Natural Seizure Remedies These are some of the natural seizure remedies that didn't work for me as well as the one that is currently work for me. Check out my journey at http://melin... By: Melinda Curle … Continue reading →

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E-Action designed for the 300,000 living with the neurological disorder1 OAKVILLE, ON, March 26, 2013 /CNW/ - Canadians with epilepsy, as well as their family, friends and caregivers, now have an exciting new information source and support network. E-Action - Taking Action Against Epilepsy strives to provide a caring and informative environment for those touched by the disorder. E-Action includes a broad range of interactive education and information resources, including a magazine, a website, a mobile application (App), and a leader program that features 10 inspirational Canadians living well with epilepsy. "Epilepsy associations across the country have been working tirelessly to help people with epilepsy live the best quality of life possible. E-Action is a fantastic resource to help us do just that," said Gail Dempsey, President, Canadian Epilepsy Alliance (CEA). "The program will go a long way in raising the profile of epilepsy, and ensuring that those living with the disorder can connect with the medical community, local epilepsy agencies, and their wider communities to obtain the best care and treatment available." E-Action is an initiative of UCB Canada Inc., a global biopharmaceutical company committed to improving the lives of people with epilepsy, one of the most common neurological … Continue reading →

Newswise COLUMBUS, Ohio. Each year, only five percent of the estimated 1.5 million children with an autism spectrum disorder in the US participate in clinical research studies. This is in stark contrast to pediatric cancer studies, which have a nearly 90 percent enrollment rate a rate that has helped advance treatment and outcomes for childhood cancers substantially in the last decade. In an effort to accelerate similar progress within the autism community, a group of academic medical centers has collaborated to launch an Autism Spectrum Disorder (ASD) sub-registry within ResearchMatch, a disease-neutral national database connecting patients with ongoing research. The new ASD sub-registry helps act as a matchmaker, linking families with autism researchers around the nation. Registration on ResearchMatch takes about 5 minutes and is open to volunteers of all ages and conditions including volunteers without health conditions. If we could raise the autism research participation level to that of the pediatric cancer community, we think we could realize similar gains in new knowledge, treatments and outcomes, said Rose Hallarn, Program Director for Clinical Trials Recruitment at the Center for Clinical and Translational Science (CCTS) at The Ohio State University and Institutional Liaison for ResearchMatch. Working with researchers at Vanderbilt … Continue reading →

A new state plan that brings autism to the forefront has given the disability much-needed recognition, and it will be up to the culture of Michigan to determine how the plan will affect real people, an author of the plan said. The Michigan Department of Community Health and the Michigan Autism Council released the Michigan Autism Spectrum Disorders Plan last week in advance of Autism Awareness Month in April. The plan was warranted because of recent legislation providing insurance coverage for autism treatment, and because the condition is on the rise, said Dr. Mary Sharp, advocacy and community development officer for the Autism Alliance of Michigan and an author of the plan. The incidence of the behavioral disorder now is one in 88 children, according to the Centers for Disease Control and Prevention, or 50,000 people in Michigan including 16,000 in schools, according to a state news release. Midlander Trisha Fenbys 13-year-old daughter, Hollie Kayden, is one of those 16,000 students. Fenbys goals for her daughter arent much different from those of other parents: to give Hollie the tools to have a meaningful life and a decent job. But Hollie is struggling, her mother said. She began in regular education, … Continue reading →

In the past year, groundbreaking research has uncovered precise genetic links between autism and Fragile X syndrome, giving families like ours hope that treatment for many of the core symptoms of both conditions is on the horizon. New drugs currently in clinical trials have been shown to have a significant effect on reducing the symptoms of severe social impairment in people with autism or Fragile X syndrome. Reducing repetitive behaviors and improving social skills would allow our family members to lead more independent lives. While most people know about autism and autism spectrum disorders, not as many are aware of Fragile X syndrome. Fragile X is closely related to autism, is the most common inherited cause of intellectual disabilities and is the most common genetic cause of autism. It is imperative that the advancements made through these groundbreaking research projects continue to be built upon. Wise stewardship of federal research dollars would encourage continued investment and expand the scope of research into the links between Fragile X and autism. The promise of this research gives hope to many of us in Utah who have family members with autism and Fragile X syndrome that independence and social acceptance are within reach … Continue reading →

Newswise PHILADELPHIA - Certified Primary Stroke Centers are three times more likely to administer clot-busting treatment for strokes than non-certified centers, reports a new study by researchers in the Perelman School of Medicine at the University of Pennsylvania. The study, published in the Journal of the American Heart Association, looked at a wide sample of hospitals across the United States, and provides insight into practice across the US health care system as experts examine ways to increase the use of this important therapy. Clot busting treatment is used to open blocked blood vessels, restoring blood flow to the brain and reducing disability after stroke. Less than half of ischemic stroke patients who are eligible for the treatment, recombinant tissue plasminogen activator (rt-PA), actually receive it. Currently, only a small percentage of stroke patients receive rt-PA therapy. "We found that primary stroke centers administered rt-PA at a much higher rate than other hospitals, demonstrating one way that certified centers are succeeding." said Michael T. Mullen, MD, the studys lead author and an assistant professor of Neurology at the Perelman School of Medicine at the University of Pennsylvania. Primary Stroke Centers, certified through The Joint Commission, used rt-PA in 6.7 percent of … Continue reading →