I'm writing this at 5 am. I haven't felt able to relax and feel the tranquillity that sleep brings. There's a pain in my head and neck. I'm not really sure exactly what's happening medically speaking. I just know that it's got everything to do with EDS. I have tears in my eyes, I'm alone and… Continue reading What you don’t see
May is EDS awareness month and if you've followed my blog for a while you may already know a bit about it, as I've talked about it in a few other posts. If you're new you may have never heard of EDS most people haven't. Which is why I feel it's really important I help… Continue reading Ever heard of EDS?
Hello Everyone, Today's post is going to be a interview style post featuring someone I reached out to on Twitter called Jane. She's a hairdresser-turned-inventor of The Keela Cup. A menstrual cup designed to be inclusive and easy to use. (I just want to point out that I asked to write this post and I'm not affiliated… Continue reading Introducing the Keela Cup
I was apprehensive about making this post. I said to myself "I'll do it if I ever get to 50 Followers". When the reality is, I could have done it even if I had 0. I realised awareness happens when anyone shares a story and takes action. So, here I am sharing mine... *DISCLAIMER POINTS*… Continue reading Living With a Chronic Illness