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The Epilepsy Advocate Community offers patients and their family members information about local Epilepsy Advocate events, plus access to the tools and resources they need to better manage daily living with epilepsy. |
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Comprehensive site with information for health care professionals, patients, and families. Includes detailed content on diagnosis (with multimedia images), medications, nonpharmacologic treatments, clinicals trials, and epilepsy-related events. |
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The Epilepsy Foundation is the national voluntary agency solely dedicated to the welfare of the 2.7 million people with epilepsy in the U.S. and their families. The organization works to ensure that people with seizures are able to participate in all life experiences; and to prevent, control and cure epilepsy through research, education, advocacy and services. In addition to programs conducted at the national level, epilepsy clients throughout the United States are served by local Epilepsy Foundation offices in nearly 100 communities. |
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Online resource center for giving educators the guidance needed to manage and discuss epilepsy in the classroom. |
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CURE is a nonprofit organization dedicated to finding a cure for epilepsy by raising funds for research and by increasing awareness of the prevalence and devastation of this disease. CURE provides research grants, workshops/conferences, advocacy, and special events focused on epilepsy and its impact. |
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The American Epilepsy Society promotes research and education for professionals dedicated to the prevention, treatment, and cure of epilepsy. Membership in the Society is made up of clinicians and researchers investigating basic and clinical aspects of epilepsy, as well as other health care professionals interested in seizure disorders.
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The International League Against Epilepsy (ILAE) is the world’s preeminent association of physicians and other health professionals working towards a world where no persons' life is limited by Epilepsy. Its mission is to provide the highest quality of care and well-being for those afflicted with the condition and other related seizure disorders. |
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The Tuberous Sclerosis Alliance is the only national organization dedicated to finding a cure for tuberous sclerosis complex (TSC), while improving the lives of those affected. During its 30-plus years of existence and growth, the TS Alliance has expanded its mission to improve the quality of life for individuals and families affected by tuberous sclerosis complex through the stimulation and sponsorship of research, the development of programs, support services and resource information, and the development and implementation of public and professional education programs designed to heighten awareness of TSC. For more information, visit www.tsalliance.org. |
