I was diagnosed with endometriosis when I was 21 after having waiting 7 years of agony for an official diagnosis. Countless doctors appointments, being told it was just a period, IBS, PCOS, etc. It got to the point where I refused to leave the doctors until he referred me for an ultrasound. I knew something was wrong but he didn't believe me! Finally, he agreed to have an ultrasound which then led to my first laparoscopy and finally a diagnosis of endometriosis. I've since had 2 further surgeries, both temporarily helping but not curing me of this chronic illness. 

Not only do I have to battle the endo flare ups but also the heavy periods, the embarrassment when I've bled through clothes, the cramping, the bloating, the depression that kicks in when you can't do anything about it! It is heart-breaking and although it is becoming more recognised and talked about, we need to do more!

I'm in pain 24/7 with this illness and by running the Great South Run on October 16th 2022, I'm hoping to raise £350 (£50 for every year it took to diagnose me) for the amazing charity as well as awareness too! 

Please help spread the awareness and any donation would be amazing <3