Kyra

lupusawareness hashtag performance

#LupusAwareness: Compassionate, empowering, informative, educational. Shares stories, boosts visibility. Fosters understanding, combats stigma. Connects community, promotes research, celebrates strength, raises funds. Supports those living with lupus.
#fyp #foryou #health #healthcare #healthandwellness #wellness #lupus #lupusawareness #symptom #sympt
Just a reminder for Lupus Awareness Month not to judge b/c you never know what someone is battling.
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Just a reminder for Lupus Awareness Month not to judge b/c you never know what someone is battling.
#autoimmune #autoimmunedisease #autoimmunewarrior #autoimmuneprotocol #chrons #ulcerativecolitis #ul
Hello I have Lupus and Sun is not my friend 😭 #lupus #lupuswarrior #lupusrash #lupusawareness #ch
Lupus warriors, we see you, we honor you, we stand with you. 💜 #lupus #lupusawareness #autoimmune
to everyone who has lupus i am here w you, as strong as i seem, lupus and RA consume me. yes i try m
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to everyone who has lupus i am here w you, as strong as i seem, lupus and RA consume me. yes i try m
Joint pain and cramps are a real thing 😭 Make sure you stretch and elevate your legs for circulat
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Joint pain and cramps are a real thing 😭 Make sure you stretch and elevate your legs for circulat
Based on a true story  🗣️Join my Living with Lupus Support Group where we’ve been discussing
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Based on a true story 🗣️Join my Living with Lupus Support Group where we’ve been discussing
Lupus Awareness Month 🦋#fyp #lupusawarenessmonth #lupusawareness #lupuswarrior #lupus #autoimmune
Lupus friendly hat! The link is on my Amazon store in my bio 🫶🏽  #livingwithlupus #lupusawaren
How I found out about my lupus diagnosis  #livingwithlupus #lupuswarrior #lupusawareness #hairloss #
Chronic illness doesn’t look one specific way, the thing about chronic illness is that there is a
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Chronic illness doesn’t look one specific way, the thing about chronic illness is that there is a
#autoimmunedisease #lupus #lupuswarrior #lupusawareness #autoimmune #singlemom
Send this to someone so they feel less alone and understand lupus a little more. You never know who
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Send this to someone so they feel less alone and understand lupus a little more. You never know who
True story. Follow my lupus journey on IG ( @lupuslivingdiaries)  #livingwithlupus #lupusawareness #
This is what having lupus and kidney disease is like 💜💚 #lupus #kidneydisease #lupusnephritis
Come with my to my rheumatologist appointment to follow up on my lupus that has started to get out o
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Come with my to my rheumatologist appointment to follow up on my lupus that has started to get out o
“You are not a victim for sharing your story. You are a warrior—setting the world ablaze with yo
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“You are not a victim for sharing your story. You are a warrior—setting the world ablaze with yo
"Lupus is like the invisible illness. Some days, I'm perfectly fine—I can do a cartwheel. And then
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"Lupus is like the invisible illness. Some days, I'm perfectly fine—I can do a cartwheel. And then
“Over the past few years, sharing visuals has been my favorite way to connect—but lately, I’ve
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“Over the past few years, sharing visuals has been my favorite way to connect—but lately, I’ve
It’s May 1st! Officially the first day of Lupus Awareness Month!! 🦋💜 #lupus #lupusawareness

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