@chronically_court: Sometimes minimizing my pain became a survival skill. Not because it hurts less, but because explaining it over and over became exhausting #ChronicIllness #InvisibleIllness #ChronicPain #LupusWarrior #spoonielife

healing_with_em :

This right here 😮‍💨

Grace :

I felt this so much

lovemadixoxoxo :

I do the same. Sometimes it’s too exhausting or overwhelming to tell people how I’m really feeling. I don’t really want to answer the follow up questions.

Sherri Constable :

I just can't afford more tests or Doctors. I just live with the pain.

GoodGirlWitAHoodPlayList :

I see you sista! RA & Graves over here! It’s the worst fucking experience I’ve ever had. It feels like a curse, or punishment.

nacguy8. :

I’m commenting twice. Sorry. But most of the time I do my best to not think on my chronic conditions. Distractions are survival. Thinking too much on them or talking about them …it’s too painful. Now I just say here. Google this research and then ask your questions. I mean I don’t. But maybe I’ll start :)

lesliestankiewicz :

I didn’t same until I finally told them I had blood in my stool. Then they took me seriously finally.

🐝✨️Eva✨️🐝 :

I wish I could find an MRI machine THAT big!!

d22woodruff :

Yessss I'm so tired of Fighting and just surviving haven't been living life for years

🐞 Kristi 🐞 :

Felt that right in my soul ❤️

Allen Millett :

that hit hard

RanD :

Yes!

Steph ✝️ Faith & Family 🐼🐻 :

I feel this in my soul and can relate all too well ❤️‍🩹

darkside444themood :

😁ME TOO

MzFrosty :

🤫

Betty :

💯 Im sorry 😞 🙏🏻

Zestyzeph93 :

nacguy8. :

🫂. It’s easier to just go with the flow than to fight constantly up stream. So yeah. The I’m peachy keeps the others happy. They just don’t know peachy means hell 🫂

Taneasha_Francis 📚✨ :

[Red heart][Red heart][Red heart]