In 2004, Kimberly Chapman suffered two ruptured brain aneurysms and was astounded by the lack of public awareness and sparse research of such a widespread and often fatal condition. Recognizing the need for brain aneurysm advocacy and other types of vascular malformations of the brain, she personally established several international support networks to provide information, resources and motivation for survivors and family members. Kim has created a patient advocacy program inside The Joe Niekro Foundation which offers patients and caregivers educational information along with a huge amount of resources to find help.This mission with the Joe Niekro Patient Advocacy Program is to help survivors realize that recovery is possible and will help patients learn what to expect during the healing process and new coping strategies.