HeadSpace (157 films)
Films made by young people affected by a brain tumour diagnosis.
Dr Helen Spoudeas introduces – The SUCCESS Charity
Success Conference – 11th November 2017
Tom talks about the importance of being on a Teenage Cancer Trust unit.
Tom’s Story – Part Two
15 year old Tom and mum, Harriet talk about Tom’s brain tumour diagnosis and treatment. Tom and Harriet also talk about how they’re are now looking into changing Tom’s diet and trying the Ketogenic Diet. ***Please speak with your GP/Care Team […]
Tom’s Story featuring Mum – Part One
18 year old Alex first thought something was seriously wrong with him whilst doing one of his GCSE exams, Alex was later to have an MRI which discovered a brain tumour. We hear how Alex dealt with his diagnosis with […]
“I was completely and utterly normal”
Alicia was eight years old when she was diagnosed with a brain tumour, now 16, Alicia talks about how at the time she didn’t really understand the implications of having a brain tumour but now she can look back and realise how […]
“It doesn’t really change me”
At aged 11, Rachel was diagnosed with a brain tumour, Rachel talks about how the support of her family and friends really helped her. Rachel explains how “Gertrude – The Brain Tumour” went away, but recently “Gertrude” has reappeared but […]
“Just Rachel”
Filmed as part of series of films highlighting the impact Cerebellar Mutism has on not only the patient but also the families. We hear from Professor David Walker, Dr. Rob Dineen and Donald Macarthur as they discuss the complexity of […]
Cerebellar Mutism – The discussion
Filmed as part of series of films highlighting the impact Cerebellar Mutism has on not only the patient but also the families. We hear from dad Tristan who talks about Antonio’s experiences.
Cerebellar Mutism – Antonio & Tristan Mosley
Filmed as part of series of films highlighting the impact Cerebellar Mutism has on not only the patient but also the families. We hear from mum Michelle who talks about Madeline’s experiences.
Cerebellar Mutism – Madeline & Michelle Blackmore
Filmed as part of series of films highlighting the impact Cerebellar Mutism has on not only the patient but also the families. We hear from dad Lee who talks about Madeline’s experiences.