Spreading Awareness & Helping Others with EDS & POTS
This is another piece I’ve just had published on the Mighty which I wanted to share with you. After working in the retail sector for as long as I have, I’ve learned that customers are inquisitive and tend to point out when something is different. In my… Continue Reading “To The Customer Who Judged Me For Sitting Down On The Job.”
Here’s a video I did for Rare Disease Day (28/02). Sorry I’m a little late putting it up on here but it’s still worth a watch 🙂 Please Subscribe to my Youtube Channel 🙂 [youtube https://www.youtube.com/watch?v=HdlsFdsahFE]
In my blog post all about 2016 I sneakily left out one of my New Years Resolutions for 2017. I left it out, firstly, because I didn’t know if I’d ever get round to doing it and didn’t want to break a resolution but… Continue Reading “My Secret Resolution”
The night before my first Blood Patch surgery, I wrote a piece for the Mighty which has just been published so I wanted to share it with you too. It’s all about the difficulties people with chronic illnesses go though when getting any sort… Continue Reading “The Most Difficult Parts of Receiving Treatment for Chronic Illness”
Is it too late to say Happy New Year? It’s still just about January so I think it’s okay 😛 I’m allowed to say it because this is my first blog post of 2017! Hope everyone is having a good year so far. I’ve… Continue Reading “New Experiences & Meeting a Fellow Zebra”
Firstly, I hope everyone had a great Christmas and Santa got them everything they asked for…and if he didn’t you managed to pick it up in the sales! I had a lovely Christmas at my Nan & Granddad’s playing games, opening gifts and eating way… Continue Reading “Two Thousand & Sixteen”
This is the 4th time I’ve sat down to try to write and finish this blog post! This has been a ridiculously busy time for me coming up for christmas, as it is for everyone, but I did all my christmas shopping, cards and… Continue Reading “Spoons for Christmas Please!”
Last Christmas my Postural Orthostatic Tachycardia Syndrome (POTS) was at its worst. (Not that I even knew what POTS was at that point let alone that I had it.) I knew I had something wrong with me I was so dizzy all the time… Continue Reading “7 things to put on your Christmas list if you’re new to POTS.”
Not being a breakfast lover I didn’t know a whole lot about breakfast. I knew I wasn’t going to like porridge but I knew I liked cooked oats as I adore Oatmeal-Raisin cookies so I thought Granola was the best option. I tried both… Continue Reading “Granola”