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The Dutch ME/CFS Cohort and Biobank consortium

NMCB is a collaboration of Dutch research institutes, medical centres and patient organisations dedicated to biomedical research of
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS).

This project is made possible by:
What is ME/CFS?

ME/CFS

ME/CFS is a serious disease that disrupts patients’ lives and causes a lot of suffering. ME/CFS patients experience continuous and intense exhaustion. In addition, symptoms worsen even after minimal mental, physical, emotional or social exertion – something known as “post-exertional malaise” (PEM).

ME/CFS symptoms:
WHAT WILL NMCB DO?

Building an international ME/CFS hub

Biomedical research

Despite the impact of ME/CFS, much is still unknown about its causes and possible treatments. NMCB recognises the need for biomedical research on ME/CFS. By establishing a national patient cohort and biobank, we are building an international infrastructure for research to improve the knowledge, diagnosis and treatment of ME/CFS.

NMCB research

In an eight-year collaboration between scientific and clinical experts, as well as patients, the NMCB will enable in-depth research divided first of all into six subprojects. In collaboration with an international research network, the NMCB will establish an international ME/CFS hub to facilitate additional research on ME/CFS.

Collaborations

Patient representatives

Patients and their experiences are an essential part of the NMCB. In collaboration with three ME/CFS patient organisations, we want to ensure that patients’ experiences remain central to our studies.

All our partners

NMCBPartners

Recent updates

News

26/08/2024

ZonMw currently has an open funding round for their ME/CFS research program. Applicants are invited to submit a project idea before 14:00 on Tuesday 24 September 2024. A detailed grant application can be submitted at a later date after the project idea has been approved.

12/05/2024

How do we ensure that the disease can be diagnosed in time and the patient’s experiences are taken seriously? A first important step in this is more education among (future) practitioners of patients with ME/CFS.
Get in Touch

Contacts

Do you have any questions about the NMCB? Feel free to reach out using the form below, or find your question at the FAQ page