In 2004, an informal partnership of a number of UK brain tumour charities came together under the banner of the United Brain Tumour Campaign. These charities worked together raising awareness and to achieve a common goal to raise funds for research into the prevention and treatment of brain tumours, as well as ultimately finding a cure.
Each of the members was galvanised into action as a result of personal involvement with brain tumours, having realised that there is relatively little being done to support brain tumour patients or carers, or towards funding research into finding a cure, compared to other more high-profile cancers.
Today, Brain Tumour Research still supports and is supported by numerous official Member Charities from across the UK that are united with us under our national banner. We embrace these collaborations and welcome any and all new Member Charities.
Our collective voice carries greater weight in media coverage and adds weight to our political campaigning action. Our Member Charities are helping us build a game-changing network of world-class Research Centres of Excellence in the UK.
Assist in the rehabilitation of children and young people who have suffered from a brain tumour or who have had brain surgery and support the funding of research into the causes, treatment and cure of childhood brain tumours.
This family-run, Suffolk-based charity was set up after Annie Hughes, a fit and healthy woman and a loving mother of two young children, was diagnosed with a high-grade brain tumour. Because of its position on the brainstem, Annie and her family were told there was no treatment available,other than palliative radiotherapy. Just eight months later, Annie passed away, aged just 29.
Annie’s Challenge funds research into all forms of brain tumour, as well as helping charities dedicated to ongoing care for those affected by brain tumours. Currently the charity is part-funding a PhD researcher at Brain Tumour Research’s Centre of Excellence at Queen Mary University of London over a three-year period.
Read Annie’s story.
Astro Brain Tumour Fundwww.astrofund.org.uk
Astro Brain Tumour Fund raises funds to support research into low-grade glioma (LGG) brain tumours. It is also working closely with charity Matthew’s Friends, providing funding and support for LGG patients wishing to undertake ketogenic dietary therapy. The charity also offers information and support via its website and closed Facebook page, which has over 300 members.
Christine for information - firstname.lastname@example.org
Mary for fundraising and donations - email@example.com
Linda for support - firstname.lastname@example.org
Brain & Spine Foundationwww.brainandspine.org.uk
Brain & Spine Foundation is a UK wide charity providing support and information on the full range of neurological conditions to patients, carers and health professionals.
Helpline - 0808 808 1000 Office - 020 7793 5900 Email: email@example.com
Explores brain tumour treatment worldwide and supports patients and their families at the point of diagnosis, brainstrust is dedicated to improving proactive care for brain tumour sufferers.
Helen Bulbeck - 01983 292405 Email: firstname.lastname@example.org
Read Meg's story.
Ellie Savage Memorial TrustHelping families living in East Anglia who have a child with cancer or a brain tumour by providing financial support and information, as well as funding research into brain tumours.
Wendy Savage - 01502 539509
The charity was set up in 2017 by Finnbar Cork’s parents after they lost their son in August 2016. Finnbar passed away aged five, just five months after being diagnosed with a brain tumour and just over a month before his birthday.
Finnbar’s Force works to support families in East Anglia who have a child diagnosed with a brain tumour. It also raises funds for research into childhood brain cancer and seeks to raise awareness of the disease and its debilitating effects and to campaign for improvements in the current standard of care and support available, as well as for more research.
Tristan and Claire Cork - 07419 369770 Email: email@example.com
Read Finnbar's story.
In Sue's Namewww.insuesname.org.uk
In Sue’s Name was set up in honour and remembrance of a very special wife, mother and daughter, Sue Blasotta, who was diagnosed with lesions on the brain in November 2010 and died just six weeks later, aged 42.
The primary aims of the charity are to raise awareness of brain cancer, the leading cause of cancer-related deaths in the UK among children and adult patients under the age of 40; to support clinical research into brain cancers; and to offer a forum of support to brain cancer patients and their families. In Sue’s Name has set a target to raise £1 million by 2027 to provide crucial research funds to support Brain Tumour Research’s Centre of Excellence at Queen Mary University of London.
Read Sue's story.
James Clifford Campling Trust
The charity, James Clifford Campling Trust, based in Grimsby, was set up by family and friends of James to continue his legacy. James was an aeromedical nurse in the Royal Air Force, who passed away from a glioblastoma multiforme (GBM) brain tumour in 2018, aged just 29. He had been diagnosed less than two years previously. James spent his life travelling the world and visited 82 countries, raising money for a variety of charities. In the 22 months since diagnosis, with the help of his friends, James raised £30,000 to support research into brain tumours and succeeded in ticking off all but 12 of 100 things on his bucket list.
James Clifford Campling Trust has three aims: it offers funding of up to £2,000 to people over the age of 18 with a life-changing condition to help them reach their life goals; it is setting up a retreat to support people with life-limiting illnesses and their families, and is funding research into GBMs.
Diane Campling – 07708 668136
Follow James Clifford Campling Trust on Facebook
Levi's Star Children's Brain Tumour Charitywww.levisstar.co.uk
Support children with brain tumours. It is also our wish to raise awareness about the symptoms of brain tumours, a truly devastating disease and support established research projects.
Vicky Ringer - 07971 932610 Email: firstname.lastname@example.org
Read Levi's story.
Matthew’s Friends was set up by mum Emma Williams MBE in 2004 after her son Matthew had suffered from hundreds of seizures a week for seven years before taking part in a trial of the ketogenic diet. Within two weeks of starting the diet, Matthew’s
seizures had reduced by 90% and within eight months he was off all medication.
The charity specialises exclusively in medical ketogenic dietary therapies to control seizures. It supports patients, families and professionals by providing information, training, research and grants to develop ketogenic services and support systems for drug resistant (refractory) epilepsy, as well as other neurological and metabolic disorders and emerging cancer types.
Send A Message (SAM)www.send-a-message.org.uk
Sam always loved getting presents. Before Sam passed away his father asked him what he would like us to do for other sick children - "give them presents". Send A Message has been set up to carry out Sam’s wishes and to raise awareness of paediatric brain tumours which can assist in easy diagnosis.
The Danny Green Fundwww.thedannygreenfund.org.uk
The Danny Green Fund was set up when his parents lost their gorgeous son Danny at the age of 11. Before he was diagnosed with a brain tumour, their beautiful, fun loving and energetic son was a typical 10 year old in every way, very much living for the moment and enjoying life. Danny went from being a healthy, lively child to needing intensive and prolonged rehabilitation to enable him to even speak and walk again following surgery to remove the tumour. Tragically they still lost him leaving a void which will never be filled.
The Danny Green Fund helps children under the age of 16 suffering from the symptoms of Posterior Fossa Syndrome as the result of a brain tumour and also provides funding for the development of research into the prevention, treatment and cure of children’s brain tumours.
Read Danny's story.
The Jane Packer Foundationwww.thejanepackerfoundation.com/
The Jane Packer Foundation will help to establish a research facility in the UK that focuses on the long term study of high-grade glioma (GBM4), with the ultimate aim of finding a cure.
Gary Wallis - 020 7935 0787 Email: email@example.com
Read Jane's story.
The Lisa Wiles Red Wellies Brain Tumour Support Fund
Set up in 2012 in memory of Lisa Wiles. Red Wellies is dedicated to raising funds for the continuing research of Glioblastoma Multiforme (GBM), so that they can find a reason for why it took her and to stop other families suffering.
Mervyn Wiles - 01553 841015 Email: firstname.lastname@example.org
The William Low Trust
The Trust was launched by Helen and Craig on the second anniversary of losing their 17-year-old son, William, to a brain tumour. Will was riginally diagnosed with a cancerous medulloblastoma at just five years of age. Helen and Craig, along with their daughter Harriet, are supporting research into finding more effective treatments and ultimately a cure for brain tumours.
Will died on 11 August 2017. He and his family had endured the crushing revelation that his brain tumour had returned, when he was 13. Will underwent further surgery, chemo and radiotherapy, as well as a stem cell transplant. Sadly, aged 16, tumours developed on his spine, and Will reached the end of the road in terms of treatment. Amazingly, despite everything, including having to learn to use his left-hand after losing the use of his right, Will achieved good grades in all his GCSEs, not least an A* in Art, demonstrating his determination to get on with his life.
Helen Forbes-Low – email@example.com