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I honestly don鈥檛 even know how to feel I鈥檝e lived with the diagnosis of lupus since 2017 I鈥檝e been treated for it. I鈥檝e taken medication for it. I鈥檝e been monitored as a lupus patient during pregnancy. I鈥檝e had symptoms that were connected to lupus And now, after finally seeing a rheumatologist again this year, I鈥檓 being told that she doesn鈥檛 see evidence that I have lupus Maybe I was misdiagnosed Maybe it鈥檚 in remission Maybe there鈥檚 a piece of the puzzle that hasn鈥檛 been found yet I don鈥檛 know
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馃 Lupus may be invisible, but the daily battles are real. Today, we raise awareness, spread understanding, and stand with every lupus warrior facing pain and uncertainty with strength. To those living with lupus: your story matters, your strength inspires, and you are not alone. 馃挏 Let鈥檚 educate, support, and advocate for better awareness and care. #LupusAwareness #LupusWarrior #InvisibleIllness
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