Seven years ago i was very excited to start my higher level education but i had no idea that one week into the school term I’d be paying my gynecologist a visit over a chronic illness i didn’t know existed.
Endometriosis is a chronic condition where tissue that behaves like the lining of the uterus is found in other parts of the body such as the ovaries, Fallopian tubes, bladder, bowel and others. For further and easier information to comprehend this, please visit https://www.medtronic.com/covidien/en-za/patient-information/explore-endometriosis.html
On my visit to the doctor, very odd tests were done and i was asked if I’d aborted before because what they were seeing was unusual. During the review he opened what i call a doctor’s dictionary and introduced me to this new word Endometriosis. I honestly wasn’t paying attention until he mentioned it has no cure and the only hope to improving the situation was giving birth. I got scared and thought at that age I’d have to get pregnant for this to go away. I remember how scared my mum was when she broke the news to my dad. My adolescent mind was racing on about how i was going to be a young mom and stuff while my mum was making phone calls to priests and other religious people she knew to start praying for me. (As would any African Mother)
There’s no cure not even in the first world countries so we are really even on this one. Anyway, there are particular pills ladies like me can take but that helps to reduce pain and balance a few hormones and that’s it. My doctor prescribed them and literally banned me from the hospital, no see me in two weeks time or visit in a month. He left me to battle it out with pharmacists asking why i need the medicine and other similar annoying questions.
During my short stay at home during the school term, we visited a doctor that specializes in herbal and organic medicine. That medicine is just as bitter as Aloe Vera or worse and i started treatment with special supervision from the school nurse. There was no skipping with that woman, she’d send over five different people to inform me that’d been summoned. I always referred to it as torture and a curse from God because why would He send me a chronic illness moreover one that was incurable.
Flash forward to the present day, i know now that the nurse just wanted me to be healthy and get better just as she’d promised my mother. The strict supervision during my treatment is why I’m not as badly off but that is a story for another day. Over the years i started doing more research about the illness and started looking for women, ladies or young girls like me. The pain i was feeling when it was that time of the month, before and after was excruciating. I thought to myself, there should be other females out there like me and i want to know how they deal with this awful pain.
Friend, if i tell you my pain is nothing compared to the stories i read as shared by different women you have to believe me. Some utilize most of their leave days from work to stay home because they can barely walk, one medically hit menopause at the age of fifteen, another quit her job because her colleagues complained about her working from home whenever it was that time of the month. Plus so many others you can check out this one https://www.healthline.com/health-news/personal-painful-ordeal-of-women-with-endometriosis-061815
The symptoms differ for every female and that’s why some get diagnosed a little later when the condition is ugly. Let me get back to why I’ve decided to write about this. This illness has so much control about pretty much everything in my life. My body physique for starters, i have a hormonal belly which is hard to shred, bad digestion process so i have to watch what i eat, anxiety and depression because i grow fat from stress and people will call me out on it as if i shove 10 butter cream cupcakes down my throat everyday. The hormonal imbalance has me loving someone today and hating them tomorrow and last but not least the intimacy situation. It’s such a load to carry but i handle it with patience and faith that it will get better.
During the lock down, i decided to study my body and assess my life from the past seven years and i realized my endometriosis situation has been controlling me the entire time. If I’d known that a while back I’d have handled life better but we make our choices and that’s not me saying i regret it. I’m proud to say my mental health is stable and I’m happy, extremly thankful to my unpaid therapists at least all our hours of talking have helped me realize what the root cause has been. I even know where I’m going with this blog journey and my life with this unfriendly illness of mine.
The story does not end here, we are going to go deeper into this chronic illness and i’ll share my experience because it feels like i’m reliving some parts. This is part one of my story and i hope you stick around. These stories need to be told and we need to be heard to find one another but most importantly to get help and offer it to those who don’t even know they need it.
Until next time,