05/03/2025
Hey bendy baddies! It's the start of May; which means it's EDS Awareness Month again. Something I would normally be excited about but it's lost its luster through the years because so many people are still not getting diagnosed, and the ones in charge are still muffling their ears on this diagnostic criteria.
Therefore, we're no longer celebrating EDS Awareness Month. No, no.. we're celebrating EDS Reckoning Month. We're aware of EDS now.. it's time to turn chronic illness into CHRONIC ICONIC. Your collagen may be chaotic but your content is about to be cute AND powerful.
Join the and show the world what living with Ehlers Danlos Syndrome really looks like.. sass, braces, and all.
From bendy joints to medical gaslighting to slaying in the face of fatigue, we're spilling the sparkly truth.
Post daily. Educate gently. Slay endlessly.
Because even when the connective tissue doesn't connect... the girls still do.
