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Our Young Adults Service for people aged 16-30 who are affected by a brain tumour diagnosis, is here to offer support and help you connect with others.
We've put together some information and advice to help ease our Community's concerns about the coronavirus situation.
The team are here to help with any information you might need and can help with researching and sending out information on topics such as tumour types, treatments and clinical trials.
We provide a listening ear when you need it, are happy to listen to your concerns or frustrations and will do our best to answer any questions you might have or point you in the direction of other services.
Receiving the news that you or a loved one has a brain tumour is something we wished no one had to hear. We're here to support you and your family, whether that's answering any questions you have or just listening to your worries.
We can connect over with you over email, Facebook messenger, telephone calls or text, so please do get in touch as we are here to help however we can.
We are also able to research information on your behalf so whether its information on tumour types, treatments, clinical trials, current research, getting a second opinion or anything else you'd like to know more about, please don't hesitate to get in touch with us and we'll look into this for you.
We can also offer information and advice on a range of other issues as well as support you to connect with other services such as our benefits clinic and other local and national services that you might find useful.
Our Young Adult Events and dedicated Young Adults Facebook Group are a great way to connect with others who are going through similar experiences, meet our Young Ambassadors and to access support from the team face to face. You can find out more about our upcoming events here, we hope you are able to join us.
Learning that a loved one has been diagnosed with a brain tumour can be a life-changing event, especially if you need to take on new caring responsibilities.
This can be a really confusing time and you may have lots of questions that you don't feel you can ask your friends and family. It's perfectly normal to experience lots of different emotions, from fear and sadness to guilt and anger - sometimes all at once.
So, whether its information you need or someone to talk things through with, our team is here to help. You may not necessarily consider yourself a carer but whether it’s a partner, parent, sibling, friend or other family member who’s received a diagnosis, this support is here for you.
We also know that it can feel isolating at times so have set up a dedicated Young Adult Carers Facebook Group where you can connect with others going through similar experiences.
We offer individual online and telephone support and are here to listen and help you find any information you might need.
You can contact the team by:
Our Support and Information Line is open 9-5 Monday to Friday, but, if you email us outside of these times we will aim to respond to you as soon as possible.
If you would like to chat to a member of our team but are unable to talk during our normal opening times, please do get in touch as we’d be happy to arrange an evening call.
If you are concerned about your health, please contact your GP immediately who may direct you to an out of hours service. Alternatively if you need to speak to someone urgently, please contact:
We are grateful to the Elliott Simmons Charitable Trust and Lewis Moody Foundation who kindly support our Young Adults Service.
If you have further questions, need to clarify any of the information on this page, or want to find out more about research and clinical trials, please contact our team:
0808 800 0004 (free from landlines and mobiles)
Phone lines open Mon-Fri, 09:00-17:00
You can also join our active online community - Join our online support groups.