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Taking risks
 The presence of any disability in a child may alter the normal dynamics in a family, and lead to the child being over-protected. Whereas this is an understandable reaction, particularly if the seizures are accompanied by injury, it is often harmful in the long run and may lead to inappropriate behaviour and over-dependence on parents. In addition, parents and teachers may try to protect the child from stress if this is felt to precipitate seizures. A more productive approach is to teach the child the skills necessary to cope with stress which is an inevitable part of everyday life.
  Concern about safety may also lead to a child being barred from workshops, laboratories and sporting activities. However, blanket restrictions on all children with epilepsy are unacceptable and the risks to each child must be assessed individually on the basis of accurate knowledge of that child's epilepsy. If the seizures are completely controlled or only occur during sleep, no restrictions are needed. Even if seizures occur during the day, almost all activities including swimming and climbing can be undertaken providing there is adequate supervision.
  Most children with epilepsy can watch TV and use VDUs quite safely, but it is sensible to find out from the doctor if the child is known to be sensitive to flashing lights (photosensitive). A Factsheet on Photosensitivity is available from the CIEN.
Careers guidance
  Advice on careers for children with epilepsy should be given early and be based primarily on aptitudes and skills. Once these are identified, the relevance of the epilepsy should be considered. The advice of specialist career adviser should be sought if the epilepsy is still a major problem. A history of epilepsy can be a bar to jobs in the armed forces, the merchant navy and those jobs requiring an aircraft pilot's licence. Moreover, any occupation that is heavily dependent on driving is not normally recommended as a single seizure while awake will lead to loss of the licence and perhaps also the job. However, many young people are very keen to learn to drive and this must be taken into account if withdrawal of medication is being contemplated as the young person approaches school leaving age. Entry into some professions such as nursing, teaching and childcare may prove difficult if there is a recent history of seizures. Moreover, if these are frequent or if there are other disabilities, job prospects are currently poor. However, it must be stressed that skills, personality and ability to present the epilepsy clearly to a prospective employer are vital to success in the job market. It is also essential for the school leaver with epilepsy to have qualifications which are on par with other job applicants. Young people with epilepsy should take full advantage of further and higher Employment Service schemes for young people.
  About 6 in every 1000 children of school age have epilepsy and 80% of these attend ordinary schools. For the majority, epilepsy does not cause enormous problems particularly if the child receives early medical attention, accurate information and appropriate counseling. There are, however, a number of areas where difficulties may arise and these are summarised in this page. For more detailed information and explanation, please contact CIEN.
Recognising Epilepsy
  A parent or teacher is likely to be the first adult to witness a seizure in a child. Most people will recognise a major convulsive tonic clonic seizure previously known as ‘grand mal’ in which the child loses consciousness and then convulses, but there are many other types of attack which are due to epilepsy. A detailed written eyewitness account is invaluable to a doctor who subsequently sees the child and makes a diagnosis. Other causes of loss of consciousness will have to be excluded and it should be remembered that some children who simply faint may also have mild convulsive movements. Absences, previously known as ‘petit mal’, are very brief interruptions of consciousness and they may be difficult to detect. Teachers and parents should be alerted to this possibility if a child suddenly appears to have vacant spells or be unusually inattentive. Focal or partial seizures may be difficult to recognise as they often appear as bizarre behaviour which may be mistaken for silliness. However such seizures are accompanied by mental confusion and tend to take the same form each time they occur. In some children, seizures only occur during sleep, and it may be some time before the true nature of the attacks is recognised.
  Although it is not always possible to identify a cause for the epilepsy, it is important to try, since the outlook may be related to the underlying reason for the occurrence of the seizures. Some forms of epilepsy are benign and will improve spontaneously as the child gets older, but this is by no means always the case.
Treatment
  Epilepsy can be completely controlled in up to 80% of cases, and all efforts should be made to achieve this at an early stage. The majority of children with epilepsy will be treated with medication in tablet, capsule or liquid form. It is important for everyone involved, including the child, to understand that treatment is not a cure for the epilepsy but is means of controlling the seizures and that medication may have to be taken regularly for several years. Most drug treatment can be given before and after school hours. Tablets taking should be regarded as essential to health rather than being a sign of illness. As soon as, possible the child with epilepsy should take full responsibility for the medication, otherwise problems may arise over taking tablets reliably, particularly during adolescence.
  Very few children who have focal epilepsy may be suitable for epilepsy surgery. This can be highly successful in controlling the seizures without causing additional problems, but a detailed assessment is required before an operation can be advised.
Communication
  The Disability due to epilepsy can be substantially reduced if there is good communication between professionals, parents, the child with epilepsy and school friends. A free interchange between teachers, parents and carers advisers is essential for all children with epilepsy and parents should not be reluctant to disclose and discuss their child’s epilepsy. Also teachers need to know more than that a particular child “has epilepsy”; this fact alone is inadequate for correct understanding and supportive care. Detailed information should be made available by the parents, school doctor and nurse, general practitioner or pediatrician, and should include a description of the seizures and their frequency, the speed of recovery, the most appropriate management for that child, drug treatment and possible side-effects.
  Parents and teachers may find it difficult to strike the right balance between providing special help when needed from time to time, and allowing the child to take risks. Children with epilepsy should experiance all the success and failures that are needed for normal growing up and an open positive attitude in parents and teachers is likely to help the child to deal with the reactions found in school friends. However, it is always difficult to decide whether other children should be told about the epilepsy. If seizures are likely to occur during school hours it is better that information about epilepsy should be included in the ordinary curriculum, such as in a health education programme, rather than taught in the agitated aftermath of an unexpected seizure in the playground or classroom. It is important to discuss with the child how they would like information about their epilepsy to be communicated to others.
  Classroom management
  A major seizure occurring at school can be very upsetting experience for all concerned. The harmful effects that may result can be minimized if the teacher acts calmly, deals with the seizure appropriately, reassures other children and comforts the child who has had the seizure. The correct management of seizures is explained in more detail in the CIEN page ‘Seizures’. The vast majority of seizures are brief and do not require emergency medical treatment.
  So children who have seizures should spend as little time as possible out of the classroom or away from school, and agreement should be reached between teachers, the child’s doctor, the parents and the child as to the most appropriate way of managing a particular child’s epilepsy.
  Learning and achievement
 Some teachers may mistakenly have a low expectation of pupils with epilepsy and inadvertently treat them differently. If the seizures are well controlled and there are no other disabilities, there is no reason to expect a child with epilepsy to under-achieve. However, research does suggest that a number of children with epilepsy perform less well than a formal assessment of their abilities would suggest. The causes of this may be complex and require assessment from a multi-disciplinary team, including an educational psychologist, to provide solutions.
 The following factors may be relevant:
 
Frequent major seizures may lead to poor school attendance, particularly if a child is removed from school inappropriately every time a seizure occurs.
Frequent absence seizures, which may be difficult to detect, can impair learning.
Children with more severe epilepsy may have episodes of disorganised brain activity, not sufficient to cause a seizure, but which may impair performance and learning.
Although the majority of children with epilepsy are of average intelligence, it is also true that children with learning disability have a high incidence of epilepsy.
If the epilepsy was caused by some localised injury to the brain, this damage may also cause other educational problems, such as poor verbal skills if the dominant half of the brain is affected (usually the left side), or poor practical skills if the non-dominant side is involved.
Incorrect or excessive drug treatment can also impair school performance, particularly if it makes the child sleepy. However, drugs should not be blamed for everything and it is often difficult to distinguish between the effects of drugs and those due to ongoing epileptic activity in the brain.
The child may have a poor self-image and inadvertently be fulfilling low expectations expressed by parents and teachers. Behaviour problems seen in some children with epilepsy may be related directly to the epilepsy but are also commonly due to difficulties in relationships within the family and with other children.
 






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