A group of young people cheers with pints of beer in a bar.

Give in celebration

Your celebration can make a difference for children and young people. 

Register today

Thank you so much for considering fundraising for Young Epilepsy through your celebration. Whether you’re getting married, celebrating a big birthday, an anniversary, an arrival of a new baby or another milestone, you can make a meaningful difference by fundraising for your special day. 

You can ask for donations instead of gifts and we’re here to help. 

Already had your celebration? You can send us your funds raised here.

How to set up your celebration fundraising

How to set up your celebration fundraising

Set up your page...

Click ‘start fundraising’ to set up your own JustGiving fundraising page or ask people to donate on the day.

How your celebration can make a difference

Your generosity will help to provide expert information, emotional support, and a community that understands.      

  • Clear, trusted information at the point of diagnosis
  • Emotional support for families in crisis 
  • A safe, understanding community to connect and share 
  • Personalised support to help children and young people manage their fears and understand their epilepsy
A mother and son in Young Epilepsy clothes smile before purple balloon, wearing Young Epilepsy merchandise.

Your celebration can help children like Dian

Stories like Dian's show how far your celebration fundraising can go.
Register your celebration

“I was diagnosed at the age of 7. I have tonic-clonic and nocturnal seizures and also drug resistant epilepsy. My epilepsy means I have seizures every day and I take medication. My epilepsy means I can't do the things that I want to do. Because someone has to be with me at all times, as it can happen anywhere.

Sometimes after having a seizure while I'm sleeping at school or with my friends, I feel scared and anxious. I worry I might have another one or get hurt.

What helps me most during a seizure and keeps me safe, is when someone like my sister, parents, or an adult knows what to do to protect me from getting hurt. I have fallen off a chair, a bed, and even a sofa during my seizure. Every second matters. 

When my seizures are over, I need to sleep because if I don't, I get a headache. After I have rested my brain, it is slow, so it takes me longer to do things. All I want to do is watch TV or build my Lego set, but it takes me longer.

Young Epilepsy has helped me by connecting me with other children from the youth club so that I can openly talk about how I feel, my worries, and how to live life with epilepsy. Young Epilepsy has set up fun activities for everyone to enjoy. It's made me feel that living with epilepsy isn't bad, and it can't stop me from doing the things I like to do."

- Dian


Thank you so much for making a difference as part of your celebration. 

If you need any help, please get in touch. You can email supportercare@youngepilepsy.org.uk or phone us on 01342 831245.

Please get in touch