When I started my nursing career in the 1960s, we did what we could to keep our heads above water. After graduation, you’re still…
In 2012, Emily Ward was diagnosed with pleural mesothelioma, a rare cancer that usually comes with a grim prognosis. She was in and out of remission twice but continued to fight for nearly 10 years. Although Ward died in 2022, her story continues to inspire other survivors of this asbestos-related cancer.
Although Ward spent 43 years as a registered nurse, she never met anyone with malignant mesothelioma cancer. It was a disease she had heard of over the years but didn’t know much about.
As Ward got older, she considered the possibility of developing cancer, but couldn’t imagine she would be one of the roughly 3,000 mesothelioma cases diagnosed in 2012.
She never worked the blue-collar jobs typically associated with this cancer. Asbestos exposure from a renovation of the hospital Ward worked at in the 1970s led to her mesothelioma decades later.
After her diagnosis, Ward didn’t ask, “Why me?” She realized there was nothing she could have done to change things. Instead, she started asking questions about treatment and how to fight back.
Shortly after her diagnosis, Ward discovered The Mesothelioma Center at Asbestos.com. As a nurse she found the website easy to understand and felt the site comfortably guided her through valuable mesothelioma information.
Ward connected with Karen Selby, a registered nurse at The Mesothelioma Center, who gave her information about treatment options in Boston and mesothelioma expert Dr. David Sugarbaker.
Her interactions with Selby resonated with Ward. She kept reconnecting with her because it was comfortable as a nurse to talk to another nurse about her mesothelioma diagnosis. They kept in touch over the years, and Selby inspired Ward to help fellow mesothelioma survivors overcome the challenges of their diagnosis. Becoming an Advocate
Ward began blogging about her experiences with mesothelioma for The Mesothelioma Center at Asbestos.com in November 2018. While challenging at times, she felt it was important to share her journey to connect and hopefully inspire other mesothelioma survivors.
Ward understood that living with mesothelioma wasn’t easy. Whether dealing with side effects of treatment, driving two hours to Boston for immunotherapy infusions, or learning how best to communicate with friends and family about her cancer, every week living with this disease presented a challenge.
Her best advice: Advocate for yourself, make decisions based on your quality of life and do what makes you happy.
The next step in Ward’s advocacy efforts was raising awareness about this rare cancer. She knew more research was needed to find a cure. She also knew it was imperative that people at high risk for mesothelioma speak up and share their history of asbestos exposure so they can get diagnosed earlier when treatment is more effective.
Living in rural Maine, Ward knew firsthand that most doctors had never treated a mesothelioma patient. They didn’t see the warning signs or know how to look for them, which led to many misdiagnoses. By increasing awareness, Ward helped change that.
More media coverage is needed to continue the discourse about mesothelioma and the dangers of asbestos exposure.
Ward belonged to a group of cancer patients who live with a grim prognosis. She knew every new study provided more encouragement for a cure, novel mesothelioma treatment option approvals and inspiring survivor stories.
Connecting with The Mesothelioma Center allowed Ward to share her story with others and shine some light on a dark disease. She was eager to share her experiences with anyone willing to listen, and her life continues to inspire and provide hope.
Press Inquiries: wpacheco@asbestos.com
When Emily wrote about her experiences, she hoped to inspire other survivors of mesothelioma who could relate to the physical and mental hardships of this cancer. She emphasized the importance of spending time with family, tending to her garden and doing whatever else made her happy. She made the most of her time and celebrated every day as if it were a holiday.
When I started my nursing career in the 1960s, we did what we could to keep our heads above water. After graduation, you’re still…
Late last year, I began a new treatment at a new facility. The medications were Opdivo and Yervoy, an immunotherapy combination recently approved…
Ward’s research on mesothelioma led her to Brigham and Women’s Hospital in Boston, where she met mesothelioma expert Dr. David Sugarbaker.
She credited Sugarbaker’s pleurectomy and decortication surgery for saving her life. Sugarbaker died six years after that procedure, and Ward expressed the utmost gratitude to him for giving her years of life most mesothelioma patients aren’t promised.
Through Brigham, Ward connected with her medical oncologist, Dr. David Jackman, at Dana-Farber Cancer Institute. He worked with her to find a treatment regimen that best fit her needs. After three rounds of chemotherapy, she started the immunotherapy drug Keytruda in April 2019 and later switched to Opdivo and Yervoy in 2020 before discontinuing treatment.
Ward’s experience with Sugarbaker and Jackman taught her the importance of working with doctors who specialize in treating this rare cancer.
To me, if you want top-notch care, you go where the research is being done.Emily WardMesothelioma Survivor
According to Ward, being diagnosed with mesothelioma completely changed her perspective on life. No longer did she worry about the hubbub surrounding holidays. Instead, she treated every day as if it were a holiday.
Ward encouraged every mesothelioma patient to do what made them happy. She believed in cherishing moments spent with family and friends and not getting lost in the details.
“Learn to say no to things you don’t want to do,” said Ward. “Don’t be afraid to ask questions or ask for help. And don’t worry about questioning your doctor or seeking a second opinion.
“It’s your health. It’s your life,” she added. “Make the best decisions for you, and deal with your cancer one scan at a time.”
Stay up-to-date on treatment, research, clinical trials, doctors and survivors
The information on this website is proprietary and protected. It is not a substitute for professional medical advice, diagnosis or treatment. Any unauthorized or illegal use, copying or dissemination will be prosecuted. Please read our privacy policy and terms of service for more information about our website.
This website and its content may be deemed attorney advertising. Prior results do not predict a similar outcome.
The Mesothelioma Center’s claim as the most trusted resource is based on our more than 150 5-star Google and BBB reviews. Our organization also helps more than half of all mesothelioma patients annually diagnosed.
Your web browser is no longer supported by Microsoft. Update your browser for more security, speed and compatibility.
If you are looking for mesothelioma support, please contact our Patient Advocates at (855) 404-4592
Our fact-checking process begins with a thorough review of all sources to ensure they are high quality. Then we cross-check the facts with original medical or scientific reports published by those sources, or we validate the facts with reputable news organizations, medical and scientific experts and other health experts. Each page includes all sources for full transparency.
Please read our editorial guidelines to learn more about our content creation and review process.