Chronically Jenni
Spreading Awareness & Helping Others with EDS & POTS
Tag: eds
New Experiences & Meeting a Fellow Zebra
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”
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”