Funding for Myalgic Encephalomyelitis Research

Summary

The motion calls for increased EU funding and coordinated research into Myalgic Encephalomyelitis (ME/CFS) to improve diagnosis, treatment, and social support.
9 18.06.2020
Other
health
economy
social policy
disabled person
research and intellectual property

Key points

  • The European Parliament calls for increased and prioritized funding specifically for biomedical research into ME/CFS.
  • There is an urgent need to develop and validate reliable biomedical diagnostic tests and effective treatments.
  • The Commission should create a European prevalence register to better track how many people are affected by the disease.
  • Improved medical education and training for healthcare professionals are necessary to ensure better patient care.
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