I have been raising awareness of Endometriosis for just over nine years after being officially diagnosed with the enervating condition in January 2015. It wasn’t really talked about back then. I hadn’t even heard of Endometriosis until I was undergoing the op. All I remember was having debilitating periods for most of my later youth years into my early twenties. Fast…
I try to raise awareness about Endometriosis every March, and apologies that I’m a little (ok, a lot) late this year. Truthfully, it doesn’t matter which month you raise awareness for a chronic illness. I’ve shared a portion through-out the past eight or so years, so I feel I’m some-what doing my bit. For those who don’t know my back…
Now who remembers this blog post? It’s an oldie, and when I first had surgery to confirm I had Endometriosis. This was back in 2015. I had been told I have stage 4 endometriosis and would need assisted help to have kids. Fast forward to now, there’s a lot more information on Endometriosis, there wasn’t back in 2015. And turns…
Its March, which means its Endometriosis awareness month according to the charity Endometriosis UK. Lets #EndotheStigma! I know a portion of you follow me because of my endo battles and my now stoma from my recent endo op. And I hope to raise as much awareness for this awful condition as I possibly can. As some may know, I was…