Invisible Merch

Ya Books - The invisible life of Addie Larue

I'm In Power Saving Mode

October is Dysautonomia Awareness Month, help us make some noise for turquoise!

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

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 © 🖤

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

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.

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

rritable bowel syndrome (IBS) is a common disorder that affects the large intestine. Signs and symptoms include cramping, abdominal pain, bloating, gas, and diarrhea or constipation, or both.

Infusion Day

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

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!

5 Star Review on Ehlers-Danlos Sydrome

Semicolon: What's left after my colostomy.

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

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!

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 am an image barrier of Christ

Stand Up For POTS... But Not Too Quickly - Funny POTS

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

Parkinson's Disease - Disability Awareness

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!

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.

Do you have a friend who has trouble with too few spoons or too high of a spoon cost to do things? Do you, personally, feel this sentiment deep in your soul? Then this is for you, from one Spoonie to another.

Lyme Disease - Disability Awareness

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.

I Would, But Flare Day