Lupus Society

Lupus Society 🧡 💜We aim to increase global awareness of Lupus
🤘🏼Spreading awareness one sale at a time! Get you

💜 Today marks the 8th year since my lupus diagnosis. 💜Another year of flares, fatigue, and hard days. But also another y...
06/02/2026

💜 Today marks the 8th year since my lupus diagnosis. 💜

Another year of flares, fatigue, and hard days. But also another year of strength, resilience, and rediscovering joy in small moments.

Lupus has been one of my hardest teachers—but it’s taught me lessons I’ll carry forever.

💜 To listen to my body.
💜 To rest unapologetically.
💜 To find joy in small things.
💜 To use my voice for others.
💜 And to remember: I am more than lupus.

To my fellow warriors: You are seen. You are loved.
💜
lupussurvivor
lupusjourney
lupusstruggle
lupusfighters
lupuselupus
lupusrash
lupusinfabula
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lupuswarrior lupussupport
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📣 Lupus Awareness Month is here! 💜Our new collection has officially dropped and it’s designed for the warriors who never...
05/29/2026

📣 Lupus Awareness Month is here! 💜
Our new collection has officially dropped and it’s designed for the warriors who never back down. Wear your strength, share your story, and look amazing doing it! 🔥
⭐️ Why you’ll love them:
• Empowering designs for the community.
• 100% Made in the U.S.A. | Premium High-Quality.
🔗 Shop the new drop via the link in our bio!

💜

05/26/2026

Tag someone who needs to see this.🥰
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📸 Source: on TikTok
(Dm for credit or removal / All rights® are reserved & belong to their respective owners)
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Tag someone who needs to see this💙
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05/25/2026

Hello 👋 This is the reason why I’ve been slowly disappearing from my social media, because I swear I wish I could do it in real life.

For about 2 months now, my health has been on a roller coaster 🎢. I look good and I feel bad, I look bad and I feel good, and so on. I’m so tired of everything and everyone 😔💔 I’m tired of pretending everything is okay when it’s obviously not. I’m tired of staying positive when everything is going from bad to worse. I’m tired of people telling me to relax, “Everything’s okay,” but no, it isn’t! Maybe it is at some point, but right now it isn’t. I’m tired of people telling me, “I see you fine,” “No, I don’t look fine.” I have a mirror in my house, I don’t need to be lied to.

To everyone who suffers from ANXIETY 🥺 You are warriors.
Because nothing is more terrifying than fighting with your own mind every day.

Lupus +1 diagnosis I’m not ready to accept ❤️‍🩹 Right now, I’m a pile of pent-up feelings I don’t know how to express.

lymphoma dermatology

Small Things That Are Big Things When You Live With Chronic Illness and/ Or Chronic Pain: ✨Someone Checking In On Yo...
05/24/2026


Small Things That Are Big Things When You Live With Chronic Illness and/ Or Chronic Pain: ✨Someone Checking In On You ✨Being Believed ✨Someone Noticing When You Get Tired ✨Getting Out Of Bed & Showering ✨Comfy Clothes That Don’t Need Ironing ✨Someone Checking Accessibility Before Booking ✨Someone Picking Up Your Prescription ✨When Out In A Group, Being Able To Walk At Your Own Pace ✨People Listening VS People Telling You What To Do ✨I Saw *This* And Thought Of You ✨Cards And Thoughtful Little Gifts In The Post / Mail ✨Non-Physical Compliments ✨Meeting People Going Through Similar Things Post by Found on Edited by me Using I’m so grateful for all of the wonderful people I have connected with on this Instagram page; so incredibly lucky for the love and the friendships we’ve all made in this safe space. I can’t wait to see what happens as our community continues to grow. 💛 Lauren . . .

Lupus doesn’t care how ambitious, educated, disciplined, or driven you are.Some battles aren’t visible. Some strength lo...
05/24/2026

Lupus doesn’t care how ambitious, educated, disciplined, or driven you are.
Some battles aren’t visible. Some strength looks like simply making it through the day. 🤍🦋
To everyone fighting silently… I see you.
:

And sometimes it's a total mystery as to what I did to cause a flare! 😐 LupusSucks chronicillness LupusLife lupu...
05/23/2026

And sometimes it's a total mystery as to what I did to cause a flare! 😐

LupusSucks chronicillness LupusLife lupuswarrior lupus lupustrust lupusawareness lupustruth lupusfacts flare

🦋 May is Lupus Awareness Month 💜Lupus is a chronic autoimmune disease where the immune system turns against the body, at...
05/23/2026

🦋 May is Lupus Awareness Month 💜

Lupus is a chronic autoimmune disease where the immune system turns against the body, attacking healthy tissues and causing widespread inflammation. It can affect virtually any part of the body from joints and skin to major organs like the kidneys, heart, and brain.

💬 It’s often called an invisible illness because many symptoms aren’t visible from the outside but the pain, fatigue, and daily struggles are very real.

⚠️ What many don’t know:
* Lupus is not contagious
* It can take years to get diagnosed
* It’s more common in women, especially women of color
* Stress, sunlight, infections, and even hormonal changes can trigger flare-ups.
* No two experiences are the same symptoms can come and go in unpredictable flares.
* It goes through a cycle of flare up and remission.

Common symptoms include:
• Extreme fatigue
• Joint and muscle pain
• Skin rashes (especially the butterfly rash)
• Fever
• Hair loss
• Organ inflammation

Behind every warrior is a story of strength, courage, and resilience. Let’s create space for lupus warriors to be seen, heard, and supported not just in May, but every day.

💜 Awareness is the first step toward understanding. Understanding leads to change.

lupuswarrior chronicillnesscommunity invisiblebutpowerful invisibleillness autoimmuneawareness autoimmunedisease spooniesupport healthadvocacy knowlupus supportnotstigma
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