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Posts that mention lupus and accounts devoted to the disease. Limited to English posts.

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  • 💙 Liked by 20 users
  • 📅 Updated about 1 year ago
  • ⚙️ Provider skyfeed.me

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@kaleidoscope-lupus.bsky.social
20 minutes ago
oday, we are excited to post an encore release of one of KFL's most popular videos, “Lupus Fatigue: Causes, Treatment and Managing Expectations" with Dr. Sharon Dowell! Here's the link: youtu.be/Fm9QFcWsnUg
Lupus Fatigue: Causes, Treatments and Management

youtu.be

Lupus Fatigue: Causes, Treatments and Management

YouTube video by Kaleidoscope Fighting Lupus

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@kaleidoscope-lupus.bsky.social
22 minutes ago
KFL's latest article, "Lupus and the Social Construction of Health" explores how social expectations can affect those living with lupus, and what can be done to make things better ... for everyone! Read the article with this link: ow.ly/f77250VKEBF
Lupus and the Social Construction of Health - Kaleidoscope Fighting Lupus

ow.ly

Lupus and the Social Construction of Health - Kaleidoscope Fighting Lupus

Introduction: How Society “Constructs” Illness The Social Construction of Lupus So, What Can We Do? In Conclusion - It Takes a Community! Introduction: How Society “Constructs” Illness It is easy to t...

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Alice Lastname
@slopcheese34.bsky.social
about 1 hour ago
He actually saved 4.8 TRILLION lives. Plus, he stopped 19 active volcanos from erupting, caused 16 hurricanes to break up, cured leprosy, lupus, and muscular dystrophy, and saved the prairie dog from extinction. All hail our savior.
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Irongranny
@irongranny.bsky.social
about 1 hour ago
Lupus is acting up today and it’s only 11:39 & need a nap!
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Asociación AMELyA Lupus Madrid
@lupusmadrid.bsky.social
about 1 hour ago
🚨 Según una encuesta llevada a cabo en 2022 por la Federación Mundial de Lupus: 🟣  El 87% de los encuestados respondió que el #lupus ha afectado a uno o más órganos principales o sistemas. ⚡ Los más afectados fueron la piel y el sistema musculoesquelético. #30DíasLupus
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Umberto2
@umberto2.bsky.social
about 2 hours ago
And when you go the doctor and he says that you’d be healthy if it weren’t for that cancer, mesothelioma, and lupus, this is the same analysis.
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Lupus Europe
@lupuseurope.bsky.social
about 2 hours ago
🧠 Brainfog is one of the most invisible symptoms of lupus, and it still has no official scale. Prof. L. Arnaud & LBFSS team, with the support of Lupus Europe, are changing that—and they need YOU. 📲 Fill the survey. Let’s make brainfog visible. 🔗 lupusresearch.limequery.org/697679?lang=en
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EarthToThien
@earthtothien.github.io
about 2 hours ago
GOTEL 2025 is just a couple of days away! Opening up a @tiltify.com auction house featuring some amazing art from Erik Krenz and Tara Hân-Trần Johnson. All proceeds go to @lupus.org. Auction Link tilt.fyi/YQshJo11qx
Carmen San Diego sitting on a throne marvelling all her successful heists. Art by Erik Krenz.
Pink cat surrounded by types of rice balls and snacks. Art by Tara Hân-Trần Johnson.
Mimikyu building a snow Pikachu. Art by Tara Hân-Trần Johnson.
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RaemiiRam 【EN Vtuber】
@raemiiram.bsky.social
about 3 hours ago
Please join us to spread awareness of this debilitating disease! Any and all donos go directly to the Lupus Foundation to help with research and resources for people suffering with Lupus. #Vtuber #Lupus #VtuberUprisings #smallstreamer #Vtubers #ENVtuber
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Mino Gozzo
@minogozzo.bsky.social
about 3 hours ago
In about 24 hours I’ll be kicking off my participation on GOTEL the largest collaborative charity event for @lupus.org . Really exited but also really nervous because it’s my first foray into charity streaming
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Cryshard
@cryshard1.bsky.social
about 3 hours ago
May starts game on to end lupus! I will be fundraising all month! I have fun incentives and milestones planned! Please join us in raising money for research. tiltify.com/@cryshard/cr...

tiltify.com

Tiltify - Made for Fundraisers

We give you the tools to engage with your donors and raise more for your charity

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Rocker_Fox
@rockerfox.bsky.social
about 4 hours ago
Going to finalize times and get a graphic out for the Game On! To End Lupus! Charity this weekend and all through the month! tiltify.com/@rocker-fox/...

tiltify.com

Tiltify - Made for Fundraisers

We give you the tools to engage with your donors and raise more for your charity

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⋆⁺₊⋆☽⋆ 𝑠𝑒𝑙𝑖𝑛𝑎 · 𝑙𝑢𝑛𝑎 ⋆☾⋆⁺₊⋆
@lunargoddessera.bsky.social
about 4 hours ago
😩 my grandma said I just need to eat saging to cure my lupus, kulang lang daw nang potassium and she keeps saying my chronic migraine is "nasa isip" ko lang. I-- I am so defeated 😂
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Grape Nuts
@poopfoot.bsky.social
about 4 hours ago
Maybe it's lupus.
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Rheum Cat
@rheumcat.bsky.social
about 5 hours ago
✅ Social media campaigns like Let’s Talk About Lupus (Latin America/PANLAR) and the ArLAR Arthritis Awareness campaigns (Middle East/North Africa) show how LMIC-led projects can educate widely. ❌ Sustainability is tough without institutional support and funding. Volunteer work is not enough.
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STDiva
@tee-ell.bsky.social
about 5 hours ago
She also breaks out in hives from the sun, but we all do, and then get diagnosed with Lupus in our 60s when all our organs are failing. Tag RFK actually, because Autism is connected to autoimmune disease, and that should be studied more, maybe.
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Lupus Foundation of America
@lupus.org
about 5 hours ago
💜 We want to thank our sponsors for supporting our CAR webinar. Together, we’re driving research, education, and hope for the lupus community. A big thank you to Bristol Myers Squibb, Cabaletta Bio, Century Therapeutics, Cullinan Therapeutics, Fate Therapeutics, Nkarta, and Novartis.
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Mx Macabre
@mxmacabre.bsky.social
about 5 hours ago
Im heading towards a complete collapse because I am never allowed to sleep and am under constant stress. Having lupus is incredibly difficult at the best of times and these are beyond not
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Sentinel Media Company
@ursentinel.bsky.social
about 5 hours ago
Lace Up for Lupus! 💜👟 Join us Sat, May 17 for the 2nd Annual Lupus Walk supporting MMRI’s lupus research! 🏃‍♀️ 1-mile walk or untimed 5K 📍 2150 Bleecker St, Utica 🕘 Reg: 9AM | Walk: 10AM Walk solo or with a team—your steps matter! 👉 runsignup.com/lupuswalk
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LoraT
@ltimonin.bsky.social
about 7 hours ago
Reminds me of the time my extreme lupus ++ coworker was invited to be the representative patient member on the experience committee ( or some such ) as a frequent flier. They uninvited her before her year was up. Got much more feedback than they wanted to deal with.
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phos ⁉️
@ennuiim.bsky.social
about 7 hours ago
s4 of house now. there's finally a lupus case🎉🙏🎉🙏🎉🙏🎉🙏🎉🙏🎉
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Oliver De'Mari
@oliverdemari.bsky.social
about 7 hours ago
Finally saw my doctor today, a follow up from my neurology appointment; 2 years of trying to find out what's wrong, crossing out all other possibilities and I finally have an answer. I have been diagnosed with Functional Neurological Disorder (FND) and there is no cure. At least it's not Lupus.
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Paul
@inthe206.bsky.social
about 8 hours ago
A few months ago, my girlfriend discovered that she also has Lupus. It’s been a challenging journey for her, and I’ve been trying to support her through it.
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