For people with ME/CFS who are single, over 18, and looking for someone special to be "more than friends" with.
If you are interested in joining, just download the Telegram app, and create an account (you'll need a mobile device).
ME/CFS/FM Singles Facebook Group
This is a group for single people, over the age of 18, with ME/CFS/FM and associated conditions who would like to meet others in a similar situation. The group is intended to be a lighthearted, fun place where you can socialize and make friends. We have a pinned post called Dating Corner where you are able to meet others looking to date, however, you don't have to date if you don't want to.
The ME/CFS Book Club Facebook Group
A friendly and calm book club group for people with ME/CFS, Fibromyalgia, Long Covid and their carers who love reading or listening to audio books
Chronic Creatives Hearing Things Facebook Group
A group for those with chronic illnesses and disabilities to share their favourite audiobooks, podcasts, and radio programmes, and hopefully discover a few new ones.
ME/CFS Game Community Facebook Group
This group is for MECFS patients to meet, connect, and share tips and tricks for how to video game with this terrible disease.
Chronically Coping Facebook Group
Sharing products, people, pages, and life-hacks that help you cope with chronic illness. Patients & Caregivers are both welcome. Specifically for patients who suffer from illnesses that are exercise intolerant and fatigue-related.
ME/CFS: Below The Threshold Facebook Group
This group is for people with ME/CFS using a heart rate monitor (HRM) to stay below their aerobic threshold (AT). The contents of this group have been compiled into "the ultimate guide to pacing with a HRM," available to download here. https://paradoxfloss.gumroad.com/l/belowthethreshold
We are focused on learning how to use Heart Rate Monitors and Heart Rate Variability (HRV) to improve pacing, living within your energy limits, and to minimise or eliminate PEM. In order to keep the focus of the group on HRMs and pacing, we don’t allow broader discussion of the experience of living with ME/CFS.