CHRONIC ILLNESS LIFE | Going to the Doctor

“On a scale from one to ten 🤪” #chronicillness #chronicpain #spoonielife #ehlersdanlos #pots #mcas #lymedisease #invisibleillness #chronicillnessawareness

[@pinkpele]

SO FREAKING RELATABLE!!

[@codih1716]

ehlers danlos life!

[@Silmarwyn]

OMG Um...I teared up because I feel this.

[@yippee8570]

I don't get much pain, mine is more fatigue (level 4-6 pain is my usual for at least a week every month, though), but of course I hide that too when I'm in a social setting, unless I literally cannot hide it any more, at which point I need to be in bed because I'm a danger to myself. The amount of masking we do so we're not perceived as weird or attention-seeking is ridiculous. Why should the disabled person have to hide? Shouldn't accessibility mean we can just be ourselves? Sorry for the rant, this one obviously hit home. Subscribed!

[@joshuaborem7063]

I’ve endured lower back pain for 25 years and this video is true. Not saying mine gets to level 10 though, but I do live with level 2-4 at all times, with regular increases to level 5,6or 7.

[@sherriouellette8832]

You forgot ‘eat healthy, exercise more, and lose weight.’