LA Times op-ed: “Being insured in America is not the same as having access to care”
One family’s experience with a GBM diagnosis.
One family’s experience with a GBM diagnosis.
Ask your employer if they match charitable gifts, many do. Here’s the info you’ll need.
We want to reach patients missing from the data, so we’re expanding our national disparities research to reach rural and underserved families often left out of the picture.
Jason Binder is a father of five and healthcare entrepreneur whose wife, Tracy, died of glioblastoma in 2025. During her illness, he built an AI tool…
Erika was thriving as a GBM survivor until it came back. She’s finding out that the options for recurrent GBM are few.
Remembering Adam Hayden, a giant in the glioblastoma community (1982-2025)
In 2025 we met with people living with GBM and their care partners, traveled to conferences, and began to tell the world about our GBM Disparities Survey.
“It was incredibly energizing to see how OBB’s work is not only documenting problems but also driving conversations and initiatives that could improve access to care and quality of life for GBM patients across diverse communities.” Jacob Ellen writes about his experience with the SNO 2025 conference where OurBrainBank presented two posters and won an award.
OurBrainBank staff will be at the ASCO (American Society of Clinical Oncology) annual meeting in Chicago to present a poster about isolation and loneliness among GBM patients and care partners.
Watch Good Morning America on Friday, April 17 to see OurBrainBank trustee Sundas Hashmi speak with host Michael Strahan about brain cancer
Help us raise funds for glioblastoma research — we collect data for tomorrow and help people today
Navigators from the Brain Tumor Network can walk you through what to expect, how to ask about clinical trials, when to get a second opinion, and more
