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10 public communities
MS Society
605 members
We're the MS Society, we're a community of people living with or affected by MS. Whether you have MS, or care about someone who does, our community is here for you through the highs, lows and everything in between. If you have any questions, don't hesitate to reach out to anyone of our admins listed below.
My MSAA Community
9,259 members
The Multiple Sclerosis Association of America (MSAA) is a nonprofit organization improving lives today for the MS community through our vital services and support. We provide direct services and ongoing support to individuals with MS, their families, and their care partners throughout the United States. Some of our free services include: Helpline with trained specialists, safety and mobility equipment distribution, award-winning educational videos and publications, cooling accessories for heat-sensitive individuals, educational programs held across the US, and more. We hope that My MSAA Community on HealthUnlocked is a safe and inviting space for you to connect with other members of the MS community in order to both find and provide support for your shared experiences.
The Australian Sjögren's Syndrome Association
2,452 members
The Australian Sjogren's Syndrome Association Inc. was incorporated in Parramatta in 2001, although due to illness of the founder, the association did not commence trading until June 2004 in Mullumbimby, Northern NSW. The name of the founder and president is Ms Beverly Norton. Background The Association was started by Beverly Norton who, in May 2000, was diagnosed with Sjogren's, a disease that Australian doctors knew very little about. Sjogren's (pronounced show-grins) syndrome is a chronic, autoimmune disorder in which the body's immune system mistakenly attacks its own moisture producing glands. The specific causes of Sjogren's syndrome are not known, but multiple factors are probably involved. These include genetics, viruses, hormones or a combination of all of these. It is critical that it is identified quickly and treated otherwise it can be fatal.
LDN Research Trust
1,414 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
Australian Pain Management Association
344 members
APMA is a health promotion charity providing advocacy, information and practical support for people living with persistent (chronic) pain and their families. APMA is the consumer health organisation for all Australians who live with persistent pain. APMA is your voice. APMA provides advice, assistance and advocacy, and works with governments, health clinicians and researchers to deliver evidence-based pain management services and ameliorate the personal and economic impact for people living with severe pain.
Borders Pain Management
170 members
We are a peer support group specifically for individuals affected by Chronic Pain within the Scottish Borders. We offer support and advice to those diagnosed with Chronic Pain as well as carers, family, friends, employers and health care professionals. We actively encourage members to post their questions to get support from others in a similar position and to feel less isolated.
Chronic Myofascial Pain
502 members
We have set up this community in order to provide support for anyone suffering from Chronic Myofascial Pain (CMP); to provide and share information about all things fascia related; to raise awareness about CMP, and fascia in general; and to bring together patients and professionals working in the field, to create a united front to campaign for better understanding of fascia and for better treatment models for CPS.
COPD Friends
3,611 members
We are peer support community for people living with COPD. Join us to share your story and experiences, ask questions and support others. Connect with others like you today!
Living with Asthma
3,643 members
Living with Asthma is a community for people with asthma who want to learn more about their condition from their peers, and help support one another. The community is run by Allergy & Asthma Network, the leading nonprofit patient education and advocacy organization dedicated to ending needless death and suffering due to asthma, allergies and related conditions. Our patient-centered network unites individuals, families, healthcare professionals, industry and government decision makers to improve health and quality of life for people with asthma and allergies.
Asthma Community Forum
22,182 members
Welcome to Asthma + Lung UK's asthma community forum (previously Asthma UK) which is a place for you to share your experience and hear from other people to support you with whatever question you have about your asthma. There's over 19000 people on the forum, so chances are, someone has been where you are.