Category: Policy & Public Affairs
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Uniting to respond to the Timms Review into PIP
We’ve united with 12 leading cancer charities to respond to the government’s Timms Review into Personal Independence Payments (PIP).
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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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“We must give brain tumour patients access to more clinical trials.”
In an article for Open Access Government, published in April 2026, Dr Simon Newman explains how we’re trying to help give more people better access to clinical trials.
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Vorasidenib approved for NHS use in England
In a positive end to Brain Tumour Awareness Month 2026, we are pleased that NICE has approved vorasidenib to treat some types of brain tumours.
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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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Vorasidenib approved for use in Scotland
We’re delighted to share the news that vorasidenib has been approved by the Scottish Medicines Consortium to treat some low grade gliomas.
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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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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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Dordaviprone – springs of hope, but a long way to go
Dordaviprone, also known as ONC201, offers new hope for treating H3 K27M-Mutated Diffuse Midline Glioma. But, there’s a long way to go before it’s ready for use on the NHS.
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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.