Support for children and families
The dedicated members of our Children and Families Team are here to help however we can. Whether you’d like information and support in relation to a new diagnosis or information about life after a diagnosis, the team are here to help every step of the way.
How to get support for children and families
We offer individual online and telephone support and are here to listen and help you find any information you might need. Unfortunately, the team are not medically trained, so please consult your GP or medical team for medical advice.
You can contact the team by:
- emailing us at childrenandfamilies@thebraintumourcharity.org
- starting a live chat by clicking the red button in the bottom corner of your screen
- calling us on 0808 800 0004 and asking for the Children and Families Service.
Opening hours
Our Support and Information Line is open 9-4 Monday to Friday, but, if you email us outside of these times we will aim to respond to you as soon as possible.
Please note, the support line will be closed from 2pm Tuesday 24th December and will reopen Thursday 2nd January at 9am.
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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:
- NHS (England) – 111
- NHS Direct (Wales) – 0845 46 47
- NHS 24 (Scotland) – 111
- If you live in Northern Ireland please dial 999 or your out-of-ours GP service
- Samaritans (UK wide) – 116 123
- Or in an emergency, visit A&E or dial 999
How we can help
Here are some of the ways in which we offer support for children and families.
Emotional support
Receiving the news your child has a brain tumour is something we wish no parent had to hear. But, we are here to support you and your family and are here to listen and help answer any questions you might have.
We also run a free counselling service, which might help. This gives you a confidential space to talk freely about your thoughts and feelings and start to find manageable ways to cope.
Connecting with others
Our Family Days and Parents Facebook Group are great ways to connect with others who are going through similar experiences 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.
Join our online community
Our online support group is a safe space online to connect with other parents who are affected by brain tumours.
Join our teenagers Instagram account
If you’re aged 13-17 and living with a brain tumour diagnosis, our private Teenagers Instagram Account is a safe place for you to share your thoughts, feelings and any questions you have.
Research requests
The team are able to research information on your behalf. This could be information on tumour types, treatments, clinical trials, current research or getting a second opinion.
If you’d like to know more about these or anything else, please don’t hesitate to get in touch with us and we’ll look into it for you.
Additional support for children and families
The team can also offer information and advice on issues with education, are able to connect you with other services such as our benefits clinic and can signpost to other local and national services that you might find useful.
Support and Information Services
Research & Clinical Trials Information
You can also join our active online community.
In this section
Recommended reading
Get your free Brainy Bag
Our Brainy Bag is a free gift for children and young people who have been diagnosed with a brain tumour, made up of a range of handpicked toys and activities!
Siblings Support Group
If you are a sibling of someone living with a brain tumour and aged 13-17 join our siblings support group on Instagram.