Endometriosis And Exercise: Your Need To Know
Every month, the endometrial lining of a women’s uterus is shed during her period - endometriosis strikes when tissue similar to that lining grows where it shouldn’t: outside the uterus, attaching to reproductive organs and sometimes spreading to other organs such as your bowel.
Endometriosis affects one in nine women and those assigned female at birth, with most diagnosed in their 30s and 40s. That’s more than 830,000 Australian women and around 200 million people worldwide!
For many, the effects are horrific and life-changing: agonising menstrual cramps, heavy periods, bowel and urinary problems and chronic pelvic pain. Debilitating fatigue and pain during sex can also be part of the endo battle.
There’s still much we don’t know about endometriosis: why some women get it and others don’t; whether there’s a genetic component; why some women with endo have no symptoms and why for some, the one sign of the disease is infertility. A study published in 2020 in BJOG – An International Journal of Obstetrics and Gynaecology found that one in three Australian women starting IVF have undiagnosed endo.
The different stages of endometriosisThe Endometriosis Foundation of America identifies four key stages of endo:
- Stage 1: minimal endometriosis with small lesions infiltrating the membrane that lines the abdomen;
- Stage 2: mild endometriosis with signs of more widespread disease, including ovarian cysts
- Stage 3: moderate endometriosis which infiltrates organs within the pelvic cavity
- Stage 4: severe endometriosis lesions and scar tissue which can affect organs throughout the body, including the bowel, appendix, heart and lungs
How is endo diagnosed and treated?While your specialist may suspect that you have endometriosis from your symptoms, the only way to be certain is through surgical intervention, and Endometriosis Australia estimates that for most women it takes six and a half years to be diagnosed.
Done under anaesthetic, a laparoscopy involves a thin, lighted tube being inserted through a small incision in your abdomen to check the size and location of any endometriosis growths. A biopsy of a sample of tissue may be done to confirm the diagnosis.
Once a diagnosis is made, your doctor will talk to you about what’s next. There’s no cure for endometriosis but treatment options can make an enormous difference to your symptoms and quality of life.
These options include:
- Non-surgical treatments, including hormonal therapies and pain medication
- Complementary approaches, such as acupuncture and diet
- Surgery, which may be done to remove endometrial lesions or, in severe cases, carry out a hysterectomy
Exercise and endometriosisWe know that exercise can help protect your body against inflammatory diseases and regulate the effect of estrogen. Given that endo is thought to be an estrogen-dependent inflammatory disease, it makes sense to think that exercise will help, right?
Truth is, more research needs to be done on what kind of exercise works best. But some studies show that exercise can support those with endo, such as a review published last year in BMC Women’s Health, which concluded physical activity and exercise may be beneficial for endometriosis symptoms.
This 2017 study in the Journal of Physical Therapy Science also found that women with endo rated their pelvic pain as significantly lower after an eight-week exercise program which included:
- Posture correction exercises
- Breathing exercises
- Stretching exercises for lower back, pelvic floor, adductors and hamstrings
- Walking on a treadmill
Reading up on working out during your period can be super helpful too. And as always, listening to your own body is crucial. If it doesn’t feel good, trust yourself!
Exercise after surgerySweat’s Head Trainer, Kayla Itsines, has shared her own experience with endometriosis since she was a teenager, with crippling period pain and other complications which have often left her bed-ridden.
In 2021, following her second round of surgery, Kayla powerfully described the impact of having to step away from her much-loved high-intensity exercise while her body recovered.
“The inability to do all the things wanted left me with an overwhelming sense of guilt, and I struggled to accept that I didn’t have control over my body—at least for now. My drive to push my physical limits was a key part of me, and I was now having trouble doing a basic ab workout.”
Following her surgery, Kayla focused on doing everything she could to make sure her body healed and embraced light walking on her treadmill.
If you do undergo surgery, it’s recommended you work with your doctor on a plan for safely returning to exercise after you have healed and recovered.
Ending the silence around endometriosisOne of the key reasons Kayla has decided to publicly share her own experience with endo, she says, is to tackle the deep social stigma surrounding this devastating condition.
For decades, many women with endo suffered in silence or had symptoms dismissed as “just period pain”. Despite being so widespread, endometriosis has long been misunderstood and overlooked – some women report visiting up to up to 10 doctors before a diagnosis is made! This 2003 study found that women with endo waited between 3 and 11 years between first reporting their pain and a correct diagnosis.
Clearly, there’s still a lot of research and education needed – a recent Alliance for Endometriosis survey of 1,800 women found a staggering 90% reported that family, friends, employers and healthcare providers often dismissed their symptoms as a “normal part” of being female.
But there is good news: millions is being poured into research, including a recent doubling of funding in the United States. And a 2020 study published in Scientific Reports found that while it’s still not perfect, that crucial wait time between first seeing a doctor about symptoms and getting the clarity of a diagnosis was shrinking.
What’s also truly inspiring is the public education campaigns shining a powerful light on endometriosis, and women everywhere speaking out about their experiences.
Singer Halsey is among those who have come forward to share their endo stories, telling of her relief at her diagnosis after “years of suffering”.
“Finding out I had endo was the most bittersweet moment because it meant I wasn’t crazy! It meant I wasn’t a “baby”!”
You’re not alone!
* Disclaimer: This blog post is not intended to replace the advice of a medical professional. The above information should not be used to diagnose, treat, or prevent any disease or medical condition. Please consult your doctor before making any changes to your diet, sleep methods, daily activity, or fitness routine. Sweat assumes no responsibility for any personal injury or damage sustained by any recommendations, opinions, or advice given in this article.