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

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

this comment is so hard for me because it ‘feels like’ cancer is taken so much more seriously and people are so much more supportive, even though chronic illnesses and rare conditions can be just as severe and debilitating 💔 inspo: @Brooke Mary 🫀 #potssyndrome #chronicillnesswarrior #invisibleillnessclub #chronicillness #mecfs #hEDS #mcas #ehlersdanlos #potsie #dysautonomia #disabledtiktok

try two ✨years✨ #potssyndrome #chronicillnesswarrior #invisibleillness #chronicillness #hEDS #mecfs #mcas #ehlersdanlos #dysautonomia #chronicfatigue #zebrastrong #nottooraretocare