Invisible illness

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Invisible illnesses aren’t always completely invisible 🙌🏻 When someone has a chronic illness, there will always be little signs here and there to look out for ⬇️ 🤍 Using mobility aids and medical devices 🤍 Sitting down more frequently than most 🤍 Taking several different medications 🤍 Needing to take many breaks 🤍 Taking things slower than others 🤍 Going to the doctor frequently 🤍 Blood pooling, shakiness, fainting 🤍 Sweating, flushing, color changes 🤍 Checking vital signs while out frequen...

Invisible illnesses aren’t always completely invisible 🙌🏻 When someone has a chronic illness, there will always be little signs here and there to look out for ⬇️ 🤍 Using mobility aids and medical devices 🤍 Sitting down more frequently than most 🤍 Taking several different medications 🤍 Needing to take many breaks 🤍 Taking things slower than others 🤍 Going to the doctor frequently 🤍 Blood pooling, shakiness, fainting 🤍 Sweating, flushing, color changes 🤍 Checking vital signs while…

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Last month I had an appointment at a rheumatologist to get evaluated for Hypermobile Ehlers-Danlos Syndrome (hEDS) or Hypermobility Spectrum Disorder (HSD). If you follow me on Twitter, you already know this did not go so well. I already knew I didn’t fit the hEDS criteria, as they’ve been made really strict in order to…

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