make a difference for severe M.E. sufferers
The 25% M.E. Group is a nationwide charity. We campaign to raise awareness of M.E. and provide services to people affected by severe M.E. (Myalgic Encephalomyelitis).
Your support is vital to our success. Join us to become a member, donate, or get involved in our campaign.
Together we are stronger
By collaborating through campaigning, education, and support, we can significantly enhance the quality of life for individuals affected by severe ME.
About
M.E
Are you suffering from Severe M.E.? What to know how it affects people? Want to understand current developments and how we can help?
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Join us today to help severe M.E. sufferers. Your donations and membership subscriptions help us do this
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We receive no statutory funding for core running costs and are solely reliant upon members’ donations, and donations from private trust funds.
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Features Include:
Latest News
Hope is the biomedical not biopsychosocial approach for ME/CFS
Suffolk and North East Essex Myalgic Encephalomyelitis, Chronic Fatigue Syndrome and Long Covid Service Contract Award
book review: ME/CFS Warrior: A Pain and Symptom Tracking Journal for Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS)Â
Our mission and vision
The following information outlines our mission, aims, values, and beliefs that guide our work and commitment to making a positive impact.
Medical rESEARCH
Advocating for Biomedical Research: We actively push for increased funding and support for rigorous, high-quality research into the underlying biological mechanisms of ME.
Awareness
Raising Public Awareness: The 25% ME Group conducts outreach efforts to educate the public about the debilitating nature of ME/CFS, seeking to dispel misconceptions and foster empathy for those living with this often invisible illness.
Policy Change
We advocate for policy changes that will improve access to healthcare, social services, and disability benefits for people with ME. This includes advocating for changes to diagnostic criteria, guidelines for medical practice, and the allocation of resources for ME specific programs.
Education
Empowerment Through Education: We foster a culture of education and empowerment, providing individuals with ME/CFS and their loved ones with access to accurate information, resources, and tools to navigate the complexities of the disease.
Care Support
The 25% ME Group acknowledges caregivers’ significant role in supporting those with ME/CFS. We offer guidance, resources, and advocacy to help alleviate caregiving’s emotional and practical burdens.
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