Hi! My name is Cordelia, I'm a 21 year old from Australia. I have had NCS for about 11 years (badly for just over 2 now) and have just been diagnosed with developing POTS in the last few months. I've tried writing on these sorts of support boards before and I find it quite hard because the conditions are so life-effecting and I feel like if I talk about it all too much I will _become_ my syncopes, rather than just dealing with them. But I now realise, I need support because it is all just too much to handle! I'm sure you all know what I mean... I look forward to getting to know you all, and reading about all your tips for dealing with all this! It can be overwhelming at times. Cordelia!
