National Brain Tumor Society
@braintumor.org
National Brain Tumor Society (NBTS) unrelentingly invests in, mobilizes, and unites the brain tumor community to discover a cure, deliver effective treatments, and advocate for patients and caregivers.
Pinned
Theo was diagnosed with medulloblastoma at the age of 1; since he was 6, Theo & his family have attended Head to the Hill, advocating for research funding & connecting with #braintumor advocates from across the country.
Join them in making a difference: Braintumor.org/Impact
Join them in making a difference: Braintumor.org/Impact
This year, advocates like Theo & his mom, Lori, rallied support in Congress, urging leaders to restore funding & advance childhood cancer legislation.
Make a gift today to unlock an additional $150K from our board & accelerate the change we so urgently need: BrainTumor.org/Impact
Make a gift today to unlock an additional $150K from our board & accelerate the change we so urgently need: BrainTumor.org/Impact
December 29, 2025 at 5:55 PM
This year, advocates like Theo & his mom, Lori, rallied support in Congress, urging leaders to restore funding & advance childhood cancer legislation.
Make a gift today to unlock an additional $150K from our board & accelerate the change we so urgently need: BrainTumor.org/Impact
Make a gift today to unlock an additional $150K from our board & accelerate the change we so urgently need: BrainTumor.org/Impact
Join our Caregiver Support Conversation on Mon, Jan 5, at 7 PM ET to connect with fellow care partners who understand the challenges of supporting someone with a brain tumor.
Share, listen & find community in a welcoming, safe space: braintumor.org/support-services/support-groups/caregiver-support
Share, listen & find community in a welcoming, safe space: braintumor.org/support-services/support-groups/caregiver-support
December 29, 2025 at 4:06 PM
Join our Caregiver Support Conversation on Mon, Jan 5, at 7 PM ET to connect with fellow care partners who understand the challenges of supporting someone with a brain tumor.
Share, listen & find community in a welcoming, safe space: braintumor.org/support-services/support-groups/caregiver-support
Share, listen & find community in a welcoming, safe space: braintumor.org/support-services/support-groups/caregiver-support
Thanks to incredible partnership from our advocates, NBTS faced down a year marked by division and championed both unity and change.
Make a gift now to support our relentless advocacy for reliable research funding in 2026: BrainTumor.org/Impact
Make a gift now to support our relentless advocacy for reliable research funding in 2026: BrainTumor.org/Impact
December 29, 2025 at 1:30 PM
Thanks to incredible partnership from our advocates, NBTS faced down a year marked by division and championed both unity and change.
Make a gift now to support our relentless advocacy for reliable research funding in 2026: BrainTumor.org/Impact
Make a gift now to support our relentless advocacy for reliable research funding in 2026: BrainTumor.org/Impact
🧠✨In 2025, NBTS launched the only brain tumor-specific research advocate program in the U.S. Patients and care partners use their voices to bridge gaps among scientists, officials, and industry, shaping research and driving impact for the community.
December 28, 2025 at 6:25 PM
🧠✨In 2025, NBTS launched the only brain tumor-specific research advocate program in the U.S. Patients and care partners use their voices to bridge gaps among scientists, officials, and industry, shaping research and driving impact for the community.
After his wife, Julia, passed from #anaplasticastrocytoma, Laurence became a passionate advocate and GNE athlete, supporting NBTS so future survivors can have a better chance.
Join him in making a difference — make a gift today: Braintumor.org/Impact
Join him in making a difference — make a gift today: Braintumor.org/Impact
December 28, 2025 at 5:29 PM
After his wife, Julia, passed from #anaplasticastrocytoma, Laurence became a passionate advocate and GNE athlete, supporting NBTS so future survivors can have a better chance.
Join him in making a difference — make a gift today: Braintumor.org/Impact
Join him in making a difference — make a gift today: Braintumor.org/Impact
NBTS is unlocking clinical trials & driving progress against #glioblastoma. In 2025, we
⭐ accelerated a Phase II trial for a promising #GBM vaccine
⭐ discovered a new vulnerability to launch a new clinical trial
Give now to help us do even more in 2026: Braintumor.org/Impact
⭐ accelerated a Phase II trial for a promising #GBM vaccine
⭐ discovered a new vulnerability to launch a new clinical trial
Give now to help us do even more in 2026: Braintumor.org/Impact
December 27, 2025 at 8:20 PM
NBTS is unlocking clinical trials & driving progress against #glioblastoma. In 2025, we
⭐ accelerated a Phase II trial for a promising #GBM vaccine
⭐ discovered a new vulnerability to launch a new clinical trial
Give now to help us do even more in 2026: Braintumor.org/Impact
⭐ accelerated a Phase II trial for a promising #GBM vaccine
⭐ discovered a new vulnerability to launch a new clinical trial
Give now to help us do even more in 2026: Braintumor.org/Impact
After his wife passed from #glioblastoma, Kabir Sethi turned grief into action. As an NBTS Board Member & GNE Athlete, he fights for patients & families.
Give today to help us unlock an additional $150K gift from our board: BrainTumor.org/Impact
Give today to help us unlock an additional $150K gift from our board: BrainTumor.org/Impact
December 27, 2025 at 7:46 PM
After his wife passed from #glioblastoma, Kabir Sethi turned grief into action. As an NBTS Board Member & GNE Athlete, he fights for patients & families.
Give today to help us unlock an additional $150K gift from our board: BrainTumor.org/Impact
Give today to help us unlock an additional $150K gift from our board: BrainTumor.org/Impact
Your gift to NBTS ensures that we can continue to serve families like Mike (patient with #glioblastoma) and Rachel (his wife) in 2026 and beyond.
Make your year-end gift now at BrainTumor.org/Impact — for everyone with a brain tumor diagnosis, it’s time for a better chance.
Make your year-end gift now at BrainTumor.org/Impact — for everyone with a brain tumor diagnosis, it’s time for a better chance.
December 26, 2025 at 8:15 PM
Your gift to NBTS ensures that we can continue to serve families like Mike (patient with #glioblastoma) and Rachel (his wife) in 2026 and beyond.
Make your year-end gift now at BrainTumor.org/Impact — for everyone with a brain tumor diagnosis, it’s time for a better chance.
Make your year-end gift now at BrainTumor.org/Impact — for everyone with a brain tumor diagnosis, it’s time for a better chance.
Erika B.’s #glioblastoma diagnosis flipped her world upside down.
In that uncertainty, she searched for and found community through the National Brain Tumor Society.
💙 Make a gift to power support for patients & their loved ones: BrainTumor.org/Impact
In that uncertainty, she searched for and found community through the National Brain Tumor Society.
💙 Make a gift to power support for patients & their loved ones: BrainTumor.org/Impact
December 25, 2025 at 3:46 PM
Erika B.’s #glioblastoma diagnosis flipped her world upside down.
In that uncertainty, she searched for and found community through the National Brain Tumor Society.
💙 Make a gift to power support for patients & their loved ones: BrainTumor.org/Impact
In that uncertainty, she searched for and found community through the National Brain Tumor Society.
💙 Make a gift to power support for patients & their loved ones: BrainTumor.org/Impact
☀️In 2025, NBTS funded our first-ever #QualityOfLife grants and also supported research to improve survival and quality of life for pediatric high-grade #glioma patients.
Make a gift to help us continue this important work in 2026: BrainTumor.org/Impact
Make a gift to help us continue this important work in 2026: BrainTumor.org/Impact
December 24, 2025 at 5:38 PM
☀️In 2025, NBTS funded our first-ever #QualityOfLife grants and also supported research to improve survival and quality of life for pediatric high-grade #glioma patients.
Make a gift to help us continue this important work in 2026: BrainTumor.org/Impact
Make a gift to help us continue this important work in 2026: BrainTumor.org/Impact
Our National Brain Tumor Society team wants to share our heartfelt gratitude for you and the incredible community we’re so proud to serve.
We know the holiday season can bring a mix of emotions — please know we’re here for you with resources and support. 💙
We know the holiday season can bring a mix of emotions — please know we’re here for you with resources and support. 💙
December 24, 2025 at 4:09 PM
Our National Brain Tumor Society team wants to share our heartfelt gratitude for you and the incredible community we’re so proud to serve.
We know the holiday season can bring a mix of emotions — please know we’re here for you with resources and support. 💙
We know the holiday season can bring a mix of emotions — please know we’re here for you with resources and support. 💙
After losing her dad, Barry, to a #chordoma, Leah joined NBTS and found a community that understood.
Now as NBTS Board Chair, she channels her grief into purpose: together with the rest of the board, she’s challenging us to raise $300K by 12/31.
Join us: BrainTumor.org/Impact
Now as NBTS Board Chair, she channels her grief into purpose: together with the rest of the board, she’s challenging us to raise $300K by 12/31.
Join us: BrainTumor.org/Impact
December 23, 2025 at 6:40 PM
After losing her dad, Barry, to a #chordoma, Leah joined NBTS and found a community that understood.
Now as NBTS Board Chair, she channels her grief into purpose: together with the rest of the board, she’s challenging us to raise $300K by 12/31.
Join us: BrainTumor.org/Impact
Now as NBTS Board Chair, she channels her grief into purpose: together with the rest of the board, she’s challenging us to raise $300K by 12/31.
Join us: BrainTumor.org/Impact
In 2025, 118 people organized Fundraise Your Way events for NBTS, raising more than $1M to fund breakthroughs.
One of these inspiring people is Kevyn, a #glioblastoma survivor who co-hosts a semiannual fundraiser, Brews for Brains Hanover.
One of these inspiring people is Kevyn, a #glioblastoma survivor who co-hosts a semiannual fundraiser, Brews for Brains Hanover.
December 23, 2025 at 5:10 PM
In 2025, 118 people organized Fundraise Your Way events for NBTS, raising more than $1M to fund breakthroughs.
One of these inspiring people is Kevyn, a #glioblastoma survivor who co-hosts a semiannual fundraiser, Brews for Brains Hanover.
One of these inspiring people is Kevyn, a #glioblastoma survivor who co-hosts a semiannual fundraiser, Brews for Brains Hanover.
💪 In 2025, our community showed up in a big way.
Nearly 21K participants joined NBTS walks & races, raising $4M+.
GNE added $1.4M+ more — incl. $85K from one Disney Marathon Weekend 🏃♀️
Help unlock $150K from our Board by 12/31!\
Give now: BrainTumor.org/Impact
Nearly 21K participants joined NBTS walks & races, raising $4M+.
GNE added $1.4M+ more — incl. $85K from one Disney Marathon Weekend 🏃♀️
Help unlock $150K from our Board by 12/31!\
Give now: BrainTumor.org/Impact
December 23, 2025 at 2:26 AM
💪 In 2025, our community showed up in a big way.
Nearly 21K participants joined NBTS walks & races, raising $4M+.
GNE added $1.4M+ more — incl. $85K from one Disney Marathon Weekend 🏃♀️
Help unlock $150K from our Board by 12/31!\
Give now: BrainTumor.org/Impact
Nearly 21K participants joined NBTS walks & races, raising $4M+.
GNE added $1.4M+ more — incl. $85K from one Disney Marathon Weekend 🏃♀️
Help unlock $150K from our Board by 12/31!\
Give now: BrainTumor.org/Impact
It is with a heavy heart that we share news of the passing of philosopher, writer, patient advocate, and NBTS board member Adam Hayden. Read about Adam’s life, legacy, and enduring impact on the brain tumor community: https://braintumor.org/news/remembering-adam-hayden/
December 22, 2025 at 9:42 PM
It is with a heavy heart that we share news of the passing of philosopher, writer, patient advocate, and NBTS board member Adam Hayden. Read about Adam’s life, legacy, and enduring impact on the brain tumor community: https://braintumor.org/news/remembering-adam-hayden/
Reposted by National Brain Tumor Society
In 2020 my life was turned upside down due to my wife's cancer diagnosis. We were fortunate to have great doctors and find an amazing group at CERN through @braintumor.org to help us navigate the waters. In June we were honored to talk about our journey. youtu.be/2af8mMPosYk?...
Megan and Mike Patterson - Speakers at the 2025 Ependymoma Awareness Day webinar.
YouTube video by CERNFoundation
youtu.be
December 19, 2025 at 3:39 PM
In 2020 my life was turned upside down due to my wife's cancer diagnosis. We were fortunate to have great doctors and find an amazing group at CERN through @braintumor.org to help us navigate the waters. In June we were honored to talk about our journey. youtu.be/2af8mMPosYk?...
Our board has given us a challenge: Raise $300K during the last 10 days of the year and they’ll donate an extra $150K to fund our work powering research, advocacy, & support for the brain tumor community.
Help us unlock this gift by December 31, give now: BrainTumor.org/Impact
Help us unlock this gift by December 31, give now: BrainTumor.org/Impact
December 22, 2025 at 1:30 PM
Our board has given us a challenge: Raise $300K during the last 10 days of the year and they’ll donate an extra $150K to fund our work powering research, advocacy, & support for the brain tumor community.
Help us unlock this gift by December 31, give now: BrainTumor.org/Impact
Help us unlock this gift by December 31, give now: BrainTumor.org/Impact
If you’re feeling overwhelmed and isolated after a diagnosis, you’re not alone.
NBTS offers many ways to find support, meet others, and get involved.
Explore 11 powerful ways to connect with the community and make a difference: https://bit.ly/4qiXrJ5
NBTS offers many ways to find support, meet others, and get involved.
Explore 11 powerful ways to connect with the community and make a difference: https://bit.ly/4qiXrJ5
December 21, 2025 at 6:35 PM
If you’re feeling overwhelmed and isolated after a diagnosis, you’re not alone.
NBTS offers many ways to find support, meet others, and get involved.
Explore 11 powerful ways to connect with the community and make a difference: https://bit.ly/4qiXrJ5
NBTS offers many ways to find support, meet others, and get involved.
Explore 11 powerful ways to connect with the community and make a difference: https://bit.ly/4qiXrJ5
⏰2025 is almost over — do you have unallocated money left in your #DAF? If so, there are still twelve days left to recommend a grant to the National Brain Tumor Society. Log in to your DAF portal today to help power the breakthroughs ahead!
December 20, 2025 at 8:25 PM
⏰2025 is almost over — do you have unallocated money left in your #DAF? If so, there are still twelve days left to recommend a grant to the National Brain Tumor Society. Log in to your DAF portal today to help power the breakthroughs ahead!
We’d be honored to share your story!
NBTS invites anyone affected by #braintumors to share this experience in writing or by video, to raise awareness and help others feel less alone.
Send us your story today at https://braintumor.org/brain-tumors/stories/share-your-story/
NBTS invites anyone affected by #braintumors to share this experience in writing or by video, to raise awareness and help others feel less alone.
Send us your story today at https://braintumor.org/brain-tumors/stories/share-your-story/
December 20, 2025 at 7:50 PM
We’d be honored to share your story!
NBTS invites anyone affected by #braintumors to share this experience in writing or by video, to raise awareness and help others feel less alone.
Send us your story today at https://braintumor.org/brain-tumors/stories/share-your-story/
NBTS invites anyone affected by #braintumors to share this experience in writing or by video, to raise awareness and help others feel less alone.
Send us your story today at https://braintumor.org/brain-tumors/stories/share-your-story/
Make an impact all year long by becoming a monthly donor!
As a special thank you, anyone who sets up a monthly gift of $25 or more will receive an NBTS umbrella as a token of our gratitude.
Join us in creating steady, meaningful change, month after month: BrainTumor.org/Impact
As a special thank you, anyone who sets up a monthly gift of $25 or more will receive an NBTS umbrella as a token of our gratitude.
Join us in creating steady, meaningful change, month after month: BrainTumor.org/Impact
December 19, 2025 at 8:56 PM
Make an impact all year long by becoming a monthly donor!
As a special thank you, anyone who sets up a monthly gift of $25 or more will receive an NBTS umbrella as a token of our gratitude.
Join us in creating steady, meaningful change, month after month: BrainTumor.org/Impact
As a special thank you, anyone who sets up a monthly gift of $25 or more will receive an NBTS umbrella as a token of our gratitude.
Join us in creating steady, meaningful change, month after month: BrainTumor.org/Impact
The Brain Tumor Investment Fund (NBTS’s venture philanthropy arm) is focused on sparking the brain tumor market to deliver treatments and cures.
Learn more about the innovative work we’re supporting at emerging and innovative companies at braintumorinvestmentfund.org
Learn more about the innovative work we’re supporting at emerging and innovative companies at braintumorinvestmentfund.org
December 18, 2025 at 4:06 PM
The Brain Tumor Investment Fund (NBTS’s venture philanthropy arm) is focused on sparking the brain tumor market to deliver treatments and cures.
Learn more about the innovative work we’re supporting at emerging and innovative companies at braintumorinvestmentfund.org
Learn more about the innovative work we’re supporting at emerging and innovative companies at braintumorinvestmentfund.org
At the The Society for Neuro-Oncology 30th anniversary annual meeting, NBTS president & CEO David Arons sat down with Dr. Rachna Malani to talk about how we’re working to advance effective treatments & advocating for patients and caregivers.
Watch now: https://www.youtube.com/watch?v=ldhzO03_Rxw
Watch now: https://www.youtube.com/watch?v=ldhzO03_Rxw
December 17, 2025 at 9:51 PM
At the The Society for Neuro-Oncology 30th anniversary annual meeting, NBTS president & CEO David Arons sat down with Dr. Rachna Malani to talk about how we’re working to advance effective treatments & advocating for patients and caregivers.
Watch now: https://www.youtube.com/watch?v=ldhzO03_Rxw
Watch now: https://www.youtube.com/watch?v=ldhzO03_Rxw
After losing her husband Jim to glioblastoma, Tracy made a promise: she would not sit on the sidelines.
Alongside her sons, Tracy supports NBTS through fundraising events and advocacy.
Give today to help her make a difference: Braintumor.org/Impact
Alongside her sons, Tracy supports NBTS through fundraising events and advocacy.
Give today to help her make a difference: Braintumor.org/Impact
December 17, 2025 at 8:06 PM
After losing her husband Jim to glioblastoma, Tracy made a promise: she would not sit on the sidelines.
Alongside her sons, Tracy supports NBTS through fundraising events and advocacy.
Give today to help her make a difference: Braintumor.org/Impact
Alongside her sons, Tracy supports NBTS through fundraising events and advocacy.
Give today to help her make a difference: Braintumor.org/Impact
Janet’s brother Michael was diagnosed with brain cancer last December & she knows firsthand how much families need support and research.
She supports NBTS because, in her words, “we have to find a cure for brain cancer so there aren’t families like mine going through this.”
She supports NBTS because, in her words, “we have to find a cure for brain cancer so there aren’t families like mine going through this.”
December 16, 2025 at 10:49 PM
Janet’s brother Michael was diagnosed with brain cancer last December & she knows firsthand how much families need support and research.
She supports NBTS because, in her words, “we have to find a cure for brain cancer so there aren’t families like mine going through this.”
She supports NBTS because, in her words, “we have to find a cure for brain cancer so there aren’t families like mine going through this.”