Popular People With Ehlers-Danlos Syndrome

Over the last years, more and more famous Hollywood stars have come out with having been diagnosed with Ehlers-Danlos syndrome, sharing their journey on social media and with the press to raise awareness. For EDS Awareness Month, Chronic Pain Partners’ Karina Sturm put together a list with popular fellow zebras, including Billie Eilish, Jameela Jamil, Yvie Oddly and many more. We hope with increased public awareness, our community keeps growing, more people will speak out about their struggles and we’ll finally get the care we need! 

1 Selma Blair

Selma Blair is an American actress known for her work in film and television. Blair’s breakthrough came with her role in the 1999 teen comedy “Cruel Intentions.” In 2018, Blair publicly revealed that she had been diagnosed with multiple sclerosis, a chronic inflammatory disease affecting the central nervous system. Since then, she has been an advocate for MS awareness and has openly shared her journey with the condition, becoming a role model for disabled people across the globe. She has shared her MS journey in her documentary “Introducing, Selma Blair.”

Recently, in January 2024, Blair shared on Instagram that she also lives with chronic pain from Ehlers-Danlos Syndrome!

Image: Screenshot from Instagram reveal of EDS diagnosis, Selma Blair

2 Billie Eilish

Billie Eilish, a woman with black shoulder-long hair all dressed in black.
Billie Eilish, Image © Glenn Francis, www.PacificProDigital.com (Wikipedia) CC BY-SA 4.0

Billie Eilish is an American singer, songwriter, and pop icon. She was born on December 18, 2001, in Los Angeles, California. Eilish gained fame in 2015 with her debut single “Ocean Eyes” and has since become known for her unique sound and edgy fashion style. Her debut album, “When We All Fall Asleep, Where Do We Go?” released in 2019, was a commercial and critical success. She has won multiple Grammy Awards, including Album of the Year. Eilish has been praised for her openness about her struggles with panic attacks and depression. In 2023, Ellis publicly talks about having been diagnosed with hypermobility. An article in Vogue shares: “Years of subsequent lower body injuries, and just as many misdiagnoses, increased the alienation Eilish felt in her own skin before she discovered, through her movement coach, Kristina Cañizares, that she has a condition called hypermobility.” [Eilish has not formally been diagnosed with EDS but with symptomatic hypermobility.]

Image © Glenn Francis, www.PacificProDigital.com (Wikipedia) CC BY-SA 4.0

3 Jameela Jamil

Jameela Jamil, a woman of color with long brown hair holding two air balloons in front of her chest.
Jameela Jamil, Image: https://abilitymagazine.com/jameela-jamil-advocate-first-actress-second/

Jameela Jamil is a British actress, model, and activist born on February 25, 1986, in London, England. She is best known for her role as Tahani Al-Jamil in the television series “The Good Place.” In addition to her acting career, Jamil is a vocal advocate for body positivity and mental health awareness. In 2022, Jamil officially came out publicly with her diagnosis of Ehlers-Danlos syndrome. She has since used her platform to raise awareness about the condition and to challenge the societal pressures that contribute to the stigmatization of illness and disability.

Jamil’s advocacy work includes the creation of the “I Weigh” movement and uses her platform to advocate for social justice and to promote self-love and acceptance for all individuals. In an interview with Sturm for Ability Magazine, Jamil said, “Ehlers-Danlos syndrome is always at the forefront of your mind because it affects every single cell in your body, and so every micro decision you make is in consideration of Ehlers-Danlos syndrome. For someone to discard that just because you look ‘Ok,’ according to their own Bible of ableism, it’s very hurtful.” 

Image: https://abilitymagazine.com/jameela-jamil-advocate-first-actress-second/

4 Yvie Oddly

Yvie Oddly, a Drag Queen with short brown hair a short colorful dress and red eyes.
Yvie Oddly, Image: DVSROSS – Dragcon-25 (Wikipedia) CC BY 2.0

Yvie Oddly is an American drag queen, performance artist, and singer. Oddly was born on May 17, 1994, in Denver, Colorado, and first gained national attention as a contestant on the eleventh season of the reality show “RuPaul’s Drag Race,” where she ultimately emerged as the winner. In addition to her drag performances, Oddly is also a singer and has released several singles and has been an outspoken advocate for LGBTQIA+ rights. Oddly came out with Ehlers-Danlos syndrome in 2019 after having to use crutches because she was in so much pain after her performance. “I’ve always been in pain as early as I can remember, and I simply thought it was growing pains. We wrote it off as such at first, but it was just so bad that I couldn’t make it through a school day from the pain or I’d come home in tears. I had to pull out of every extra curricular activity I have ever done because the pain was getting far too much to handle,” she said in an article in Out.

Image: DVSROSSDragcon-25 (Wikipedia) CC BY 2.0

5 Halsey

Halsey, a woman with curly brown long hair and a colorful outfit on a stage with a microphone in her hand.
Halsey, Image: Justin Higuchi from Los Angeles, CA, USA – Halsey @ Grammy Museum 09/23/2019, CC BY 2.0, Wikipedia

Halsey is an American singer and songwriter. Born on September 29, 1994, in Edison, New Jersey, Halsey began her music career by self-releasing music on social media platforms, which led to her signing with Astralwerks in 2014. Halsey gained mainstream success with her debut studio album “Badlands” in 2015, which included hit singles such as “Gasoline” and “Colors.” She has since released several more successful albums. In addition to her music career, Halsey is also known for her advocacy work, particularly around issues related to mental health and sexual assault. She has also been open about her own experiences with bipolar disorder, endometriosis, and miscarriage. “I was hospitalized for anaphylaxis a few times and had some other stuff going on. Basically, after seeing like 100,000 doctors, I got diagnosed with Ehlers-Danlos syndrome, Sjogren’s syndrome, Mast Cell Activation Syndrome (MCAS), POTS (postural orthostatic tachycardia syndrome),” they said on Instagram in May 2022.

Image: Justin Higuchi from Los Angeles, CA, USA – Halsey @ Grammy Museum 09/23/2019, CC BY 2.0, Wikipedia

6 Cherylee Houston

Cherylee Houston, a woman with curly brown hair and long eye lashes.
Cherylee Houston, Image by Cherylee Houston (https://abilitymagazine.com/cherylee-houston-writers-and-performers-with-disabilities-eds/)

Cherylee Houston is a British actress born on April 29, 1975, in Morecambe, Lancashire, England. Houston is best known for her role as Izzy Armstrong in the long-running soap opera “Coronation Street” and as Maz, a character in Houston’s BBC Radio 4 comedy series “Tinsel Girl”. Houston is a wheelchair user and has always been outspoken about her diagnosis of Ehlers-Danlos syndrome (EDS). She quickly became a spokesperson for raising awareness of the condition. Since her diagnosis, Houston has continued to act in “Coronation Street” and other TV shows and incorporates her experience with EDS into her shows! She has also become an advocate for disability rights and inclusion in the arts. “In my early teens, I was told I had a growing disability, then arthritis and MS, and then they decided I was making it up. For ten years, they said it was a mental health issue. I got to the point where I stopped speaking about being in pain, even though I was in severe pain. This part was tricky and impacted my identity quite a lot because I’d struggle, but I couldn’t tell people how much I was struggling,” Houston says in an interview with Sturm for ABILITY Magazine

Image by Cherylee Houston (https://abilitymagazine.com/cherylee-houston-writers-and-performers-with-disabilities-eds/)

7 Sia

Sia, a woman with blonde hair and a white shirt with her mouth open as if she was singing.
Sia, Image: Charlie Llewellin, CC BY-SA 2.0 via Wikimedia Commons

Sia, who was born on December 18, 1975, in Adelaide, South Australia, is an singer-songwriter best known for her hits like “Chandelier” and “Elastic Heart.” She began her music career in the 1990s as a member of the band Crisp, but gained mainstream success as a solo artist with her 2014 album “1000 Forms of Fear,” which featured the hit single “Chandelier.” She has since released several more albums. In addition to her music career, Sia is also known for her distinctive visual style and often wears oversized wigs that cover her face in public appearances and performances. She has written songs for popular artists such as Rihanna and also (co-)directed several music videos for herself and other artists, including Maddie Ziegler’s iconic performance in the “Chandelier” video. On October 4, 2019, Sia shared she lives with Ehlers-Danlos syndrome. On Twitter, she wrote: “Hey, I’m suffering with chronic pain, a neurological disease, Ehlers-Danlos and I just wanted to say to those of you suffering from pain, whether physical or emotional, I love you keep going. Life is f*cking hard. Pain is demoralizing, and you’re not alone.” 

Image: Charlie Llewellin, CC BY-SA 2.0 via Wikimedia Commons

Just because a public person has EDS does not automatically make them a good spokesperson for the whole community. While we all agree that public attention is needed, we also realize there are some controversies around some of the people in this list. For instance, we moved Sia to he back of the list since her film “Music” has been widely criticized by the autistic community to misrepresent people with autism. Many people with EDS also have autism and therefore, we felt it was important to mention this. We think it’s crucial to be aware of  all a person stands for. So when choosing your favorite public spokesperson with EDS, get well informed, make up your own mind and decide for yourself  who represents you the best. We hope over the years and with improved awareness, we’ll see many more stars come out with EDS and publicly speak about our struggles. 

10 thoughts on “Popular People With Ehlers-Danlos Syndrome”

  1. Mary obrien says:

    My sister and I were diagnosed about 9 or 10years ago but our doctor doesn’t think there’s such a thing as eds. My sis was taken yo hospital in April for chest infection unfortunately it was a heat attack, she was taken to different hospital and they decided to do open heart surgery as all tests showed it was a hole in the heart. When they got her down to theatre they couldn’t find a hole, further tests showed back of her heart at the bottom was like butter, they couldn’t fix her, and they said it was down to eds, never got to speak to her again.. now I’m worried as my family are, about my eds, but if my doctor and most docs here think it’s a nonsense and there’s no such thing…. what chance have I got….?

  2. Gloria Hartsoch says:

    I have EDS and where I live there is no help no one cares because rare diseases do not generate money it’s put on the shelf and forgotten. That’s How I feel put on shelf way in the back and forgotten.

  3. Tina M Zemla says:

    Where do you live, Mary? I live in Upstate New York, and every doctor I see (and there are several) have heard of Ehlers-Danlos Syndrome. It is a well established, real genetic disorder. There are around nine different types of EDS, and most can be detected with a genetic test. The most common, Hypermobility Type, does not yet have a genetic test, but can be diagnosed using clinical knowledge and the Brighton test for joint hyperextension. Please find new doctors. I am so sorry to hear about your sister. You need to find competent medical professionals who take you seriously.

  4. Anne-Marie Glover says:

    Hello Mary this is heart breaking to hear firstly if I were you I would I would find a different GP your condition is real and I know every day will be a living struggle for you my sister suffers from EDS and one consultant in the hospital thought her condition was psychological but later on a scan proved she was not in imagining what she was going through and he ended up having to appologise to her, stay strong,Sending love and healing light your way,
    Anne-Marie

  5. Juli says:

    This comment has been edited based on our comments policy.

    I was diagnosed at a university genetic center in Pennsylvania, but there seems to be some further problems at that school being brought up with the latest global climate. I had noticed that some people really haven’t studied science, a big problem in America is seen with dishonest and pushed pharmaceutical realms, placing some ingredients through streamlining agriculture and what health food is through expensive stores like Wholefoods. If it weren’t for the studies and progress done outside of America, such as the high need and use of MEDICAL GRADE HONEY, the UK seemingly paying more attention and taking real global action than capitalistic America (sorry, ‘MURICA… where everything is either bipolar, adhd, schizophrenia or just a mental gaslighting/medical gaslighting before they send people out their doctor’s appointment it took months to a year to reserve (if you’re 15 minutes late after all that waiting, too, you’re screwed for another 6 months to a year).

    Finally being diagnosed, however, changed my life, so I could be aware of what my body was doing, be strong and save my own life. All you can do is manage your condition with its comorbitities, basically you adapt through trial and error (also risky! But better than never knowing what your body’s true mechanical problems are, lol!).

    I’m ecstatic to hear there is some more American awareness in New York, which makes sense too, it seems there would be caring and cerebral, conscious folk who would rather honestly save lives and make a difference to our everyday world rather than perpetuate the deadly entity that is capital-focused healthcare… period.

  6. chandler s. says:

    well yall first thing i am a man who was diagnost with h.E.D.s. also called type three. i am in kansas and i have a dr who has exp. with people with E.D.s. also there is a center for people cwith conective tissu disorders in wichita ks. i share this for those people who are having issues with their doctors. i was finnaly diagnost with heds at 34 now i am 38 and trying to keep going.

  7. Maura says:

    This comments has been edited based on our comments policy.

    Hello!
    I was diagnosed in 2009, and have been searching ever since to build a team of reliable and knowledgeable Healthcare professionals who actually believe in the disorder.
    It’s sad, because I am from Cleveland, where we have a world reknown clinic, yet they don’t diagnose it there.
    In fact, I was told by a geneticist there, back when I searched far and wide to find out what was ailing me, that there is no such thing as EDS, it is just a manifestation of ones own mind.
    I have never been so disappointed in the treatment as I have from that clinic.
    It’s awful.

    I now have a pretty solid team, all from another hospital group, including the best PT on God’s green earth.
    She has become an ambassador for us zebras, and has helped give us a voice.

    All major cities don’t have great Healthcare.
    I dealt with so much gaslighting and now have PTSD to the point of not even going into an ER, due to the treatment I have had in my past.

  8. Mary Buoy says:

    I thought Billie Eilish is a Canadian from ‘down east’?

  9. SufferinginVirginia says:

    Our doctors here, in the US, don’t care about EDS either. They truly do make you feel placed on a shelf and forgotten. It’s all about the money, sadly. There needs to be more doctors willing to LISTEN to patients, do more than bend their thumb as the sole diagnostic test and actually CARE to find them relief. This is very sad, only 4 responses on here. We must do better and start advocating for ourselves and others struggling! Speak up about EDS and all the complex health issues involved.

  10. Alice Martin says:

    Mary, get in touch with the EDS Society, they should be able to send info to you and your doctor.

Leave a Reply

Your email address will not be published. Required fields are marked *

Get Webinar Announcements And Our FREE Guide

Support EDS Awareness

See all upcoming events

Current Poll

How long until you received a proper diagnosis for EDS?

View Results

Loading ... Loading ...