Living with endometriosis

So yeah, I inadvertently got diagnosed (unofficially) last summer. The extreme pain got too great for me to handle and I was desperate. The fun thing about endometriosis is that you can get it at anytime, at any age apparently. Mine got triggered by having the Mirena IUD for some reason, and then it was a full-on ride to pain town for years. 😦 It does not respond to painkillers, at all. I have burned a hole in my stomach from trying to use ibuprofen with Tylenol to try to function, and it never worked.

On bad days I am vomiting in pain with extreme bloating and discomfort. I have chronic fatigue with terrible back pain with flare-up days and my stomach is in a turmoil with IBS-like symptoms. It’s miserable.

On good days I can function, I am not dizzy and incredibly fatigued, my stomach looks NORMAL and sometimes even *gasp* Good??

Sadly, even with a new medication (Visanne) that I started taking about 5 months ago, I don’t have all good days. It started off terrible- horrible periods that hemorrhaged, awful cramps, bloating, back pain, exhaustion- and then for about 2 blissful months I had nothing! It felt incredible!

And then it immediately relapsed and now I have bad weeks again. 😦 the doctor I am seeing- who is a specialist- said to hang on and it should be getting better, but so far it has NOT gotten better. My bad days aren’t as bad as they were, but they still suck a 100000% worse than those good 2 months I had.

I am starting to wonder if Visanne is enough, or I should start looking at other options, like a surgical intervention. This is a life-altering disease, and causes severe, chronic pain and discomfort. I hate living with it, and it greatly affects my personal quality of life.