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SHOP AYAHUASCA RETREATS BLOG

Endometriosis and Work: The Hidden Career Cost No One Talks About

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Fiona Holloway
September 8, 2026


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Picture this: you wake up at 6 a.m. with a cramping pain that radiates from your lower back through your pelvis, sharp enough that standing feels like a negotiation. You have a full day ahead. A team meeting at 9. A deadline at 4. You already used your last sick day two weeks ago. So you swallow the painkillers, put on real clothes, and try to look like a person who isn't quietly falling apart at her desk.

For roughly one in ten women of reproductive age, this isn't a bad-luck morning. It's Tuesday. Endometriosis — a condition where tissue similar to the uterine lining grows in places it shouldn't — is one of the most under-discussed drivers of chronic pain in working-age women. And a study out of Hungary just put a number on what many of us have suspected for a long time: it's costing women a month's salary a year. At least.

What the researchers actually measured

The team compared 566 women with endometriosis to 447 women without it, all of them working. Instead of just counting sick days, which is the usual lazy metric, they went broader. They looked at absenteeism (hours missed entirely), presenteeism (hours you're technically at work but functioning at maybe 60 percent), and something called work ability — a self-assessment of whether you actually feel capable of doing your job given your current health.

That last piece matters. Anyone who has tried to write a coherent email while their uterus feels like it's being wrung out knows that “showing up” and “working” aren't the same thing. The Hungarian researchers took that reality seriously, which is more than most workplace studies bother to do.

The numbers came out ugly. Women with endometriosis missed an average of 12.7 hours of work every four weeks because of health issues. Women without it missed 5.7. Translated into lost income, that's roughly €1,757 a year in Hungary — about $2,040, or a full month's average paycheck. And that's just the hours they were physically absent. It doesn't count the days they dragged themselves in and produced half the output, or the money spent on scans, specialists, hormonal treatments, and the years of misdiagnosis so common with this disease.

Why this is a health story, not just an HR story

Forty-two percent of women with endometriosis in the study fell into the “poor” work ability bracket, compared to just under 18 percent of women without it. That gap isn't a rounding error. It's a signal that something is being systematically ignored — by employers, by healthcare systems, and honestly by the culture at large.

Endometriosis takes an average of seven to ten years to diagnose. Which means most women are navigating career-defining decades — their twenties and thirties, when promotions, raises, and reputations are being built — with a condition nobody has named yet. They're being labeled unreliable, dramatic, or “not a team player” when they're actually managing a serious inflammatory disease that no one has bothered to identify.

And here's the part that doesn't make it into corporate wellness slides: chronic pain grinds people down. It affects sleep, mood, cognition, libido, relationships, everything. Over time, it can drift into depression and anxiety, and it often does. Which brings us to a conversation that's been quietly gaining traction — how women with long-standing pain conditions are looking beyond conventional treatment for relief.

Small waterfall hidden in jungle, framed by ferns and orchid... | ShopAyahuascaRetreats

Where plant medicine enters the conversation

This isn't going to be a “ayahuasca cures endometriosis” pitch, because it doesn't, and anyone selling that is either misinformed or lying. But there's a real and growing conversation among women with chronic pelvic pain, autoimmune conditions, and treatment-resistant depression about what psychedelic and plant-medicine work can offer alongside — not instead of — proper medical care.

What ceremony seems to help with, based on what facilitators and participants consistently report, is the layered exhaustion that comes from years of not being believed. The trauma of being dismissed by doctors. The grief around fertility questions. The rage at a body that feels like it's working against you. The pattern of overriding your own pain signals to keep functioning in a workplace that never asked how you were actually doing.

Ayahuasca, psilocybin, and San Pedro have all been used by women navigating chronic illness as a way to process the emotional weight the illness carries — the isolation, the internalized guilt, the sense of being a burden. None of that is the same as curing the disease. But if you've lived with endometriosis long enough, you know the disease and the psychological residue it leaves aren't easy to separate.

A few honest caveats before you book anything

  • If you're on hormonal treatments, GnRH agonists, or SSRIs — extremely common for endometriosis management — talk to a knowledgeable retreat facilitator before drinking. Some combinations are dangerous. A reputable retreat will ask about your medications in the intake and turn you away if there's a risk.
  • The ayahuasca dieta and the ceremony itself can be physically demanding. Purging, long ceremonies, sometimes sitting on the floor for hours. If pain flares are unpredictable for you, ask specifically about how the retreat handles participants who need to lie down, leave the maloca, or take breaks.
  • Menstrual cycles are treated differently across traditions. Some Shipibo lineages ask women not to drink while bleeding; others don't. This isn't superstition to those traditions — it's part of the framework. Ask about the retreat's approach before you arrive, especially if your cycle is unpredictable.
  • Integration matters more than the ceremony. If you're processing years of medical trauma, plan for real aftercare — a therapist, a support group, or a coach who understands both chronic illness and psychedelic integration.
Coca plant leaves in bright morning sunshine, sharp green de... | ShopAyahuascaRetreats

What workplaces still don't get

Zooming back out: 54 percent of women in the Hungarian study said their employer knew little or nothing about endometriosis. Only 17 percent felt their workplace was clued in. When asked what would actually help, the women didn't ask for anything wild. Flexible hours. Remote or hybrid options. Menstrual leave. Managers who don't roll their eyes when someone needs to work from home during a flare.

None of this is expensive. None of it is complicated. And yet a decade into the mainstreaming of remote work, most companies still treat chronic-pain accommodations like a personal favor rather than a basic operational reality for roughly ten percent of their female workforce.

There's a broader point in here too. The wellness industry loves to talk about “burnout” as if it's a spa-weekend problem. But for a lot of women, what looks like burnout is actually untreated or undertreated chronic illness dressed up in more socially acceptable language. Fixing that requires better diagnosis, better workplace policy, and — for some — deeper healing work that goes beyond the strictly medical.

What to do if you're in it right now

If you're reading this while sitting on a heating pad, a few practical things:

  1. Track your symptoms. Not in a vague way. A cycle app plus a pain-and-fatigue log gives you data to bring to a doctor who might otherwise wave you off.
  2. Find a specialist, not just a GP. Endometriosis is chronically underdiagnosed by generalists. If you can access an excision surgeon or an endo-focused gynecologist, that's the standard of care.
  3. Advocate at work early, even before diagnosis. You don't need a diagnosis to request flexibility. Frame it around productivity outcomes and it lands better than framing it around pain.
  4. Look at the whole picture. Nutrition, sleep, stress load, pelvic floor physio, and yes — for some women — deeper psychological or spiritual work all move the needle. No single intervention fixes this. Layered ones sometimes do.

For women exploring the psychological and spiritual side of living with chronic illness, curated plant-medicine and healing retreats can be browsed on our marketplace here. Not as a cure. As one more tool in a life that's had to hold too many things at once.

Endometriosis isn't a niche condition, and it isn't just a “women's issue” tucked politely into the corner of the health beat. It's a mainstream, career-shaping, income-draining, life-altering disease that ten percent of women are quietly managing while the rest of the world acts like their tiredness is a personality flaw. The Hungarian numbers are a wake-up call. Whether workplaces — and the rest of us — actually wake up is another question.

Mist hanging low over a tropical valley at sunrise | ShopAyahuascaRetreats


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Fiona is a globe-trotting psychonaut who’s been cultivating her passion for meditation and promoting collective consciousness throughout her adult years. A seasoned traveler and mindfulness advocate, she's found inner peace in diverse cultures across the globe.