My 16month old baby boy was diagnosed with Epilepsy last Christmas and then in March with the SCN1A Gene and likehood of Dravet, This has been a challenging time for our family and with the support of Epilepsy Action within their counselling services , support groups and training for families and friends we are getting through much easier as a family as they have been our lifeline and always a phone call away , so I am joining hundreds of people challenging themselves to get reading 30 minutes a day in October, to help ensure nobody has to face living with epilepsy alone, by raising funds and awareness for Epilepsy Action.