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im a uk potsie and there are a number of us on here now. Im probably not the best person to bombard with questions as im still on a rather steep learning curve myself but i know a few of the others would be great for that.xx

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I'm on the South coast of the UK and have had POTS pretty much my whole life but only suffered very badly with it for 5yrs and only diagnosed then too.

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Hi,

Im from the UK and I am in the Southwest. I am without diagnosis and struggling as I now seemed to have developed gastroparesis as well now. My main battle is that my GP doesn't believe Pots exists and that he believes your heart rate going from 80bpm resting to 135bpm on standing is completely normal. I bought the book the fainting phenomena and lent it to him, so I await his response.

I am currently waiting for tests on the gastro symptoms.

I find this forum so helpful its my lifeline and the only way that I know I am not going mad.

Rach

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