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Ménière's disease is described by its major symptoms: vertigo, tinnitus and deafness. Individuals have the symptoms with different intensities, variable over time and not necessarily all active at the same time. Currently there is no clear understanding of how the disease develops and hence there is no way of halting or curing it; although it may spontaneously go into remission. As the disease is little understood and is not common (about 0.1% of the population suffer), medical care and support can vary depending on the patient's location. As there is no obvious line of research to follow to cure the disease the Society spends a considerable part of its budget on research to help sufferers and their carers manage the disease better. Consequently research in the following areas is supported:
The Society continues to seek, evaluate and support worthwhile projects. Funding is available to help stimulate interest in Ménière's disease for medical staff.