EDS is complicated, not rare.
We’re not going anywhere.
No matter what they take from us.
Take our care, we'll fight harder.

#EDS #EhlersDanlos #DisabilityRights #ChronicIllness #WeAreNotRare #DisabledAndProud #pots #mcas #heds #spoonie #hypermobility #mariannequilez #edscommunity #mthfr

✨ You’re doing your best, and that truly is enough.
Your symptoms are real. Your voice matters. Your story deserves to be heard. 🌿

#ChronicIllness #EDS #heds #MTHFR #SelfAdvocacy #MedicalGaslighting #ChronicPain #POTS #MCAS #InvisibleIllness #SpeakUpToolkit #SymptomTracker #EDSCommunity #spoonie

The Tangled Web of Sleep Apnea and Ehlers-Danlos Syndrome: Unraveling the Connection Imagine settling into bed after a long day, expecting the sweet embrace of sleep, only to find yourself jolted awake repeatedly, gasping for air. Now, add to this scenario a body whose connective tiss...

Struggling to sleep, breathe, or function? It might not just be “bad sleep.” Let’s untangle the hidden link between EDS and sleep apnea.
#SleepApnea #EDS #ChronicIllness #RareDisease #UnremarkableMe #InvisibleIllness #EDSCommunity #BeKindToYourself #hEDS

www.unremarkableme.com/post/the-tan...