Eds Awareness Posters and Art Prints

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.

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

Show awareness for ehlers danios syndrome.

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

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.

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!

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.

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

Ehlers danlos syndrome warrior...Eds awareness gift

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.

My original Everything Hurts Ehlers-Danlos Syndrome awareness design features a zebra head motif with a vintage worn look. Pretty awesome way to spread awareness about this genetic connective tissue illness!

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.

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."

The perfect gift for Ehlers-Danlos syndrome awareness! This funny design features two EDS ribbons with the text, “I don’t look sick? You don’t look stupid! Looks can be deceiving. Ehlers-Danlos Syndrome”. This design makes a great gift for those with EDS, spoonies and those interested in the spoon theory, chronic pain and invisible illness awareness, friends, and family.

Perfect for those with Ehlers Danlos Syndrome and know what life is like because of it, What Life With EDS Is Like – The Jackass features a common issue encountered by people with invisible disabilities. Shine a light on this misconception about what disabilities should look like with this awesome design!

This ribbon is perfect for showing support and raising awareness about the cause. It's a symbol of strength for you and for family, friends, co-workers, classmates or neighbors. Lupus Awareness

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!

Perfect for those with Ehlers Danlos Syndrome and know what life is like because of it, What Life With EDS Is Like – Ran Out Of Spoons is based on the Spoon Theory. Show off this design at support meetings, doctor visits, and EDS Awareness Month in May!

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!

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

How many spoons are left in YOUR batteries? Now you can tell people with just ONE FINGER... No - not like that - by pointing at the appropriate spoon battery 😆

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!

Life With Ehlers-Danlos Syndrome - Snap Crackle Pop is based on a true story and features what dealing with EDS is like using stick figures. Help support and spread awareness about Ehlers-Danlos Syndrome with this unique design!

Ehlers-Danlos Syndrome and its related disorders don't really show up well on lab reports. There will be one thing that's a little high or low, but nothing that medical professionals seems to care to investigate. Help fight for patient rights with the help of this design!

Perfect for those with Ehlers Danlos Syndrome and know what life is like because of it, What Life With EDS Is Like – Snap Crackle Pop is based on the daily injuries sustained from having Ehlers Danlos Syndrome, one of the many issues that people with EDS face on a daily basis.

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

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!

Bend Don't Break, Ehlers Danlos Resilience - EDS Awareness

Life With Ehlers-Danlos Syndrome - I Slept is based on a true story and features what dealing with EDS is like using stick figures. Help support and spread awareness about Ehlers-Danlos Syndrome 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!

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

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!

Our joints subluxate and dislocate which can cause us to inexplicably fall. Sometimes we are asked why we are so clumsy and the real reason is simple: Ehlers-Danlos Syndrome. Help spread awareness about EDS!

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!

Rare Disease Awareness - I'm So Rare I'm Practically Mythical-Zebra Ribbon - Ehlers-Danlos Syndrome Tee for Rare Disease Warrior Gift