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Top Epilepsy Sites

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For International Epilepsy Day 2016, we ran a special photography competition with the theme ‘YES, I CAN’, to demonstrate achievement in overcoming obstacles, or achievement despite obstacles. The best photographs will form the International Epilepsy Day exhibition, taking place in the European Parliament in Strasbourg from Monday to Friday, February 1 to 5, 2016. All entries are in our...
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Epil-K9, The All Breed Canine Epilepsy List was founded in 1996 by Alicia Wiersma-Aylward. It is now co-owned and managed by: Marion Mitchell, Chris Desmedt, Alisa Arnoff, Jeanette Tunstal, Kathy Linder, and Jean Collinson. The purpose of Epil-K9 to is to discuss canine epilepsy and seizures. List members are encouraged to ask questions and/or give information on these disorders according to...
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The first step is an interview with a good neurologist or epileptologist, a neurologist who specializes in epilepsy. The neurologist’s first tool in diagnosing epilepsy is a thorough medical history of the patient, including family history of seizures, if any; an observer’s account of what the...
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Researchers at Case Western Reserve University may have found a new way information is communicated throughout the brain. Their discovery could lead to identifying possible new targets to investigate brain waves associated with memory and epilepsy and better understand healthy physiology. They...
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Be a part of the 30th anniversary of the Chocolate Ball! An evening of chocolate, wine, dinner and dancing -- all to support epilepsy and other programs at EPI. Contact Shaunta Collier-Santos at (585) 442-6420 x2227 or scollier-santos@epiny.org for more information. Buy tickets or sponsor today!...
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Northeast Regional Epilepsy Group New York and New Jersey. Treatment of epilepsy in children and adults. To accomplish our second goal of treatment built around patient needs, we listened carefully to our patients. They spoke of encountering obstacles and even sometimes discrimination because of their epilepsy. We heard from parents that they needed help with their children's schools, adults...
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The Epilepsy Foundation of Connecticut will help ensure that people with seizures are able to participate in all life experiences. Thank you for a wonderful inservice program today. The Norwalk school nurses could not speak more highly of your presentation. We all learned so much about the different types of seizures, treatment modalities, and implications for care in the school setting. It was...
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EFEPA provides education, support and advocacy for people with epilepsy and their families. To stop seizures and SUDEP, find a cure and overcome the challenges created by epilepsy through efforts including education, advocacy and research to accelerate ideas into therapies. Number of people with epilepsy who live with uncontrollable seizures because no available treatment works for them. The...
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Forum for people living with epilepsy to discuss treatment options and offer peer support. What a difference a year makes - Stacy managed to go tonic-clonic seizure free throughout 2010! She’s gotten *much*, much better at managing her diet, meds, sleep and overall life/stress/schedule balance. She still occassionally has a small CP seizure (maybe once a week or two). By small, I mean they are...
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The International League Against Epilepsy (ILAE) is the world's preeminent association of physicians and other health professionals working toward a world where no person's 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. NMDAR antibody encephalitis is characterized by...
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Door to Door Campaign The Door to Door Campaign is now in full swing. High school students can gain career hours while helping out a non-profit organization. Anyone can participate across the island. For those interested, please call Elaine 709-722-0502 Calendar Campaign The Calendar Campaign is now closed for the 2015 year. If you still have donations to submitted, please do so. We would like...
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The rules governing epilepsy and driving vary somewhat from province to province; this document is specific to Ontario. As this document shows, having epilepsy does not mean a person cannot drive. Most provinces now follow these CCMTA guidelines. This document can be used to document facts relevant to a workplace seizure before, during and after the fact. This reference information could be...
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EFNJ Scholarship Winners Announced: Ashley Kulikowski from Glassboro High School, Alisa Harada Pascack from Hills High School, Makenzie Bayless from Robbinsville High School, Naomi Schachter from Summit High School and Josue Leon from Essex County Vocational Technical School! Good luck to all in their new school year! Epilepsy Foundation of NJ is proud to announce our Get FIT program has been...
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While epilepsy occurs in 1 out of every 100 persons worldwide, persons with epilepsy and their loved ones often spend their lives working against misconceptions that prevent them from accessing appropriate medical care, education, employment, and other community resources. Persons who suffer other kinds of seizures also face huge challenges, misconceptions and stigma regarding their condition....
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The 200TH camp was held on 8TH November at Ratan nagar where National Epilepsy Day was celebrated. As reported by Dr R.K. Sureka a Exhibition depicting the various facets of Epilepsy was organized and visited by residents of the village and about 590 patients and their relatives where people were educated about Do’s and Don’ts. Similarly an audio visual film was also run for the Epileptics. A...
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People with epilepsy and those with developmental disabilities will attain the highest quality of life and gain full acceptance and understanding from the community. The Mission of the Epilepsy Center of Northwest Ohio is to improve the lives of people affected by epilepsy and those with developmental disabilities. Vision. We offer a wide range of services aimed to better the life of people...
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Do you have a child with epilepsy? Are you searching for answers? Are you feeling overwhelmed or stressed? The Kids and Family Program is a free service designed to help parents overcome obstacles in managing a child’s epilepsy. The service is provided by an Epilepsy Association social worker who will meet with you privately in the comfort of your own home or at the Epilepsy Association office....
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The Epilepsy Foundation will ensure that people with seizures are able to participate in all life experiences; and will prevent, control and cure epilepsy through services, education, advocacy and research. Epilepsy is a central nervous system disorder (neurological disorder) in which the nerve cell activity in your brain is disturbed, causing a seizure during which you experience abnormal...
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Since 1978, the Epilepsy Association of Oklahoma has been incorporated as a nonprofit health agency with the mission of helping Oklahomans who have epilepsy and their families. I call epilepsy a “stealth” disease, but it’s difficult to imagine how so few people can know about a disease that affects so many. For example, few people know:. Epilepsy affects over 3 million Americans of all ages –...
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The Epilepsy Foundation of Mississippi leads the fight to stop seizures, find a cure, and overcome challenges created by epilepsy. This foundation is dedicated to the prevention and cure of seizure disorders, the alleviation of their effects and the promotion of an independence and optimal quality of life for people with epilepsy, through education, advocacy, research and direct client service....
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