Episode 9 - What's it like to get diagnosed as a child?
In this episode we hear from Rosie who was diagnosed with a brain tumour when she was just 8 years old. She shares what it was like to be a child going through treatment, how it affected her friendships, going to school and the long term impacts both mentally and physically of having a brain tumour at such a young age.
If you would like more information about our Children and Families Service you can go to our website https://www.thebraintumourcharity.org/living-with-a-brain-tumour/get-support/children-and-families-service/ or contact the team directly by emailing childrenandfamilies@thebraintumourcharity.org
For more information about our Young Adults Service https://www.thebraintumourcharity.org/living-with-a-brain-tumour/get-support/young-adult-service/ or email the team at yas@thebraintumourcharity.org
If you would like to speak to a member of our support team you can call 0808 800 0004 or email support@thebraintumourcharity.org
