What do you give someone who has heard "get well soon" a few too many times?
A blanket to sink into, a lavender candle, a crochet bouquet, and a purple ribbon that says "I see you." π
#LupusWarrior#LupusAwareness
Research week is here. So are the refills, the appointments, and the Monday you still showed up for.
Lupus Warrior. Fighting Every Day. π
#LupusWarrior#SpoonieLife
Holiday spoon math: one sleep mask + one lavender candle + tulips that never wilt = permission to rest. π·
The gift that says "rest is allowed," not "get well soon."
#LupusWarrior#Spoonie
Lupus is 2-3x more prevalent among Black, Latina, Native American & Pacific Islander women than White women (LFA). Their strength matters, and so does being heard early. π #LupusAwareness#HealthEquity
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Lupus picked a fight with the wrong one. π¦
Flares, fatigue, cancelled plans, and still showing up in purple. Wear the receipts.
#LupusWarrior#Spoonie
It takes nearly 6 years on average to be diagnosed with lupus (LFA). If you kept advocating for yourself, that was strength. We're proud of you, warriors. π #LupusAwareness
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63% of Americans have never heard of lupus or know little about it (LFA). It isn't contagious or cancer, and symptoms are often invisible. Share one lupus fact this week. π #LupusAwareness
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Some days lupus is visible. Most days it isn't. π¦ The butterfly rash is real, but fatigue, pain and brain fog stay hidden. About 1.5M Americans live with lupus. We see you, warriors. #LupusAwareness
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Some of the strongest things happen where nobody can see them.
Unseen. Unbreakable. Unstoppable. A purple watercolor butterfly for the wall of every lupus warrior's recovery corner.
#LupusWarrior#InvisibleIllness
Dear Santa: no socks. Just spoons. π₯π
Some of us are budgeting energy for every holiday plan, and we're not sorry about it.
#SpoonieLife#LupusWarrior
You didn't cause this.
And the appointment-day bag can say so. Butterfly + wolf lupus tote with boxed corners, 3 sizes, 5 handle colors.
#LupusAwareness#Spoonie
Supporters: listen without fixing, check in without expecting a reply, and say "I'm here." That can mean everything to someone with lupus. π
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#LupusAwareness#LupusSupport
Depression and anxiety are common in people with lupus. Feeling heavy isn't weakness. You can ask for help. Your feelings are valid. π
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#LupusAwareness#MentalHealth
Rest isn't giving up. It's strategy.
Light the candle, dim the day, let the flare day be quiet. Purple ribbon + butterflies, 12 scents.
#LupusAwareness#Spoonie
Want to help lupus research? Ask your care team about clinical trials, support trusted lupus orgs, and share accurate info. Every action helps. π¬π
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#LupusAwareness#LupusResearch
Lupus research is moving: a 2025 study of subcutaneous anifrolumab showed a 56% response vs 37% for placebo, and phase 3 trials of new therapies are underway. π¬π
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#LupusAwareness#LupusResearch
Nobody tells you the hardest part of loving someone with lupus is not knowing what to say.
So say it with a layer that holds them: purple ribbon hands, a cozy crewneck, zero words required. π
#LupusWarrior#LupusAwareness