Real stories from people and families affected by ganglioglioma.
Here you can read and listen to personal experiences of symptoms, seizures, diagnosis, brain surgery, treatment, recovery and life after a ganglioglioma diagnosis.
Gangliogliomas are rare, usually slow-growing brain tumours made up of both nerve cells and supporting glial cells. They are most often found in children and young adults and are commonly linked with seizures, especially when they develop in the temporal lobe.
Every person’s experience is different. These stories are shared to help others understand what living with a ganglioglioma can involve and to help people and families affected by this rare diagnosis feel less alone.
Browse the stories below and hear directly from people and families affected by ganglioglioma.
