Tag: Joint hypermobility

While many people have never heard of it, an estimated 1 in 5,000 individuals are affected by Ehlers-Danlos syndrome (EDS), and the hypermobile type (hEDS) is seen with increasing frequency. For those living with this genetic connective tissue disorder, the question 'How do people with EDS feel?' reveals a complex reality extending far beyond simple joint flexibility.

As a group of inherited disorders affecting connective tissue, Ehlers-Danlos syndromes (EDS) result from faulty collagen, the body's most abundant protein. These defects lead to a wide spectrum of issues affecting nearly every body system, meaning the problems caused can vary significantly between the different EDS types.

Affecting approximately 1 in 5,000 individuals, Ehlers-Danlos Syndrome (EDS) is a group of inherited connective tissue disorders that primarily affects the skin, joints, and blood vessel walls. The question of whether this condition is a degenerative disorder is complex, as its impact on the body is often progressive, with symptoms evolving and potentially worsening over a person's lifetime.

While a specific condition known as 'Eldens' disease does not exist in medical literature, the term is a common misspelling that likely refers to Ehlers-Danlos syndromes (EDS), a group of rare, inherited disorders that affect connective tissues. The confusion may also stem from online searches related to the fictional “Scarlet Rot” ailment in the popular video game *Elden Ring*.

Though exceedingly rare, affecting as few as 17 in one million people, it is medically possible to be born without certain ligaments. While the body relies on these fibrous tissues for joint stability and movement, some individuals have a congenital absence of ligaments. So, can you have no ligaments? The answer is yes, though it is the exception and not the rule.