In 2009, world-renowned oncologist Dr. Vincent DeVita was diagnosed with advanced prostate cancer. Dr. DeVita – who developed the first chemotherapy for Hodgkin’s lymphoma and wrote the book on The Death of Cancer – simply froze. He was paralyzed with shock.
Eventually, Dr. DeVita appointed a care champion to advocate on his behalf. But his story illuminates a major challenge in oncology: a cancer diagnosis is emotionally crippling, no matter who you are or what you know. And when we consider complex challenges with health literacy, cultural nuances, and the sheer logistics of navigating care, one thing is clear.
The current system places undue and unjust burden on patients and their loved ones as they face one of the worst experiences imaginable.
When all is said and done, life-changing medicines are useless if they cannot reach the patients who desperately need them. Change is needed to close the gaps for patients, physicians, and the system itself.
Today, despite major gains in access to health information, cancer leaves many patients feeling powerless and lost. According to All.Can, a not-forprofit organization dedicated to improving the efficiency of cancer care: