Why Exercise Often Makes POTS or MCAS Symptoms Worse in EDS

If you live with Ehlers-Danlos Syndrome (EDS) or hypermobility, you may recognise this pattern:

You try to exercise in a “gentle” or graded way.
One session feels okay.
The next leaves you dizzy, exhausted, flared, or unwell for days.

You’ve been told:

  • “Just keep moving”

  • “Your fitness will build over time”

  • “It’s deconditioning”

  • “You just need to be consistent”

But for many people with EDS, especially those with POTS, dysautonomia, or MCAS-type symptoms, movement intolerance isn’t a willpower issue.

It’s a systems-level load problem.

 

The Overlap Between EDS, POTS and MCAS

People with EDS frequently experience overlapping conditions, including:

  • POTS (Postural Orthostatic Tachycardia Syndrome)

  • dysautonomia

  • mast cell activation syndrome (MCAS)

  • chronic fatigue and exercise intolerance

While these conditions are different, they often coexist because connective tissue, circulation, and nervous system regulation are closely linked.

When one part of the system struggles to manage stress, symptoms can cascade.

 

What Is POTS — and Why Exercise Can Trigger Symptoms

POTS is characterised by difficulty regulating heart rate and blood pressure when upright.

Common POTS symptoms include:

  • dizziness or light-headedness

  • rapid heart rate

  • chest pressure

  • breathlessness

  • fatigue

  • poor heat tolerance

  • symptom worsening after exercise

In EDS, exercise can worsen these symptoms when movement increases circulatory demand without sufficient mechanical support.

If force is leaking through joints and posture, the autonomic system has to compensate — raising heart rate, breathing demand, and stress output.

This makes even low-intensity exercise feel overwhelming.

 

MCAS and Movement Intolerance

Mast cell activation syndrome (MCAS) involves inappropriate or exaggerated inflammatory responses.

Common mast cell activation symptoms include:

  • flushing

  • fatigue

  • headaches

  • gastrointestinal upset

  • “flare” responses to stress or exertion

In people with EDS, poorly tolerated movement can act as a mechanical stressor, triggering downstream immune or inflammatory responses.

This is why some individuals feel worse after:

  • repetitive exercise

  • long periods of standing

  • poorly coordinated strength training

  • breath-holding or bracing strategies

It’s not that movement is harmful — it’s that how movement is organised matters.

 

Why “Gentle Exercise” Still Isn’t Always Appropriate

Gentle does not automatically mean low stress.

When mechanics are inefficient:

  • even low loads accumulate irritation

  • repetition compounds instability

  • the nervous and autonomic systems stay on high alert

  • recovery capacity is exceeded quietly, then suddenly

Many people with EDS report that:

  • symptoms don’t appear during exercise

  • they flare hours or days later

  • tolerance feels unpredictable

This delayed response is a hallmark of system overload, not failure.

 

Movement, Mechanics and Autonomic Load

Movement intolerance in EDS is often driven by a combination of:

  • inefficient gait mechanics

  • poor postural organisation

  • excessive muscular guarding

  • altered breathing strategies

  • unstable load transfer through the pelvis and trunk

When these factors are present, the body must work much harder to produce the same movement.

That extra cost shows up as:

  • fatigue

  • dizziness

  • breathlessness

  • shutdown or flares

This is why improving mechanical efficiency often reduces physiological stress, even without increasing fitness.

 

Rebuilding Tolerance Without Crashes

For people with EDS, POTS or MCAS-type symptoms, progress depends on:

  • sequencing before strengthening

  • coordination before repetition

  • gait before conditioning

  • tolerance before intensity

Effective progression should:

  • avoid forced stretching

  • avoid maximal effort early

  • build capacity gradually

  • prioritise consistency over volume

  • respect recovery signals

The goal isn’t pushing through — it’s expanding what the system can tolerate without backlash.

 

Where Assessment Fits In

Because symptoms overlap and vary day-to-day, generic exercise advice often misses the mark.

A biomechanical assessment looks at:

  • posture and load distribution

  • walking mechanics

  • breathing patterns

  • balance strategies

  • how stress accumulates across the system

This allows movement support to be tailored — rather than guessed.

➡️ If you want to understand how this applies to you, our EDS & Hypermobility Support assessment focuses on mechanics, tolerance, and safety — not pushing symptoms.

Book An Assessment
Louis Ellery

Just a man trying to make the world more functional and less painful.

https://www.functionalpatternsbrisbane.com
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Why Gross Motor Control Matters More Than Strength in EDS & Hypermobility