top of page

hEDS Posts

Search

Heart Palpitations with POTS Causes, Feelings of Weakness, and How to Find Relief

Writer: zebrathemiddleaged
zebrathemiddleaged
1 hour ago
5 min read

A racing heart can feel alarming, especially when it shows up after something as simple as standing, showering, or walking across the room. For many people with Postural Orthostatic Tachycardia Syndrome, often called POTS, heart palpitations are one of the most noticeable and frustrating symptoms.


POTS affects how the nervous system controls blood flow, heart rate, and blood pressure when the body changes position. The result can be a fast or pounding heartbeat, dizziness, shakiness, brain fog, and a heavy sense of weakness. These symptoms are real, and they can improve with the right mix of daily habits, medical guidance, and symptom tracking.



Eye-level view of a person sitting on a bed with a hand resting over their chest.
Palpitations with POTS often happen during ordinary daily moments.

Why POTS can make the heart pound


In POTS, the body has trouble adjusting to gravity when standing. Normally, blood vessels tighten slightly to help push blood back toward the heart and brain. In POTS, that response may be weaker, delayed, or uneven.


When blood pools in the lower body, less blood returns to the heart. The body tries to compensate by increasing heart rate. That faster rhythm can feel like:


  • Fluttering in the chest

  • A pounding or thumping heartbeat

  • Skipped beats

  • A racing pulse after standing

  • Palpitations after meals, heat exposure, or mild activity


This fast heartbeat is often the body’s attempt to maintain blood flow, not a sign that the heart itself is damaged. Still, new, severe, or changing palpitations should always be checked by a clinician.


Several factors can make palpitations worse in POTS:


Low blood volume


Many people with POTS have lower circulating blood volume. When there is less fluid in the bloodstream, the heart may beat faster to move enough blood through the body.


Blood pooling


Standing still, warm weather, hot showers, and long periods upright can allow more blood to settle in the legs and abdomen. This can trigger the familiar surge in heart rate.


Adrenaline surges


Some forms of POTS involve a stronger stress-hormone response. This can create a shaky, wired feeling along with a pounding heart.


Deconditioning


When symptoms lead to reduced activity, the heart and muscles may lose some conditioning. Over time, even small tasks can feel more demanding.


Triggers from food, sleep, and stress


Large meals, dehydration, alcohol, poor sleep, infection, and emotional stress can all increase symptoms. Menstrual cycle changes may also affect symptom patterns for some people.


How palpitations can lead to weakness


Weakness with POTS is not “just being tired.” It often comes from the same circulation problem that causes the fast heart rate.


When blood does not return efficiently to the heart and brain, the body has to work harder to stay upright. Muscles may receive less steady blood flow. The brain may get less oxygen-rich blood for short periods. The nervous system may also stay in a heightened state, which drains energy.


That can create symptoms such as:


  • Heavy legs

  • Trembling or shakiness

  • Lightheadedness

  • Nausea

  • Shortness of breath

  • Sudden fatigue after standing

  • Feeling better when lying down


The cycle can be discouraging. Palpitations can make a person avoid movement, but too much rest can worsen conditioning. The goal is not to “push through” severe symptoms. The goal is to support circulation, reduce triggers, and build tolerance slowly.


If palpitations come with chest pain, fainting, severe shortness of breath, confusion, or a new irregular rhythm, seek urgent medical care.

Daily habits that may reduce symptoms


Many POTS treatment plans start with lifestyle changes because they directly support blood volume and circulation. A clinician can help tailor these steps, especially for anyone with kidney disease, heart disease, high blood pressure, or pregnancy.


Close-up view of a water bottle, electrolyte packet, and salty snack on a kitchen counter.
Hydration and sodium intake are common parts of many POTS care plans.

Hydrate early and often


Fluids help increase blood volume. Many people with POTS do better when they drink water throughout the day rather than waiting until they feel thirsty. Some care plans include electrolyte drinks, especially during heat, illness, or exercise.


Ask about sodium


Higher sodium intake may help some people hold onto fluid and maintain blood pressure. This should be discussed with a healthcare professional, since it is not safe or appropriate for everyone.


Use compression garments


Waist-high compression tights, abdominal binders, or compression leggings may reduce blood pooling. Garments that include the abdomen often work better than socks alone.


Change positions slowly


Moving from lying down to sitting, then standing, gives the nervous system more time to adjust. Before standing, try flexing the calves, squeezing the thighs, or crossing the legs to help push blood upward.


Avoid overheating


Heat relaxes blood vessels and can worsen palpitations. Cooler showers, fans, breathable clothing, and avoiding long periods in hot environments may help.


Eat smaller meals


Large meals can pull more blood toward digestion. Smaller, more frequent meals may reduce post-meal racing heart and weakness. Some people notice worse symptoms after high-carbohydrate meals, though triggers vary.


Exercise can help, but it needs the right starting point


Exercise is often part of POTS care, but the wrong approach can backfire. Upright workouts may feel impossible at first. Many people start better with recumbent or semi-recumbent activity.


Options to discuss with a clinician or physical therapist include:


  • Recumbent biking

  • Rowing machine workouts

  • Swimming or water walking

  • Floor-based strength exercises

  • Gentle resistance training for legs and core


Short sessions count. A few minutes of tolerated movement can be a valid starting point. Progress may come slowly, and symptoms may fluctuate. The focus is consistency, recovery, and avoiding repeated crashes.


Strengthening the legs and core can support blood return over time. This may reduce the heart’s need to compensate so strongly when standing.


Medical treatments may be part of the plan


Lifestyle changes help many people, but they are not always enough. A healthcare professional may evaluate heart rhythm, blood pressure patterns, medications, anemia, thyroid issues, vitamin levels, and other possible contributors.


Depending on the person’s symptoms and health history, treatment may include medications that:


  • Help the body retain fluid

  • Narrow blood vessels to reduce pooling

  • Lower excessive heart rate

  • Support blood pressure

  • Reduce certain nervous system surges


Commonly discussed options in POTS care can include beta blockers, ivabradine, fludrocortisone, midodrine, pyridostigmine, or other medicines. Each has risks and benefits. Medication choices should be individualized and monitored.


Symptom tracking can make appointments more useful. A simple log might include:


What to track

Why it helps

Heart rate lying down and standing

Shows position-related changes

Blood pressure if available

Helps identify low or unstable pressure

Fluids and sodium intake

Connects habits with symptom changes

Meals, sleep, heat, and stress

Reveals personal triggers

Flares and recovery time

Guides pacing and treatment decisions


Finding relief starts with understanding the pattern


Heart palpitations with POTS causes weakness because the body is working hard to keep blood moving when upright. The pounding heart, shaky legs, and sudden fatigue are connected. They often reflect circulation and nervous system strain rather than a lack of effort or willpower.


Relief usually comes from layers of support: better hydration, appropriate sodium, compression, trigger management, careful conditioning, and medical treatment when needed. Small changes can matter. So can patience, because POTS symptoms often improve in steps rather than all at once.


If palpitations are frequent, worsening, or interfering with daily life, bring a clear symptom log to a healthcare professional. The right plan can reduce the fear around symptoms and help the body feel steadier again. If your symptoms are a source of worry for you always seek medical advice to ensure that your palpitations are not something that requires further treatment.


 
 
 

Comments


Stay Connected

Disclaimer

This site is strictly a blog and information website about HEDS. It does not provide medical advice, diagnosis or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website.

  • Facebook
  • Instagram
  • Link
  • Link
bottom of page