Story
I am running the Great North Run to raise vital funds for Endometriosis UK!
Endometriosis is the name given to the condition where cells similar to the ones in the lining of the womb (uterus) are found elsewhere in the body. It is a chronic and often debilitating condition that can cause painful periods, painful sex and pelvic pain outside of periods. It may also lead to infertility, fatigue and bowel and bladder problems.
Endometriosis affects 1 in 10 women and those assigned female at birth, that's as many as diabetes yet very few people have even heard of it.The impact can be felt for life and there is no cure.It takes an average of 8 years to get a diagnosis of endometriosis in the UK, that's too long!
I was diagnosed at 29 however I had been displaying symptoms since I was 11! I was always told what I was experiencing was normal so I gave up trying to find answers until my symptoms became so bad I was reliant on pain relief 24/7 and was not able to function. I was diagnosed with stage 4 uterus, ovarian, pelvic and bowel endometriosis and also had some nerve and vascular involvement.
Endometriosis UK put me in touch with an amazing surgeon who helped to diagnose and treat me and I’m feeling much better post surgery. The support groups have allowed me and Steffan to come to terms with my diagnosis and what it means for our future. They have also given us tips on managing my symptoms, because yes, I still have flares and very bad days but they’re nothing compared to my pre op symptoms.
Your donations will mean that Endometriosis UK can continue to support those affected by Endometriosis through national support groups, information provision and their helpline as well as continue to campaign for change, fairer treatment and eventually a cure.