Living with POTS: What It’s Like for a Spouse | Dysautonomia & Chronic Illness Support

Living with POTS: What It’s Like for a Spouse | Dysautonomia & Chronic Illness Support

What is it really like to love someone living with POTS and dysautonomia?

In this episode of Let’s Talk About The POTS Life, my husband Cale shares what it was like watching me navigate years of undiagnosed Postural Orthostatic Tachycardia Syndrome (POTS) — the ER visits, the “normal” test results, the adrenaline dumps at night, and the slow decline that didn’t make sense.

We talk openly about what dysautonomia and autonomic nervous system dysfunction looked like from his perspective — the tachycardia, tremors, chronic fatigue, insomnia, and living in constant fight-or-flight. From the outside, POTS can look like “just dizziness.” But inside, it affects every part of life — including marriage and family.

In this episode, we discuss:

  • Supporting a spouse with POTS
  • Understanding invisible illness and dysautonomia
  • Nighttime adrenaline surges and anxiety
  • The emotional impact of chronic illness on relationships
  • How to validate someone with autonomic dysfunction
  • Practical advice for partners, caregivers, and family members

If you are newly diagnosed with POTS, living with dysautonomia, or trying to help your spouse or loved ones understand what this condition really feels like, this conversation will resonate deeply.

POTS affects the autonomic nervous system, but it also affects relationships. And understanding changes everything.


Connect with Us:

⁠⁠⁠⁠Our Website⁠⁠⁠⁠

Facebook: The POTS Life

Instagram: @thepotslife_

Tik Tok: thepotslife

Tämä jakso on lisätty Podme-palveluun avoimen RSS-syötteen kautta eikä se ole Podmen omaa tuotantoa. Siksi jakso saattaa sisältää mainontaa.

Jaksot(63)

The Invisible Burden of Chronic Illness

The Invisible Burden of Chronic Illness

Hosts Kelsey and Britney discuss the invisible burden of living with chronic illness, including POTS, and the challenges of diagnosis, treatment, and explaining symptoms when you look fine. They share...

3 Marras 25min

Electrolytes: The Key to Proper Hydration with Redmond's Darryl Bosshardt

Electrolytes: The Key to Proper Hydration with Redmond's Darryl Bosshardt

In this episode, Kelsey and Redmond’s Darryl Bosshardt discuss the significance of salt and electrolytes, particularly for individuals with POTS. They explore the historical context of salt, its essen...

20 Loka 40min

From Misdiagnosis To Management: Ryenn’s POTS Journey

From Misdiagnosis To Management: Ryenn’s POTS Journey

In this episode, Ryenn shares her journey from misdiagnosis to managing POTS and vascular conditions, highlighting the importance of persistence, proper diagnosis, and lifestyle modifications. Her sto...

6 Loka 36min

POTS, Marriage, and Motherhood - What We Learned Along The Way

POTS, Marriage, and Motherhood - What We Learned Along The Way

In this episode, Kelsey and her husband Cale discuss the journey of living with POTS, diagnosis, treatment, and how it has impacted their family life. They share insights, challenges, and advice for o...

22 Syys 38min

The Hidden Connections Between POTS, EDS, Hypermobility & Chronic Pain with Dr. Linda Bluestein

The Hidden Connections Between POTS, EDS, Hypermobility & Chronic Pain with Dr. Linda Bluestein

Living with chronic pain, hypermobility, POTS, or other complex conditions can make it difficult to connect the dots. In this episode, I sit down with Dr. Linda Bluestein, a board-certified physician ...

4 Elo 28min

Accepting Life After a POTS Diagnosis: Grief, Control & Building Your Support Team

Accepting Life After a POTS Diagnosis: Grief, Control & Building Your Support Team

Receiving a POTS diagnosis can be both validating and overwhelming. After finally getting answers, many people are surprised to learn there isn't a quick fix and that managing POTS often requires cons...

20 Heinä 19min

Dr. Marie-Claire Seeley on POTS, EDS & Changing the Future of Care

Dr. Marie-Claire Seeley on POTS, EDS & Changing the Future of Care

Dr. Marie-Claire Seeley is a registered nurse, researcher, Founder and Volunteer CEO of the Australian POTS Foundation, and one of the leading voices advancing POTS research, education, and advocacy.I...

30 Kesä 51min

Learning to Trust Your Body Again with POTS

Learning to Trust Your Body Again with POTS

How do you start trusting your body again after a POTS diagnosis?In this episode, Kelsey and Brit talk about the fear of doing everyday activities when your symptoms feel unpredictable. From weddings ...

16 Kesä 16min

Suosittua kategoriassa Terveys ja hyvinvointi

unicast
aamukahvilla
meditaatiot-suomeksi
vakeva-elama-viisaampi-mieli-vahvempi-keho
psykopodiaa-podcast
tiedenaiset-podcast
rss-kuumilla-aalloilla
rss-uplevel-by-sonja-hannus
katilon-kahvitunti
rss-pt-paahtio
rss-rentoudu-podcast-rentoutumiseen-hanna-viljanmaa
voi-hyvin-meditaatiot-2
rss-adama-mindful-hetki
selviytyjat-tarinoita-elamasta
rss-mighty-finland-podcast
rss-sanelunpurku-podcast
rss-taysi-voima
rss-hereilla
junnut-pelissa
terapiassa