Invisible T-Shirts

My EDS Awareness Typographic Zebra features the stripes of a zebra making up the letters EDS. show off this awesome and unique design to help spread awareness about this connective tissue disorder!

Time to Believe is a campaign by the Invisible Disabilities Association. People living with invisible disabilities are often disbelieved, because they can't readily "see" their illness or pain. We strive to bring awareness and education, so people will believe and support friends, family, co-workers and strangers living with invisible disabilities!

The universal monsters invisible man, that's it

All profits go to the National MALS Foundation to help us in our mission to educate and spread awareness about Median Arcuate Ligament Syndrome. Designed by Laura Gilmore @mals.foundation

All profits go to the National MALS Foundation to help us in our mission to educate and spread awareness about Median Arcuate Ligament Syndrome. Designed by Laura Gilmore @mals.foundation

All profits go to the National MALS Foundation to help us in our mission to educate and spread awareness about Median Arcuate Ligament Syndrome. Designed by Laura Gilmore @mals.foundation

All profits go to the National MALS Foundation to help us in our mission to educate and spread awareness about Median Arcuate Ligament Syndrome. Designed by Laura Gilmore @mals.foundation

Immerse in the ethereal allure of a trapped mime within an invisible, glass-like interactive layer of graphic design. Unseen yet palpable, this enigmatic creation invites you to explore the boundaries between reality and illusion, where the mime's gestures echo in a mesmerizing dance beneath the surface.

Can Joe Diamond Read Your Mind? The REAL question is, did you spot the second “YOUR” on the first read?

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!

Folks with chronic illnesses (EDS, fibromyalgia, chronic fatigue, and so many others) use “spoons” as a unit of energy. We only have so many spoons in a day. It takes spoons to cook, shower, work, socialize, and play. If you’re “saving spoons,” it means you can’t do too much today because you know you need to do stuff tomorrow! Thanks for supporting a spoonie artist! Feel free to send me a message if there’s anything you’d like to customize! I can change colors and scale and all kinds of things. Don’t hesitate to get in touch!

From one spoonie to another. If you would like a custom colour (design or background) just drop me a message :) For more chronic creations check my page or follow me on insta and don't forget to tag me in your posts @spooniespecies. ©spooniespecies

Myalgic encephalomyelitis is easier to day than to live with

Embrace the power of unseen beauty with this captivating design inspired by a timeless tale. Discover the essence of what truly matters. #InvisibleBeauty #WisdomWithin #PrintOnDemand

Spoon Theory helps folks with chronic illnesses talk about energy levels! "I'm saving spoons today because I have a big presentation tomorrow." "I think it'll take too many spoons to shower today, so I'll just use dry shampoo today and shower tomorrow." "I used up my spoons faster than I thought today, so I think I'd better go home." Thanks for supporting a spoonie artist! Feel free to send me a message if there’s anything you’d like to customize! I can change colors and scale and all kinds of things. Don’t hesitate to get in touch!

Semicolon: What's left after my colostomy.

All profits go to the National MALS Foundation to help us in our mission to educate and spread awareness about Median Arcuate Ligament Syndrome. Designed by Laura Gilmore @mals.foundation

All profits go to the National MALS Foundation to help us in our mission to educate and spread awareness about Median Arcuate Ligament Syndrome. Designed by Laura Gilmore @mals.foundation

I Wear Purple For Lupus Awareness

A fun take on living with Postural orthostatic tachycardia syndrome, after a family member referred to us as this.

Always falling over? Me too! Perfect for the spoonie in your life, or as a treat for yourself!

I am an image barrier of Christ

All profits go to the National MALS Foundation to help us in our mission to educate and spread awareness about Median Arcuate Ligament Syndrome. Designed by Laura Gilmore @mals.foundation

Inspired But Tired

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

Parkinson's Disease - Disability Awareness

This design is a tribute to the Spoon Theory, a metaphor often used by individuals with chronic illnesses to describe their limited energy and daily struggles. The phrase "All Out of Spoons" signifies the depletion of physical or mental energy and serves as a reminder of the challenges faced by those living with chronic illnesses.

A picture of a brain with a nervous facial expression and what looks to be liquid rising inside with the words "Under Pressure" under it.

If you want to add colour drop me a DM via insta :) From one spoonie to another, for more chronic creations check out my shop and follow me on insta for updates @spooniespecies © 🖤

I Would, But Flare Day

Fibro fighter; keep going, or have a nap. Whichever makes you feel better!

Another way of showing off our immune compromised bodies with a bit of style from the Galaxy.

As someone with a complicated pituitary disorder, I have to take a LOT of medications to replace the many crucial hormones my body can't make on its own. Over the years, I've had a few "helpful" "wellness experts" tell me that I would "feel so much better" if I wasn't "taking so many pills". Y'all, these miracles of modern medicine keep me ALIVE. Keep your uncalled for advice to yourself before you really hurt somebody. This design was inspired by that, and all the other uncalled for judgements of anyone who takes any medications to manage their disease, chronic pain, depression, whatever. I see you, spoonies. We've got enough going on without the being judged by others for taking care of ourselves. This one's for you.

Lyme Disease - Disability Awareness

People with chronic illnesses use "spoons" as a way to measure and budget their energy. It takes spoons to work, socialize, cook, clean, and more. Spoonies are strong! Thanks for supporting a spoonie artist!

Yes I’m Still in Pain