Brain Aneurysm Foundation BAF Changemaker: Alison Woodruff
Alison Woodruff from Midland, Michigan.
After experiencing a rupture on May 15, 2018, and navigating a long, challenging recovery, Alison turned that life-altering moment into a source of strength—raising awareness and showing up year after year for the Brain Aneurysm Foundation community. Alison has been attending BAF Michigan Walks over the years, and this year stepped into the role of Event Coordinator, working closely with BAF staff to make this year’s event the first to feature a timed 5K run. Alongside her team, “Team Bucky!,” Alison has helped raise more than $11,000 since 2022 in support of brain aneurysm awareness, research, and support programs. Her story is a reminder of why awareness matters, how resilience can inspire action, and what it truly means to work toward a world without ruptures.
BAF: Tell us a little about your connection with brain aneurysms.
AW: A little about me – my connection with brain aneurysms is deeply personal. I am a survivor of a grade five brain aneurysm rupture. Going through that ordeal and the long road of recovery has given me a profound appreciation for the value of awareness, early detection, and support. The journey was incredibly challenging, but it has also become my source of strength and motivation to give back.
BAF: When did you first learn about the BAF?
AW: I first learned about the Brain Aneurysm Foundation in the summer of 2019. A family friend had told me about the Michigan 5K that was to be held in Clare, MI that following May and said that she would let me know the details when they were available. Being a survivor, I wanted to help support this worthy cause. I registered and raised money. I have done so every year since! And now, the Michigan 5K will be held in my hometown, Midland, Michigan.
BAF: Have you participated in any BAF events? What did that experience mean to you?
AW: As mentioned previously, yes, it has become a passion of mine to participate in the Michigan Brain Aneurysm 5K since 2019. My family and I look forward to it every year. Being a survivor, I am passionate about helping others and raising money to do so. It really makes me feel that I am giving back.
BAF: How do you explain the importance of brain aneurysm awareness to people who may not know much about it?
AW: I usually start by sharing that brain aneurysms are more common than many people realize—and that they often have little or no warning. I’m living proof that this can happen to anyone. I was 39 years old, and my son was only 11 years old at the time. Awareness matters because recognizing the signs of a rupture and taking symptoms seriously can save a life, and knowing your family history and risk factors can lead to conversations with a doctor before an emergency happens. I also emphasize that awareness leads to research and education—so fewer families have to experience what mine did.
BAF: What does the BAF community mean to you?
AW: The BAF community means hope, understanding, and connection. It’s a place where survivors, caregivers, and families don’t have to explain the unexplainable—we’re simply understood. Being part of this community reminds me that I’m not alone, and it gives purpose to my experience. It’s also incredibly motivating to see people show up—walking, running, donating, and sharing stories—because it turns something scary into something powerful: support, action, and progress.
BAF: If you could share one thing with the world about brain aneurysms, what would it be?
AW: Please don’t assume “it could never happen to me.” Brain aneurysms can be silent, and a rupture is a medical emergency. If you ever experience a sudden, severe headache—especially one that feels different than anything you’ve had before—go to the nearest emergency room! Trust your instincts and seek care immediately. Being a survivor, my word of advice is, hug your loved ones every chance you get. Every day is a gift.