Brain Cancer Justice

04/09/2026

Still time to be counted.
Brain cancer gets just 1% of research funding. Patients, families, friends: add your voice.

https://eu.surveymars.com/q/TeYaxWDvA

04/09/2026

Encouraging news in Australia (again)

But two questions:

1. Why is this going to take 6-10 years to reach patients? What’s the challenge / red tape?

2. Is there enough collaboration amongst scientists, going on around the world, that enables insights to be shared - so we can improve the speed of processes such as this one?

Australian scientists are developing a breakthrough treatment for b...

03/09/2026

We will not sit by any longer.

Help us map every family brain cancer has touched across the UK 🇬🇧

It only takes 2 mins 👊
https://eu.surveymars.com/q/TeYaxWDvA



P.S. don’t stay silent
&

03/09/2026

Patient. Family member. Carer. Loved one. However brain cancer has touched your life, you’re part of this fight and we want to find you. Help us build the UK’s first true picture of who this disease affects.

Link in bio - or copy this:
https://eu.surveymars.com/q/TeYaxWDvA

Together, we can turn terminal to treatable.

02/09/2026

Patient. Family member. Carer. Loved one. However brain cancer has touched your life, you're part of this fight and we want to find you. Help us build the UK's first true picture of who this disease affects:

https://eu.surveymars.com/q/TeYaxWDvA

Together, we can turn terminal to treatable.

02/09/2026

Burnham: "There is so much more we need to do on brain cancer.
"You can be sure from me, madam deputy speaker, that I will always do that in the name of my good friend Tessa Jowell, whose family still work on these issues."

Words are encouraging
Delivery is essential.

01/09/2026

This is the harsh reality for brain cancer patients. We are thinking of you Jack.

If others are going through a similar process and have a spare two minutes, then please answer these quick questions:
https://surveymars.com/q/TeYaxWDvA

Jack has been told he only has a year left to live.

After suffering with double vision earlier this year, the 25-year-old, from Derbyshire, was diagnosed with an inoperable brain tumour.

Now, he's hoping he can receive experimental treatment abroad: https://bbc.in/4gzstck

01/09/2026

All around the world there are huge challenges facing brain cancer patients - but there is also hope on the horizon to turn terminal into treatable. The ABC shares that there is a new customised vaccine trial taking place in Australia. But young Coby cannot access it.

Brain Tumour Alliance Australia says there need to be more options for people like Coby, including drug companies providing free access to experimental treatments and greater support for drug cancer trials.

Potential is out there, but we need Pharmaceutical industry to recognise this and get behind it.

Read this story to find out more.


Brain Tumour Alliance Australia ABC News
Head to Facebook to access the link

01/09/2026

Thank you for sharing 🫂💔🫂

💛 SEPTEMBER — CHILDHOOD CANCER AWARENESS MONTH 💛

September is Childhood Cancer Awareness Month.

And this year, it feels very different.

Because until you have a child diagnosed with cancer, you can never truly understand what those words mean.

Around 2,000 children in the UK are diagnosed with cancer every year. Around five children every single day.

This year, one of those children was my beautiful Max.

Except Max was never a statistic.

He was my boy.

He was 14 years old. Funny, cheeky, loving, football-mad and full of life. He had dreams, plans, a family who adored him and a whole future ahead of him.

Then, in November, cancer changed everything.

For nine months we fought.

We searched for treatments. We chased hope. We raised money. We travelled. We prayed. We held onto every possibility we could find.

And Max fought with everything he had.

But on 8th August 2026, at 13:24, our beautiful boy died from his brain tumour.

Now, when I see the statistics, I don’t just see numbers.

I see children.

I see families.

I see parents sitting beside hospital beds, desperately wishing they could take their child’s pain away.

I see the future that was stolen from Max.

And I think about how much more needs to be done.

More research.
More funding.
More treatment options.
More hope.
More children coming home.

So this September, I will wear the gold, share the message and say my son’s name.

MAX. 💛

Because he deserves to be remembered.

Not as a statistic.

Not as a diagnosis.

But as the beautiful boy he was.

Our boy.

Forever 14. 💛🎗️