Together, we support, uplift, and empower those living with M.E. CFS, fibromylgia, PVFS and their families and carers in and around Milton Keynes.
About Milton Keynes M.E. Group (MK MEG)
The Milton Keynes M.E. Group is a caring local network dedicated to supporting individuals and families affected by Myalgic Encephalomyelitis (M.E.), CFS, fibromylgia and PVFS. Founded by people who understand the challenges of living with a chronic illness, our group is built on compassion, understanding, and mutual encouragement.
Our mission is to create a safe, welcoming space where members can share experiences, access reliable health resources, and find comfort among others who truly understand. We believe no one should face M.E. alone, and we strive to make a positive difference in every member’s wellbeing.
We offer regular meetings, both in-person and online, to help members connect, share stories, and find practical advice. Through our events and resources, we aim to empower individuals to navigate daily life with confidence and hope.
At the heart of our group is a commitment to building a supportive, informed, and inclusive community. Whether you’re newly diagnosed, a carer, or seeking connection, you’ll find understanding and friendship here.
Through MK MEG, you will be able to meet other people who are living with these illnesses, chat with them about common experiences and share coping strategies.
We are a friendly, informal group, run by people who understand what you’re going through. Although we can’t offer medical advice, members will share their experiences of treatments, offer suggestions on how best to manage the illness and give moral support.
Membership is open to everyone affected by, or with an interest in, ME/CFS/PVFS/FMS. Most of our members live in and around Milton Keynes, but we welcome members and supporters from any area.
Our Journey and Legacy
The Milton Keynes M.E. Group was established in response to a growing need for connection, understanding, and advocacy for those living with Myalgic Encephalomyelitis (M.E.) in our local community. We are small gathering of individuals seeking mutual support and dedicated to improving wellbeing.
Over the years, our group has evolved to provide not just emotional support but also a safe space for sharing experiences. We have organized regular meetings, try to raise awareness campaigns, and community events that bring people together, fostering hope and resilience among members.
Key milestones in our history include expanding our outreach to families and caregivers, collaborating and adapting to the changing needs of our members. Every step of our journey has been shaped by the compassion and determination of our group, making us a lifeline for so many in Milton Keynes.
How We Support You
Empowering those with M.E. in Milton Keynes to connect, learn, and thrive together.
Discover the unique ways Milton Keynes M.E. Support Group uplifts, connects, and informs people living with Myalgic Encephalomyelitis. Our welcoming community is here for you—whether you’re newly diagnosed, supporting a loved one, or seeking ongoing encouragement.
Warm Community Connections
Join a safe, understanding space where you can share experiences and find friendship with others who truly understand life with M.E.
Regular Group Meetings
Take part in supportive meetings—online and in-person—designed to reduce isolation, provide updates, and offer uplifting discussions.
Trusted Information & Resources
Access reliable information about M.E., and self-care strategies, tailored to your needs.
Join Our Caring Community
Support, Understanding, and Friendship Await