How I Get By When My Endometriosis Turns to Anger


Endometriosis is by no means a picnic in the park. Bouts of pain, mood swings and exhaustion make it difficult to get through the day. It’s frustrating not knowing if I will wake up to my old self or the chronic monster I have become. Controlling my reactions to everyday situations is tough. Since my endometriosis diagnosis, I find I experience bouts of anxiety and depression. I now take offense to things I used to be able to laugh about. I become defensive and angry if someone is just trying to give me advice or help.When did this monster become so controlling? Why have I become so angry?

How I Cope With My Anger

All of this bottled-up anger makes it hard to work, sustain relationships and do things I normally love to do. But as I slowly work on myself and my health, I have found ways to cope when I am having a rough time.

1. Personal development books

Reading has always been a wonderful hobby. If I didn’t get chronic migraines, I could read all day. Whenever I am feeling discouraged, I turn to personal development books. They are always filled with words of wisdom, support and positivity. It helps me snap out of my funk, and brings me back to life. Sometimes, it even gives me a kick in the rear end that I need. Most of the time, I forget what I was even angry at, and become motivated to become a better version of myself. Along with personal development books, I find that books about endometriosis or other chronic illnesses help. One of my personal favorites, “The Doctor Will See You Now,” can be found on Amazon — it is such a great read.

2. Take a walk through nature

The best place for me to clear my head is outside. Walking through nature has always calmed my soul. Taking breaths of fresh air and looking at the world around me, I begin to realize my problems are so small. Whatever I’m angry at diminishes into the trees. On days that it is rainy or my body aches too much for a walk, I enjoy “Relaxing Nature Sounds.”

3. Find someone to talk to

I know this can be a hard thing to find for many of us. Not many people truly understand what it is like living in pain every single day. I have found endometriosis support groups on Facebook to be helpful. I am also lucky that my mom is always there to listen and give advice when I need it the most. It may also help, if you are comfortable, to find a therapist you can talk with on days when you just cannot control your emotions. I have found having a therapist who allows online/email sessions is very helpful for me.

4. Breathing exercises

This is something I never believed in until I tried yoga and realized how much it truly helps. When my mind is racing and my heart is pumping fast, I close my eyes, take a deep breath in from my nose, count to seven and then let the breath out through my mouth. I do this however many times I need to until I feel relaxed. This is one of my favorite coping mechanisms because I can do it anywhere at anytime.

Getty Image by Cheremuha

Follow this journey on My Endo Journey.


Find this story helpful? Share it with someone you care about.


Related to Endometriosis

Woman's hands typing on a computer.

Why I Write About My Endometriosis

We live in the age of online social networking, where we share even the most mundane elements of our lives. Not much is kept secret from our peers. But it is still deemed inappropriate to discuss your health problems online, for the world to see. I didn’t start out with the intention of sharing my [...]
hot water bottle and cover, and pelvic seat cushion

14 Products People With Endometriosis Swear By

When you struggle daily with the pain of endometriosis, it can quickly become frustrating and exhausting – especially since there is no cure. Finding a product or technique to help ease your symptoms is often an ongoing process of trial and error that usually involves a combination of treatments rather than one single “fix.” Although there is [...]
woman in a red dress holding her hands over her pelvic area

What Endometriosis Pain Feels Like for Me

It’s difficult to describe pain. When we talk to our doctors, we usually try to describe pain with words like “sharp” or “dull,” or by using a pain scale from one to 10. I’ve never felt I’ve been able to fully convey how endometriosis actually feels, and I’m often left with the sense others think [...]
profile portrait of a woman with dark hair

Why I Spent 12 Years in Silence About My Endometriosis

Honestly, that’s a loaded question, but I think it’s important to talk about because staying silent is no longer an option. It’s scary to talk about because sometimes it feels as if there is a lot at stake. Hopefully this will make it easier to understand why so many women struggle in silence: 1. It’s [...]