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Epilepsy Action provides freephone and email helplines and a wide range of information booklets, web pages and e-learning courses. It has around 100 local support groups across England , Wales and Northern Ireland and a network of volunteers working in the community.
In 1983, the facility was renamed to the Central Virginia Training Center. [14] The institution's mission statement emphasized, "The Central Virginia Training Center is committed to providing effective, compassionate and individually responsive services to persons with intellectual disabilities...empowering safe, healthy and enriched lives for ...
An epileptologist is a neurologist who specializes in the treatment of epilepsy. [1] Epileptologists are experts in epileptic seizures and seizure disorders, anticonvulsants, and special situations involving seizures, such as cases in which all treatment intended to stop seizures has failed and epilepsy (especially poorly controlled epilepsy) in pregnant women.
Opinion: Children with epilepsy should be able to feel safe at school, and teachers shouldn't have to fear seizure response, writes Dr. David Moore. 4,400 Iowa kids have epilepsy. Schools need ...
The National Association of Epilepsy Centers is an association of Comprehensive Epilepsy Centers - academic departments of epilepsy in the United States that meets certain criteria and has certain resources available for the care of the most complicated patients with epilepsy. [1] It is based in Washington DC.
Epilepsy is a group of non-communicable neurological disorders characterized by recurrent epileptic seizures. [10] An epileptic seizure is the clinical manifestation of an abnormal, excessive, and synchronized electrical discharge in the neurons. [1]
Research into the causes, diagnosis and treatment of epilepsy. Research focuses on brain imaging and genetics. [2] Epilepsy information, a national helpline and awareness raising programmes. [3] Campaigning on issues to help all people affected by epilepsy live as full a life as possible [4] Epilepsy training to external organisations. [5] [6]
The Epilepsy Foundation received anecdotal reports of patients experiencing seizures and side effects after switching drugs, and tried to convince the U.S. Food and Drug Administration (FDA) in 1999 that there was a problem, but the FDA decided there was no evidence. In 2006, foundation leaders convened a committee of medical experts, and its ...