People with MPDs and MPD specialists talk about ET, PV and MF in these videos.
Albert talks about living with myelofibrosis (MF) and taking a JAK2 inhibitor drug currently under trial.
John, a cyclist, talks about his diagnosis with polycythaemia vera (PV) and how he’s stayed active and fit in spite of PV.
Rachel talks about how having essential thrombocythaemia (ET) has impacted her life and how she’s making a contribution by fundraising.
David talks about his diagnosis of Myelofibrosis (MF), and the impact it had on his life and how he copes.
Leading MPD specialists talk about what the characteristics of Essential thrombocythaemia (ET), Myelofibrosis (MF) and Polycythaemia vera (PV) are.
Why MPDs (myeloproliferative disorders) were reclassified as MPNs (myeloproliferative neoplasms) by the WHO.
Leading MPN specialists talk about the symptoms patients present with and the ways MPNs are diagnosed.
Leading MPN specialists talk about the problems and risk factors patients face and how they gauge these factors and then treat them.
Leading MPN specialists explain the importance of the JAK/STAT Pathway prominence in the pathogens of MPNs.
Leading MPN specialists talk about the recent JAK 1 and 2 study results and what they mean for patients.
Leading MPN specialists talk about the prognosis for patients with MF and the impact it has on their day to day living.
Leading MPN specialists give an overview of the symptoms patients with MF may suffer from.
Watching videos of other people with MPDs has meant a lot to me.