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We aim to make a positive difference to people with epilepsy. We do this by letting policy makers know how their policies may have an impact, either directly or indirectly, on people affected by epilepsy.
All of the policy work which we do is based on evidence. Evidence comes from a variety of sources; from our members, from our helpline and people we support, from our clinical contacts and from partner organisations.
You can help us by letting us know your own views on public consultations. We will take these views into account when writing our own responses to public consultations.
If you want to be part of this process, email us on firstname.lastname@example.org