Share our vision
It’s simple really; we just want a brighter future for everyone living with epilepsy.
We want to make sure people with epilepsy have expert healthcare and treatment for their condition and that they can lead their lives free of stigma, prejudice and discrimination.
But to do this we need your help.
Of every £100 we need to raise we rely on getting £34 from gifts people have left in their wills.
When you’ve remembered your loved ones, please remember Epilepsy Action in your will.
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"When mum died in 2012, she left a letter which asked us to give to Epilepsy Action. It was just her way of saying ‘thank you’" - read more Sandra Hough |
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“I wrote my will simply because life is moving on and I am not getting any younger. Knowing that I have made a gift to Epilepsy Action in my will makes me feel positive that progress will be made when I am gone.” Steven Tummons |
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"It’s really important to me that they are able to continue to help people with epilepsy... This is why I decided leave a legacy to Epilepsy Action." - read more Alison Jackson |
Our legacy adviser
If you need more information about our work before you make a decision about leaving a gift in your will, please get in touch.
Comments: read the 2 comments or add yours
Comments
My son is having head drop type convulsions.It started from the month of 8 and now he is 30months still it is not stopped. We are based in India and need your help to stop this problem my child is facing.Please help !
Hi
Is your son seeing an epilepsy specialist? If not, is it possible for him to see one? Epilepsy Action isn’t aware of what epilepsy services there are in India, but you might be able to find this out from Indian Epilepsy Association.
We have a section of our website for parents who have children with epilepsy. Although some of the information may be related to children in the UK, there is also some general information that you might find helpful.
Advice and Information Team