Jump to content

Uk Potsies


Recommended Posts

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.

Link to comment
Share on other sites


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.


Link to comment
Share on other sites

Join the conversation

You can post now and register later. If you have an account, sign in now to post with your account.

Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

  • Create New...