In Fundraising

Well done to our team brainstrust runners in this year’s Great Manchester Run. You were all amazing.

We had a last-minute addition to the team when Claire Bushell, our support specialist for children and families, decided to run. Moved by the attacks in Manchester, Claire wanted to support the Manchester community, while raising money to help people living with a brain tumour.

This is Claire’s story.



Last Thursday, on a bit of a whim, I decided to take part in the Great Manchester Run for brainstrust. As a proud Mancunion for 7 years now, I’ve been really affected by the attack in Manchester – so when our Northern Fundraiser Michael challenged me to take up a place in the 10k – I didn’t take much persuading.

The chance to join my city in a huge event and show the world that the awful events have only brought us closer was really one I couldn’t ignore. It was also a fantastic opportunity to raise a bit of cash for brainstrust. So now there was only one problem – I’ve never run 10k. In fact, I’ve barely run 5k before! And I only had 3 days to go.

As the support specialist for children and families, I’ve seen and heard first-hand how devastating a brain tumour diagnosis can be. This carries so much more weight than just the ‘c word.’ For many, it means a shortened life, ongoing cognitive and neurological deficit, mobility problems, worries about siblings and more. It carries the certainty of an uncertain future. For families, all of this can result in a loss of control.

At brainstrust, the work we do helps families to regain some of that control. Our work helps them to find the right support, so that with their uncertain future they can live well, and feel less alone. The families we support surprise and inspire me every day with their strength and resilience. I feel really lucky to be able to help them in the way we do, and so I wanted to do something inspiring for them too.

Back to the training. This involved a tailored plan of
a) lots of sleep
b) lots of water
c) a few gins for the bank holiday
d) pizza on Saturday (I heard carb loading is important before a big race)

And before I knew it, I was at the start line! The atmosphere was incredible, and a group warm up was followed by a minute’s silence and an inspiring poem by Tony Walsh And then, we were off! Crowds lined the Manchester streets and, as I got into my rhythm, we headed out of the city through Castlefield. My main hope was to run as much of the course as possible – so at my steady jog I was shocked to get to the 4k mark at Old Trafford and still be running! Even on the quieter sections of the course members of the public cheered on as many people as they could. I lost count of the number of high 5s I’d got by this point! Music stations added to the entertainment / distraction too – with brass bands, steel bands and DJ booths blasting out 90s Manchester classics.



As we swooped around Old Trafford Stadium and Salford Quays and headed back towards Manchester – I wondered if I might just be able to run the whole thing…was I really enjoying myself? At 8km the crowds started building up – and with my shuffle-jog now perfected I knew I could do it. The last 1km was a breeze – there’s nothing like Mancunion strangers telling you how proud they are to give you a boost!

The atmosphere was really special, and I even managed a ‘sprint’ finish and made it over the line in 1.15.52 – a personal best of course! I collected my medal and swiftly grabbed a glass of bubbly and a well-deserved burger before sinking into the longest bath of my life.

I’m so proud to have taken part in such a wonderful day with Manchester and thrilled that I’ve raised over £200 for brainstrust in just 4 days, which is enough for 4 of our fantastic brain boxes for families who are coming to terms with huge challenges of their own.

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The Brain Tumour Data Dashboard lets you explore up -to-date, population level data about the brain tumours diagnosed in England between 2013 and 2015. Using the drop down menus on the left you can select different groups of patients to view in the charts below. In these charts the number of patients for every 100 diagnoses is displayed as images of people. Patients have been grouped by date of diagnosis, type of tumour, age, gender, and region in England.

For each group of patients you can explore the different routes to diagnosis, the proportion of those who received chemotherapy or radiotherapy, as well as the survival of the patients within each group. For more information about what these metrics mean please see the glossary.

How to use

  1. Select the year of diagnosis using the drop down menu.
  2. Select your patient group of interest from the four drop down menus in the following order:
    1. Tumour group
    2. Age at diagnosis
    3. Region of England
    4. Gender of patient
  3. To view a second chart to compare different groups of patients, click the ‘compare’ button.The second chart will appear below the first chart.

*Note that the tool is best used on a laptop or tablet rather than a mobile phone*

Unavailable data

Some of the data in these charts is not available.There are two main reasons for this:

  1. How the data has been grouped

If you cannot select a patient group from the drop down menus, the data is unavailable because of how the data has been organised.

Public Health England has grouped the data like a branching tree. The bottom of the tree contains all the patients with brain tumours, and then each branch divides the data by a certain characteristics, like age, or location of tumour. But the data is divided in an order, starting with location of the tumour (endocrine or brain), then by age, region, and gender. Age is at the start because it makes a bigger difference to survival rates and treatment rates than gender or region. Sometimes, after the data has been split by type of tumour and age, there is not enough data to be split again. This is because to protect patient confidentiality groups cannot contain less than 100 patients. Because some groups cannot be split further, you cannot create ‘totals’ for everyone by region or gender. For example, you cannot see results for all ages by region, or all brain tumours by gender. If these totals were calculated and released, it might be possible to identify patients, which is why Public Health England cannot release this data.

  1. Statistical reasons and data availability

If you can select a patient group from the chart menus, but the chart does not display, the data is unavailable for one of several reasons:

  1. Data is not yet available for the selected year from Public Health England.
  2. Data is not available because the data quality is too poor to release this statistic.
  3. Data is not available as the statistic is not appropriate for this group.
  4. Data is not available because the standard error of the estimate was greater than 20% and so the estimate has been supressed.

Up to date brain tumour data

Brain tumour data may influence the decisions you make about your care. Data also helps you understand the bigger picture, or landscape, in which you find yourself.

Brain tumour data and statistics influence the focus, and work of organisations like brainstrust. The information helps us to understand the scale and impact of the problems we are setting out to solve.

This tool helps you understand the landscape in which you find yourself having been diagnosed with a brain tumour. This landscape can be particularly tricky to navigate as there are many different types of brain tumour, all of which have a different impact.

The information you see represents the most up-to-date, official, population level brain tumour data available for England. Over time we will be adding to the brain tumour data available and publishing reports, with recommendations, as a result of what we learn from this data.

The data behind this content has come from Public Health England’s National Cancer Registration and Analysis Service (NCRAS) and is a direct result of the ‘Get Data Out’ project.

This project provides anonymised population level brain tumour data for public use in the form of standard output tables, accessible here:


The number or rate (per head of population) of new cases of a disease diagnosed in a given population during a specified time period (usually a calendar year). The crude rate is the total number of cases divided by the mid-year population, usually expressed per 100,000 population.


Malignant tumours which grow by invasion into surrounding tissues and have the ability to metastasise to distant sites


The number or rate (per head of population) of deaths in a given population during a specified time period (usually a calendar year). The crude rate is the total number of deaths divided by the mid-year population, usually expressed per 100,000 population.


Not cancerousNon-malignant tumours may grow larger but do not spread to other parts of the body.


The length of time from the date of diagnosis for a disease, such as cancer, that patients diagnosed with the disease are still alive. In a clinical trial, measuring the survival is one way to see how well a new treatment works. Also called ‘overall survival’ or ‘OS’.

Routes to Diagnosis

Under the ‘Routes to Diagnosis’ tab in the Brain Tumour Data Dashboard, you can explore the ways patients have been diagnosed with brain tumours. There are many ways, or routes, for cancers to be diagnosed in the NHS. A ‘route to diagnosis’ is the series of events between a patient and the healthcare system that leads to a diagnosis of cancer. The routes include:

  1. Two Week Wait

Patients are urgently referred by their GP for suspected cancer via the Two Week Wait system and are seen by a specialist within 2 weeks where they are diagnosed.

  1. GP referral

Diagnosis via a GP referral includes routine and urgent referrals where the patient was not referred under the Two Week Wait system.

  1. Emergency Presentation

Cancers can be diagnosed via emergency situations such as via A&E, emergency GP referral, emergency transfer or emergency admission.

  1. Outpatient

Outpatient cancer diagnoses include diagnoses via an elective route which started with an outpatient appointment that is either a self-referral or consultant to consultant referral. (It does not include those under the Two Week Wait referral system).

  1. Inpatient elective

Diagnosis via an inpatient elective route is where diagnosis occurs after the patient has been admitted into secondary care from a waiting list, or where the admission is booked or planned.

  1. Death Certificate Only

Diagnoses made by Death Certificate Only are made where there is no more information about the cancer diagnosis other than the cancer related death notifications. The date of diagnosis is the same as that of the date of death.

  1. Unknown

For some patients with a cancer diagnosis, there is no relevant data available to understand the route to diagnosis.


More information

If any of the statistical terms in this section of the brainstrust website are hard to understand, we recommend looking them up here:

Cancer Research UK’s Cancer Statistics Explained

If you are looking for help understanding terms relating specifically to brain tumours, and treatment, then the brainstrust glossary is available here: