{"id":628177,"date":"2026-10-12T10:12:11","date_gmt":"2026-10-12T10:12:11","guid":{"rendered":"https:\/\/www.newsbeep.com\/nz\/628177\/"},"modified":"2026-10-12T10:12:11","modified_gmt":"2026-10-12T10:12:11","slug":"we-cant-deal-with-it-in-canada-some-women-turn-to-mexico-for-endometriosis-care","status":"publish","type":"post","link":"https:\/\/www.newsbeep.com\/nz\/628177\/","title":{"rendered":"&#8216;We can\u2019t deal with it in Canada&#8217;: Some women turn to Mexico for endometriosis care"},"content":{"rendered":"<p class=\"paragraph-b3GxD html-paragraph\">Noelle Menu, 37, says the pain began to darken her reality at a pivotal moment in her life \u2014 once she and her husband decided to try for kids, when she was 26.\u00a0<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">She stopped taking her birth control, which she had been on for a long period, and said she began experiencing pain she&#8217;d never had before.<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">The pain came to define and limit her life, she said, and it seemed nothing could relieve it. She suffered through delays in diagnosis, as well as emergency room visits, a hysterectomy and being placed on waitlists stretching years to see specialists and receive treatment.\u00a0<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">At that point, it was &#8220;literally destroying my life,&#8221; she said, &#8220;and to hear it\u2019s about three to four years to see somebody here, I was just so emotional, so devastated.&#8221;<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">Soon, she realized: &#8220;We can\u2019t deal with it in Canada.&#8221;<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">So Menu and her husband pulled from their savings and went into debt to seek private treatment at EndoGlobal in Tijuana, Mexico, which cost about $35,000 including airfare, a multi-day hotel stay and other costs.\u00a0   <\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">It\u2019s a journey some Canadian women suffering from endometriosis are taking because they feel their health-care system has failed them.<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">The condition affects one in 10 women, and Canada is doing a &#8220;poor&#8221; job at providing them care, according to a November 2025 report by the House of Commons <a class=\"link-_o8iA html-anchor\" href=\"https:\/\/www.ourcommons.ca\/Content\/Committee\/451\/HESA\/Reports\/RP13774304\/hesarp02\/hesarp02-e.pdf\" target=\"_blank\" rel=\"nofollow noopener\">health committee<\/a> \u2014 and in addition to causing undue pain, the lost productivity due to the disorder costs the Canadian economy some $2.5 billion a year.\u00a0<\/p>\n<p>Gender bias plays a role<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">Endometriosis is a chronic condition where tissue similar to the lining of the uterus begins to grow and spread to other parts of the body.\u00a0This tissue thickens and breaks down according to a woman&#8217;s menstrual cycle, and can cause severe inflammation, scarring and pain during periods.<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">It can take an average of five years to be diagnosed with endometriosis in Canada, the parliamentary committee found, while some people have waited for up to 20 years before doctors linked their pain to the disease.\u00a0<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">Even after that, it can take, on average, between six to 18 months to see a specialist and up to 24 months for surgery, it said.\u00a0<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">It can be difficult to diagnose because its symptoms can resemble other conditions, and the level of reported pain sometimes doesn&#8217;t match detectable tissue growth.<\/p>\n<p>WATCH | Similar issues in P.E.I.:<img decoding=\"async\" src=\"https:\/\/www.newsbeep.com\/nz\/wp-content\/uploads\/2026\/10\/1791799929_407_default.jpg\"  alt=\"\" class=\"thumbnail\" loading=\"lazy\"\/><\/p>\n<p class=\"video-item-title\">Islanders with endometriosis say it&#8217;s taking too long to get medical care<\/p>\n<p>Some people on P.E.I. living with endometriosis say they&#8217;ve been waiting a long time to get the specialized treatment they need. For some, it\u2019s been years. CBC&#8217;s Gwyneth Egan has more.<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">The report found that gender bias plays a significant role in those issues \u2014 along with a taboo around discussing menstrual issues, it is often assumed that this kind of pain is &#8220;just part of being a woman.&#8221; <\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">Menu, a supply-chain systems adviser, said she was forced to reduce her workday in half because of the pain. Sometimes, she could barely make it through to the evening.\u00a0<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">&#8220;This disease is just debilitating for some women, and I really wish there was more awareness around it and that doctors would take us women seriously.&#8221;<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">Days before her flight, she told CBC News, &#8220;It\u2019s hard to be so hopeful just because of the previous surgeries I\u2019ve had, but I\u2019m feeling a lot more hopeful this time.&#8221;<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">Dr. Jorge Zavala is one of the founders of EndoGlobal, and he says endometriosis mimics cancer in the way that it spreads, without being as destructive.\u00a0<\/p>\n<p><img decoding=\"async\" loading=\"lazy\" alt=\"A man in doctor scrubs sits on a chair and gestures with his hands.\"   src=\"https:\/\/www.newsbeep.com\/nz\/wp-content\/uploads\/2026\/10\/1791799930_341_default.jpg\" style=\"aspect-ratio:1.7777777777777777\" data-cy=\"image-img\"\/><\/p>\n<p class=\"imageCaption-oOSXz\">Dr. Jorge Zavala, one of the founders of EndoGlobal, says there is a general lack of awareness around endometriosis among doctors who don\u2019t necessarily know what to look for in a patient to get to an accurate diagnosis. (Alessandro Molatore\/CBC)<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">Zavala said doctors generally lack awareness about the condition, which is why diagnoses can take so long.\u00a0<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">&#8220;As a doctor, if you\u2019re not trained in something, you\u2019re not going to be able to diagnose it. It could be poking your eye, but if you are not trained to see it, you\u2019re not going to see it,&#8221; said Zavala.\u00a0<\/p>\n<p>2-year wait time for surgery<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">Vanessa Papiernik, 42, says it took about 30 years for her to arrive at her diagnosis \u2014 and it came with a cancer scare.\u00a0<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">Papiernik, a veterinarian in Victoria, said she suffered through nine months of &#8220;significant&#8221; and &#8220;debilitating&#8221; pain until she landed an appointment for a colonoscopy.\u00a0<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">&#8220;I was purely in survival mode,&#8221; said Papiernik.<\/p>\n<p><img decoding=\"async\" loading=\"lazy\" alt=\"A woman sits with her arm stretched as a masked nurse takes her blood.\"   src=\"https:\/\/www.newsbeep.com\/nz\/wp-content\/uploads\/2026\/10\/1791799930_477_default.jpg\" style=\"aspect-ratio:1.7777777777777777\" data-cy=\"image-img\"\/><\/p>\n<p class=\"imageCaption-oOSXz\">Vanessa Papiernik, 42, undergoes pre-surgery exams at the EndoGlobal treatment centre. She says it took about 30 years for her to arrive at her endometriosis diagnosis and it came with a cancer scare. (Alessandro Morbato\/CBC)<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">She would take Advil, put on maternity clothes because of the bloating and strap a heating pad around her waist to go to work.\u00a0<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">&#8220;I would push the pain aside, but as soon as I got home, I would realize, &#8216;Wow, this is very dangerous, what I\u2019m going through right now.'&#8221;<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">Her colonoscopy found a mass. For two weeks as she waited for the biopsy results, she feared it was cancer; her sister had died from colon cancer 10 years earlier.\u00a0However, the results showed it was endometriosis that had infiltrated through the layers of her colon.<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">She was referred to a centre in Vancouver, but faced a one-year wait to see a specialist, plus another year for surgery, said Papiernik.<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">&#8220;Living like this for two years was just not an option for me,&#8221; she said.\u00a0<\/p>\n<p><img decoding=\"async\" loading=\"lazy\" alt=\"A brithly lit room in a hospital with several curtained-off rooms on the periphery and medical staff desks in the middle.\"   src=\"https:\/\/www.newsbeep.com\/nz\/wp-content\/uploads\/2026\/10\/1791799931_410_default.jpg\" style=\"aspect-ratio:1.7777777777777777\" data-cy=\"image-img\"\/><\/p>\n<p class=\"imageCaption-oOSXz\">The post-surgery recovery floor at EndoGlobal in Tijuana. (Alessandro Morbato\/CBC)<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">She eventually booked a trip to the same centre as Menu, landing the same week the Calgary woman was scheduled for her own procedure.<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">There were more than 30 Canadian women receiving treatment there within the same timeframe, said Papiernik.\u00a0<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">&#8220;We need to really come face to face with the fact that this is, to some extent, it\u2019s discrimination against women,&#8221; said Dr. Nicholas Leyland, president of Obstetricians and Gynaecologists of Canada.\u00a0<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">&#8220;If this were happening with the same degree of pain in a male, it would have been fixed a long time ago.&#8221;<\/p>\n<p>&#8216;Complex surgical issues&#8217;<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">Leyland said that there are not enough specially trained gynecologists in Canada to deal with &#8220;the complex surgical issues,&#8221; and that the condition requires a multidisciplinary approach to care, including psychologists and physiotherapists.<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">The House of Commons report\u2019s top recommendation called on Ottawa to &#8220;develop a national action plan on endometriosis&#8221; to deal with the &#8220;gaps and barriers that hinder awareness, diagnosis and treatment.&#8221;<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">The <a class=\"link-_o8iA html-anchor\" href=\"https:\/\/www.ourcommons.ca\/content\/Committee\/451\/HESA\/GovResponse\/RP13951853\/451_HESA_Rpt2_GR_PDF\/451_HESA_Rpt2_GR-e.pdf\" target=\"_blank\" rel=\"nofollow noopener\">federal government responded<\/a> saying that <a class=\"link-_o8iA html-anchor\" href=\"https:\/\/www.statcan.gc.ca\/en\/survey\/household\/5448\" target=\"_blank\" rel=\"nofollow noopener\">Statistics Canada would<\/a> gather data on conditions like endometriosis; the agency has been collecting responses since Sept. 28 and will do so till Jan. 15, 2027.<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">The Canadian Institute of Health Research has also invested $4.9 million in endometriosis research between 2020 and 2025, Ottawa said.<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">Shortly before her procedure, Menu said doctors in Mexico found a large mass that threatened to block her bowels and send her into septic shock. She said she was two weeks away from emergency surgery.\u00a0<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">&#8220;For me to hear that I could have been in emergency surgery and my specialist appointment [in Canada] was a 30- to 40-month wait\u2026. It makes me so mad,&#8221; said Menu, in a late-September interview with CBC News after her surgery.<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">With the help of her husband, Menu took a walk around the post-surgical floor, which has about 14 beds.<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">Most of her neighbours were Canadian women. They greeted each other as they passed.\u00a0<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">&#8220;I was just so grateful that they were able to find everything,&#8221; said Menu.<\/p>\n<p class=\"paragraph-b3GxD html-paragraph\">&#8220;I\u2019m on the other side of it now. I\u2019m really happy for that.&#8221;<\/p>\n","protected":false},"excerpt":{"rendered":"Noelle Menu, 37, says the pain began to darken her reality at a pivotal moment in her life&hellip;\n","protected":false},"author":2,"featured_media":628178,"comment_status":"","ping_status":"","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[34],"tags":[134,527,111,139,69],"class_list":["post-628177","post","type-post","status-publish","format-standard","has-post-thumbnail","category-healthcare","tag-health","tag-healthcare","tag-new-zealand","tag-newzealand","tag-nz"],"_links":{"self":[{"href":"https:\/\/www.newsbeep.com\/nz\/wp-json\/wp\/v2\/posts\/628177","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.newsbeep.com\/nz\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.newsbeep.com\/nz\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.newsbeep.com\/nz\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.newsbeep.com\/nz\/wp-json\/wp\/v2\/comments?post=628177"}],"version-history":[{"count":0,"href":"https:\/\/www.newsbeep.com\/nz\/wp-json\/wp\/v2\/posts\/628177\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.newsbeep.com\/nz\/wp-json\/wp\/v2\/media\/628178"}],"wp:attachment":[{"href":"https:\/\/www.newsbeep.com\/nz\/wp-json\/wp\/v2\/media?parent=628177"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.newsbeep.com\/nz\/wp-json\/wp\/v2\/categories?post=628177"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.newsbeep.com\/nz\/wp-json\/wp\/v2\/tags?post=628177"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}