Ehlers-Danlos syndrome

What is Ehlers-Danlos Syndrome?

Ehlers-Danlos Syndrome (EDS) is a rare genetic disorder that affects the connective tissues in your body. Connective tissues are like the glue that holds your body together, making your skin, joints, and blood vessels strong and flexible. People with EDS have a problem with their connective tissues, which can cause a range of symptoms.

Diagnosing Ehlers-Danlos Syndrome

Diagnosing EDS can be challenging because it can vary from person to person. Doctors will look for certain signs and symptoms, such as hypermobile joints (joints that can move beyond the normal range), stretchy skin, and easy bruising. They may also perform genetic tests to confirm the diagnosis. If you or your child have any of these symptoms, it's important to see a doctor for a proper diagnosis.

Treating Ehlers-Danlos Syndrome

While there is no cure for EDS, there are ways to manage the symptoms and improve quality of life. Treatment options may include physical therapy to strengthen muscles and improve joint stability, pain management techniques, and assistive devices like braces or splints. It's important to work closely with your healthcare team to develop a personalized treatment plan that suits your needs.

Preventing Ehlers-Danlos Syndrome

Since EDS is a genetic disorder, there are no specific preventive measures to avoid developing it. However, if you have a family history of EDS, it's important to talk to a genetic counselor before planning a pregnancy. They can provide information and guidance on the chances of passing the condition to your children. Additionally, maintaining a healthy lifestyle with regular exercise, a balanced diet, and avoiding activities that may put excessive strain on your joints can help manage symptoms and prevent complications.