This article is more than 4 years old.

Halifax doctor agrees endometriosis should be treated like cancer

New study published in Canadian medical journal says endometriosis patients should be taken more seriously

5 min read
caption Photo illustration of someone experiencing endometriosis pain
Lesli Tathum

Jennifer Sheppard never thought she would see herself having to have a hysterectomy at the age of 35.

She was 12 years old when she was told she might have endometriosis, a condition affecting one in 10 women. She was given the choice to start birth control but at the time her father said no.

“He just didn’t understand,” she said.

Over the years the speculation grew, and in 2008 she had her first surgery, an abdominal laparoscopy. This is a procedure that requires cutting small incisions in the abdomen and pelvis with a camera. The doctor actually diagnosed her with endometriosis, but never told her, until she found out from another doctor 10 years later. The diagnosis was mentioned in a footnote of the 2008 surgical report.

Related stories

“I had zero quality of life,” Sheppard recalled.

Ten years later, Sheppard lost her business due to the severity of her pain. She made an appointment with a local doctor in Cape Breton.

“I said to them ‘Either I am pregnant or I have a tumor,’” she said.

After an ultrasound, she was told for the first time she had endometriosis and cancer.

The World Endometriosis Society (WES) website describes it as “a condition in which tissue similar to the lining inside the uterus (called “the endometrium”), is found outside the uterus, where it induces a chronic inflammatory reaction that may result in scar tissue.”

WES states that symptoms of this condition include “painful periods, painful ovulation, pain during or after sexual intercourse, heavy bleeding, chronic pelvic pain, fatigue, and infertility.”

In 2018, Sheppard had surgery to remove an endometrioma, a cyst that forms on the ovary due to endometriosis. According to the WES, these cysts are not cancerous and can be found in 17 to 44 per cent of endometriosis patients and can create infertility.

Dr. Elizabeth Randle, a Halifax gynecologist, performed two of Sheppard’s surgeries. Randle said the wait time to meet with a gynecologist in Halifax is about nine months.

Sheppard thought all her problems were solved until she found herself in the operating room only six month later. She had hydrosalpinx, a blockage in the fallopian tube. She had the tube removed.

“I was a rapid regrower, so basically all of the adhesions and endometriosis that Dr. Randle removed was back,” she said.

She said she felt no relief.

‘I couldn’t do this anymore’

She said she and her husband tried to preserve her fertility as they had no children, but last month, she found herself back in the doctor’s office in Cape Breton.

“I told her I couldn’t do this anymore, so I had a radical hysterectomy at age 35,” she said.

Last month, an article was published in The Journal of Obstetricians and Gynaecologists of Canada (JOGC) by Dr. Mathew Leonardi, a gynecologist currently practicing in Australia. He said that endometriosis patients should experience the same care as a patient with gynecological cancer.

“We, as a medical system, are failing people with endometriosis,” Leonardi said in the article.

Leonardi said since endometriosis is non-cancerous, it has gone “under the radar” and has not required a gynecological specialist. He said the medical system should create an integrated multidisciplinary program to help those with endometriosis. The program would include: pain specialists, psychologists, physiotherapists and other specialities to help endometriosis patients.

He said “until endometriosis care is considered as high a priority as gynecological oncology management and this care predominantly takes place in centres of expertise…we will continue to fail our patients.”

Randle agrees. She said treating endometriosis patients as a more complex issue like cancer would work more effectively.

“I would 100 per cent agree that endometriosis patients will find better outcomes when treated with multidisciplinary expertise,” she said.

caption Dr. Mathew Leonardi is a gynecologist currently working in Australia.
Courtesy of Dr. Mathew Leonardi

Randle said endometriosis is a form of chronic pain and is not always seen as an urgent matter. She also said Nova Scotia currently does not have multidisciplinary programs for pelvic pain. There are only chronic pain clinics that cater to a variety of pain patients. This results in very long wait times.

Randle said she and Dr. Allana Munro, an anesthetist, received a Translating Research Into Care (TRIC) grant from the IWK Foundation to look into an integrated multidisciplinary program for chronic pelvic pain patients at the IWK Health Centre.

They hope to supply a program that will integrate gynecologic management and chronic pelvic pain from an anesthesia, physiotherapy and psychological standpoints.

In a Twitter message to The Signal regarding his recent journal article, Leonardi said “The response has been outstanding. There was such a demand to read the full article from people on social media and ResearchGate that JOGC made the article free access.”

He said there are two things that need to happen in order for places to make this change in management. First, there needs to be more training for the managing of endometriosis and other complex gynecological problems. Second, those without specific training and skill need to learn “it is better for the patient if the patient is referred to someone with expertise.”

“Regular residency training may be okay to manage some patients with endometriosis, but it is not enough for a lot of patients,” he said. “Our traditionally taught clinical and diagnostic tools are inadequate to aid gynecologists in determining whether a patient is actually an appropriate patient for them to treat.”

Sheppard said her hysterectomy was life changing, and for the first time in 23 years she has been without pain. She said she was aware of Leonardi’s article and had heard about it in passing.

“I think he is exactly right,” she said.

Share this

About the author

Lesli Tathum

Lesli is from the Cayman Islands. She is in her fourth year of journalism at the University of King's College and is a member of the King's Women's...

Have a story idea?

Join the conversation

  1. A

    Alena

    I have suffered with severe Endometriosis since 1991, and was diagnosed by laparoscopy in 1994 with stage 4 Endometriosis. I had just completed my masters degree in school counseling and as a teacher, couldn’t even stand up to lead my class any longer. We tried IVF, multiple rounds, after 6 months of Lupron (chemotherapy drug) which made it worse Plus added fibromyalgia, CFS, and restless leg disorder to my list of conditions. . I would pass out regularly from the pain but each doctor I visited only would prescribe ibuprophen and antidepressants. Then one doctor said she thought it had become cancerous, in 2003, and did an emergency surgery where I woke up with no ovary on one side because she thought it was a cancerous tumor. It wasn’t. I also developed a staph infection with high fever a week after that one and almost died, waiting in the ER for 21 hours in horrible pain, vomiting and screaming for them to please help me. I was admitted and placed on strong antibiotics for weeks to help me fight the infection. After that my health went downhill. I have been to 29 ob-gyn doctors in the past 25 years. None of them helped me with pain. My husband left for a younger, more fertile wife. I was alone with our two adopted kids and couldn’t work. Now I am starting menopause and am bedridden for two years. I am on strong opioids to be able to get out of bed and outside once a week. It hurts to digest my food because it has grown throughout my abdomen with adhesions binding everything together in my bowel. It seems to be never ending. I’d i could just call it ‘cancer’ others would sympathize more, because the level of pain in cancer is nothing compared to this. I was never able to get pregnant but my current husband has never known me without this pain. He is a wonderful caregiver. My daughter stopped speaking to me 8 years ago because she said she was ‘tired of being around sick people.’ There is nothing but loss after loss with this disease. It’s good to see doctors taking it more seriously. It’s manmade from all the plastics, chlorine, and toxins in our food and water supply. Only diet change and supplements seem to make any difference at all in whether or not I am able to get out of bed each morning.
  2. S

    SMH

    I was fortunate enough that my gynecologist knew what endometriosis looked like and diagnosed me while removing my fallopian tubes due to hydrosalpinx. Unfortunately he prescribed medication (vissane and orlissa) instead of referring me to a specialist. Luckily I found Nancy's nook on Facebook not long after being diagnosed and i started researching. I immediately requested and recieved a referral to an excision specialist 2.5 hours away (the closest specialist) but the wait time is 18-36 MONTHS just for a consult let alone a surgery date. I fear the progression of my endometriosis and the symptoms it brings while I wait. We need more excision specialists in Canada. We need physicians to be better informed about this disease and the medication they prescribe that only mask the symptoms. Just because the pain may be gone while on the meds it is not a "win" while our bodies potentially endure the horrid long term side effects. I am one of the lucky ones who was diagnosed early and taken seriously right from the start but my journey with endometriosis is far from over. I agree with Dr. Mathew Leonardi in that endometriosis patients should experience the same care as a patient with gynecological cancer. Thank you for writing this article.
  3. M

    Missy

    Dr Randle performed my hysterectomy for Adenomyosis and dense adhesions caused by c-sections and endometriosis. I am thankful for her work, and efforts to increase and diversify the care,but Nova Scotia has a long way to go! I was brushed off for 11 long agonizing years!! Even by a different doctor at the IWK in 2009! I have missed out on so much of my life suffering debilitating pain. I am also very thankful for Nancy Peterson's work through her FB page: Nancy's Nook Endometriosis Education, it has been a wealth of useful information to make smart decisions about your own healthcare. We must be advocates for ourselves!
    • n

      nancy petersen

      Missy, thanks for your comments, can you send me in. a PM in Nook, Dr Randle's address or if she is on Facebook, alert her to Nook, we have now many physicians who have joined after AAGL and since they are looking at a multidisciplinary approach there may be others doing this that she would benefit from liking up with. thankss
      • M

        Missy

        Will do!
  4. L

    Lada Phillips

    I live in Moncton, New Brunswick. I grew up in Saint John. I doubled over in pain as a teenager and told yo calm down that I was having a miscarriage. My mother slapped me... I was a virgin. Later I was told it was a cyst. My doctor had me on different birth control pills to help with my periods. I’ve always had horrible periods. My nurse practitioner told me no one likes them, exercise and loose weight, I would avoid paps; they left me in tears. Again, told that no one enjoys them. I started dating my husband and was put on depot shots. I was told because of my Mom and family history with breast cancer they this was my only birth control option. I gained major weight, on top of already being obese. I had lapband surgery; went off depot. Had an IUD; oh the pain, Removed the IUD to try and start a family,.. no luck. 2017 had the lapband removed and had gastric bypass, On my own and with weight loss surgery I’ve lost 170lbs. When we tried again for children, we were referred to Conceptia. We waited a whole year and got there on my 40th birthday. I was asked about endometriosis and I said I didn’t know. I started to advise my history of infertility, pain with sex, horrible periods. I was told that if I had endometriosis I would know. My husband and I decided not to pursue IVF for financial reasons. A few months later I started bleeding from my belly button. After a year of blood work, X-rays, various versions of ultra sounds, and a biopsy, I was referred to gynaecologist got the first time in my life. Who said I most likely have endometriosis. He attempted an internal exam that cause me to scream and instant tears. He put me on Zoladex and said 6 months will dry up the endometriosis and I’ll be cured. Those 6 months... I was pain free and no periods, I had hot flashes, moods, no sex drive. Honestly because of the pain; I’m not a fan of sex. Well, 6 months up.., 2 months later and my period comes back with all the pain and bleeding belly button,. It’s even worse now because after pain free for 6 months it’s hell. Now waiting to see the gyno again after 3 months because he wanted another mri. I experience pain every day. My periods leave me curled up in tears. I’ve been told to just take ibuprofen. I’ve had my knees buckle in pain. I’ve taken oxy, naproxen, Motrin. I’ve never done cannabis but I wonder if it would help. I’ve never been doing my own research since the Zoladex was a lie. I was never offered a lap or excision. Nancy Nook and the Canadian Facebook site show no options in Atlantic Canada. I asked for a hysterectomy and was told that’s a last option and they don’t like doing them. During my periods it is excruciating to have a bowel movement. I bleed through overnight pads. I have pain in my groin, hips, and down my leg right to my heel. Plus I bleed through my belly button. It stinks, becomes sore and raw a week before, during, and after my period. I feel like my issues were ignored because I’m fat. Now I’m not sure if the gynaecologist I was assigned is even qualified or knowledgeable enough to treat me because they don’t seem to care that I’m in pain. I’m sick and tired of being told take a pill and suck it up. By the way my threshold for pain let me pass 24 kidney stones with 1 oxy pill.... but my period or ovulation that leaves me popping pills and barely walking is just “normal.” Or something to live with. Frustrated in New Brunswick
  5. A

    A

    More doctors need to be properly informed of endometriosis. I have seen so many doctors that have very little or incorrect knowledge on endo.... Saying if they can't feel it, it's not there, or it's just a pulled muscle, it's "just period pain, part of being a woman". I have left doctors offices in tears from the horrible comments they make, saying it's all in your head or that your creating the pain and anxiety... It's hard enough to have pain daily but for doctors to treat you like you are crazy and blow you off... Then they wonder why we are depressed!
    • A

      Amber

      Seriously. The medical community should be ashamed of this situation and want to change, as opposed to a few outspoken doctors that we all have to fight to see. At the VERY least they should be willing to admit they aren’t skilled or informed enough to deal with endo and refer them elsewhere, as opposed to just shoving useless pills at them...or worse, operating on them when they have absolutely no business doing so. It’s just so incredibly frustrating and horrible!
Comments closed.