Endometriosis Awareness Month
Endowarrior is what we say,
But it doesn’t even begin to portray,
The many pains, frustrations, and disbelief,
From society and far wider than the school Dean. Yeah, back during gym sessions, class of strict teachers, and all those runs to the lo. “No more to the toilet for you”. Bleeding through tampons, pads, and jeans. We were just teens. So little empathy given for the young; “period pains are part of womanhood” came out from their tongue.
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So often we’re met with disbelief,
For apparently normality is what they all portray it and it seems.
But pains like these are far too much,
To be anything but normal as such.
Still doctors tells you no,
Even when you’ve done the research and almost know. A few tests and the right gyno could solve a lot, but then they lack knowledge of such.
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Cries, vomit, and unexplainable pain,
Will make any people go insane.
Far worse than pain itself,
Is the disbelieve in oneself.
Is all just in my head like they all ensured and said to me,
Or is the fault in lack of knowledge of thee?
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It’s time to wake up and fight,
Fight for a human right.
Right as a woman to be heard,
Not met with absurd.
Knowledge of doctors and society we must,
Let’s lift the problem and trust.
When someone has excruciating pain,
Don’t make them feel far from sane.
Hear their words and reassure,
Though they might lack the knowledge to find,
They will acknowledge you, and contact people who could figure out what’s “wrong with you”. Rather admit to the boundaries of knowledge, than just saying no.
Endometriosis awareness month, but let’s lift it to science of female health. Health is your greatest wealth after all, and I’m sure we’ll find it profitable for all. Investors, society and women around the world, knowledge must be power for sure. When one in ten females has the disease, I question how come we haven’t researched more and found a better cure? Painkillers, the pill, and operations are only useful for a while,
But there should be something more worthwhile.
Until then,
Fight your way through life,
For who says you can’t dance in life while still fighting a strife?
March is the #EndometriosisAwarenessMonth – join the conversation!
The aim is to increase awareness and highlight the symptoms of the condition that affects about one in ten women, with average of about 7 years to get diagnosed.1 The difference between endometriosis and adenomyosis is where the tissue grows, but the two are not mutually exclusive as adenomyosis is seen in 20-89% of women with endometriosis. Adenomyosis is when endometrial-like tissue grows into the muscle of the uterus, while endometriosis is when endometrial-like tissue grows outside the uterus (like on the ovaries, fallopian tubes)2.
My personal story
Last year I got very sick with a lot of different viruses and bacterial infections, resulting in severe constipation, vomiting, fainting, ER visits, and more. One part of the total package of examinations was testing for endometriosis and/or adenomyosis due to a gynecologist who had previously that year found tissue evidence supporting the diagnosis. Before this gynecologist, I’ve been to several different ones and GPs regarding my period pains and flood, but all previous healthcare professionals have turned down my inquiry for testing and been certain in their knowledge that I did not have either, or. Even the doctor who gave me coagulation pills as a teenager, nor the gyno whom I meet at 16 years old for pains. Teachers at my schools were harsh when I had to run to the toilet so much, even though my mother had given a note in advance… even when I was one of the few at secondary school who followed every lecture with a hawk’s eye and sharp pencils writing down every word….
One year ago, right after the first doctor who acknowledged me, I wrote the poem above. One year ago, I didn’t have the courage to publish it. After all last year, I grew, and this year, it’s out. This year I have the courage to stand by it and every word in it. This year, I’m taking a stand – we need to invest more in #womenhealth!
Resources
I’ve collected a few information resource links below, but please note that I’m not a doctor and to use critical thinking when searching the web. Moreover, please contact a doctor you trust or ask for a GP and/or a gynecologist with experience in the field if you resonate with the above and suspect it could be Endometriosis or Adenomyosis:
Videos for educational purposes found on Youtube:
• Endometriosis: Causes, Pathophysiology, Symptoms, Diagnosis & Treatment by JJ Medicine here. Short and to the point with info-graphics.
• Endometriosis – Overview (pathophysiology, differential diagnosis, investigations and treatment) by Armando Hasudungan here. Easy to follow drawing video, but a bit longer than the first video.
• Why Medicine Often Has Dangerous Side Effects for Women | Alyson McGregor | TED Talks here.
• What is endometriosis? A Mayo Clinic expert explains here.
• Nurse With Endometriosis Shares Painful Journey To Diagnosis | TODAY here. You’ll feel less alone with this one.
Websites
• Global Forum for news and information, endometriosis.org
• Endometrioseforeningen (Norway)
• Legeforeningen (in Norwegian, but check the references for sources)
• Google Scholar search here
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References
- Endometriosis Awareness Month 2023. (n.d.). Awareness Days Events Calendar 2023. Retrieved February 16, 2023, from https://www.awarenessdays.com/awareness-days-calendar/endometriosis-awareness-month-2023/
- EMajak, B., G., Tellum, T., Ringen, M., I., Veddeng, A., Langeland, K., Alvirovic, J., Omtvedt, M., & Aas-Eng, K. (2021). Endometriose og adenomyose. Norsk gynekologisk forening. Retrieved February 15, 2023, from https://www.legeforeningen.no/foreningsledd/fagmed/norsk-gynekologisk-forening/veiledere/veileder-i-gynekologi/endometriose-og-adenomyose/
Love & Light / CG
My debut book “A Poetry Collection of The Broken and The Divine” is out for sale on Amazon (paperback and e-book). Keep posted for my upcoming book launch event in the near future.


































