Risk of second cancers in patients with PV and ET

A very recent article in the journal Nature, 'Cancer history and second cancer risk in polycythemia vera and essential thrombocythemia' reminds us of the risk that PV and ET patients face regarding other cancers.

Updated MPN patient guidelines from the US

The 2026 US physician guidelines were released earlier this year and the 2026 US patient guidelines for MPNs have recently been released and are free to access.

Work and cancer: monthly support groups

A team at Peter MacCallum Cancer Centre in Melbourne will be running a monthly peer support group about work and cancer. The group is available both in-person and online.

Rare Cancers Awareness Day 26 June

Rare cancers struggle for visibility, and without targeted funding, progress is slow. Your support helps change that.

Low serum cholesterol and MPNs

US cardiologist Dr Orly Leiva has a special research interest in MPNs and cardiovascular issues and has published several articles on this emerging area of MPN management. His latest article was published on 26 May 2026 and is free to access.

Modern and multidisciplinary care in polycythemia vera

In April 2026, a review article was published from Italian haematologists titled, ‘Modern and multidisciplinary care in polycythemia vera’ (PV).

Welcome to the MPN Alliance Australia website

MPN stands for myeloproliferative neoplasms – a group of rare, chronic blood cancers that include essential thrombocythaemia (ET), polycythaemia vera (PV), and myelofibrosis (MF).

MPN Alliance Australia is a volunteer organisation run by people living with MPNs, for people living with MPNs and their families.

Our website aims to provide support, connection, and reliable, up-to-date information in one place.

We are also committed to supporting Australian MPN research and hope to raise funds to help advance new discoveries and improve outcomes for people living with an MPN.

We welcome your feedback and ideas. If you would like to suggest improvements to the website, resources or share your experiences, please get in touch.

Together, we can continue to build a supportive and informed MPN community.

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