Educating Others With Clinical Knowledge and Personal Experience


Although a gynecologic oncologist has spent a good part of her career helping patients during their cancer journeys, she took it upon herself to take one step further to educate women on how they can advocate for themselves and potentially prevent cancer before it impacts their lives.

Dr. Valena Wright has specialized in gynecologic oncology for the past 25 years. When her sister, Debbie, received a diagnosis of ovarian cancer, she gained a new perspective on what patients and their families go through throughout the process.

Unfortunately, her sister died from ovarian cancer, but Wright used this opportunity to teach others what can be learned from her sister’s experience by writing her book “It’s Time You Knew.” In the book, Wright speaks with her own patients about their cancer journeys, discusses major takeaways from their experiences and explores ways to potentially reduce their risk for cancer, among other topics.

CURE®spoke with Wright to learn what women need to know to protect themselves from women-related cancers and the importance of potentially preventing cancers versus treating it.

CURE®: What inspired you to write your book?

Wright: My family story really inspired me to write the book. I'm a gynecologic oncologist, so I've trained both in obstetrics/gynecology and then (did my) fellowship in women's cancer surgery and chemotherapy. I take care of women that have different gynecologic cancers, which include ovarian cancer, uterine cancer, (cervical) cancer, vulvar cancers, those are the most common. When you study and practice all of these years, and a member of your family is diagnosed with ovarian cancer, which is the most serious or difficult to treat, I got to see things from a different perspective. I learned so much from being with my sister during her battle with ovarian cancer. I was disappointed in some of the interactions that she had with the medical system. And I thought, if I wrote our story, it could help other people avoid some of the same problems. There are a lot of things about ovarian cancer that aren't well understood, but the more that women understand and know about ovarian cancer, I hope it helps them to learn what they can do to avoid ever having to deal with that diagnosis.

What were some of the things that you wish were different with your sister’s communication with her doctor, and what do you want women to take away from this book?

A lot of times with ovarian cancer, it's really difficult to diagnose. … It can take up to two years for women to have symptoms before they get diagnosed. And it's always been controversial, whether the symptoms aren't clear, if there are no symptoms that are recognized early or if it's a problem (related to cysts).

When my sister was first diagnosed, she was living in Germany and she was told she had an abnormal cyst on the ovary. She didn't follow up right away because she's in the middle of traveling. When she came back to Canada, a follow-up ultrasound showed the cyst had enlarged dramatically. Because of that, her doctors recognized something was really wrong and that she should have surgery.

With ovarian cancer, some of the symptoms are very subtle like (an) increase in urinary frequency. … Often the symptoms are more related to digestion, like a little bit of bloating, feeling full. (With) these symptoms, people don't think of the ovary. If people have those symptoms, they end up sometimes being triaged into gastroenterology, to colonoscopies, to urology, but people don't think about it in the differential diagnosis.

There are some tests that can help diagnose ovarian cancer. Ultrasound and a tumor marker called CA 125 are our two best tools. If (my sister) had understood the importance of follow-up at that first visit, maybe she wouldn't have had a delay. I think it was six months from her first abnormal ultrasound to follow up. Part of that was not having symptoms that she recognized, but even if you have no symptoms or no recognized symptoms, sometimes medical tests will come back abnormal. Just because you feel fine doesn't mean you should ignore an abnormal medical test; it means something requires follow up, and not (following) up can put your health at risk.

When someone has ovarian cancer, they should consider genetic testing. The reason for that is up to 20% of ovarian cancers have a familial component. If you do genetic testing, you can identify yourself as being at increased risk if you have (what) we call it a deleterious gene mutation. Debbie didn't have (genetic testing) with the (other) testing that was done. It was several years ago, so the testing is better now. But family history alone, even without genetic testing, shouldn't be ignored because there's some gene mutations that we just haven't studied or identified as being deleterious yet.

With that knowledge, in women who are at high risk for ovarian cancer (and) have a gene mutation, you can do risk-reducing surgery to decrease the risk of ovarian cancer, which is removal of the fallopian tubes and ovaries. Fortunately, my younger sister Shirley did that and was so lucky to be diagnosed when she had no symptoms with a very early precursor to ovarian cancer. It's called fallopian tube carcinoma in situ, which is a really small, microscopic tumor in the fallopian tube that is impossible, really, to diagnose. When researchers looked at women with gene mutations who were undergoing this risk-reducing surgery, it was discovered that a lot of the what we call ovarian cancer actually starts in the distal end of the fallopian tube as a microscopic lesion. It spills those cells into the abdominal pelvic cavity. And those cells can land on the ovary creating a mass that is then attributed to the ovary, even though it really started in the fallopian tube.

She was very fortunate she didn't require any further treatment or chemotherapy. I'm so glad she's with us today because of that. One of the frustrating things, though — as I do as an oncologist, I was encouraging her to do that. She was concerned about side effects of menopause, and she delayed (surgery) for several years. When she pursued it, it was when she was getting close to the time of menopause, but her general practitioner told her it wasn't necessary. Other people told her it was necessary. … Because we know so much more now, it's really important to be an advocate for your own health and consider genetic testing.

There's a lot we're learning based on genetics and advances in the field. It's hard for all doctors to keep up on different aspects of care. If you do have a positive family history, it's really important to talk about it with your family members and see if you qualify for genetic testing. It doesn't mean you have to have risk reducing surgery, but perhaps it will mean that you would be screened differently. And if you don't know or if you don't explore that option, you might miss an opportunity that could actually have a huge impact and save your life.

That background is really the motivating factor for me to write this book, because I really want women to understand their risk and what the options are to do something about it.

Throughout your book, you focus on a variety of women-related cancers. Why do you find it so important to cover this topic with a broader approach?

The numbers of women affected by breast cancer is higher than the number of women with these other cancers. When we look at health and health outcomes, medicine wants to divide everything up into body parts or different areas, but our health is really a constellation of many things and it's not divided down by one system. I think obesity is such a good example of that because it affects all of our body parts in different ways. There's risk of obesity and the comorbidities that we've seen associated with it. Even the COVID-19 pandemic highlights that.

Having more of an emphasis on health and lifestyle interventions to prevent risk rather than waiting for cancer to develop and playing catch up is really another reason I thought this book was is really important. Nobody wants to be diagnosed with cancer, and it's not just being diagnosed with cancer, it's the ability to have good health. That's probably our most important asset because without good health, we're really limited in our ability to enjoy life in many different ways. Knowing over time (the) actions that you can take to prevent cancer over a lifetime, it really adds up.

This interview has been edited for clarity and conciseness.

To hear more of our conversation with Dr. Wright, listen to the episode of the “CURE® Talks Cancer” podcast.

For more news on cancer updates, research and education, don’t forget to subscribe to CURE®’s newsletters here.

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