The webinar took place on 18 February 2021 and it is the first in a set
of members-only meetings for MPN patient advocates to equip you with
all the recent information you need to pass on to your respective organisation.
Many thanks also to our own Kapila Viges (MPNRF, United States)
and Ken Young (MPN Alliance Australia) for co-moderating this informative session!
MPN Advocates Network was founded by representatives from several MPN patient support groups as a way of creating and maintaining collaboration between these organisations and providing a platform for joint activity.
The objective of the organisation is to enhance MPN patient care by collaboratively:
MPN Advocates Network operates purely for the benefit of MPN patients and acts independently of any other organisation or company. MPN Advocates Network aims to be supported by a broad base of sponsorship & funding.
We welcome all organizations that represent MPN patients, whether as part of a larger organization for blood disorders or as an MPN-specific group
“Together we have a stronger voice!“
The current members of the organization are listed below.
Do you want to become a member? Please email firstname.lastname@example.org
Please fill out the Membership application form and email it to email@example.com. Your application will be reviewed by our membership committee and you will be contacted when it’s approved.
MPN Advocates Network
c/o Münzgraben 6, P.O.B. 453,
CH-3000 Bern 7,