Jameela Jamil, a British actress, has spoken out about her struggle with Ehlers-Danlos syndrome (EDS), a rare condition that affects the body’s connective tissues. On Tuesday, the actress posted a video of herself on social media pulling her cheeks to demonstrate the elasticity and flexibility of the skin.
She intended for the video to spread awareness of the problem and to encourage people to seek treatment because undiagnosed or untreated cases of the condition can be fatal. In a video that Jameela Jamil posted, she can be heard saying:
“Hello, have a look at this. This is not a filter or program. Look at how elastic my face is—me. I have EDS, HEDS 3, and the H because I’m so hypermobile, which is why it’s so elastic. She discussed her joints and demonstrated how nothing bends “the right way.” She uttered:
“Even though people like to make fun of me because of my condition, I still want to talk about it. It’s a dangerous condition to have if you don’t know you have it because it affects every aspect of your body and mind.
Jameela Jamil’s Symptoms? Detailing Ehlers-Danlos Syndrome
Even though Jameela Jamil’s disease is relatively uncommon, she explains in her video that, if undiagnosed or untreated, it can be pretty hazardous. According to experts, the illness is a collection of hereditary disorders that result in aberrant collagen function.

These may also impact the connective tissues that often support and form the skin, joints, bones, and even blood vessels. People with this illness have unusually mobile joints and flexible, brittle skin that is prone to breaking, as shown in Jameela Jamil’s video.
According to experts, there are roughly 13 different types of EDS. Hypermobility is one of them, and the Good Place actress has it. In addition, there are various forms, such as spondylodysplastic, classic-like, cardiac-vascular, vascular, brittle cornea, etc. Regarding symptoms, the most prevalent ones are floppy joints, elastic skin, and delicate skin.
However, if a person has excessive muscle discomfort, muscle weariness, easily bruised skin, or issues with their heart valves, they should see a doctor right once. A few mobility tests, genetic tests, a skin sample, and an echocardiography test can all be used to make a quick and accurate diagnosis.
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View The Signage. “It can save your life,” Jameela Says About EDS
Jameela Jamil stated in her video that raising awareness of the rare disorder was the only reason she made the video. The She-Hulk actor yelled about the warning signals and symptoms:

“The way it affects bleeding, bruising, and healing, as well as if you want to get pregnant… I don’t use drugs, drink, or smoke. I’m concerned about my health, which puts me at a disadvantage. It indicates that you experience joint dislocation, difficulty cleaning your teeth, migraines, and sporadic allergies.
She also tried to raise awareness of the condition and encourage individuals to seek medical attention if they experienced any symptoms. “I’m not a doctor, but I want you to see one. If you constantly have accidents with your joints, please look at the symptoms. You could end up living—the folks who have it look good. I love you. I’m with you. Go get checked!”
This is not the first time that Jameela Jamil has spoken about her ailment. When she posted a video about it on social media in 2019, she addressed the problem. In an interview with Parade in 2021, she discussed it once more and referred to it as an “invisible sickness.” You can also check Auditory Processing Disorder Symptoms: How is it Tested and Treated?
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