Brain Aneurysm Foundation BAF Changemaker: Danisha Henry
Danisha Henry from Richmond, Texas
Dani’s journey is one of resilience, faith, and finding purpose after unimaginable challenges. She survived a ruptured brain aneurysm that changed the course of her life, and exactly eight years later, to the day, endured an ischemic stroke. Still living with an unruptured aneurysm, she chooses every day to lead with gratitude and determination.
BAF: Tell us a little about your connection with brain aneurysms.
DH: I am both a survivor and someone still living with a brain aneurysm. I survived a ruptured brain aneurysm that completely changed my life. And exactly eight years later, to the date, I survived an ischemic stroke. Those two life-altering events taught me the true meaning of strength, faith, and gratitude. I’m still living with another unruptured aneurysm, and I’ve learned to approach each day as a gift and an opportunity to raise awareness for others who may not yet know they’re at risk.
BAF: When did you first learn about the BAF?
DH: I first connected with the Brain Aneurysm Foundation just three weeks before the 7th anniversary of my rupture. Out of the blue, I received an email from the Foundation inviting me to Advocacy Day in Washington, D.C.—and it happened to take place on my aneurysm anniversary. It felt like more than a coincidence; it felt like a purpose. That invitation became a turning point in my journey of healing and advocacy.
BAF: Have you ever participated in any BAF events?
DH: Yes, I’ve had the honor of participating in several BAF events, including Advocacy Day in Washington, D.C., the Annual Support Conference, and local awareness walks. Each one has been a powerful reminder of how connection and community can fuel change. Meeting other survivors, families, and advocates face-to-face—sharing stories, tears, and laughter—has been both healing and inspiring. It reaffirmed that we are stronger together and that our collective voices truly matter.
BAF: How do you explain the importance of brain aneurysm awareness to people who may not know much about it?
DH: I tell people that brain aneurysms are more common than they realize—and often silent until it’s too late. Awareness and education are everything. When people know the signs, understand the risks, and advocate for early detection, lives can be saved. My goal is to turn my survival into purpose by helping others recognize that what they don’t know could change everything.
In October of 2024, I had the opportunity to share my story on The Portia Show. (watch video below) The show highlighted how brain aneurysms disproportionately affect women and helps explain what brain aneurysms are and what steps can be taken to protect ourselves. Sharing this message on a public platform reinforced my belief that informed communities are empowered communities—and that awareness truly has the power to save lives.
BAF: What does the BAF community mean to you?
DH: The BAF community means hope, healing, and belonging. It’s a family bound not by blood, but by survival and shared purpose. Through BAF, I’ve found a space where my story has meaning and where advocacy can drive real change—from research and legislation to the way aneurysms are classified and treated. It’s a community that reminds me I’m not alone, and that my voice has power.
BAF: If you could share one thing with the world about brain aneurysms, what would it be?
GD: If I could share one thing, it would be that brain aneurysms don’t discriminate—and awareness can save your life or the life of someone you love. Every conversation, every story, every bit of advocacy helps move us closer to a world where no one has to experience the pain, fear, or loss that so many survivors and families endure. Awareness isn’t just important—it’s lifesaving.