ME Research UK
ME Research UK[edit | edit source]
ME Research UK is a charity based in the United Kingdom that focuses on funding and promoting research into Myalgic Encephalomyelitis (ME), also known as Chronic Fatigue Syndrome (CFS). The organization aims to advance scientific understanding of the disease, improve diagnosis, and develop effective treatments.
History[edit | edit source]
ME Research UK was established in 2000 with the mission to "energise ME research". Since its inception, the charity has funded numerous research projects across the globe, contributing significantly to the body of knowledge surrounding ME/CFS.
Objectives[edit | edit source]
The primary objectives of ME Research UK include:
- Funding high-quality biomedical research into the causes, consequences, and treatment of ME/CFS.
- Raising awareness of the disease among the public, healthcare professionals, and policymakers.
- Providing information and support to patients and their families.
Research Focus[edit | edit source]
ME Research UK supports a wide range of research initiatives, including:
- Investigating the pathophysiology of ME/CFS.
- Exploring potential biomarkers for diagnosis.
- Evaluating the effectiveness of various therapeutic interventions.
Achievements[edit | edit source]
Over the years, ME Research UK has funded over 50 research projects, leading to significant advancements in understanding the disease. Some notable achievements include:
- Identification of potential biomarkers for ME/CFS.
- Insights into the immune system dysfunction associated with the disease.
- Development of new diagnostic criteria and tools.
Collaboration[edit | edit source]
ME Research UK collaborates with various academic institutions, healthcare providers, and other charities to further its research goals. The organization is a member of several international consortia focused on ME/CFS research.
Public Engagement[edit | edit source]
The charity actively engages with the public through events, publications, and social media. It aims to educate the public about ME/CFS and advocate for increased research funding and better healthcare services for patients.
Related pages[edit | edit source]
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