Personal stories from the pages of Narrative Inquiry in Bioethics
To read stories from parents who have faced the challenges associated with a childhood brain tumor, click here.
"Deeply moving and fierce, with hope on every page."
-- Terra Trevor, author and Voices contributor
A family's emotional lifeline when a child is diagnosed with a brain tumor
We Can brings together families of children diagnosed with brain tumors in order to share information and pesonal stories, allowing young patients, their siblings and parents to nurture and empower one another to face treatment, recovery, long-term survival, end-of-life issues or bereavement. Our programs include:
hospital and clinic visits
Kidshops for patients and their siblings
teen and young adult group activities
parent education and support meetings
"I have had the privilege of working with We Can and have come to recognize how indispensable this organization has become to children with brain cancer and their families."
-- Jonathan Finlay, MD, past director, Neural Tumors Program, Children's Hospital Los Angeles
Based in Los Angeles and serving all of California, We Can includes families with newly diagnosed patients, those with children and teenagers who are still in treatment and recovery, and those with older children who were treated more than a decade ago. Our network also includes families who have experienced end-of-life care, death and bereavement.
"We Can has been a critical team member caring for our brain tumor patients, survivors and their families by adddressing their unmet psychosocial needs... and has allowed UCLA to be one of the few pediatric oncology centers that is caring for the 'whole' child."
-- Jacqueline Casillas, MD, MSHS, Director, Life After Cancer Clinic at UCLA's Jonsson Cancer Center
The Marion Rose Foundation
The Linda Tallen and David Paul Kane Education and Research Foundation
We Can is a project of Community Partners, a 501(c)3 nonprofit organization.
(c) 2014 We Can. All Rights Reserved