Dumfries & Galloway ME and Fibromyalgia Network

Registered Charity No. SC030641

You are not alone, join our community for some local support;

Meetings – All physical meetings are cancelled until further notice due to Covid-19. In the meantime we are holding virtual meetings to members of the Network and our Facebook page every Thursday for about an hour from 2pm using Zoom Meetings. Zoom is available for app for smart phones and tablets, and in your browser or by app on PCs, laptops and Macs. We find it works best on PC, laptop or Mac, followed by tablet, as there’s more screen space to see all participants.

Come along and say hello, bring your questions, your concerns, and bring some cheer and banter to the lockdown! The Zoom link is available on our Facebook page or you can get it by emailing admin@dgmefm.org.uk

When we return to normal, see Upcoming Events for details of meetings and any discussion themes and guests. Click here for our video on how to access the meeting room at Turning Point Scotland, 22 Newall Terrace, Dumfries.

Newsletter – click for the March edition of our Newsletter, and see the Newsletter page for earlier issues.

Contact us;

  • by phone: 07437 602610;
  • E-mail us:  admin@dgmefm.org.uk; Or
  • Complete the form in the ‘Contact Us’ tab above

Facebook – ask to join our Facebook page (closed group)
Facebook http://www.facebook.com/groups/dgmefm

How do I sign up for Facebook?

Blog click on the heading below for our latest Blog

May 2020 Facebook Blog.

    Well thats another month of lockdown gone. At least now we have a flicker of light at the end of the tunnel. Hopefully the new measures will bring back some form of normality into our lifes. Still a long way off from a coffee and cake with friends but that will come. Please continue to follow the Government guidelines and social distancing rules. Wonder how the New Normal will turn out and affect us.  Its sad to hear of some Covid-19 patients are still struggling with symptoms of fatigue. The only positive is that this may bring in more funding for research into ME/CFS and Fibromyalgia. STAR OF