives that improve the overall quality of care for MPN patients. View videos from our past events.
In addition, take a minute to tour our website, mpnadvocacy.com, it provides a wealth of information on MPNs, including videos from our MPN patient education programs, FAQs, local support group contacts, and many other useful resources. You can also view and sign up for our online monthly newsletter.
If we can be of any help or you wish to receive additional materials, please do not hesitate to contact us.
