MPNS MADE NEWS AT ASCO THIS YEAR
The American Society of Clinical Oncology has its big meeting each year in Chicago in early June. In the past solid tumor cancers have received… Read More »MPNS MADE NEWS AT ASCO THIS YEAR
MPN PREVALENCE
MPN PREVALENCE
MPN CLINICAL TRIAL HIGHLIGHTS FOR SUMMER 2015
If you have MF, PV or ET but don’t need medication now, you may think that clinical trials don’t matter to you. But that could… Read More »MPN CLINICAL TRIAL HIGHLIGHTS FOR SUMMER 2015
WHAT’S NEXT FOR MPN RESEARCH?
Before there was knowledge of the JAK2 mutation, there was the MPN Research Foundation. Both the Foundation and MPN patients had the nerve to demand… Read More »WHAT’S NEXT FOR MPN RESEARCH?
FEARS: DISEASE PROGRESSION
We’ve started a new guest blogger feature. Please welcome Lina of linampn.com When I was first diagnosed, I knew absolutely nothing about MPNs. And for a… Read More »FEARS: DISEASE PROGRESSION
NOT YOUR MOTHER’S PV: A YOUNG PATIENT’S BATTLE WITH POLYCYTHEMIA VERA
Special guest post by PV patient Donna B. The polycythemia vera part of my story began in August 2006, when I was diagnosed. I… Read More »NOT YOUR MOTHER’S PV: A YOUNG PATIENT’S BATTLE WITH POLYCYTHEMIA VERA
CAN ENVIRONMENTAL CAUSES BE BEHIND SOME CASES OF POLYCYTHEMIA VERA?
By Ann Brazeau In August 2008, ATSDR and PADOH organized a meeting with a panel of experts in Philadelphia. Medical researchers, environmental scientists, and public health professionals met… Read More »CAN ENVIRONMENTAL CAUSES BE BEHIND SOME CASES OF POLYCYTHEMIA VERA?
INTRODUCING THE MPN FOUNDATION’S OFFICIAL BLOG
The MPD Foundation is a decade old this year. We are currently waiting for proposals to arrive for the 2011 grant cycle and are looking… Read More »INTRODUCING THE MPN FOUNDATION’S OFFICIAL BLOG