Life for patients with myelofibrosis: the physical, emotional and financial impact, collected using narrative medicine—Results from the Italian ‘Back to Life’ project

Using survey data from patients with primary or post-essential thrombocythemia/post-polycythemia vera and their caregivers, Italian researchers suggest that better relationships between health care team members and patients can lead to more focused care and better financial support for patients.

 Quality of Life Research

By continuing to browse this site you permit us and our partners to place identification cookies on your browser and agree to our use of cookies to identify you for marketing. Read our Privacy Policy to learn more.