Lochaber ME/CFS Support Network is here to help people in the Lochaber area whose lives are affected by this illness - people with the illness and their carers, families and friends.
We are a friendly and down-to-earth group. Being a grass-roots group, we're not medically trained and don't give medical advice. However, we can provide information and members can share tips on what's worked for them. Our members range from those who are mildly affected to people who are housebound and severely ill. We hope you find the information on this website useful
Membership is free and open to all – people with ME/CFS, their carers, families and friends.
What is ME / CFS? Our leaflet might answer your questions.
Myalgic Encephalomyelitis (ME), Chronic Fatigue Syndrome (CFS) and Post Viral Fatigue Syndrome (PVFS) are all names for what is probably the same debilitating and poorly understood illness.
We are not currently meeting because of Covid-19, but please contact us to join our mailing list. We welcome new members who have long Covid
In the photo, a few members at one of our regular group meetings at Lochaber Hope (before the Covid crisis)
The aims of Lochaber
ME / CFS Support Network are to:
Membership is free and open to all – people with ME / CFS, their carers, families and friends.