Driving research of Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME / CFS),
Post Treatment Lyme Disease Syndrome (PTLDS), and Fibromyalgia.

OMF Worldwide Tour Coming to Denmark

Dear Danish OMF Friends,

Being the mother of a sick daughter, I am well aware of how important hope is for all of you with ME / CFS. I will once again embark on a European Tour of Hope in June and will be visiting Denmark (following the IIME in London).

I would love to meet as many patients, parents, caregivers and doctors/healthcare personnel as possible! I will be giving an exciting OMF research update to learn what we are doing to unravel ME / CFS, share hope, raise awareness and encourage everyone to collaborate to be part of the solution. At the end of my talk, I will be available to answer your questions and for a personal meet and greet.

OMF is the leading international research organization fundraising to support research to end ME / CFS and related chronic complex diseases. We are committed to open and collaborative research. I am looking forward to seeing you soon in Copenhagen to exchange hope and ideas to conquer this terrible disease, together!

OMF’s End ME / CFS Worldwide Tour in Denmark – Accelerating Collaborative Research:

Date: Sunday, 2 June 2019. Time: 14.00u-16.00u.

Speaker: Linda Tannenbaum, Founder & CEO/President, OMF

Location: Valby Kulturhus (Cultural House), Valgårdsvej 4, 2500 Copenhagen

Host: ME Foreningen.

For more information about the program, please visit: https://me-foreningen.dk.

To register: Please send an email to Karin Christensen: sekretariat@me-foreningen.dk. Kindly register by May 26. This event is free for ME Foreningen members and 50DKK for non-members.

With hope for all,

Linda Tannenbaum

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