National Brain Tumor Society

National Brain Tumor Society We are a nonprofit organization committed to conquering and curing brain tumors--once and for all.
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“You’re so lucky it’s not cancer.”Many people with benign brain tumors have heard this statement — but benign doesn’t me...
01/23/2026

“You’re so lucky it’s not cancer.”

Many people with benign brain tumors have heard this statement — but benign doesn’t mean harmless.

Even noncancerous tumors can cause serious, long-term symptoms and significantly affect quality of life.

This January, in honor of Quality of Life Month, we’re raising awareness of the realities faced by people living with benign brain tumors.

💡Learn more:
https://braintumor.org/news/benign-is-not-fine-common-misconceptions-about-noncancerous-brain-tumors/

Are you living with a benign brain tumor? Share your experience in the comments below.

Head to the Hill is back! 🏛️ Register today at BrainTumor.org/HeadtotheHill to join the National Brain Tumor Society and...
01/23/2026

Head to the Hill is back!

🏛️ Register today at BrainTumor.org/HeadtotheHill to join the National Brain Tumor Society and fellow volunteer advocates from May 3-5, 2026, on Capitol Hill in Washington, D.C.

Share your story, raise your voice, and urge policymakers to take action on the issues that matter most to the brain tumor community.

NBTS is honored to exhibit at the 13th Neuro-Oncology Brain Tumor Symposium on Friday, January 30.This educational event...
01/22/2026

NBTS is honored to exhibit at the 13th Neuro-Oncology Brain Tumor Symposium on Friday, January 30.

This educational event brings together medical professionals, patients, caregivers, and advocates to learn current innovative approaches to brain tumor care.

The symposium can be attended in person or virtually — register today at: med.upenn.edu/brain2026/

🏀⚽⛳ Turn your favorite sport into a force for good! From lacrosse and golf tournaments to pickup games and everything in...
01/20/2026

🏀⚽⛳ Turn your favorite sport into a force for good!

From lacrosse and golf tournaments to pickup games and everything in between, sports fundraisers are a powerful way to rally your community and help accelerate world-class brain tumor research with the National Brain Tumor Society.

Learn how other supporters have made an impact—and how you can organize your own sports fundraiser: https://braintumor.org/news/how-to-fundraise-through-sports-for-the-brain-tumor-community/

Have you or a loved one enrolled in a clinical trial after a brain tumor diagnosis?NBTS wants to connect with patients a...
01/18/2026

Have you or a loved one enrolled in a clinical trial after a brain tumor diagnosis?

NBTS wants to connect with patients and caregivers who have gone through the process to help educate others on what to expect.

If you’re willing to share your experience for possible inclusion in future NBTS content, please complete this brief form: https://braintumor.org/brain-tumors/stories/clinical-trial-experience/

01/17/2026

Melissa runs with Gray Nation Endurance in memory of her late aunt Debbie, who passed from glioblastoma.

She’s turning her loss into action, putting meaning behind her miles by running and fundraising for NBTS. 💙

Watch her story to see why every mile matters.

Learn more about Gray Nation Endurance and how to put meaning behind your miles at: BrainTumor.org/GNE

“It’s powerful, isn’t it, sharing stories with others who’ve gone through similar experiences,” said acclaimed British a...
01/17/2026

“It’s powerful, isn’t it, sharing stories with others who’ve gone through similar experiences,” said acclaimed British actor/writer and brain tumor survivor Miles Jupp.

“People come up to me after [my show] and say it meant so much to feel seen — and even to laugh a bit in the process.”

This week, NBTS’s Anne was honored to attend Jupp’s comedy show, *On I Bang,* at the SoHo Playhouse in NYC. Jupp was diagnosed with a meningioma after collapsing while filming in London.

The witty, warm *On I Bang* tells the story of his diagnosis and brain surgery experience while sharing some side-splitting moments about the life of an actor, son, husband, and father of five.

🎭 NYC-area brain tumor community, tickets are still available for shows tonight, Saturday, and Sunday!

Stay after the applause to talk to Miles; he’d love to hear your story, too: https://www.sohoplayhouse.com/see-a-show/miles-jupp-on-i-bang

Special thanks to Soho Playhouse for the tickets, and to the The International Brain Tumour Alliance and The Brain Tumour Charity for inviting us to the show.

01/16/2026

Take an activity you love — such as golfing, running, baking, or enjoying happy hours — and turn it into a fundraising event that will help drive brain tumor research, advocacy, and support for patients and caregivers.

Learn more at BrainTumor.org/FundraiseYourWay

“If someone is considering starting a fundraiser in honor of their loved one, I would say do it. It’s been one of the most meaningful things in my life. It’s meant a lot to my family. It’s meant so much to me. It’s been meaningful to the National Brain Tumor Society, and we really think it’s helped make a difference.” — Lido Ramadan

“My brother was my hero from the day I was born.” — Pat S.After Pat’s beloved brother Emilio passed away due to  , she f...
01/16/2026

“My brother was my hero from the day I was born.” — Pat S.

After Pat’s beloved brother Emilio passed away due to , she found healing through tin punching — an art form that became more than just a creative outlet.

Now, the proceeds from every piece she sells are donated to NBTS to support brain tumor research, in the hopes that other families will not have to endure the same heartbreak.

Read her story: https://braintumor.org/news/tin-punching-out-glioblastoma-through-my-art/

As we step into 2026, we’d like to thank you for the incredible work you've done in 2025.Your advocacy has made a real i...
01/14/2026

As we step into 2026, we’d like to thank you for the incredible work you've done in 2025.

Your advocacy has made a real impact for the brain tumor community. Here's a quick look back and a peek at the road ahead:

In 2025, we saw record-breaking engagement, with 7,313 advocates responding to our action alerts! From Head to the Hill to Advocate From Your State, over 500 volunteers across 46 states shared their stories with Congress, pushing for key issues like:

- Increasing medical research funding
- Advancing the BRAIN Act
- Supporting pediatric cancer research
- Ensuring continuity of critical pediatric brain tumor research

Learn more: https://braintumor.org/news/update-from-the-capital-2025-nbts-policy-and-advocacy-wrap-up-and-2026-look-ahead/

“At least it’s benign.”For Amanda B., those words didn’t match the reality of living with a brain tumor.She shares how a...
01/14/2026

“At least it’s benign.”

For Amanda B., those words didn’t match the reality of living with a brain tumor.

She shares how a meningioma diagnosis reshaped every part of her life — from treatment decisions and long stays away from home, to permanent side effects, parenting, finances, and learning how to slow down and accept help.

Her message is clear: benign is not fine, and brain tumors can have a lasting impact on someone’s life.

👉 Read Amanda’s full story: https://braintumor.org/news/how-a-benign-brain-tumor-reshaped-my-life/

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What is our mission?

WHY WE ARE DIFFERENT

We believe we can move the needle faster and drive more new discoveries by influencing and funding research, and actually bringing together policy makers, researchers, clinicians doctors and industry organizations to collaborate and share information in order to find better treatments and a cure for brain tumors. We are the only brain tumor organization that has an active public policy agenda, and we directly advocate to policymakers to give brain tumor patients a voice in Washington, D.C.

We are intimately connected with top brain tumor researchers, academics and clinicians. Some of the top brain tumor experts are scientific advisors on our programs, and we hire PhDs to help create informative content and translate new research developments into language that brain tumor patients and their families can understand and act on.

We don’t just write blank checks. We drive a thoughtful research agenda and hold our researchers’ feet to the fire by monitoring their progress and having them report on findings to the community to justify funding.