#spoonieproblems résultats de recherche
Straight away to the point blue shine on my internet screen so lived it so much balance #spoonieproblems #cfs #pain #chroniclife #spooniewarrior #spooniestrong #painsucks #autoimmune #fibromyalgia #crps #heretohelp
You know it's bad when you are pouring through anatomy books trying to find any kind of clues for your leg pain. It turns out I honed in on the right areas and was right, but how desperate is it that?! Out. Of. Control. Pain. #SpoonieProblems #RicketyBones #MySeveralWorlds
Today's high was 93 degrees - then when thunderstorms began, it rapidly went down to 68. Holy barometric pressure changes!! #Spoonies #SpoonieProblems #ChronicPain #ChronicIllness
Being a Spoonie is basically a nonstop tug-of-war: youtube.com/shorts/ACMp9I4… 🧠 Brain fog vs. fatigue 💊 Insurance battles vs. symptoms ⏰ Rest vs. productivity guilt Which side wins in your life? 👇 #SpoonieProblems #ChronicIllness #DisabilityHumor #BoatTugOfWar
youtube.com
YouTube
Spoonie Tug-of-War: Chronic Illness in a Boat
I may have made a huge mistake but I actually have some plans over the next month or two starting with tomorrow - let’s see if they actually come to fruition and life doesn’t get in the way #chronicillness #spoonie #spoonieproblems #invisibleillness
My biggest challenge is not to get ill when my mom has a health problem. She had cancer and now she is really better, but when she fell ill It was a hard time, and after her recovery, I was almost a month in the hospital. #spoonie #spoonieproblems
How many of my chronic illness friends are primary caregivers for a parent or another disabled family member (spouse, child, aunt, grandparent) ? What’s your biggest challenge? Working on a teaching conference and would find your stories helpful. Thanks for sharing.
I'm Indie Publishing A Little Less Invisible Because #5: When the cute new boy looks at you like that–all frazzled and slightly annoyed–and you thought the heart palpitations were bad before 😅 I want to see more #SpoonieProblems in books #AmWriting #YAFantasy #ChronicIllnessRep
Really wish I could scrape up a few spoons so I could write and talk about my Detroit concert experience. I must be getting worse than I thought if one day’s trip can flare me and knock me out like this… 🥺😭#spoonieproblems
Flare-up brain: ☑️ Can’t remember if I ate ☑️ Forgot what day it is ☑️ BUT I can rate my pain on a scale of 1–10 like a champ 🙃 📘 Painfully Organised was made for days like this. No pressure. 🔗 amazon.com/dp/B0F5BFFH27 #ChronicIllness #BrainFog #SpoonieProblems #FlareUpLife
amazon.com
Painfully Organised: A Flare-Up and Symptom Tracker for Chronic Illness
Living with chronic illness is unpredictable — but this journal helps you find patterns, take control, and track what matters most. Whether you’re managing daily symptoms, tracking flare-ups,...
Recently someone told me how difficult is to have a life like mine. Everytime this is told by people I think their intentions are compassive but it feels like "are you reminding me how difficult is my life to make me feel better?" #spoonie #spoonieproblems
Just in case you needed to hear it: Telling a sick and disabled person that we’re strong because you would’ve ended your life if you had to live like us isn’t a compliment
CRAP. Y'all, if your doctor ever offers you a #Shingles vax 💉 (esp if, like me, you are immunocompromised from an autoimmune condition) FREAKING DO IT. YOU DO NOT WANT THIS MISERY. This is now my 3rd case and it FEELS LIKE I'M ON FIRE!!! 🔥 #SpoonieProblems 🥄❤️🩹♿🤕
I miss Sparks a lot cuz he was family & my best buddy 🤟... but I ALSO very much miss the freedom & safety having him gave ME! I miss being able to go out with him to the stores & traveling. It's SO hard now, if not impossible. 😭♿❤️🩹🤕💉🐕🦺💊🥄😷🩸 #SpoonieProblems #Disability
I just wish it wasn’t such a struggle to afford life and I hate hate hate relying on the help of others. Sigh. #spoonieproblems
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