Independent global EDS information & community project · working titleMedical information policy →
Knowledge hub

Understand EDS without needing twelve browser tabs.

Plain-language guides built from recognised medical and patient-organisation sources, with visible review dates and links back to the source.

Start here

What are the Ehlers-Danlos syndromes?

A plain-English introduction to a group of inherited connective tissue disorders.

Reviewed 2026-10-06 →
Diagnosis

hEDS diagnosis: why there is no single test

hEDS is currently diagnosed clinically rather than through a confirmed diagnostic genetic test.

Reviewed 2026-10-06 →
Living with EDS

Fatigue can be one of the hardest symptoms to explain

Severe tiredness is commonly reported in hEDS, but it can have more than one cause.

Reviewed 2026-10-06 →
Symptoms

Joint pain, instability, subluxations and dislocations

Hypermobility is not simply being flexible — for some people it comes with instability and pain.

Reviewed 2026-10-06 →
Symptoms

Skin, bruising and wound healing

Skin features differ by EDS type, and can be much more significant in some types than others.

Reviewed 2026-10-06 →
Associated problems

Dysautonomia and orthostatic symptoms

Some people with EDS or HSD also experience symptoms such as dizziness, palpitations or faintness when upright.

Reviewed 2026-10-06 →
Living with EDS

Sleep and the cycle of pain and fatigue

Poor sleep can amplify fatigue, concentration problems and pain.

Reviewed 2026-10-06 →
Living well

Braces, splints and mobility aids are tools, not failures

The right support can reduce strain and make participation possible.

Reviewed 2026-10-06 →
Families

Children and young people with symptomatic hypermobility

Growing bodies need age-appropriate assessment rather than simply applying adult labels.

Reviewed 2026-10-06 →
Research

EDS knowledge is changing — and the site should show that

The next major diagnostic framework is due in December 2026, followed by care guidance in 2027.

Reviewed 2026-10-06 →