Living with POTS: Back to the start
I've realised recently just how unknown POTS is. Unless you know someone with it, you probably have no idea what it is and even when you know...you don't really know. As such...I thought I'd do a couple of posts about what is is, where you can find out more info, how it affects me day to day and the like. So first off...symptoms and diagnosis. It was around 2006/2007 when I first started having episodes of fainting - my GP and the paediatrician we saw put it down to my height and therefore my blood pressure dropping when I was stood. Quite a logical solution and I was told it'd improve with time - which it did. However, I still seemed incredibly prone to fainting and once at University they realised my postural drop and resolved yet I was still having these faints. In September 2011, I was generally unwell and had multiple collapses over the course of a few days. During which I hit my head. After CT and MRI scans I was transferred to the local neurology specialist...