Chronically Jenni
Spreading Awareness & Helping Others with EDS & POTS
Tag: postural orthostatic tachycardia syndrome
The Most Difficult Parts of Receiving Treatment for Chronic Illness
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”
Two Thousand & Sixteen
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”
Spoons for Christmas Please!
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!”
7 things to put on your Christmas list if you’re new to POTS.
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.”
My Invisible Journey
Wow, it’s been a while! My excuse for not having posted anything in such a long time was going to be that I haven’t been very well, but , of course, that’s a bit of a rubbish excuse, seen as, I wouldn’t have ever… Continue Reading “My Invisible Journey”