POTS Recovery Stories:
Patient POTS Stories with a difference!

Experience an chronic disease like POTS (Postural Orthostatic Tachycardia Syndrome) can be tough to deal with, so often patients seek POTS stories to see what it is is like for others living with POTS.  Unfortunately there are not enough POTS recovery stories on the internet.

This site shares POTS stories that specifically focus not just on what it is like to live with POTS, but it focusses on how people discovered their POTS recovery strategy or 'cure'.

So every POTS story here, is in fact a POTS recovery story and every story is different.

When I was sick, one of the most upsetting things was not hearing other people recover from POTS, so I believed it wasn't possible. (because we all know there isn't a one fits all cure for POTS!) Hence one of the things I really wanted to do was collect and share POTS Recovery Stories to give hope to people still suffering with this illness.

If you know someone who has recovered from POTS, please ask them to contact me to share their story or if you yourself have recovered from POTS, please contact me directly here.

Besides POTS recovery stories, I also share stories of recovery from Fibromyalgia, PVFS, ME/CFS, MCS and other similar syndromes.  You can see the full list of recovery interviews and recovery stories.

Best wishes,



Please note that the people sharing their stories here have gone through their own journey of recovery from POTS independently from the author of this website and related content. They are simply offer the experience of their POTS recovery story and are not responsible for, nor are they endorsing the content on this website or other related products. Similarly, we do not take responsibility for the content on their respective sites or products and make no implied endorsement.

Kiki overcomes POTS, MECFS with Chronic Lyme after 10 years of illness
Kiki (@chronicallyhealed) tried lots of cures for POTS but nothing really worked for years. Finally, she cured POTS and ME/CFS in stages over a period of 3 years and regained her health despite being diagnosed with Chronic Lyme Disease. In this interview, she tells her story.
Mollie recovers rapidly after 4½ years of MECFS (POTS)
Mollie shares her experience with the ANS REWIRE program after 4 years of failed approaches to return to health in an inspiring interview.
James learns how to heal from Myalgic Encephalomyelitis after 9 years of illness
After 8 years of suffering, James' life had hit hit rock-bottom. “I couldn’t see a future for myself”. It was an understandable outlook for a young man whose life was in shambles and who had never experienced what it was like to be an adult and have normal health. But against all odds, he then changed his approach, his outlook, his whole life and 9 months later he was recovered.
My Story – Dan Neuffer’s CFS Recovery Story
My Story – Dan Neuffer’s CFS Recovery StoryFor Recovery Story Disclaimer, please see the main page here!I thought that the[...]

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