Living with an Invisible Illness? From the moment I was told by my GP that I may have endometriosis I was straight on the internet and advice forums. One of the most commonly used phrases I found was "living with an invisible illness". When I first read this I felt like fist bumping the air and shouting YES! at the top of my voice. Suddenly I wasn't just the only one who felt like this. I had always felt like a bit of a whimp for being so rubbish that I couldn't just get on with my life during Painful monthly periods. I saw my friends and family get through it without any trouble or moaning and not having to even take paracetamol. I on the other hand was doubled over in pain, dosed up on codeine with a hot water bottle and bleeding so heavily sometimes that I couldn't move from the toilet. Why was I so different? Then the pain just carried on. It didn't matter where in my cycle I was and it was suddenly all around my abdomen, sharp and stabbing in my ba...
I was 30 when endometriosis began to take over my life. I have spent 3 years in and out of hospitals, having operations, trying to control my pain and mainly getting more frustrated and depressed day by day. With this blog I hope to help others get through the days of sheer agony and sadness of being an Endo Sister and maybe even bring a smile and a laugh to their days.