MPN Hub Launches Open Access Resource

The MPN Hub is an open-access online resource, dedicated to providing balanced, credible, and up-to-date medical education in MPN

by David Wallace

The MPN Hub is an “open-access” online resource, dedicated to providing balanced, credible, and up-to-date medical education in MPN.  The aim is to enhance knowledge in MPN, through the multichannel dissemination of global advances related to their classification, diagnosis, treatment, and management.

The MPN Hub shares new data, evidence-based articles, therapy approvals, expert opinions, and international congress coverage to treatment teams and researchers around the world.

Overview

The website offers a rich mix of recent, relevant information about MPN clinical advances, pathophysiology and therapy.  Delve into the mysterious world of MPN mutations, while discovering detailed information on the latest clinical trials and therapeutics.

When I interviewed Dr. Jean-Jacques Kiladjian at ASH 2019, we discussed the upcoming rollout of this exciting new resource.  Dr. Kiladjian is an annual contributor to PV Reporter via interviews held at the American Society of Hematology (ASH) conference over the last several years.  Although geared towards healthcare professionals, fellow MPN patients and advocates will find plenty of outstanding information to pour over and broaden your knowledge.

Contributing MPN Experts include:

An “all-star” line up of contributing physicians.

  • Aaron Gerds
  • Jacqueline Garcia
  • Jean-Jacques Kiladjian
  • John Mascarenhas
  • Ruben Mesa
  • Tiziano Barbui

Scientific Education Support launches the MPN Hub at the 25th European Hematology Association (EHA) Annual Congress.

A live event feature page helps you keep up to date with the latest in MPN, fresh from worldwide congresses.  Check out the freshly minted website and further your MPN education.


 

About David Wallace

Founder of PV Reporter, a resource for Myeloproliferative Neoplasm (MPN) patients and caregivers. After being diagnosed with Polycythemia Vera (PV) in 2009, I utilized social media to connect with "informed patients" and develop a better understanding of emerging treatment options. My philosophy on patient care is straight forward - "educating the patient is essential, so the patient can guide their physician to meet his or her needs." PV Reporter is a comprehensive resource hub giving visitors vital tools to become "empowered patients."

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