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Press release

Less than 20% of those diagnosed with a brain tumour survive beyond five years

Bereaved son’s story heard at House of Commons as brain tumour impact highlighted

Bereaved son’s story heard at House of Commons as brain tumour impact highlighted

A man from north-west London, who lost his father to a brain tumour, was at Westminster as MPs were told of the “unbearable” burden of the disease.

The poignant words of David Peters were presented at a meeting of the All-Party Parliamentary Group on Brain Tumours (APPG-BT) on Tuesday 20 November, as it published a hard-hitting report on the devastating economic and social impacts faced by patients and their families.

His father, Norman Peters, was diagnosed in June 2007 with an aggressive and incurable glioblastoma multiforme (GBM) brain tumour. Norman, a retired doctor, was told his tumour was inoperable and he started a course of palliative radiotherapy. His family subsequently paid for private surgery to extend his life but Norman, aged 73, continued to deteriorate and passed away in December 2007, just six months later, at the North London Hospice.

David, an entrepreneur in the food and drink industry, said: “I very much welcome this report which, for the first time, attempts to quantify the economic and social impacts of brain tumours. I was living and working abroad at the time of my father’s diagnosis but returned to London and moved into my parents’ home to help care for my father. My mother also had to give up her job and our regular lives came to an abrupt halt, while we tried to deal with the financial, social and emotional fallout of my father’s illness. This not only impacted our ability to earn a living and therefore generate income tax revenues but also our ability to consume and generate VAT revenues. This demonstrates it is not just the patient and their family that is impacted by a brain tumour, but the whole of society. The APPG-BT’s report draws attention to the wider impacts of this devastating disease and will hopefully lead to increased funding, both for research, so that we may one day find a cure, and specialist financial and care support for patients and their families.”

Brain tumours – a cost too much to bear? is the report of a Parliamentary inquiry into the economic and social impacts of brain tumours which received more than 200 online submissions from patients and their families and comprehensive written submissions from charities and academics. It also held oral evidence sessions during June and July from researchers, doctors, surgeons, academics, representatives of drug companies as well as brain tumour patients of all ages and their families.

Its key findings include:

  • The incapacitating nature of a brain tumour, a cancer of the body’s most important organ, can see patients faced with an immediate financial burden and the severity of the disease all too often means people contribute less to the economy and society at large.
  • Costs range from loss of income through to higher domestic bills and costly home modifications. Additionally, patients are required to surrender their driving licence, leading to a loss of independence.
  • The experience of children, teenager and young adult patients is dismaying; they will experience more ‘social’ issues as the disease affects them at an important stage of their development and they have to bear its burden for the rest of their lives.

Derek Thomas, MP for St Ives, who is chairman of the APPG-BT, said: “It was impossible not to have been personally affected by the wealth of emotionally compelling personal stories we heard during the course of this Inquiry and my most heartfelt thanks go to all of the brain tumour patients and their families who helped us with this report. For those of us who were privileged to hear this evidence first hand it was an experience that will stay with us for a very long time. Over the coming months and years, we will use the results of this Inquiry to keep brain tumours on the political agenda and improve outcomes for brain tumour patients.”

Sue Farrington Smith, Chief Executive of the charity Brain Tumour Research, said: “We are extremely grateful to David for sharing his personal story which demonstrates why we must continue to highlight this issue and do everything we can to improve outcomes for brain tumour patients.

“Understanding the very high ongoing costs of brain tumours is vital and the Government must find additional ways to minimise these costs. We will continue to influence and find ways to minimise this unique burden through a combination of further research funding, earlier diagnosis, additional benefits, and improved post-treatment support for brain tumour patients and their families.”

 

For further information, please contact:
Farel James at Brain Tumour Research on 01908 867221 or 07592 502708 or Farel.James@braintumourresearch.org

 

Notes to Editors

Brain Tumour Research is the only national charity in the UK dedicated to raising funds for continuous and sustainable scientific research into brain tumours, and we are a leading voice calling for greater support and action for research into what scientists are calling the last battleground against cancer.

We are building a network of experts in sustainable research at dedicated Centres of Excellence whilst influencing the Government and larger cancer charities to invest more nationally.

We welcome recent funding announcements for research into brain tumours from the UK Government and Cancer Research UK – £65 million pledged over the next five years. However, this potential funding of £13 million a year comes with a catch – money will only be granted to quality research proposals and, due to the historic lack of investment, there may not be enough of these applications that qualify for grants from this pot.

We want research funding parity with breast cancer and leukaemia. We are calling for a £30-35 million investment every year for research into brain tumours in order to fund the basic research groundwork needed to accelerate the translation from laboratory discoveries into clinical trials and fast-track new therapies for this devastating disease.

The Brain Tumour Research charity is a powerful campaigning organisation and represents the voice of the brain tumour community across the UK. We helped establish and provide the ongoing Secretariat for the All Party Parliamentary Group for Brain Tumours (APPGBT). We are supporting the crucial APPGBT 2018 Inquiry into the economic and social impacts of brain tumours and will publish their report in the autumn. We are also a key influencer in the development strategy of the Tessa Jowell Brain Cancer Mission. 

Key statistics on brain tumours:

  • Brain tumours are indiscriminate; they can affect anyone at any age
  • Brain tumours kill more children and adults under the age of 40 than any other cancer
  • Historically, just 1% of the national spend on cancer research has been allocated to brain tumours
  • In the UK, 16,000 people each year are diagnosed with a brain tumour
  • Brain tumours kill more children than leukaemia
  • Brain tumours kill more men under 45 than prostate cancer
  • Brain tumours kill more women under 35 than breast cancer
  • Less than 20% of those diagnosed with a brain tumour survive beyond five years compared with an average of 50% across all cancers

Please quote Brain Tumour Research as the source when using this information. Additional facts and statistics are available from our website. We can also provide case studies and research expertise for the media.

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