Hi I’m Linda aka Stella aka Linda Stella aka Ella aka Kelly (Only one person calls me that) Two months ago I thought up a blog series Brave Women Unique Tales which at the time was meant to be a quick series of only three people. Along the way more ladies reached out to me and it lasted longer than I expected.
Episode or Part 7 is the last tale of the first BWUT series but it is not the end. Feel free to visit the blog and read all the stories that have been shared if you have not already. Link to our last story is here.
This is a bonus story which is also my story. (Could not end the series without mine) Following the question prompts that were used in all seven parts, here is my unique tale on living with hormonal imbalance and a chronic illness.
1. When did you learn that you had hormone imbalance?
Seven years ago on a doctor’s visit after my periods had lasted for about two months. It was the beginning of my second last year in high school.
2. How do you normally explain your hormonal imbalance induced chronic illness to people?
Normally I say I have complicated and prolonged periods. That’s for people who ask and don’t seem interested to know more. When I sense interest I’ll go all out and give them the 411 on everything endometriosis. (Its fun watching their facial expressions)
3. How would you describe your pain and what is it really like living with a chronic illness/hormonal imbalance?
The pain is excruciating and very annoying. It’s too much and also very unbearable. Personally the pain killers don’t work for me, taking them is such a waste of time. I use ginger, hot water and cinnamon. That’s just to reduce the pain not stop it. Living with a chronic illness is really tough but lately I prefer to say it’s challenging (both in a good and bad way) I would not know the things I know now if I was normal. That’s why i prefer to call it challenging.
4.Have you ever explained your pain to a guy? If yes how?
I’ve told only four guys. I’ll name them A,B,C and E for identification. Guy A is an ex boyfriend who really didn’t take our conversation about my condition seriously. Guy B found out after i’d cancelled a number of our scheduled appointments. I was going through it and my guilt was going over the roof so i had to explain why i was a no show. I don’t remember how i shared to Guy C and E.
5.What was their reaction?
Guy A’s reaction was disrespectful. Guys B,C and E handled it rather well. One of them even went to YouTube to watch a visual representation of what i was going through. (How sweet!!)
6. What coping mechanisms have helped you survive life with hormone imbalance/chronic illness?
Truth be told all my coping mechanisms are trial and error. This month they’ll work and three months down my body will play numb to them. A few include eating nut free meals during a flare up, avoiding caffeine of all sorts (I’m addicted to coffee) and not owning bright colored clothes to save myself the embarrassment.
7.Has the hormonal imbalance/chronic illness affected your eating habits?
After my extensive research on endometriosis i learned that i’d been consuming tonnes of food high in inflammation. Yes it has affected my eating. Now my focus is much on anti-inflammatory foods, fruits, vegetables, healthy proteins and fiber. I don’t think my tongue can taste ice cream anymore.
8.What myths /assumptions have you heard people say about your hormonal imbalance?
In regards to the long and heavy periods caused by hormonal imbalance, we are the most fertile women. That is such a myth other wise we would not be worried about conceiving, would we?
9.What would you want the world to know about living with a chronic illness/hormonal imbalance?
It’s special. Before I got so interested in my illness I lived normally. By that I mean, wait for my heavy almost two months long periods and the excruciating pain then sit back for three months and wait for the cycle to repeat itself. After researching, reading a couple of blogs and watching stories of women dealing with such conditions. I’m proud to say we are special, despite our differences we are special and so are our conditions.
10.Lastly, two people you would like to thank for supporting you when times with the illness get tough.
God tops my list. There are times I deliberately didn’t pray because I was angry at God. Kept asking myself why me, how can you give one person this much pain and all the other rants you are familiar with by by now. I’m not healed biologically but there’s a special healing I feel. It’s only God’s love and grace which has given me that feeling.
My family (not one person but rules are meant to be broken) They’ve been there and listened to my rants not forgetting how patient they were with me. Some have felt the pain with me. They call and ask if anything has changed. You are the best and I love each one of you.
PARTING WORDS (Only to end the series): Thank you so much to all the contributors. You are amazing, uniquely and wonderfully made. Now more than ever i believe in the phrase “there is power in numbers”. Thank you so much to all our readers, those who shared and even those who reached out to me when i had taken a break.
There’s so much more on the way and i’d love for all of you stick around and enjoy what is yet to come. Visit akellolinda.com search for Brave Women, Unique Tales to read all our stories on the series.
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