Brain Aneurysm Foundation BAF Changemaker: Geneva Dickerson
Geneva Dickerson of Mount Vernon, NY, at the 2nd Annual Support Conference in Scottsdale, AZ
As Brandon Dickerson’s oldest sister, I want to share my brother’s inspiring journey as a 34-year-old survivor. Born on January 29, 1991, he is the youngest of four siblings and the only boy in our family. Growing up in Long Island, New York, I watched Brandon develop a quiet strength, often showing his feelings through his love of singing and sports.
Before his health challenges, Brandon enjoyed working as a Line Haul Driver. I treasure the meaningful phone conversations we had; he had a special way of making every talk feel easy, his calm presence providing comfort and understanding.
When he became ill, Brandon was living in Louisiana, exploring new opportunities. However, it became important for him to come back home to New York for medical treatment and to be close to family. I am proud to have been there for him during this difficult time, and I admire his strength and courage as he continues to navigate his journey as a survivor. I am grateful for the chance to share his story with you. – Geneva Dickerson
BAF: Tell us a little about your connection with brain aneurysms.
GD: My connection to brain aneurysms is personal and comes from a difficult family experience. It all started when my younger brother, Brandon Dickerson, a 34 year old brain aneurysm survivor, had a ruptured brain aneurysm in March 2022. Watching the severe effects of this life-threatening condition on him has been both traumatic and life-changing. Brandon’s journey as a survivor has opened my eyes to the about advocacy. I aim to raise awareness about this often-misunderstood condition and highlight the need for education and support for families affected by it. The emotional and physical struggles he faces every day inspire me to make sure others know the risks and feel empowered to take action.
BAF: When did you first learn about the BAF?
GD: I first learned about the Brain Aneurysm Foundation (BAF) during my brother’s recovery process. As I navigated the complexities of his condition, I realized the necessity of understanding brain aneurysms and their potential impact. My search for knowledge led me to discover the BAF, whose mission to support research, raise awareness, and provide resources for survivors and caregivers resonated deeply with me. The foundation’s commitment to making a difference in the lives of people affected by brain aneurysms inspired me to engage with their work and to become a part of a community focused on education and advocacy.
BAF: Have you ever participated in any BAF events?
GD: I have taken part in several important BAF events that have strengthened my advocacy work. In 2023, I joined the Brain Aneurysm Foundation’s 5K run/walk and led a team called “Team Brandon,” raising over $3,000 for research and awareness. I have also traveled to Washington, DC, for the past two years for Advocacy Day, where I supported Ellie’s Law, a law named after a brave 14-year-old girl who sadly died from a brain aneurysm. These experiences have deepened my dedication to this cause and connected me with others who are equally passionate. I also attended the BAF’s Annual Research Grant Symposium & Support Conference in Boston and Scottsdale, where I was able to lead my first support conference. These events have allowed me to share stories, learn from medical experts, and build connections within the community. They confirm my belief in the importance of working together for advocacy and support..
BAF: How do you explain the importance of brain aneurysm awareness to people who may not know much about it?
GD: When discussing brain aneurysm awareness, I highlight its importance through my brother’s experience. I explain the significant challenges that come after a ruptured aneurysm and how it can change lives. I also point out that brain aneurysms affect the African American community disproportionately, leading to higher risks and worse outcomes. This emphasizes the need for focused awareness efforts. I stress that early detection and treatment are vital; educating people about the signs and risks can save lives. By promoting awareness, I empower individuals to recognize symptoms and seek help quickly, improving their chances of survival. Ultimately, I aim to foster a culture of awareness and proactive health management for everyone.
2. Ana Metzger- BAF Advocate, Arlicia Albert- Survivor and BAF Board Member & Geneva at the 2025 Research Grant Symposium in Scottsdale, AZ.
3. Christine Buckley, Sharon Epperson – Survivor and CNBC Sr. Personal Finance Corespondent & Geneva at the NBC Studios in Washington, DC during Advocacy Day.
BAF: What does the BAF community mean to you?
GD: The BAF community gives me support, hope, and a sense of togetherness. It brings together people and families affected by brain aneurysms, creating a helpful network for sharing experiences and encouragement. This community allows everyone to talk about their struggles, learn from each other, and find important resources. Being part of this group makes me feel included and reminds me that no one has to face this alone. Together, we work to raise awareness and support research, and I am proud to be involved.
BAF: If you could share one thing with the world about brain aneurysms, what would it be?
GD: If I could share one important message about brain aneurysms, it would be the need for early detection and taking care of your health. Knowing the risk factors, recognizing the symptoms, and seeking medical help right away can greatly improve outcomes for those affected. I encourage everyone to take charge of their health, stay informed, and take preventive steps. This way, we can help reduce the number of brain aneurysms and ensure that those affected get the care and support they need.
To hear more of Geneva’s caregiver journey, watch the video below.