#lupus search results
๐ Have a vehicle youโre no longer using? Donate your car, truck, boat, or RV to the Lupus Foundation of America and help fund critical #lupus research, support programs, and resources. ๐ Itโs an easy way to make a lasting difference. Learn more: buff.ly/Kegvid4
๐ #LupusAwarenessMonth is almost here! LFA Ambassadors Racquel and Linda joined @12OnYourSide to share their #lupus journeys, shed light on the realities of living with an invisible illness, and highlight ways to get involved this May. ๐ฅ Watch now: buff.ly/a61pL6X
#MakeLupusVisible this May for #LupusAwarenessMonth! ๐ While many symptoms of #lupus aren't visible, the impact is real. Join us all month long as we raise awareness for the millions living with this cruel disease. Learn more: buff.ly/3OCV73t
Constantly torn between not wanting to let my health issues control everything and needing to listen to my body and rest. ๐ฅบ #chronicillness #lupus
DYK the Lupus Foundation of America leads #lupus awareness on a global scale? As coโfounder & Secretariat of the World Lupus Federation, we unite 200+ organizations across 90 countries for #WorldLupusDay. On May 10, join lupus warriors & use the toolkit: buff.ly/cA4kIRC
May is #Lupus and #Fibromyalgia Awareness Month. Weโre grateful to the @CityofCoachella for recognizing this month and helping bring visibility to illnesses that are too often misunderstood. At @Looms4Lupus, we remain committed to advocacy, education, and community every single
We are only 2 weeks away from #GOTEL2026! Once again, content creators from around the world are uniting to use their platforms to help end #lupus - streaming video games, making music, crafting and getting creative. Join us May 1โ3 or anytime in May: buff.ly/f6F6soJ
Wear your strength and show up for the #lupus community! ๐ Introducing our newest partner, @littlewordsproj. $5 from every Fearless! bracelet purchased April-June 2026 supports the LFA and helps the millions affected by lupus. Shop now: buff.ly/gqywvvf
The start of #LupusAwarenessMonth is just days away! Join us and people like Kay Dudley to #MakeLupusVisible this May! Kay has been bravely sharing her #lupus journey and amplifying lupus awareness. As we head into May , we're grateful to have her voice in this fight.
#FactFriday ๐ #Lupus can affect women's reproductive health at every stage of life. The more we know, the better we can advocate for ourselves and our loved ones. Learn more about lupus and women's reproductive health: buff.ly/PZkPzLq
๐ฎ Meet @8bitDee. #GOTEL organizer, streamer, and #lupus warrior. Diagnosed in 2019, she found a way to help lupus warriors while building community. Moving in to another year of GOTEL, she can't wait for the month ahead. Join Dee May 1โ3 or all May long: buff.ly/Li8XhuH
New research reveals a potential link between gut bacteria and inflammation in #lupus nephritis. Findings point to a microbiome-driven pathway that may open the door to more targeted treatments. Read the study: buff.ly/679ponc
๐จ ICYMI, the National #LupusAdvocacy Summit starts tomorrow! Thereโs still time to register and join #lupus advocates virtually as we come together to raise our voices and make an impact. ๐ Register here: buff.ly/W15PV8H
๐๏ธ Today is #NationalHealthcareDecisionsDay โ a reminder that your voice matters in every part of your care. If you live with #lupus, learning to speak up, ask questions, and make informed decisions is key. ๐ ๐ Read our self-advocacy tips: buff.ly/ze2lmaS
#LupusAwarenessMonth is 2 days away! ๐ There's no better time to start a Facebook fundraiser and rally your community. Every dollar you raise helps fund research, education, and support for the #lupus community. ๐ Start your fundraiser: buff.ly/jNOVSyH
#LupusAwarenessMonth kicks off tomorrow! ๐ Don't miss out on a full month of content dedicated to raising awareness and making #lupus visible. Make sure to follow us on all our social media platforms so you never miss a post: buff.ly/JzFuHG3
๐The National #LupusAdvocacy Summit is live! ๐Our CEO, Louise Vetter, is kicking off the day with opening remarks, setting the stage for powerful conversations on #lupus advocacy, research and care. Tune in now: buff.ly/NHjJcn5
We want to thank everyone who helped make the National #LupusAdvocacy Summit a success! A special thank you to our sponsors: @AstraZeneca, @Biogen, @CabalettaBio, @EMDGroup, @Genentech, @GSK, @Novartis, @PhRMA, @UCBUSA, & @ViatrisInc for your commitment to the #lupus community.
Rachel was told treating her #lupus could make pregnancy nearly impossible. 10 years later, she welcomed a healthy baby girl. As an LFA Ambassador, she joins the Walk to End Lupus Now to fund research that made her story possible. Read more in @People: buff.ly/AmqUhxE
๐จ The National #LupusAdvocacy Summit kicks off today. If youโre joining digitally, the livestream starts at 9:00 a.m. ET. Join fellow #lupus advocates and connect with the community in the chat. ๐ Access the livestream and join us now: buff.ly/yT4FIAv
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Lupus Foundation of America
May is #Lupus and #Fibromyalgia Awareness Month. Weโre grateful to the @CityofCoachella for recognizing this month and helping bring visibility to illnesses that are too often misunderstood. At @Looms4Lupus, we remain committed to advocacy, education, and community every single
Constantly torn between not wanting to let my health issues control everything and needing to listen to my body and rest. ๐ฅบ #chronicillness #lupus
This clip akin to me knowing that May is #LupusAwarenessMonth when @selenagomez shares about #Lupus & #MentalHealth on 5/3! โFierce females are a FORCE.โ
Full footage of trainer Cherie DeVaux watching Golden Tempo win the Kentucky Derby! DeVaux is the first female trainer to ever win the Kentucky derby.
The last drug approved for cutaneous lupus was in the 1950s. Biogen just posted its SECOND positive Phase 2 trial for litifilimab. The science is ready. Is the FDA? thetownhall.news/federal-news/bโฆ #Lupus #FDA #Biogen
Thank you @selenagomez Raising #Lupus Awareness. Supporting @LupusResearch #LupusAwareness during May!
โจ ยกHola! Tercer dรญa de mayo, mes de concientizaciรณn sobre el lupus ๐ฆ La Dra. Felicia Almada nos habla acerca de los signos y sรญntomas de los pacientes con lupus eritematoso sistรฉmico. #Lupus #Concientizaciรณn #AtenciรณnPrimaria #Medicina #Salud
I still have this severe wound on my leg that wont heal that i had surgery for + a million antibiotics. I see my wound care team on tues. But every day when i have to clean and reprep the site is literal torture. Writhing around from the pain nearly puking from the pain #lupus
We are live today with @LupusOrg โs VP of Research, Joy Buie (2pm for interview EDT) for a real conversation about the science of #lupus and LFA research as we raise money for science! @tiltify link: tilt.fyi/A8YwXeChIn twitch.tv/sciants_streams
๐WE ARE LIVE WITH #GOTEL2026 DAY 3!๐ Weโre raising awareness & money for @lupus.org to fight #Lupus!! ๐ Join us @ twitch.tv/zeldaquinn7 Weโre playing Peak w/ frens & cc If u want 2 donate & support a wonderful cause, u can do so here: tilt.fyi/wBEFB9NTEO #LupusIsPoopus
Itโs Lupus Awareness day 3 ๐๐ฆ The mega dose of antibiotics I took yesterday at the dentist wreaked havoc on my stomach. Iโm in pain big time and my intestines feel like sharp knives are in them. Please pray for #Painmanagment is important with #Lupus
Der Lupus 365 Termin zum Thema Fatigue wurde auf den 12. Mai verschoben. Alle, die angemeldet sind, sollten auch eine Mail erhalten haben. Wenn ihr noch nicht angemeldet seid, holt das auf unserer Website nach! Hier findet ihr die Infos: lupus-rheumanet.org/lupus-365/ #lupus #fatigue
#NUESTRAGENTE | Lyssette Rodrรญguez Ornelas, investigadora de la UAZ, lidera el Proyecto Mariposa para visibilizar el lupus en Zacatecas. ๐ฆ๐ #Lupus #Salud #Zacatecas #EcoDiario ecodiario.mx/noticia/lideraโฆ
โจ Friend and lupus advocate @selenagomez shares a heartfelt message with the global #lupus community on what #HopeInAction means to her as we kick off #LupusAwarenessMonth. ๐ Join us and get involved today at LupusResearch.org.
The Asian American and Pacific Islander (AAPI) community encompasses diverse cultures and languages. They face a disproportionate burden with #lupus. Lupus-related death rates among Asian women are 4โ6 times higher than the general population.
Lupus Awareness Month in May raises understanding of lupus, a chronic autoimmune disease. It highlights symptoms, early diagnosis, and treatment options while addressing the challenges faced by those affected. World Lupus Day is May 10. #Lupus #LupusAwareness #PMILOC
#Lupus clinical research has been problematic due to the lack of basic understanding of the disease, reliable biomarkers, and uniform control groups, as well as clinical outcome measure limitations and the heterogeneity of the patient population. #lupusawareness #autoimmune
Vom 04. bis zum 10. Mai findet der diesjรคhrige Lupus Butterfly Run statt. Wir freuen uns schon auf diese Aktion mit euch. Meldet euch gerne an - weil jeder Schritt zรคhlt! #lupus #butterflyrun #2026
Y como lo hemos hecho desde que estamos por estos lares, en el mes de mayo, activamos toda la baterรญa con campaรฑas para hacer visibles: #Lupus #Fibromialgia
Happy Lupus Awareness month! ๐๐ฆโ๏ธ๐๐พ Hello welcome to my Journey with #Lupus gofund.me/805457249
The Asian American and Pacific Islander (AAPI) community encompasses diverse cultures and languages. They face a disproportionate burden with #lupus. Lupus-related death rates among Asian women are 4โ6 times higher than the general population.
May is #LupusAwarenessMonth. ๐ #Lupus affects 1.5 million Americans.Yet lupus and its signs and symptoms remain widely misunderstood. Help us raise awareness. Take the Know Lupus Quiz and explore more ways to help us #MakeLupusVisible all month long: buff.ly/VI6iO8o
#LupusAwarenessMonth kicks off tomorrow! ๐ Don't miss out on a full month of content dedicated to raising awareness and making #lupus visible. Make sure to follow us on all our social media platforms so you never miss a post: buff.ly/JzFuHG3
We are only 2 weeks away from #GOTEL2026! Once again, content creators from around the world are uniting to use their platforms to help end #lupus - streaming video games, making music, crafting and getting creative. Join us May 1โ3 or anytime in May: buff.ly/f6F6soJ
Meet @3llebelle โ #GOTEL organizer, streamer, & driving force behind the largest #lupus charity fundraiser on Twitch. 3llebelle and nearly 200 streamers raise awareness & change the lives of lupus warriors everywhere. Join Elle May 1โ3 or all month long: buff.ly/f6F6soJ
DYK the Lupus Foundation of America leads #lupus awareness on a global scale? As coโfounder & Secretariat of the World Lupus Federation, we unite 200+ organizations across 90 countries for #WorldLupusDay. On May 10, join lupus warriors & use the toolkit: buff.ly/cA4kIRC
Clinical research is key to better #lupus outcomes โ and your voice is part of that. Researchers and opinion leaders at the National #LupusAdvocacy Summit discuss the latest in #lupusresearch, drug development, and the role patients play. Watch now: buff.ly/NHjJcn5
The start of #LupusAwarenessMonth is just days away! Join us and people like Kay Dudley to #MakeLupusVisible this May! Kay has been bravely sharing her #lupus journey and amplifying lupus awareness. As we head into May , we're grateful to have her voice in this fight.
#MakeLupusVisible this May for #LupusAwarenessMonth! ๐ While many symptoms of #lupus aren't visible, the impact is real. Join us all month long as we raise awareness for the millions living with this cruel disease. Learn more: buff.ly/3OCV73t
๐ Have a vehicle youโre no longer using? Donate your car, truck, boat, or RV to the Lupus Foundation of America and help fund critical #lupus research, support programs, and resources. ๐ Itโs an easy way to make a lasting difference. Learn more: buff.ly/Kegvid4
If your company has an employee matching gift program, you can maximize your support for the #lupus community throughout the year by doubling or even tripling your next donation to the LFA! Visit our site to learn if your company has a similar program: buff.ly/SewOK90
3 days until #GOTEL2026 kicks off! ๐ฎ๐ Hundreds of content creators are uniting to raise awareness & funds for #lupus research & support. We can't wait to see the creativity & community spirit this year! Sign up to stream May 1โ3 or join all May long: buff.ly/tbYsnF1
๐ฎ Meet @8bitDee. #GOTEL organizer, streamer, and #lupus warrior. Diagnosed in 2019, she found a way to help lupus warriors while building community. Moving in to another year of GOTEL, she can't wait for the month ahead. Join Dee May 1โ3 or all May long: buff.ly/Li8XhuH
Apolipoprotein L1 High-Risk Genotypes are Associated With #Lupus #Nephritis Incidence doi.org/10.1016/j.ekirโฆ #KIRResearchLetter #APOL1
We're excited to announce the recipients of our Clinical Referral Mini-Grant, helping connect more people with #lupus to our SELF app and self-management tools through their care team. Congratulations to @MedUnivSC, @MountSinaiNYC, @UABNews, and @UCSFChildrens!
#LupusAwarenessMonth is two weeks away!ย Get ready to make #lupus visible with our toolkit โ sample posts, shareable graphics, and resources to help spread awareness all May long. ๐ฒ Explore the toolkit: buff.ly/uS9yAQx
Wipe that โSMILEโ away! #hydroxychloroquine did NOT โ reduce onset of #SLE #lupus In people w 2 or 3 #criteria for lupus & +ANA Smile trial sad ๐ข Dr Judith James #CCREast
Wear your strength and show up for the #lupus community! ๐ Introducing our newest partner, @littlewordsproj. $5 from every Fearless! bracelet purchased April-June 2026 supports the LFA and helps the millions affected by lupus. Shop now: buff.ly/gqywvvf
We were proud to present Dr. Lindsey Criswell, former Director of @NIH_NIAMS, with the Lupus Research Hero Award at the National #LupusAdvocacy Summit. ๐ Her dedication to #lupus research has driven meaningful progress for the community.
Managing #lupus while navigating work, disability benefits, or finances can be overwhelming. We've compiled a list of resources, from job accommodations to legal support, to help you find assistance. Explore employment and disability resources: buff.ly/dAokFPl
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