Emily's Story
In an instant, everything changed.
Emily is a 21-year-old pre-med student at Boston University who was diagnosed with Glioblastoma Multiforme (GBM), WHO grade IV — the most aggressive malignant brain tumor. It all started in June 2026, when 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 in the Boston University pre-med program, she was rushed to the Neurosurgery Department at Massachusetts General Hospital.
Emergency cranial MRI revealed a 4.2 cm mass in her right frontal lobe with characteristic ring enhancement and perilesional edema. Stereotactic biopsy and molecular analysis confirmed the diagnosis: 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 (subtotal 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, beginning concurrent radiotherapy (30 sessions over 6 weeks) with daily temozolomide in late July. She completed that concurrent phase in early September and has now started her first cycle of maintenance temozolomide. Because MGMT promoter unmethylation confers resistance to alkylating chemotherapy, standard temozolomide offers only limited survival benefit. Her family sought consultation with a specialized center in Germany providing autologous dendritic cell vaccines.