MPN Cancer Connection
a resource for MPN patients
Information. Community. Opportunity.
Welcome to MPN Cancer Connection, where the future is bright for the MPN community, filled with opportunity with new clinical trial treatments, offering a wide range of MPN resources and information, all for improved patient care and quality of life.
MPN-CC was founded to serve patients, care partners, physicians, and your healthcare team. We help empower patients to be proactive and to be your own health advocate by asking questions from your healthcare team.
New Patient Resources Available
David Wallace, MPN Cancer Connection CEO and Founder
Learn about the new downloadable resources that have been recently added to the website! The resources cover what you should know about Myelofibrosis causes, symptoms, and changes over time along with treatment options and questions to use in discussions with your doctor
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Clinical Trial Finder
Free, No Personal Information Required
Search for MPN Clinical Trials that may help you find new treatments and medical approaches for your myelofibrosis (MF), polycythemia vera (PV) or essential thrombocythemia (ET).
ClinicalTrials.gov is difficult to use for patients, as it is primarily a resource for doctors and clinicians. Our Clinical Trial Finder restructures the trial information – providing “easy access” while improving patient’s understanding of the trial.
David Wallace on Patient Advocacy
MPN Cancer Connection, CEO and Founder
David Wallace is honored to receive the Cure Magazine 2016 MPN Hero Award for his commitment to the broader MPN community for his work on PV Reporter founded in 2013 and MPN Cancer Connection, a non-profit organization founded in 2015. He is committed to helping newly diagnosed patients with myeloproliferative neoplasms (MPNs) learn more about their condition. He shares his experience as an “outspoken patient advocate” to help fellow patients get up to speed quickly and have the tools necessary to make educated decisions on treatment options.