What is POTS? (Postural Orthostatic Tachycardia Syndrome)

Learn what POTS (Postural Orthostatic Tachycardia Syndrome) is, including symptoms, causes, diagnosis, and what it actually feels like to live with it.

Living with POTS (Postural Orthostatic Tachycardia Syndrome) can feel confusing, overwhelming, and often misunderstood—especially because many of its symptoms are invisible.

This page is here to help you understand what POTS is, why it happens, and what it can actually feel like to live with it.


What is POTS?

POTS is a form of dysautonomia, which means the autonomic nervous system isn’t functioning properly. With POTS, the body struggles to regulate these functions—especially when moving from lying down to standing.

The autonomic nervous system controls things your body is supposed to do automatically, like:

  • Heart rate

  • Blood pressure

  • Breathing

  • Temperature regulation

  • Digestion

Autonomic Nervous Dysfunction

POTS involves autonomic nervous system failure causing abnormal heart rate increase upon standing. Heart rate jumps abnormally high (often +30 beats per minute or more within 10 minutes of standing)

Baroreceptor Reflex Impairment

Impaired baroreceptor reflexes reduce blood vessel constriction, disrupting normal blood flow control.

Blood Pooling and Symptoms

Blood pools in the lower extremities, causing brain hypoperfusion, dizziness, and rapid heart rate in POTS patients.

There is no cure for POTS, only treatments and lifestyle changes to help manage symptoms.

What Exactly Happens in POTS?

When a healthy person stands up:

  • Blood vessels tighten

  • Blood moves efficiently to the brain

  • Heart rate adjusts slightly

With POTS:

  • Blood pools in the lower body

  • Less blood reaches the brain

  • The heart compensates by beating much faster

This leads to a rapid increase in heart rate (tachycardia)—often 30+ beats per minute within 10 minutes of standing.

Common Symptoms of POTS

POTS affects each person differently, but common symptoms include:

  • Dizziness or lightheadedness (especially when standing)

  • Rapid heart rate or heart palpitations

  • Fainting or near fainting

  • Severe Fatigue

  • Brain fog or difficulty concentrating

  • Shortness of breath

  • Chest pain

  • Headaches or migraines

  • Nausea or digestive issues

  • Temperature sensitivity

  • Shakiness or weakness

POTS Symptoms can become worse in certain conditions or situations:

  • Being in high heat (showers, hot tubs, saunas)

  • Standing for periods of time (standing in line)

  • Strenuous exercise

  • Being sick or having an infection

  • Menstruation

What Does POTS Feel Like?

POTS is more than just “feeling dizzy.”

It can feel like:

  • Your body isn’t keeping up with simple movements

  • Standing takes effort your body can’t sustain

  • Your energy disappears without warning

  • Your heart is racing even when you’re not doing much

For many, it’s not just physical—it’s also emotional:

  • Frustration from limitations

  • Feeling misunderstood

  • Loss of independence

What Causes POTS?

Researchers aren’t exactly certain yet, but POTS has be linked to:

  • Viral illness or serious infections

  • Autoimmune conditions

  • Pregnancy

  • Trauma

  • Surgery

POTS is far more common in women, usually affecting people ages 15-50.

How is POTS Diagnosed?

POTS is typically diagnosed using:

  • Tilt table test (most common)

  • QSART (measures the autonomic nerves that control sweating)

  • Autonomic breathing test (measures your blood rate and pressure response during exercise)

The key diagnostic criteria is:

  • A sustained increase in heart rate of 30+ beats per minute (40+ in teens) within 10 minutes of standing

  • Without a significant drop in blood pressure

Living with POTS

The unpredictability can be one of the greatest challenges. POTS doesn’t always look the same from day to day. Some days may feel more manageable. Others may feel like your body has completely shut down.

It’s not just standing, but how your body responds to everything:

  • Movement

  • Stress

  • Heat

  • Energy use

If you’re living with POTS, your experience is real. Even if others can’t see it or don’t fully understand it.

There is a growing community of people managing this alongside you, learning how to adapt, adjust, and rebuild life in a body that doesn’t feel like their own.

If this helped you understand what you’re going through, or helped you explain it to someone else, consider sharing it or subscribing for more.

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Disclaimer: This content is for educational purposes only and is not intended as medical advice. Always consult with a qualified healthcare provider for diagnosis and treatment.