Brain Tumor Awareness Month: How Do We Get From Surviving to Thriving?
As I march into Awareness Month this May as a mother of a brain tumor survivor and an advocate for all pediatric survivors and their parent-caregivers, I have come to the realization that I am simply not feeling it this year. I am at a low in this journey. I will refer to it as battle weary.
Survivors of a Rare Brain Tumor and Their Families Meet Up in Ocean City
Ocean City, MD — Survivors of craniopharyngioma, a rare and complex benign brain tumor, and their families joined together for the inaugural East Coast Cranio Survivors Picnic at Northside Park in Ocean City on Saturday. The group also included spouses, parents, siblings and grandparents, who provide support to each other on Facebook as part of a group page specific to the tumor. The picnic was organized in part by the Raymond A. Wood Foundation (RAWF), whose mission is to provide quality-of-life support for survivors of childhood brain tumors and their families.
RAWF Director “Heads to the Hill”
Washington, D.C. — Amy Wood, director of the Raymond A. Wood Foundation, joined the Maryland contingency to “Head to the Hill” Tuesday with the National Brain Tumor Society to advocate for legislation to fund brain tumor research. Wood is mother to Alex, a 6-year-old brain tumor survivor and kindergartner at Ocean City Elementary School.