Is the BAF in Your Plan?

We are thrilled to announce the launch our new planned giving program, the Brain Aneurysm Foundation Legacy Society.

The BAF Legacy society allows donors to make a lasting impact on our work through estate planning and ensures that brain aneurysm research, education, support, awareness, and advocacy continue for years to come. Your planned gift can help provide a lasting legacy of support and hope to those affected by brain aneurysms.

In the summer of 2022, the BAF received the largest gift in its 28-year history from the estate of brain aneurysm survivor Renee Joyce prompting the establishment of the Legacy Society for those who wish to include the BAF in their planned giving. Joyce, a talented writer, editor, and researcher who succumbed to pancreatic cancer on August 31, 2021, at the age of 67, donated $230,000 to the foundation in support of essential research through her estate plans.


“Bequests will allow us to expand our reach and impact through groundbreaking studies focused on early detection, improved treatment modalities, and the technological advances that will ultimately improve outcomes.”

– Christine Buckley, BAF Executive Director


By joining the Brain Aneurysm Foundation Legacy Society, you too can be assured that the foundation will use your gift to further its mission to promote the early detection of brain aneurysms, provide support networks for patients and families, and fund further research that will improve patient outcomes and save lives. 

To learn more about the Brain Aneurysm Foundation Legacy Society, please visit our website HERE
Support for Ellie's Law

Ellie's Law (H.R. 902) was introduced to the 118th Congress on February 9th by Representative Yvette Clarke (D-NY) and 18 co-sponsors. We are grateful for their commitment to the cause and for their support of this bipartisan bill.

As a reminder, if you can join us in person for our annual Advocacy Day on Capitol Hill on March 23, 2023, there is still time to register! By joining our efforts, you will be advocating for increased funding for brain aneurysm research, connecting with policymakers, and helping to ensure that critical research is supported.

Please CLICK HERE to learn more or to register.
2023 Webinar Series

On February 8th, Executive Director, Christine Buckley hosted a webinar: The Hope and Unknown of Brain Aneurysm Genetics, with Rebecca Middleton from HBA Support (Hereditary Brain Aneurysm Support) and William Gibson, MD, from BC Children's Hospital. The conversation addressed the genetics behind hereditary brain aneurysms, research that is happening now, and discussions you should have with relatives. You may view the webinar HERE

Keep an eye on your inbox for updates about our March webinar.
Upcoming Events
April 13, 2023

Celebrate the Brain Aneurysm Foundation's Chicago area champions with us at the Union League of Chicago. Honorees include Congressman Sean Casten and Dr. William Ares. Please CLICK HERE to learn more or to purchase tickets.
April 30, 2023

Join us for the Brain Aneurysm Foundation Run/Walk - New England at Castle Island in Boston, MA, as we come together to celebrate survivors and honor those lost to brain aneurysms. Please CLICK HERE to learn more or to register.
September 21, 2023

Save the date for the 2nd Annual Brain Aneurysm Foundation Day of Engagement. Last year was a big success, and we hope you will take part again this year.
Your donation to the Brain Aneurysm Foundation, the nation's only nonprofit organization solely dedicated to providing critical awareness, education, support, and research funding to reduce the incidence of brain aneurysm ruptures, can make a difference in the lives of those affected by brain aneurysms in many ways.