Muscular Dystrophy Ireland (MDI) is a voluntary organization which was established in 1972 by a small group of people in the west of Ireland to support families who had a member with muscular dystrophy. Since then it has grown considerably and it now has a membership of over 750 members […]
MS Ireland is the national organisation providing information, vital services and support to the MS community. We provide a wide range of specialised services and resources on a national, regional and local level. Services include; Regional Community Worker programmes for one-to-one support; physiotherapy; symptom management courses; newly diagnosed sessions and the […]
Migraine Association of Ireland are Ireland’s only patient charity providing support, education, information and reassurance to people suffering from migraine and other headache disorders. They provide free educational courses on self management and understanding migraine for people with migraine, and certified health professional courses for GPs and other HCPs. They […]
The Irish Heart Foundation are leading the way in the fight against heart disease and stroke in Ireland. They campaign to influence government policy to improve care for patients and for real change for those affected by heart disease and stroke. As the national charity fighting heart disease and stroke […]
If you are living with Huntington’s disease, at risk, or caring for a loved one HDAI is here to help. We can support you to access the health and social services you need, provide information to you and your health professionals, and champion your rights. We will also work with […]
Headway is an Irish registered charity and an internationally accredited brain injury services organisation that supports adults (18+) who are affected by brain injury. A bit more… We were founded in 1985 as a support group by families and interested professionals to address the needs of people with brain injuries and their […]
Guillain Barré & Associated Inflammatory Neuropathies Receiving a diagnosis of Guillain-Barré syndrome or CIDP can be a terrifying and isolating experience, bringing with it many questions and an uncertain future. GAIN is the only organisation dedicated to helping people affected by these conditions in the UK and Ireland. We are […]
“Welcome to Ataxia Foundation Ireland (AFI), the New Voluntary National Support Group for people affected by Friedreich’s Ataxia (The most common Genetic Ataxia) and up to 50 other Ataxia’s. The organisation was founded by four people with Ataxia, to form the board of directors and trustees, we have recently increased the board to seven, […]
The aims of Dystonia Ireland are to promote and encourage scientific research into the causes and treatments of dystonia, raise the level of awareness amongst the general public and the medical profession, offer support and information to all people with dystonia and their families nationwide. As the national support group […]
Epilepsy Ireland was established in 1966 with the goal of improving the quality of life of people with epilepsy in Ireland. Today, we provide a range of services across the Country from headquarters in Dublin and via our regional offices in Cork, Dundalk, Galway, Kerry, Kilkenny, Letterkenny, Limerick, Sligo and Tullamore. Vision Epilepsy Ireland’s vision is to achieve a society where no […]
