The Waterloo Wellington Myalgic Encephalomyelitis Association (WWMEA) is a Canadian nonprofit organization dedicated to providing support and information to individuals affected by Myalgic Encephalomyelitis (ME) and Chronic Fatigue Syndrome (CFS). Established to assist those living with these chronic illnesses, the association organizes support group meetings and disseminates educational resources to help patients and their families cope with the challenges associated with ME and CFS.

Operating primarily in the Kitchener and surrounding Waterloo Wellington region, the WWMEA focuses on fostering a community of support and advocacy for affected individuals. As a registered Canadian nonprofit, its business registration number is 892825969RR0001. The association’s activities are geared toward creating awareness, offering emotional and social support, and providing up-to-date information related to the illness, its management, and ongoing research.

The WWMEA is recognized for its commitment to members and the broader ME community by maintaining accessible support channels and educational efforts tailored for patients, caregivers, and healthcare providers. Through regular meetings and outreach, the organization plays a vital role in enhancing the quality of life for those impacted by ME and CFS in the Waterloo Wellington area.

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[1] http://www.wwmea.ca [2] http://www.wwmea.ca/aboutwwmea.html [3] http://www.wwmea.ca/aboutme.html [4] https://wwema.org [5] https://www.wwhealthline.ca/displayService.aspx?id=214711