ME/CFS and Lyme Association of WA

Located within the QEIIMC campus, the ME/CFS and Lyme Association of WA, Inc. stands as a beacon of support and knowledge for individuals grappling with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Lyme disease. The association is unwavering in its commitment to assist those affected, offering a variety of resources, educational materials, and support services tailored to meet their unique needs.

With a dedicated team of professionals and volunteers, the association works tirelessly to increase public awareness and understanding of these complex conditions, advocating for better care, support, and research. Their holistic approach ensures that individuals and their families receive comprehensive assistance, empowering them to navigate their health journey with confidence and resilience.

The ME/CFS and Lyme Association of WA, Inc. plays a crucial role in building a supportive community, fostering connections, and championing the rights and well-being of all those impacted by these conditions.

• Support and Advocacy: Providing a strong voice and support network for individuals affected by ME/CFS and Lyme disease.
• Education and Resources: Offering educational materials and resources to enhance understanding of ME/CFS and Lyme disease.
• Community Building: Creating a sense of community and connection for individuals, families, and caregivers.
• Awareness Campaigns: Engaging in public awareness initiatives to increase understanding and reduce stigma associated with these conditions.
• Research and Development: Supporting and promoting research efforts to better understand and find effective treatments for ME/CFS and Lyme disease.