Pots diagnosis

Living with POTS / dysautonomia can be challenging. This post gives my story, tests, diagnosis and lifestyle measures to discuss with your doctor.

#10TipsForHealthyLife

The Poor Man's Tilt Table Test You suspect that you may have a form of dysautonomia called POTS, or Postural Orthostatic Tachycardia Syndrome. However, you haven’t been diagnosed with it officially. You’ve heard stories from other people talking about their experiences living with POTS and you’re starting to connect the dots that something may be amiss. You may have also heard that it could take up to seven years (!!) to get an official diagnosis. That’s the incredibly disappointing average…

Spring tends to bring with it increased POTS symptoms. As we gear up for warmer weather, I want to share my tips for living with POTS.

Running a 5k with POTS is challenging, but I did it! Read my blog with journal entries describing my training leading up to race day!

Managing a diagnosis like POTS can include a few, some, or all of these, and this isn’t everything! But for those who don’t believe POTS is… | Instagram

5 doctors and 3 ½ years later, my medical ‘mystery’ solved: I have Postural Orthostatic Tachycardia Syndrome. My POTS Syndrome diagnosis story.

My name is Lisa and this is my life with POTS (Postural Orthostatic Tachycardia Syndrome)