“I’ve had the medication for weeks,” she wrote in an op-ed for CNN. “I am not suicidal. If I were, I would have consumed that medication long ago. I do not want to die. But I am dying. And I want to die on my own terms.”
On New Year’s Day, Maynard, 29, was diagnosed with brain cancer. Nine days later, doctors performed a partial craniotomy and a partial resection of her temporal lobe to keep her tumor from growing. She was given up to 10 years to live. Then in April, doctors learned that the tumor had returned. Her initial diagnosis was elevated to a stage 4 glioblastoma, a malignant brain tumor. And the prognosis was grave — only six more months.
Maynard qualified for physician-assisted suicide in Oregon, one of a handful of states that permits it under its Death with Dignity Act. Since it was enacted in 1997, 1,173 people in the state have had prescriptions written for lethal medications. Only 752 of them have used the drugs to die as of 2013.
Four other states — Montana, New Mexico, Vermont and Washington — have similar laws. Bills have been introduced in seven other states.
Maynard was living in San Francisco with her husband, Dan Diaz, 42, when she began having debilitating headaches and soon learned the cause: brain cancer. Doctors explained her options, none of which would save her life.
“Doctors prescribed full brain radiation,” she wrote in the op-ed. “I read about the side effects: The hair on my scalp would have been singed off. My scalp would be left covered with first-degree burns. My quality of life, as I knew it, would be gone.”
She also looked into hospice care. However, there were no guarantees she wouldn’t suffer — she could lose her ability to speak or use her own body. And, because she is so young, she could physically hold on for a long time.
“After months of research, my family and I reached a heartbreaking conclusion,” she wrote. “There is no treatment that would save my life, and the recommended treatments would have destroyed the time I had left.”
That’s when Maynard chose doctor-assisted death. But California, like most states, does not have a law that allows terminally-ill patients to end their lives. So earlier this year, she and her family relocated to Oregon.
Maynard had to find new physicians and a new home. She had to change her driver’s license and voter registration. Her husband had to take a leave of absence from work.
“The amount of sacrifice and change my family had to go through in order to get me to legal access to death with dignity – changing our residency, establishing a team of doctors, having a place to live – was profound,” she told People. “There’s tons of Americans who don’t have time or the ability or finances and I don’t think that’s right or fair.”
Maynard is using her last days to help others in similar situations, volunteering for Compassion & Choices, an advocacy organization for terminally-ill patients in California, Colorado, Connecticut, Massachusetts and New Jersey. She has launched the Brittany Maynard Fund to fight for death-with-dignity laws in other states. Later this month, she plans to videotape a testimony for California lawmakers and voters, People reported.
Some opponents of physician-assisted suicide have cited moral and religions concerns. Others worry that patients who are depressed will use such laws to end their mental anguish, among other things. In a poll conducted by the New England Journal of Medicine last year, about 67 percent of the 1,712 medical experts surveyed in the U.S. were against the practice. But Diaz said it’s a comfort knowing that his wife has the option.
“Death with dignity allows for people who are in the predicament of facing a lot of suffering that they can decide when enough is enough,” he said in a campaign video.
Maynard has the option to change her mind, she doesn’t think she will.
“Now, I’m able to move forward in my remaining days or weeks I have on this beautiful Earth, to seek joy and love and to spend time traveling to outdoor wonders of nature with those I love,” she wrote. “And I know that I have a safety net.”