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Experiences with
Cinchocaine / Prednisolone hexanoate
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Communities
32 public communities
USAnaphylaxis
102 members
USAnaphylaxis is a community for people who are at risk for life-threatening allergic reactions, or anaphylaxis, and want to learn more about their condition from their peers. 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.
ABDA
551 members
American Behcet's Disease Association - we aim to support patients with Behcet's disease and their families.
Children with Allergies
331 members
The Children With Allergies Support Group was established in 2010 to give children with allergies a chance to talk and play with other children who also live with allergies. Children have the opportunity to talk about having allergies with others who understand what it is like, and gain support from making friends with children who are going through the same experiences.
Partners for Behcet's
523 members
We are a community dedicated to supporting those with Behcet’s Syndrome, which is a rare disease that sees the blood vessels become inflamed.
Allergic to Glycols
213 members
This is a support community for people learning to live with allergies to glycol compounds: Polyethylene glycol (PEG, PPG), propylene glycol (PG), ethylene glycol, and butylene glycol. Here we share our experiences living with allergies that are uncommon, often hidden, and often life-threatening. We offer support, understanding, and share ways we've succeeded living with an allergy to these inactive ingredients.
EFA
2,070 members
European Federation of Allergy and Airways Diseases Patients’ Associations. We are a community dedicated to supporting those impacted by allergy and airway diseases, such as asthma.
Bronchiectasis Support
906 members
The Bronchiectasis Support Community is run by HealthUnlocked and is an online peer-to-peer support network for people affected by bronchiectasis or their carers and families. Please join the community for information, support or advice.
SarcoidosisUK
428 members
We are an online support community for people who experience Sarcoidosis. Join today and get support, help others, and discuss your personal experiences! This community is run by SarcoidosisUK.
USAllergies
422 members
USAllergies is a community for people who experience seasonal and/or environmental allergies and want to learn more about their condition from their peers. 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 (such as hay fever) 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.
The Australian Sjögren's Syndrome Association
2,435 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.
Vasculitis UK
7,783 members
Vasculitis UK is the UK's number one Vasculitis charity, run by people with Vasculitis for people with Vasculitis. We promote a national network of support groups, have a website, social media resources and a near 24 hour helpline that all help the trust to achieve its aims; offering support to sufferers, their families and friends both at home and abroad by providing information, advice and the means to contact each other. We work with other organisations and medical professionals to improve the recognition, diagnosis and treatment of Vasculitis. We raise awareness of Vasculitis among medical professions and the general population. We encourage and support the formation and development of local independant Vasculitis support groups. We raise funds in order to support research into the causes and effects of vasculitis, into improvements in the diagnosis of vasculitis and into the treatment of people suffering from all the different types of vasculitis.
Sjogren's Support
700 members
This community is a safe space for members to chat about their experience with Sjogren's syndrome.
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