Emily's Story
In an instant, everything changed.
Emily is a 21-year-old pre-med student at Boston University, dedicated to training as a neuro-oncologist. In June 2026, she began experiencing persistent morning headaches accompanied by nausea and blurred vision in her left eye. On June 20th, after a seizure during a lecture at Boston University's pre-med program, she was rushed to the Neurosurgery Department at Massachusetts General Hospital.
Emergency cranial MRI revealed a 4.2 cm heterogeneously enhancing lesion in the right frontal lobe with perilesional edema. Stereotactic biopsy and molecular analysis confirmed: Glioblastoma Multiforme, IDH-wildtype, WHO CNS Grade 4, with an unmethylated MGMT promoter — the most unfavorable molecular subtype, meaning reduced response to chemotherapy.
"I wanted to become a doctor to help people. Now I'm learning what it means to be a patient — and how unbearable it is to know that a treatment exists that could save you, but you can't access it. Every donation isn't just money — it's time. Time I get to keep living. If I make it through this, I promise to dedicate my life to neuro-oncology, so no one else has to go through what I'm going through."
Emily underwent partial surgical resection on July 10, 2026 at Mass General — complete removal was not possible due to the tumor's proximity to functional speech areas. She then followed the Stupp protocol with concurrent radiotherapy and temozolomide. Her doctors were honest: with unmethylated MGMT, response to temozolomide is expected to be limited. Median survival with standard treatment is 12-15 months. Her family identified a specialized dendritic cell immunotherapy program at a certified oncology center in Germany — a treatment not covered by any insurance plan in the United States.