Who We Are
Our mission is to fight ovarian cancer on all fronts
Education – uniting and educating individuals, the medical community and organizations about the symptoms and risk factors for ovarian cancer to achieve earlier diagnosis, better treatment and ultimately a cure.
Advocacy – working with policy makers at the local, state and national levels to ensure the needs of women with ovarian cancer are met. We advocate for adequate and sustained funding for ovarian cancer research, awareness programs, legislation that improves quality of life and access to care for cancer patients.
Support – creating and promoting resources for support, networking and education for women diagnosed and their families.
•We publish a comprehensive resource guide for women on Cape Cod and the Islands diagnosed with ovarian cancer.
• Renee’s Fund – a financial assistance program for ovarian cancer patients.
• Survivors Teaching Students® – a chance for survivors to share their stories with medical students to increase understanding of ovarian cancer symptoms and risk factors so that they can diagnose the disease when it is in its earlier, most treatable stages.
• Bags of Hope and Comfort – complimentary bags include information and items intended to provide support and comfort to Cape Cod and Islands women who receive an ovarian cancer diagnosis.
On April 21, 2010 life seemed “normal”, until I found my mother laying on her living room floor, confused and hallucinating. We called 911 and took her to the emergency room. After four long hours of waiting and wondering, we got a diagnosis…a metastatic brain tumor. Everyone assumed it was a result of her breast cancer returning 8 years later. A few days following the surgery to remove the tumor the pathology came back. It was NOT breast cancer but was in fact ovarian cancer. The tests were even repeated as ovarian cancer rarely spreads to the brain.
The results of a full body scan showed cancer in various lymph nodes, chest, hip, shoulder and liver. Her oncologist was cautiously optimistic yet really would not talk about a timeline, but a year or better seemed to be the consensus. We were told that she could not start chemotherapy until the 6 week mark when she completed the radiation treatments for the brain tumor.
Two weeks after brain surgery her hip broke by simply standing up as a result of the tumor at her hip and she needed femur replacement surgery. She then spent a few days in the hospital and then a week in a rehab facility before returning home.
The following week we went to the doctors to have her chemotherapy port put in and I noticed she was acting more confused again. Her oncologist did some blood work and we went home. The next day was even worse and I called the doctor to get the blood test results. I was informed my mother was suffering “multiple organ shutdown” and it was suggested I call in hospice.
My mother passed away 3 days later, 1 day before she was scheduled to begin her chemotherapy and 5 weeks after being diagnosed.
I think about the symptoms she complained of – bloating, incontinence, bowel irregularities, reflux, shoulder & hip pain and yet – who would have ever guessed cancer? I think about the diagnoses she’d been given, irritable bowel syndrome, gastroesophageal reflux disease (GERD) and menopause. Since making ovarian cancer awareness my goal in life, I’ve heard the same story over and over again and every time I want to cry because almost every time women didn’t know what they needed to save their lives!
~ Diane Riche, Founder/President