EHLERS DANLOS SYNDROME

Ehlers Danlos Syndrome (EDS) is a rare genetic disorder of connective tissue that causes unusually flexible joints, very elastic skin, and fragile tissues.

There are six major types of EDS. Hypermobile or Type III is the most common type. Symptoms of Hypermobile EDS include loose, unstable joints and long-term joint pain. People who are “double-jointed”, that have joints that move well beyond the normal range, may in fact have a form of EDS. Symptoms of Classical EDS, the second most common type, include highly elastic and delicate skin that tears and bruises easily.

For more information on EDS, check out our blog- Is There Such a Thing as Being Double Jointed?

Symptoms

• Your joints are hyper-flexible and move well beyond the normal range of motion
• Your skin is stretchy and elastic
• Your skin is easily damaged and doesn't heal well
• You have joint pain

What Can I Do About It?

Protecting your joints and skin is crucial in managing your EDS. Sunburn and injuries to the skin are difficult to skin that is fragile. Wounds must be tended with great care and infections treated and prevented. Contact sports, such as football, and exercises, like running, that heavily impact the joints, should be avoided. Braces/Splints that help support stable joints without limiting function may be helpful.

Splints and Braces That Can Help (Click on the box below)