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Latest News and Stories
Elizabeth's Journey - From a 1% Chance of Survival After a Brain Aneurysm Rupture to Supporting Others Through Advocacy
"I have 75 percent of a brain left," she says. "But I think my brain is better now than it ever was before my stroke. We have to make the most of what we have got, rather than worry about what we haven't. If I can help just one person feel less alone, then it's worth it."
Living With Scan Anxiety: A decade after my first brain aneurysm scan, it still takes work
“Scan‑anxiety” is real. Wherever you are in your journey - newly diagnosed with a brain aneurysm, years into monitoring, post‑treatment, or supporting someone you love - your feelings around scan time are valid. They are shared. And you are not alone.
Families living with familial (hereditary) brain aneurysms: Lily George’s research
Research study exploring what it means to live with familial (hereditary) intracranial aneurysms (FIAs) by Lily George, MSc Genetic and Genomic Counselling at Cardiff University
Introducing our new Patient and Family Brain Aneurysm Advisory Panel – Your Community Needs You!
Hereditary Brain Aneurysm Support is proud to launch the Patient and Family Advisory Panel (PFAP), a new voluntary group bringing together the voices of people and families affected by brain aneurysms to help shape the future of our work.
We Need Your Support Today!
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