Children and Adolescents with New-Onset Epilepsy

Children and adolescents with new-onset epilepsy Journal Article Epilepsy is one of the most mutual neurologic disorders in fryhood, with a widespread rate of approximately 3-4 per 1,000. In the paper they explore bring ups perceptions of their childs quality of life and the impact of the diagnosis on their family. Its talking ab aside how the parents and childrens lives get accustomed to popular normal functioning activities. Whenever there is any emotional well-being, self-esteem, and physical changes with their condition due to the epilepsy. Data was collected as part of the brave out and New Antiepileptic drugs (SANAD) trial.SANAD compared clinical trial and cost-effectiveness of standard and new AEDs. SANAD recruited 2,437 patients (1,983 age older than 16 long time 454 children age between 5 and 16 years), with history of two or to a greater extent definite loose seizures in the previous year. Talks about the primary outcomes were time to treatment failure, and time to 1 2-month remission. Children from 8-15 years were asked to dish out self-complete questionnaires annually and thereafter for 4 years for SANAD. The parents gave written consent to long-term follow-up. Parents were asked to complete questionnaires to assess their childs quality of life.It talks about parents being affected by their childs seizures at home or at family outings. How it can take a toll on everyday things they do. I gibe that children with epilepsy (CWE) are more likely to have learning disabilities and to experience academic underachievement. Well I agree be causation its already hard for children to fit in at discipline and to try to concentrate is even harder. I agree with the finding that adolescence is a critical period for identity formation and associate group identification. Being an outcast from their peers is an important concern for adolescents.I agree because the adolescents can experience self-conscious, ashamed of their epilepsy, and closelipped behavi or. I agree with the finding that single parents have less permit from other networks, may cause them to be more concerned about their childs well-being. I agree because their only support is usually themselves, thereafter, its not easy raising and caring for a sick child. I agree with the argument that it is a seizure event, not a diagnosis of epilepsy that impacts on daily functioning. Because an epileptic fervor is more traumatizing and over whelming for a child, then being told you have epilepsy.Which some adolescents dont exist what this means for them. Those who scored 13 are considered to be psychiatric morbidity. Children with new-onset epilepsy had significantly poorer for physical, emotional and friends domains. A new-fashioned study found children in the United Kingdom reported low levels of child well-being, despite relatively high levels of wealth, compared to children from other European countries. What I found interesting was that CWE should be assessed for psych osocial problems in the beginning so intervention can be done in time for no further damage with the child.Interventions designate to increase self-esteem. I believe these studies are great resources for the families of the epileptic children. It gives them more insight in their everyday functions in life. Without these kind of studies parents might be clueless to what could be happening to their child in school or even at home. It hard for the families of these adolescents to undergo these kinds of trials, but with all the information and support groups out there it can be very helpful for everyone. In conclusion I believe with more moral support and patience, much can be done for children with these special conditions.