brook

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

So close! but that is not actually how that works! #chronicillnesswarrior #potssyndrome #invisibleillness #invisiblenotimaginary #dysautonomia #potsie #potssyndromeawareness

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

get the mobility aid🫶🏼 #dysautonomia #chronicillnesswarrior #potssyndrome #invisibleillness #mecfs #hEDS #ehlersdanlos #mobilityaid

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

it doesn’t matter how fit, athletic or healthy you are. life can change in an instant. don’t take it for granted. #chronicfatigue #dysautonomia #chronicillnesswarrior #potssyndrome #invisibleillness #mecfs #hEDS #ehlersdanlos

Lmk what else you guys want to see in p2 😌 #chronicfatigue #chronicillnesswarrior #potssyndrome #invisibleillness #chronicillness #mecfs #hEDS #ehlersdanlos #mcas #dysautonomia #chronicillnessawareness

i love this trend i wanna hear all your guys stories 😅 #chronicfatigue #dysautonomia #potssyndrome #chronicillnesswarrior #invisibleillness #mecfs #hEDS #ehlersdanlos #invisiblenotimaginary

It is running rampant and no one wants to talk about it 🚩 #dysautonomia #chronicillnesswarrior #potssyndrome #invisibleillness #mecfs #hEDS #ehlersdanlos #chronicfatigue