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Our Fundraising Groups
16,000 people diagnosed with a brain tumour every year
Our amazing family of Fundraising Groups
Championing the fight against brain tumours and raising thousands for our cause, helping us build network of experts in sustainable research at dedicated Centres of Excellence and supporting us as we influence the Government and larger cancer charities to invest more nationally.
Leah's Fairy Fund
Leah’s Fairy Fund was set up by the family of Leah Martin who was diagnosed with a high-grade medulloblastoma at the age of two. Several operations, as well as chemotherapy and radiotherapy, have left Leah with long-term side effects including problems with her speech and mobility.
Mum and Dad, Joanne and Wayne, want better options and outcomes for brain tumour patients and in particular are keen to support the research being funded at Brain Tumour Research’s Centre of Excellence at University of Plymouth.
Read Leah's story.
Mum and Dad, Joanne and Wayne, want better options and outcomes for brain tumour patients and in particular are keen to support the research being funded at Brain Tumour Research’s Centre of Excellence at University of Plymouth.
Read Leah's story.
Retired Fundraising Groups
Our Fundraising Groups are set up by families who have lost loved ones to brain tumours or have a loved one with a brain tumour diagnosis. Sometimes there comes a time when a family may wish to continue their work of raising awareness and funds, but in a less formal way.
We are grateful to all our Fundraising Groups, past and present, for the invaluable work they do within their communities to promote the brain tumour cause and make a difference in our mission to find a cure for all types of brain tumours.
The following are Fundraising Groups who have retired from active duty, but remain very much a part of our brain tumour community:
Leah's Fairy Fund
Leah’s Fairy Fund was set up by the family of Leah Martin who was diagnosed with a high-grade medulloblastoma at the age of two. Several operations, as well as chemotherapy and radiotherapy, have left Leah with long-term side effects including problems with her speech and mobility.
Mum and Dad, Joanne and Wayne, want better options and outcomes for brain tumour patients and in particular are keen to support the research being funded at Brain Tumour Research’s Centre of Excellence at University of Plymouth.
Read Leah's story.
Mum and Dad, Joanne and Wayne, want better options and outcomes for brain tumour patients and in particular are keen to support the research being funded at Brain Tumour Research’s Centre of Excellence at University of Plymouth.
Read Leah's story.