Joints that move beyond their end range. Example when standing, knees locked, shoulder forward, everything hanging. You may also be able to do “Party tricks” with moving your joints.

You could have no other symptoms or it could be part of a larger connective tissue syndrome

It is thought joint hypermobility affects approximately between 1 in 4 to 1 in 10 people.

Ehlers-Danlos Syndrome (EDS) is a genetic connective tissue syndrome. There are currently 13 types of EDS, Hypermobile EDS is one of these.​ Most types are thought to have the common features of joint hypermobility (stretches beyond normal range) and tissue fragility. 

Hypermobile Ehlers-Danlos Syndrome (hEDS) is the most common type of EDS.

Symptoms of this type may include:

- Joint hypermobility, Joint pain,Skin hyperextensibility
- Easy bruising
- Chronic Exhaustion
- Digestive problems
- Heart problems, dizziness and lightheadedness

Research is still ongoing, but scientists think that certain genes might not work the way they should. These gene changes can affect how proteins are made, which then affects the structure and function of connective tissue. In people with hEDS, this may cause the connective tissue to become too stretchy and fragile.

Think of connective tissue like the rubber bands that hold everything together inside your body. These “rubber bands” support and connect your joints, skin, organs, and more. In people without EDS, the rubber bands are strong and stretchy just enough to do their job. But in people with hEDS, the rubber bands might be too loose or too thin. This can make joints unstable, organs less supported, and systems in the body not work as well.

Because connective tissue is found all over the body, when it's not working properly, it can cause symptoms in many different areas—not just the joints.

There is unfortunately no cure. However with our management strategies, many individuals are able to manage their symptoms and live fulfilling lives.

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