TEAM EMILY: thought it was just a headache
In January 2013 our daughter Emily was diagnosed with a rare brain tumor in her pineal gland. It took several complicated surgeries, 9 weeks in the ICU and months of rehab, but she made a full recovery after about eight months.
It’s been 10 years and we will be supporting the National Brain Tumor Society’s NY Brain Tumor Walk on Saturday, September 30, 2023 at Jones Beach. Emily will be speaking at the event as a 10-year survivor.
Please join our team, or consider donating (any amount is appreciated) to help foster awareness and education about brain tumors.
I am uniting with others to make a difference in the fight against brain tumors. I am passionate about this cause, so I’m taking action. I need your help in this fight. National Brain Tumor Society will not rest until a cure exists - but more needs to be done. Please join in my effort!
National Brain Tumor Society is fiercely committed to finding a cure for brain tumors. They are aggressively driving strategic research and advocating for public policies that meet the critical needs of the brain tumor community. Your support ensures this important work will continue.
