Tag: policy
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Working with the new Scottish government to improve outcomes for people affected by brain tumours
We welcome a new Scottish Parliament, share an update on recent activity in Scotland as well as our call for a National Brain Tumour Strategy.
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What does a new Welsh government mean for the brain tumour community?
While the newly elected Members of the Senedd settle into their roles and Plaid Cymru form the next government, we’re taking stock of the progress made in improving brain tumour care and outcomes across Wales. This new government brings a critical opportunity to shift the dial for brain tumour care, diagnosis, treatment and research in Wales.
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Eight recommendations to unlock brain tumour innovation in the UK
Our new report explains how to unlock brain tumour innovation in the UK and the systemic barriers holding it back.
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Celebrating The Rare Cancers Act officially being enshrined in law!
We’re celebrating the news that the Rare Cancers Act has now become law and the transformative potential this has for the brain tumour community.
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A National Cancer Plan for England Published: what it means for brain tumours
Following a consultation by the Department of Health and Social Care, in which we fed back your experiences of brain tumours, we welcome the publication of the National Cancer Plan for England and its explicit focus on rare and less survivable cancers, including brain tumours.
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Holding on to Hope: From Diagnosis to Advocacy
In August 2025, Mark joined The Brain Tumour Charity’s Scottish Steering Committee. Here he shares why he joined the Committee and what he hopes can be achieved.
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Vorasidenib – an update
We provide an update on the latest developments surrounding the appraisal process related Vorasidenib.
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Why approving vorasidenib matters
We’ve sent your feedback to the consultation on NICE’s draft guidance on vorasidenib. These are just some of the powerful testimonies we received that formed part of that.
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Thanks for helping shape our response to NICE’s draft decision on vorasidenib
Despite the disappointing draft guidance published by NICE, there’s still hope that vorasidenib will be available through the NHS in England.
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Enabling Faster, Better Diagnosis: The Scottish Steering Committee’s Renewed Commitment
We provide an update on the Scottish Steering Committees decided ambitions and objectives that members will seek to achieve.
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Campaigning together: pushing for change as Parliament returns
In this post we provide an update on recent Campaigns activity including on the Rare Cancers Bill and the NIHR-funded National Brain Tumour Research Consortium.
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Update for the brain tumour community on the National Brain Tumour Research Consortium
Following our previous statement in April 2025, we share the latest update on activity linked to the National Brain Tumour Research Consortium
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Gathering insights on potential barriers to innovation
This week we hosted a roundtable with representatives from the life sciences sector to begin to understand potential barriers to innovation across the UK.
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National Cancer Plan: Targeting the challenge
We explore the upcoming National Cancer Plan targets and their potential impact on survival gaps in cancer treatment.
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New Scottish guidelines aim to speed up brain tumour diagnosis
NHS Scotland has published updated referral guidance for suspected cancers – including brain. We share information on some of the key changes that have been made.
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The Government’s Welfare Reform: what’s happening and how does it impact the brain tumour community?
We’ve broken down what the proposed reforms were, what’s changed, and what it means for our community.
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Urgent: The Rare Cancers Bill is at risk and we need your help!
The Rare Cancers Bill is at risk of falling – we urge supporters to get in touch with their MP to ensure it progresses.
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What the 10 Year Health Plan means for the brain tumour community
Following the launch of the UK Government’s 10 Year Health Plan, we analyse some of the key announcements that may impact the brain tumour community.
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A Bill of Hope: Rare Cancers Bill Passes Committee Stage
“The Rare Cancers Bill, led by Scott Arthur MP, has passed Committee Stage – bringing hope to those affected by rare and less survivable cancers, including brain tumours.”
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Six ways to remove the barriers to research participation
If we’re going to improve survival rates and quality of life for people with a brain tumour, research must be shaped by those who are eligible to take part.
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Maintaining momentum: A busy week of campaigning activity and actions
We share information on activity that has taken place across the UK in the drive to improve outcomes for all those affected by brain tumours.
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Our submission to the National Cancer Plan consultation
The Government is working on a National Cancer Plan to improve patient experience for those affected. Here we share what our submission to the Government’s Consultation included.
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Exploring GP Access to Brain Scans
Today we publish new research into the barriers GPs face in being able to diagnose people with a brain tumour. Read our blog overview of our findings.
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Consortium to build sustainable pipeline of trials for new brain tumour therapies
A brain tumour consortium, funded by the National Institute for Health and Care Research (NIHR), with the vision to make the UK a “testbed for oncology innovation by accelerating the development of treatments for patients with brain tumours” is being developed and is aiming for real progress in “the soonest time frame possible.”