Dear Mayo Clinic: I was recently diagnosed with vascular Ehlers-Danlos syndrome. My doctor said there's no cure, and that it's genetic. What can be done to treat this? I have two young children.

The actress made a TikTok to raise awareness of Ehlers-Danlos syndrome. Jameela Jamil visits SiriusXM Studios on September 13, 2022 in New York City. Santiago Felipe/Getty Images North America ...

Three years ago, I wrote about my daughter Sarah being diagnosed with a connective tissue disease known as hyper-mobile Ehlers-Danlos syndrome, one of 13 variations of this rare condition. We ...

Hypermobile Ehlers-Danlos syndrome is a connective tissue disorder. When Sarah Lazarus’ daughter was diagnosed with it, she discovered that the majority of cases are going undiagnosed for decades.

CHESAPEAKE, Va. — Ehlers-Danlos Syndrome (EDS) is a connective tissue disorder that impacts about 1 out of every 300 people, ... It is also hereditary —all four of her kids have it.

Ehlers-Danlos syndrome can be a devastating disease in patients who are severely affected — a situation made worse by the current scarcity of treatment options. “The life expectancy for those ...

Olivia was born with a severe form of Ehlers-Danlos Syndrome (EDS), a rare genetic disorder that causes her joints to be hyper-flexible -- so flexible that her hips and knees would regularly ...

A Tulsa teenager has been diagnosed with a rare condition called Ehlers-Danlos Syndrome. The disease can cause one to lose teeth, and Meadow Hill is asking for fundraising help for what doctors ...