“If you handle it well, they tend to forget that you’re handling it at all… It doesn’t mean that I’m okay… I still have to deal with my #chronicillness(es) and handle everything… I still have way too many medical appointments and way too much #pain.” https://t.co/t9QORp6ULB
“The thing with #ChronicPain is that it is utterly exhausting. I’m not talking “a little bit tiring,” I’m talking the kind of tiredness that no amount of sleep seems to cure. The kind of tired which makes every single atom of your body ache and cry out.” https://t.co/sY8RzFYDIN
“The problem with so many people who live in my world of #chronicillness is that we never fake being ill—but we’re masters at faking being well. I think it makes people uncomfortable if I’m honest about how I’m feeling.” https://t.co/pnq7UymAjh #ChronicPain#InvisibleIllness
“#ChronicPain can change on a day to day basis. Pain can even change on a minute to minute basis… Just because a person looks healthy, that doesn’t mean that they feel 100 percent. People with chronic pain are very good at hiding their pain and emotions.” https://t.co/07Zl3dECGk
“#ChronicPain can disrupt sleep, which in turn, exacerbates the pain, creating a distressing cycle. This disruption heightens #anxiety, reduces pain tolerance, and diminishes emotional resilience, making day-to-day coping a challenge.” https://t.co/I98MOCg95g #MentalHealthMatters
“When someone with #chronicillness says that they are tired, it means something very different than when someone without chronic illness says the same thing. There is no guarantee that our energy will be replenished after sleeping.” https://t.co/DKvORl92A6 #chronicpain#spoonie
“As research continues to show, pain is biopsychosocial—a lived experience. We’re more than our physical pain and #ChronicPain is more than just a rating on a pain scale. A number doesn’t capture our struggle with pain.” Letter to Pain Providers https://t.co/IRKBjM88Og #cpp
“It takes a lot of energy to be in pain all the time… You can’t know what it’s like living with #chronicpain unless you have it, and understanding what it’s like […] dramatically affects how you treat someone who lives with it.” https://t.co/UUdev4BWcv @kmitchellauthor#spoonie