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Hypermobility Spectrum Disorders

Bendy joints, frequent sprains, and pain that moves around? Hypermobility is common and often unremarkable — but when it comes with pain and instability, it needs a specific approach.

Overview

What Is Hypermobility?

Joint hypermobility means joints move beyond the usual range. It is common, present in a substantial minority of the population, and frequently causes no problems at all — it can even be an advantage in dance, gymnastics and music. A hypermobility spectrum disorder is diagnosed when hypermobility is accompanied by symptoms such as pain, recurrent injuries or instability, and other conditions have been excluded. Hypermobile Ehlers-Danlos syndrome sits at the more involved end of the same spectrum.

increasing overload Healthy Reactive Degenerative

Use the buttons to see the main areas that need addressing.

Most common

Joint Symptoms

Recurrent sprains and subluxations, joints that feel unstable or give way, and pain that moves between joints. Symptoms often worsen with fatigue and improve with strength. Strengthening through the full available range is the mainstay of management.

Symptoms

How It Tends to Feel

Hypermobility spectrum disorders present with a characteristic mix of joint and systemic features:

Joints That Move Too Far

Ability to bend joints beyond the usual range, often noticed since childhood.

Recurrent Sprains and Subluxations

Joints partially slipping out and back, particularly shoulders, kneecaps and fingers.

Pain That Moves Around

Widespread or shifting joint pain rather than one consistently painful area.

Fatigue

Often the most disabling symptom, and frequently more limiting than the pain itself.

Poor Balance or Clumsiness

Reduced joint position sense makes coordination and balance harder.

Worse After Activity

A tendency to overdo things on good days and pay for it afterwards — the boom-and-bust pattern.

Causes & Risk Factors

What Drives It

Hypermobility is largely inherited, and symptoms arise from the interaction between joint laxity and the demands placed on the body.

01

Genetic Connective Tissue Variation

Differences in collagen structure are inherited, which is why hypermobility often runs in families.

02

Reduced Muscular Support

Where ligaments provide less passive stability, muscles must work harder — and weakness has a disproportionate effect.

03

Reduced Proprioception

Joint position sense is measurably reduced in hypermobile people, contributing to injury and instability.

04

Deconditioning Cycle

Pain leads to reduced activity, which reduces strength, which increases symptoms — a cycle that is very common and very breakable.

05

Hormonal Influences

Symptoms frequently fluctuate with the menstrual cycle and during pregnancy, reflecting hormonal effects on connective tissue.

The Approach

How Management Differs

The principles aren’t exotic, but the execution needs care. Progressions are slower, ranges are controlled, and pacing matters more than in most conditions.

Understanding

Get the framework right

  • A clear explanation of what hypermobility is and, importantly, what it isn’t
  • Establishing a realistic baseline of activity that doesn’t provoke flares
  • Identifying the boom-and-bust pattern if it’s present
  • Screening for features that warrant specialist referral

Tap through the stages. Slower progressions and better pacing are the main adaptations.

How We Can Help You

Treatment & Management

Management is about building active control where passive stability is reduced — and doing it patiently enough that the programme is sustainable.

Thorough Assessment: Assessing hypermobility formally, identifying which joints are symptomatic, and screening for features warranting specialist referral.
Education: Understanding the condition, and specifically that hypermobility is not fragility, which changes what people feel able to do.
Progressive Strengthening: Building muscular control, starting in mid-range and progressing carefully. This population is frequently under-loaded rather than over-loaded.
Proprioceptive Training: Specific balance and joint position work, which addresses a measurable deficit and is distinct from strengthening.
Pacing and Activity Management: Practical strategies for breaking the boom-and-bust cycle, which is often the single biggest change.
Onward Referral: Where systemic features are prominent, referral for specialist assessment of connective tissue disorders.

What the evidence says

Exercise-based interventions have the strongest evidence for symptomatic joint hypermobility, with trials showing improvements in pain, function and quality of life. Programmes emphasising strengthening and proprioceptive control outperform generic advice.

There is no evidence that hypermobile joints need to be protected from loading — the opposite is true. Progressive strengthening is safe and effective, though progressions generally need to be smaller and more gradual than in the general population.

When to Seek Help

Red Flags — Don’t Ignore These

Hypermobility itself is benign. Some features warrant specialist assessment:

⚠ Seek medical assessment if you notice:

  • A family history of aortic aneurysm, sudden cardiac death, or bowel or uterine rupture (needs specialist genetic assessment)
  • Unusually fragile skin, poor wound healing, or widened scars
  • Recurrent joint dislocations requiring reduction
  • Marked dizziness or fainting on standing, or persistent digestive symptoms
  • Neurological symptoms including new numbness, weakness, or changes to bladder or bowel control

Most hypermobility is benign. A family history of vascular or organ rupture, or unusually fragile skin, warrants assessment for rarer types of Ehlers-Danlos syndrome via your GP.

Common Questions

Frequently Asked Questions

Should I avoid exercise to protect my joints?

No — and this is the most important thing to get right. People with hypermobility are frequently under-loaded rather than over-loaded. Muscular control is what compensates for reduced ligamentous stability, so building strength is directly protective.

Should I stretch?

Generally, less than you might think. Hypermobile joints already have plenty of range, and stretching into end range can increase instability and irritation. Building strength and control through the range you have is far more useful.

Is this the same as Ehlers-Danlos syndrome?

They sit on a spectrum. Hypermobility spectrum disorder and hypermobile Ehlers-Danlos syndrome share the core features and the same management approach, differing in specific diagnostic criteria. Rarer types of EDS involve vascular and skin fragility and need specialist assessment.

Why am I so tired?

Fatigue is one of the most commonly reported symptoms, and it’s genuine. Holding hypermobile joints stable requires more continuous muscular work, and disrupted sleep from pain compounds it. Building endurance and improving pacing both help substantially.

Build Control, Not Protection

A programme that builds the strength and control hypermobile joints need — progressed carefully enough to be sustainable.

Book Your Initial Assessment

This page is for general information only and isn’t a substitute for individual medical advice. If you’re experiencing any of the warning signs above, contact your GP or seek emergency medical care as appropriate.