Eds Phone Cases - iPhone and Android

Designed for EDSers! Spread the awareness of Ehlers Danlos Syndrome with this bold Straight Outta Collagen shirt! Featuring epic distressing texture and ink splatter for an edgy, worn look. This is the perfect gift for anyone affected by EDS. Help raise awareness of EDS and EDHS with this shirt.

EDS sufferers show how you aren't going to let Ehlers-Danlos Syndrome win you are a warrior. This invisible illness may make your days harder but you are stronger than the disease.

EDS sufferers show how you aren't going to let Ehlers-Danlos Syndrome win you are a warrior. This invisible illness may make your days harder but you are stronger than the disease.

EDS sufferers show how you aren't going to let Ehlers-Danlos Syndrome win you are a warrior. This invisible illness may make your days harder but you are stronger than the disease.

EDS sufferers show how you aren't going to let Ehlers-Danlos Syndrome win you are a warrior. This invisible illness may make your days harder but you are stronger than the disease.

EDS Ehlers-Danlos Syndrome, Not your average Zebra. Everyone in the EDS club whether it is hypermobility or vascular EDS, know what its like to suffer with an invisible chronic illness. Wear your illness with pride or support someone who is living with this disease. Help raise EDS awareness.

EDS sufferers show how you aren't going to let Ehlers-Danlos Syndrome win with this Zebra Strong design. This invisible illness may make your days harder but you are stronger than the disease.

Ed's crew

For those with Ehlers Danlos Syndrome

Loose Joints, Stretchy Skin EDS Strong - Ehlers Danlos Syndrome Awareness

Promote awareness of Ehlers-Danlos Syndrome by wearing Rosie the EDS warrior.

Show awareness for ehlers danios syndrome.

EDS sufferers show how you aren't going to let Ehlers-Danlos Syndrome win you are a warrior. This invisible illness may make your days harder but you are stronger than the disease.

MJ Fox. Raising awareness doesn't need to be dull.

Perfect for those with Ehlers Danlos Syndrome and know what life is like because of it, What Life With EDS Is Like – Just Walking is based on a true story about injuries sustained while walking, one of the many issues that people with EDS face on a daily basis.

Just because my legs don’t work, you assume incorrectly that my brain doesn’t either

white captial text reads "Nobody knows I have EDS" referring to Ehlers-Danlos Syndrome being an invisible or non-apparent illness

Also available as the quote by itself. From one spoonie to another... Follow me on insta @spooniespecies for more chronic creations and dont forget to tag me in your buys! ©

EDS sufferers show how you aren't going to let Ehlers-Danlos Syndrome win you are a warrior. This invisible illness may make your days harder but you are stronger than the disease.

Pixel art of Ed, Edd n Eddy

The Ehlers Danlos Syndrome Zebra Posse design features a group of zebras ready to take on the world! Perfect for spreading awareness about this invisible illness.

Ehlers-Danlos Syndrome makes it difficult to perform basic tasks or ones that are necessary. Sometimes we fix one thing just to break another, usually in the form of a dislocated joint or a cut that doesn't heal properly.

Juggling comorbidities is no picnic. One diagnosis leads to another, which triggers the next, and so on. Managing each diagnosis on its own is enough work, let alone managing several different disorders and syndromes. We might as well have some fun with it.

Perfect for those with Ehlers Danlos Syndrome and know what life is like because of it, What Life With EDS Is Like – I Slept is based on a true story about injuries sustained after sleeping wrong, one of the many issues that people with EDS face on a daily basis.

If you've ever been a student at the University of Utah, needed a downtown late night pick me up or ordered the hangover special of the Gadawful or a Sex Panther espresso before an exam then you know what an icon Big Ed's was. Celebrate your time at the U and great memories of college in Salt Lake City Utah with this Big Ed's design.

The coolest New York gang icons of all time...as icons!

Perfect for people with Ehlers-Danlos Syndrome to show your support and help spread awareness about EDS and educate people about this connective tissue disorder! Show off this design at support meetings, doctor visits, and EDS Awareness Month in May!

The greatest 80s cartoon icons of all time...as icons!

A really amazing guy died last month. You probably did not know him. I didn't know him well enough. He loved riding his boke. He was kind beyond measure. He loved Hermann Hesse. He was my uncle and now that he is gone I am turning to books and authors he loved to stay in touch with him. I have an invisible disability and it keeps me home. (Ehlers Danlos, Fibromyalgia, POTS, and MCA) It keeps me lonely and frustrated. The incredible civil war between my body's limitations and my soul's needs and goals is one I will fight a long time. This quote makes me think of my uncle that maybe he understood what I am going through.

Perfect for people with Ehlers-Danlos Syndrome and other invisible disabilities, this design features a zebra kick with the words "don't confuse my invisible disability with laziness I will find the strength to kick you."

Ehlers Danlos Syndrome - You're in trouble if the doctor looks your disorder up on the internet features a hand drawn zebra and a quirky fun typeface. Help spread awareness about this disorder with this unique design!

Perfect for people with Ehlers-Danlos Syndrome to show your support and help spread awareness about EDS and educate people about this connective tissue disorder! Show off this design at support meetings, doctor visits, and EDS Awareness Month in May!

In all lowercase letters, across the chest text reads, "ambulatory wheelchair users exists" and beneath that symbols depicts a wheelchair user getting up to walk away

Perfect for those with Ehlers Danlos Syndrome and know what life is like because of it, What Life With EDS Is Like – Putting Up Hair is based on a true story about injuries sustained trying to put hair up in a ponytail, one of the many issues that people with EDS face on a daily basis.

My Ehlers-Danlos Syndrome My Face design features a smiling Zebra in profile with the phrase "My Face When I Finally Get A Diagnosis." Show support and help spread awareness about this rare connective tissue disorder!

Invisible illness club