brook

Disabled but make it ✨contextual✨ ⚠️EXPLANATION POSTED⚠️ #ambulatory #wheelchairuser #potssyndrome #chronicillnesswarrior #hEDS #dysautonomia #invisibledisability #invisibleillness #ChronicIllness #holyairball #airball

Replying to @The_quad_father Yes, I can walk. No, that doesn’t mean I don’t need my wheelchair. - you wouldn’t walk 3 hours to work when you could drive, so why would I choose to damage my body by standing when I could use my wheelchair? - for me, standing and walking is a calculated risk I may or may not choose to take depending on how my body is feeling that day. #ambulatorywheelchairuser #potssyndrome #chronicillnesswarrior #hEDS #dysautonomia #POTS #mcas #mecfs #ChronicIllness #myalgicencephalomyelitis #invisibleillness #invisiblenotimaginary #ambulatorywheelchairusersexist

Thought these were just random? Nope— it could be POTS😅#POTS #ChronicIllness #chronicillnesswarrior #potssyndrome #potsawareness #dysautonomia #chronicillness #hEDS #invisibleillness #invisiblenotimaginary #potssyndromeawareness #potsie

She loves teaching people about POTs I literally adore her- how did i get so lucky 🫶🏼🥹 #chronicillnesswarrior #disabilityawareness #disabilityadvocate #ambulatorywheelchairuser #hEDS #mecfs #dysautonomia #invisiblenotimaginary #ChronicIllness

It seems fine. Until someone in a wheelchair shows up. That “just a minute” parking, means that someone who actually needs it can’t park there, and may be stuck. It’s convenience for you, but crucial to us. #chronicillnesswarrior #disabilityawareness #disabilityadvocate #ambulatorywheelchairuser #hEDS #dysautonomia #mecfs #invisiblenotimaginary #chronicillness

leaning on Jesus (and the floor) #chronicillnesswarrior #potssyndrome #potsawareness #potssyndromeawareness #dysautonomia #tachycardia #presyncope #chronicillness #invisibleillnessclub #hEDS