I was diagnosed with Endometriosis over twenty-years ago and I was amazed (and saddened) when I visited The Fife Endometriosis Support Group in 2016, that nothing seemed to have changed in terms of general awareness…or the way in which women are treated by the medical profession. I vowed to do something about this! So, I have teamed up with Claire and her girls to bring you their incredible (and at times) heartbreaking stories.
Endometriosis: our pain is real will be available from Autumn 2017. Here is a brief extract from Claire’s story.
“I started getting symptoms of endometriosis when I was aged around fifteen or sixteen but wasn’t diagnosed until the age of thirty-one! I had all the classic signs including heavy periods, pain in my lower back and hips as well as lower stomach pain with the pain getting gradually worse, the older that I got. Things reached a breaking point when I was in so much pain during sex that I was constantly bursting into tears...”
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