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9 public communities
Myalgic Encephalomyelitis Community
2,043 members
Myalgic Encephalomyelitis (ME) Community is a peer support community for people who living with ME, aka chronic fatigue syndrome (CFS). Join to connect with others who understand. Share your experiences and get tips and advice from others like you. Why not introduce yourself today - healthunlocked.com/meandcfssupport/write
EDMESH
2,023 members
We are a charity primarily focused on helping patients and their families with ME (Myalgic Encephalomyelitis) and CFS (Chronic Fatigue Syndrome) living in Edinburgh, Scotland. We welcome members from around the UK and the world with an interest in ME and CFS friends – indeed, anyone with an interest in M.E. or CFS.
Fibro Friends WSM
1,060 members
Fibro Friends WSM is registered with the Fibroduck Foundation Our aim is to reach out to others in the area with Fibromyalgia, Chronic Fatigue and Similar Conditions. We run Regular Coffee Mornings and Meetings and occasionally invite guest speakers to come along and talk to us, to help us have better understanding of our conditions and how to manage them. We Meet Twice a Month: On The Second and Last Tuesday Every Month At 11am 1 in 4 People 39 Oxford Street. Weston Super Mare
Foggy's "Invisible Illness" Support
5,569 members
With charitable donations, we are able to provide 2 Hydrotherapy sessions per week, for our paid members. We are dedicated to providing support, raising awareness and promoting positivity, for invisible conditions primarily for: Arthritic Condition's Chronic Fatigue Syndrome Chronic Widespread Pain Fibromyalgia Giant Cell Arteritis Long Covid M. E. Myalgic Encephalopathy Myofascial Pain Polymyalgia Rheumatic Condition's
FieryBones - RA Community
696 members
Rheumatoid Arthritis, or RA, is a type of auto-immune disease where the body's immune system starts attacking its own tissues and joints. It can happen at any age and is one of the most common form of arthritis. Some of the common symptoms are painful and swollen joints, fatigue and weakness. For people living with RA, it is a daily struggle to balance their personal and professional lives with the unpredictability of this painful disease. FieryBones has been created to connect all the RA warriors and caregivers throughout the world on a single platform. Nothing makes us feel better than reading inspirational blogs of how our RA peers are coping with this illness and sharing our story with the community that truly understands!
Neuro Support
1,994 members
Welcome to the Neuro Support Community. This community exists to improve the quality of life of people affected by any neurological condition, including: ALS, Alzheimer’s disease, Back pain, Bell's palsy, birth defects of the brain and spinal cord, brain aneurysm, brain injury, brain tumors, cerebral palsy, chronic fatigue syndrome, concussion, dementia, disk disease of neck and lower back, epilepsy, Guillain-Barré syndrome, migraine, multiple sclerosis, muscular dystrophy, neuralgia, neuropathy, neuromuscular and related diseases, Parkinson's disease, scoliosis, seizures, spinal cord injury, spinal deformity, spinal disorder, spine tumors and stroke. Whether you're affected directly, caring for someone or know someone affected, everyone is welcome. Join today to share your experiences, receive support and exchange advise in a community of people who truly understand. Introduce yourself today: https://healthunlocked.com/neuro-support/write
The York ME Community
82 members
Andover Fibromyalgia & ME Community Group
2,788 members
Welcome to AFMCG community! :) Here you can share your experiences about living with Fibromyalgia & M.E in a non-judgemental friendly environment. AFMCG members can be from all over UK, the world however the group was initially founded for a place in Hampshire called Andover, The philosophy of the group to treat one another with respect & understanding focusing on bringing the FMS/ME community together to provide support for one another. We aim to post relevant information or signpost members to other organisations that may give the appropriate advice. We are passionate about raising awareness & often post relevant campaigns to help spread the word including petitions. To find out more please visit www.afmcg.org. Please can we kindly ask you adhere to the guidelines to make the community a supportive place for one & all. Any questions please contact our Volunteer Admin via the private message facility or alternatively email admin@afmcg.org
LDN Research Trust
1,405 members
The primary aim of the Trust is to initiate Clinical Trials of Low Dose Naltrexone. Whilst working to raise funds for trials, we have helped over 16,000 people to obtain LDN from a General Practitioner or Neurologist, either through the National Health Service or by private prescription. We have also been able to help people, not just in the UK but in countries throughout Europe, as well as USA, Canada, West Indies, Australia, New Zealand, and others. By using this website and from our downloadable newsletters, you will be able to read the stories of some of these people. We have helped many people with MS, Crohn's, IBS, ME and Cancer to name a few. The use of LDN is spreading. Our ultimate goal is for everyone to be prescribed LDN globally for all conditions where LDN could be of benefit