The Citizen (Gauteng)

The pain of being a woman...

- Asanda Matlhare

It’s something people don’t like to talk about in open company, but it is something which regularly invades my world and removes me from reality because I become bedridden. Endometrio­sis has disrupted my life. Every now and again when I am on my period, I experience abdominal and spinal pain, but my mood swings and nausea get to the point where I don’t drink water as often as I should or eat supper because of fear that I will throw up.

This is also a time where I am highly self-conscious because I usually have a heavy flow that I always need to look out for and make sure I don’t leave traces of it on anything I sit on.

March is Endometrio­sis Awareness Month, launched by the Endometrio­sis Associatio­n in 1993. It’s now observed worldwide through activities such as education, fundraisin­g and marches. The awareness month is symbolised by a yellow ribbon.

The condition affects one in 10 women a year.

In an article written by Abdul Wadood Mohamed and medically reviewed by Dr Valinda Riggins Nwadike, endometrio­sis is described as a disorder in which tissue that normally lines the uterus grows outside the uterus. The lining of the uterus is called the endometriu­m.

Mohamed explained how the condition is formed:

“Endometrio­sis occurs when endometria­l tissue grows on your ovaries, bowel and tissues lining your pelvis. It’s unusual for endometria­l tissue to spread beyond your pelvic region, but it’s not impossible.

“Endometria­l tissue growing outside of your uterus is known as an endometria­l implant.”

The most common symptoms are discomfort with bowel movements, painful periods and cramps around menstruati­on.

Ever since my teenage years, I have experience­d debilitati­ng period pains. The last straw for me to seek medical help from my gynaecolog­ist (who later diagnosed me with endometrio­sis) was when I was in high school.

The doctor used an abdominal ultrasound as an additional step for him to be sure that I suffered from the condition.

The period pains I experience­d were so bad I could not walk or sit up straight and anything I ate was followed to a dreaded trip to the toilet.

Looking back, I really wish my sexual health teachers had spoken more about such conditions. Growing up, I have always thought menstruati­on had to be extremely painful as it was simply “part of the process”.

I still suffer from the condition, but I can manage it with prescripti­on tablets and painkiller­s and don’t need surgery – yet.

Another weird observatio­n is how my cycles differ. One month I feel like ripping out my uterus and the next, I forget that I suffer from endometrio­sis.

It’s extremely important for women to pay attention to their bodies and visit their gynaecolog­ists as often as they can, as this will help them take better care of themselves.

Lastly, to all my endometrio­sis worriers, I know it is difficult coping with this painful condition while trying your best to be a daughter, friend or parent, but you are not alone and deserve comfort while navigating through life with endometrio­sis.

It’s extremely important for women to pay attention to their bodies and visit their gynaecolog­ists as often as they can, as this will help them take better care of themselves.

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