Tomorrow LaVita will be hosting a lupus awareness table at the Health & Wellness Expo in Wadsworth, IL. If you are attending please make sure to stop by and say hi! She has tons of great information about lupus and LSI. She is also handing out candy. #healthexpo #lupus #lupusawareness #wadsworth #lupuseducation #lupuscommunity #lupuswarrior
Lupus Awareness Month, fact of the day, May 17th! #LSILupusAwareness #lupus #lupusawareness #lupuswarrior #lupuseducation #lupussupport
A good readfor one of many bed days. #lupus #lupuswarrior💜 #lupusawareness #chronicillness #chronicpain #cardiomyopathy #NHS @ #isolation #lupuseducation #lupusuk #lupusbutterfly #lupuscommunity #itslupus #lupusbooks
Empowering Lupus Patients Educational Event Saturday, May 18, 2024 9:30am - 1:00pm Three topics covered: SOCIAL SECURITY DISABILITY: CHANGE AND CONFUSION Presented by: Jeffrey A. Rabin THE LATEST IN LUPUS RESEARCH & THE IMPORTANCE OF RESEARCH & SAFETY OF CLINICAL TRIALS Presented by: Irene Blanco, M.D. CLINICAL TRIALS: A LUPUS PARTICIPANT'S PERSPECTIVE Presented by: Stacey Kennedy-Conner https://ow.ly/l0tO50RBTNx #lupus #lupusawareness #lupuscommunity #lupuseducation #chicago #freeevent #stxavieruniversity
Stress can make you feel overwhelmed and isolated. But remember that you’re not alone, and there are people who can help. Try these tips to find support: Ask your health care team about ways to manage stress — or about getting mental health treatment or seeing a therapist or counselor. Reach out to friends and family — talking and spending time with loved ones can be a great stress reliever. MAKE LUPUS VISIBLE Credit - Lupusorg #liridonaautoimmunefoundation #worldlupusday #lupus #lupuswarrior #lupusadvocate #lupuseurope #lupusawarenessmonth #livingwithlupus #lupusawareness #lupuswarriors #lupusadvocacy #lupuscure #lupusresearch #lupusflare #lupusproblems #makelupusvisible #lupusnigeria #lupuseducation #lupustreatment #endlupus #treatment #joinus #lupusresearchalliance #getinvolved #lupusorganisation #cure #hopebeginshere #worldwide #lupusencyclopedia #worldlupusfederation
Lupus Awareness Month, fact of the day, May 16th! #LSILupusAwareness #lupus #lupusawareness #lupuswarrior #lupuseducation #lupussupport
Lupus Awareness Month, fact of the day, May 15th! #LSILupusAwareness #lupus #lupusawareness #lupuswarrior #lupuseducation #lupussupport
Lupus Awareness Month, fact of the day, May 14th! #LSILupusAwareness #lupus #lupusawareness #lupuswarrior #lupuseducation #lupussupport
Lupus awareness isn’t just a month; it’s a movement. Let’s keep the conversation going. 💜 Dedicated to my Makeup Sister @makeup_bysugg 💜 Products Used: ✨ @mezbeauty -Auto Brow Liner (Dark Brown) -Limited Edition 1509 Palette (Colors Souvereign and Dim Dim) -Coleur Kweyol Palette (Color Gros Pwell) -Swarthy Palette (Color Iced for highlighter) -Kat Palette for blush -Pinky Lipgloss https://mezbeauty.com (USE CODE DESI22)✨ @breazys_lashes -White and Black Magical Glue @glamandbeautybyyaneth Number 7 Setting Powder @ivybeauty.official @ienvylashes_official -VLuxe Airy Mink Lashes in the style Ethereal @anastasiabeverlyhills Glitter Adhesive @jlaruecosmetics White Diamonds Loose Pigment @oliva__cosmetics -V. Jeroe Contour Palette 🩵 @threadbeauty -Cover It Multi-Use Complexion Fluid Number 4 (Tan Golden Beige) for concealer🩵 @maybelline -Baby Skin Instant Pore Eraser -Super Stay Active Wear 30H Foundation (Colors 332 and 340) @benefitcosmetics -Badgal Bang Volumizing Mascara (Intense Black) @rimmellondon Exaggerate Waterproof Eye Definer (Blackest Black) in waterline @urbandecaycosmetics All Nighter Setting Spray @elfcosmetics -Power Grip Primer -Brow Lift, Clear Eyebrow Shaping Wax #mezbeauty #desiglamups #threadbeauty #MakeupGoals #MNYitlook #makeup #benebabe #benefitclubpink #benefit #ivybeauty #ivybeautizen #ienvy #fyp #foryou #LupusAwareness #KnowLupus #support #FightLupus #LupusFighter #LupusStrong #LupusSupport #LupusAwarenessMonth #LupusLife #LupusCommunity #LupusAdvocacy #LupusSurvivor #LupusAwarenessCampaign #LupusAwarenessDay #LupusEducation #LupusResearch
Empowering voices, inspiring hope: it’s time to shine a light on lupus. 💜 Top 5 Lupus Facts: 1. Lupus is an autoimmune disease where the immune system attacks healthy tissues, leading to inflammation and damage in various parts of the body. 2. Lupus can affect anyone, but it is most common in women of childbearing age (15-44) and people of color, particularly African American, Hispanic, and Asian descent. 3. Symptoms of lupus can vary widely and may include fatigue, joint pain, skin rashes, fever, and organ damage. 4. There is no single test to diagnose lupus, and it can often be challenging to diagnose due to its varied symptoms. Diagnosis usually involves a combination of medical history, physical examination, and laboratory tests. 5. While there is currently no cure for lupus, treatment aims to control symptoms and prevent flares. Medications, lifestyle changes, and regular medical care can help manage the disease and improve quality of life for those affected. #desiglamups #foryou #instagood #instadaily #purple #Lupus #LupusAwareness #KnowLupus #LupusWarrior #LupusFighter #LupusStrong #LupusSurvivor #LupusLife #LupusSupport #LupusCommunity #LupusAdvocacy #LupusEducation #LupusResearch #LupusAwarenessMonth #LupusAwarenessDay #LupusAwarenessCampaign #LupusAwarenessWeek #LupusSucks #LupusWarrior #LupusFight #LivingWithLupus #LupusAwarenessRibbon #LupusAwarenessBracelet #LupusAwarenessWalk #LupusAwarenessFundraiser
Invisible but not silent: raising awareness for lupus warriors worldwide. 💜 Products Used: ✨ @mezbeauty -Auto Brow Liner (Dark Brown) -Limited Edition 1509 Palette (Colors Souvereign and Dim Dim) -Coleur Kweyol Palette (Color Gros Pwell) -Swarthy Palette (Color Iced for highlighter) -Kat Palette for blush https://mezbeauty.com (USE CODE DESI22)✨ @breazys_lashes -White and Black Magical Glue @ivybeauty.official @ienvylashes_official -VLuxe Airy Mink Lashes in the style Ethereal @anastasiabeverlyhills Glitter Adhesive @jlaruecosmetics White Diamonds Loose Pigment @benefitcosmetics -Badgal Bang Volumizing Mascara (Intense Black) @elfcosmetics -Brow Lift, Clear Eyebrow Shaping Wax #mezbeauty #desiglamups #threadbeauty #MakeupGoals #MNYitlook #makeup #benebabe #benefitclubpink #benefit #ivybeauty #ivybeautizen #ienvy #fyp #foryou #LupusAwareness #KnowLupus #support #FightLupus #LupusFighter #LupusStrong #LupusSupport #LupusAwarenessMonth #LupusLife #LupusCommunity #LupusAdvocacy #LupusSurvivor #LupusAwarenessCampaign #LupusAwarenessDay #LupusEducation #LupusResearch
Thursday night!! Join @lupusfoundationnewengland for Let’s Talk Lupus: A Lupus Health Seminar, being held May 16th at the YMCA of Greater Boston from 6-8pm. #lupus #lupustalk #lupussupport #lupuseducation #lupuscommunity #communityhealth #lupusawareness #lupusawarenessmonth #livewellwithlupus #lupuslightsne
Lupus Awareness Month, fact of the day, May 13th! #LSILupusAwareness #lupus #lupusawareness #lupuswarrior #lupuseducation #lupussupport
Do not be too timid and squeamish about your actions. All life is an experiment. The more experiments you make the better. What if they are a little coarse and you may get your coat soiled or torn? What if you do fail, and get fairly rolled in the dirt once or twice? Up again, you shall never be so afraid of a tumble. Ralph Waldo Emerson MAKE LUPUS VISIBLE #liridonaautoimmunefoundation #worldlupusday #lupus #lupuswarrior #lupusadvocate #lupuseurope #lupusawarenessmonth #livingwithlupus #lupusawareness #lupuswarriors #lupusadvocacy #lupuscure #lupusresearch #lupusflare #lupusproblems #makelupusvisible #lupusnigeria #lupuseducation #lupustreatment #endlupus #treatment #joinus #lupusresearchalliance #getinvolved #lupusorganisation #cure #hopebeginshere #worldwide #lupusencyclopedia #worldlupusfederation
It’s Lupus Awareness Month (Day 12) The year was 1998 and this was my first photo shoot for a hair magazine. Yes! This is my real hair. 😉 (I was 6 months pregnant with my 1st born, Iman Jolie) Did you know that Lupus may cause hair loss? I’ve had a bald patch, and my hair would fall out throughout the years. #iHateLupus #33YearLupusConqueror #DiagnosedWithSLEIn1993 #LupusSucks #LupusAwareness #LupusEducation #PurpleIs4Lupus 💜💜💜 #BeforeITurnedCompletelyGray #iDyedMyHairEvery3Weeks #iDidntWant2LookOld #MyHairWouldFallOut #iAmJLaTrina www.JLaTrina.com
Lupus Awareness Month, fact of the day, May 12th! #LSILupusAwareness #lupus #lupusawareness #lupuswarrior #lupuseducation #lupussupport
One week from today!!! Empowering Lupus Patients Educational Event Saturday, May 18, 2024 9:30am - 1:00pm Three topics covered: SOCIAL SECURITY DISABILITY: CHANGE AND CONFUSION Presented by: Jeffrey A. Rabin THE LATEST IN LUPUS RESEARCH & THE IMPORTANCE OF RESEARCH & SAFETY OF CLINICAL TRIALS Presented by: Irene Blanco, M.D. CLINICAL TRIALS: A LUPUS PARTICIPANT'S PERSPECTIVE Presented by: LSI Associate Board prez Stacey Kennedy-Conner Type in this link to attend. We hope to see you next Saturday! https://ow.ly/l0tO50RBTNx #lupus #lupusawareness #lupuscommunity #lupuseducation #chicago #freeevent #stxavieruniversity
In honor of Lupus Awareness Month, we are pleased to show this encore release of the KFL educational video, “Lupus Nephritis: The Road to Diagnosis!” Lupus nephritis is not only a serious condition for those living with lupus, but it is a particularly challenging one to diagnose. In this video, nephrologist German Hernandez, MD, guides us through the process of a lupus nephritis diagnosis with helpful insights and expert advice. You can view this video on our YouTube channel by following this link: https://youtu.be/ettgRan-hwc� We thank our presenting sponsor, Aurinia Pharmaceuticals, for their generous support in making this video possible. #kaleidoscopefightinglupus #lupus #sle #spoonie #lupusfighter #lupuslife #spoonielife #lupuscommunity #invisibleillness #butyoudontlooksick #autoimmunediseases #chronicillness #autoimmunedisease #lupusawareness #lupuseducation #lupusblogs #lifewithlupus #lupuslife #livingwithlupus #autoimmune #lupusstrong #lupustruth #livingwithlupus #lupusinformation #lupusawarenessmonth #lupusawarenessmonth2024 #lupusnephritis #nephritislupus #kidneys #kidneydisease
One week from today!!! Empowering Lupus Patients Educational Event Saturday, May 18, 2024 9:30am - 1:00pm Three topics covered: SOCIAL SECURITY DISABILITY: CHANGE AND CONFUSION Presented by: Jeffrey A. Rabin THE LATEST IN LUPUS RESEARCH & THE IMPORTANCE OF RESEARCH & SAFETY OF CLINICAL TRIALS Presented by: Irene Blanco, M.D. CLINICAL TRIALS: A LUPUS PARTICIPANT'S PERSPECTIVE Presented by: Stacey Kennedy-Conner https://ow.ly/JcIG50RBTNA #lupus #lupusawareness #lupuscommunity #lupuseducation #chicago #freeevent #stxavieruniversity
Lupus Awareness Month, fact of the day, May 11th! #LSILupusAwareness #lupus #lupusawareness #lupuswarrior #lupuseducation #lupussupport
Yoga practice can have a positive impact on the immune system, which is crucial for individuals with lupus. Studies have shown that regular yoga practice can reduce inflammation and modulate immune function, thereby potentially minimizing lupus flares and supporting overall immune health. The best is restorative yoga, which helps loosen ligaments and muscles that can get really tight and compromised. MAKE LUPUS VISIBLE #liridonaautoimmunefoundation #worldlupusday #lupus #lupuswarrior #lupusadvocate #lupuseurope #lupusawarenessmonth #livingwithlupus #lupusawareness #lupuswarriors #lupusadvocacy #lupuscure #lupusresearch #lupusflare #lupusproblems #makelupusvisible #lupusnigeria #lupuseducation #lupustreatment #endlupus #treatment #joinus #lupusresearchalliance #getinvolved #lupusorganisation #cure #hopebeginshere #worldwide #lupusencyclopedia #worldlupusfederation
Let’s spread awareness and support for those battling lupus this month and beyond. Together, we can make a difference! 💜 Visit us at Kalyani Hospital Pvt Ltd or Reach Out to Us for Your Healthcare Needs: 📍 Location: @kalyanihospitalpvtltd 📞 Contact: 9873666799 - 0124-4666999 📧 Email: [email protected] Your well-being is our priority. Connect with us for comprehensive healthcare services. #LupusAwarenessMonth #FightForACure #LupusAwareness #KnowLupus #LupusWarrior #AutoimmuneDisease #LupusFighter #ChronicIllness #LupusSupport #LupusWarrior #LupusStrong #InvisibleIllness #LupusAwarenessMonth #LupusCommunity #LupusLife
El lupus puede ser difícil de diagnosticar porque sus signos y síntomas generalmente son similares a los de otras enfermedades. El signo más distintivo del lupus es una erupción cutánea en el rostro que se asemeja a las alas de una mariposa en ambas mejillas y se presenta en muchos casos de lupus, pero no en todos. Esto se llama eritema malar, y en los pacientes se dice “mariposa Lupica”. En general es una enfermedad autoimmune donde el sistema de defensas de tu cuerpo está alterado y eso genera que se auto ataque, produciendo síntomas como la inflamación o el dolor. Además, puedes compartir que es una enfermedad crónica como la diabetes o la hipertensión, y te va a acompañar durante toda tu vida, sin embargo, hoy podemos controlar la enfermedad de manera efectiva con diferentes tratamientos. Los gatilladores del lupus pueden provenir de diferentes hábitos como la alimentación, altos niveles de cortisol (hormona del estrés), la carga tóxica, efectos secundarios de la medicina tradicional, ausencia de conocimiento sobre el manejo en forma natural 🌱, etc. Hoy es el #DíaMundialDelLupus y en #Chile y en todo el mundo elevamos la #ConcienciaLupus. Como #GuerrerosDelLupus, luchamos con #FuerzaLupus y apoyamos la #InvestigaciónLupus. Unidos en la #ComunidadLupus, somos #LupusFuertes. ¡Juntos, pongamos #FinAlLupus! 💜 #LupusChile #LupusAwareness #LupusResearch #LupusSupport #LupusCommunity #LupusFighter #LupusLife #LupusSurvivor #LupusAdvocacy #LupusEducation #LupusHeroes #LupusAwarenessMonth #LupusThrive #LupusJourney #LupusHope #LupusLove #LupusStrongerTogether #LupusFacts #LupusDay #LupusAdelante #MesDeConcienciaLupus
How are you celebrating World Lupus Day? #lupus #lupusawareness #lupuscommunity #lupuseducation
May 10th is World Lupus Day! 💜 Lupus is a chronic, autoimmune disorder that affects kids and adults of all nationalities, races, ethnicities, genders, and ages. To support kids in understanding Lupus, whether for their own diagnosis or for a loved one or peer who is affected, it is helpful to use concrete language, visuals, and play activities. These strategies will allow for opportunities for repetition and make the concept of Lupus more concrete or physical and less abstract. Seem overwhelming? Worried you might not know what words to use? Anxious about your child’s response? All completely normal and we are here to help. Here is some starting language to use, as always feel free to reach out and we can provide individualized support!
Lupus Awareness Month, fact of the day, May 10th! #LSILupusAwareness #lupus #lupusawareness #lupuswarrior #lupuseducation #lupussupport
🌍🎗️ Ever noticed how superheroes are always battling something invisible? Well, so are many people around us, fighting battles you can’t see. That’s why World Lupus Day isn’t just another observance on your overcrowded calendar. It’s a call to action, because believe it or not, autoimmune diseases like lupus are on the rise, and they’re as sneaky as any comic book villain. Why spotlight lupus? Because it affects over 5 million people globally, and scientists believe the number could be much higher, as many go undiagnosed. In the U.S. alone, at least 1.5 million have lupus, with more than 16,000 new cases reported annually. And here’s a fun (or not-so-fun) fact: autoimmune diseases have been ticking up over the past 50 years – faster than you can say “immune system gone rogue.” So, this World Lupus Day, let’s bring out the purple ribbons, folks! Let’s educate, advocate, and donate to turn the tide against this invisible adversary. Remember, knowing is half the battle—the other half is not forgetting about it once the day is over. #WorldLupusDay #LupusAwareness #AutoimmuneWarrior #InvisibleIllness #FightLupus #LupusResearch #ChronicIllness #AutoimmuneDiseases #SpoonieLife #HealthAwareness #LupusSupport #ImmuneSystem #LupusWarrior #PurpleRibbon #LupusAdvocacy #HealLupus #LupusFacts #UnderstandAutoimmune #AutoimmuneStats #ProtectYourHealth #LupusEducation #RaiseAwareness #LupusLife #AutoimmuneAwareness #AdvocateForHealth #LupusFighter
Let’s shine a light on this often misunderstood condition. 💜 Lupus affects millions worldwide, yet many still don’t fully grasp its impact. Lupus can cause a variety of symptoms, including pain, often due to inflammation in the joints and muscles, resulting in joint pain, muscle pain, and stiffness. Managing pain in lupus typically involves a combination of medication, lifestyle changes, and other treatments. It’s important for individuals with lupus to work closely with their doctor to develop a comprehensive treatment plan tailored to their specific needs and symptoms. Let’s educate, advocate, and support those living with lupus, spreading awareness and understanding every step of the way. Together, we can make a difference. #LupusAwareness #knowLupus #lupussupport #lupusstrong #autoimmuneawareness #chronicillness #invisibleillness #lupusfighter #lupuscommunity #lupusadvocacy #lupuslife #spreadpurple #endlupus #lupusawarenessmonth #lupuseducation #lupusresearch #lupusawarenesscampaign
World Lupus Day 2024: World Lupus Day is observed on 10 May every year to raise awareness about the autoimmune disease lupus. The day is also dedicated to spreading awareness about the need for research to find a cure for the disease. This day serves as a platform to shed light on the condition, its impact on individuals, and the urgent need for increased research funding to find a cure. It also aims to provide support and understanding to those affected by lupus and their families. Lupus is a complex and debilitating autoimmune disease that affects millions of people worldwide. It is characterized by the immune system attacking the body’s own tissues, leading to inflammation and damage to various organs. MAKE LUPUS VISIBLE #liridonaautoimmunefoundation #worldlupusday #lupus #lupuswarrior #lupusadvocate #lupuseurope #lupusawarenessmonth #livingwithlupus #lupusawareness #lupuswarriors #lupusadvocacy #lupuscure #lupusresearch #lupusflare #lupusproblems #makelupusvisible #lupusnigeria #lupuseducation #lupustreatment #endlupus #treatment #joinus #lupusresearchalliance #getinvolved #lupusorganisation #cure #hopebeginshere #worldwide #lupusencyclopedia #worldlupusfederation
World Lupus Day 2024: World Lupus Day is observed on 10 May every year to raise awareness about the autoimmune disease lupus. The day is also dedicated to spreading awareness about the need for research to find a cure for the disease. This day serves as a platform to shed light on the condition, its impact on individuals, and the urgent need for increased research funding to find a cure. It also aims to provide support and understanding to those affected by lupus and their families. Lupus is a complex and debilitating autoimmune disease that affects millions of people worldwide. It is characterized by the immune system attacking the body’s own tissues, leading to inflammation and damage to various organs. MAKE LUPUS VISIBLE #liridonaautoimmunefoundation #worldlupusday #lupus #lupuswarrior #lupusadvocate #lupuseurope #lupusawarenessmonth #livingwithlupus #lupusawareness #lupuswarriors #lupusadvocacy #lupuscure #lupusresearch #lupusflare #lupusproblems #makelupusvisible #lupusnigeria #lupuseducation #lupustreatment #endlupus #treatment #joinus #lupusresearchalliance #getinvolved #lupusorganisation #cure #hopebeginshere #worldwide #lupusencyclopedia #worldlupusfederation
Every day with lupus is a new opportunity to educate, inspire, and support. #WorldLupusDay #LupusEducation #InspireLupus #SupportNetwork #DailyStrength
"Uniting for Lupus 💜 Together, let's strive for understanding, early detection, and improved management. Enhance the quality of life for those affected. 🌍🦋 #LupusAwarenessDay" Today, on World Lupus Day, we unite to raise awareness about lupus, a challenging autoimmune disease that requires our attention and compassion. By fostering better understanding, promoting early detection, and working towards improved management, we can significantly enhance the quality of life for those living with lupus. 🌟🩺 Let’s educate ourselves and others, support research, and offer hope to every individual facing this condition. Every step we take together makes a brighter, more supportive world for lupus warriors. 💜💪 For more details: Contact us at: @vijayatraumacare Address: GJ4H+M7G, Kundanpally, Secunderabad, Hyderabad Telangana 501301 Visit: www.vijayatraumacare.com Mobile: 9703769769 . . #WorldLupusDay #LupusAwareness #LupusSupport #AutoimmuneWarrior #FightLupus #EarlyDetection #ImprovedManagement #ChronicIllnessAwareness #SupportLupusResearch #HopeForLupus #LupusEducation #UniteForLupus #PurplePower #RaiseAwareness #TogetherWeCan #services #rehabilitation #medicalservices #criticalcareservices #besttraumacarecenter #traumacare #emergencycarecenterinhyderabad #traumacareexpert #india #hyderabad #vijayatrauma #instapost #instagram
World Lupus Day is observed annually on May 10th to raise awareness about lupus, a chronic autoimmune disease that affects millions of people worldwide. --- _ _ World Lupus Day serves as an opportunity to educate the public about lupus, its symptoms, and the challenges faced by those living with the disease. Lupus is a complex condition where the immune system attacks healthy tissues and organs, leading to inflammation, pain, and damage throughout the body. It can affect various systems, including the skin, joints, kidneys, heart, lungs, and brain. Despite its prevalence, lupus remains widely misunderstood and underdiagnosed. Many people with lupus experience periods of remission and flares, where symptoms worsen unpredictably. Managing lupus often requires a multidisciplinary approach involving medication, lifestyle changes, and regular monitoring by healthcare professionals. On World Lupus Day, organizations and individuals around the globe come together to raise awareness, provide support, and advocate for better research, diagnosis, and treatment options for lupus. It's a time to honor the strength and resilience of lupus warriors while striving for greater understanding and improved quality of life for everyone affected by this challenging condition. #medmanpharmaceuticals_pvt #medmn #medmanpharmaceutucals #WorldLupusDay #LupusAwareness #KnowLupus #LupusWarrior #FightLupus #AutoimmuneDisease #ChronicIllness #HealthAwareness #SupportLupusResearch #LivingWithLupus #LupusCommunity - #raiseawareness #LupusEducation - #LupusResearch
. Celebrating World Lupus Day! 🎗Together, let's raise awareness and support for those living with lupus. Through understanding and advocacy, we can make a positive impact on the lives of lupus warriors everywhere. Let's stand united in the fight for a cure! . . . . 📍Visit us : 1ST FLOOR, Param Ratan Building, APARTMENT, Haji Zakaria Rd, opp. POST OFFICE, Malad, Navy Colony, Mamledarwadi, Malad West, Mumbai, Maharashtra 400064 . . . #LupusDay #LupusAwareness #LupusWarrior #SupportLupus #AutoimmuneDisease #ChronicIllness #HopeForLupus #LupusEducation #LupusAdvocate #HealthMatters
TODAY the Lupus Foundation of New England presents the Lupus Medical Educational Symposium at the Beechwood Hotel in Worcester! 🗓️ You can still register! Don't miss this incredible opportunity to gain valuable insights from leading experts, discover the latest advancements in Lupus research, and connect with fellow fighters in our community. 💜 Whether you're a patient, caregiver, or healthcare professional, this symposium promises to be informative and empowering. Let's come together to learn, share, and inspire hope in the fight against Lupus! See you there! 👋 #LFNEMedSymposium #LupusEducation #WorcesterEvent #TogetherWeCanBeatLupus
During Lupus Awareness Month, it is especially important to share these facts. Help spread awareness and understanding of lupus everywhere! #kaleidoscopefightinglupus #lupus #sle #spoonie #lupusfighter #lupuslife #spoonielife #lupuscommunity #invisibleillness #butyoudontlooksick #autoimmune #autoimmunediseases #chronicillness #autoimmunedisease #lupusfact #lupusfacts #lupuseducation #lupusproblems #lupusstrong #lupustruth #livingwithlupus #lupuseducation #lupusinformation #lupusinfo #lymphoma #lupusandcancer #lupusawarenessmonth #lupusawarenessmonth2024
Lupus Awareness Month, fact of the day, May 9th! #LSILupusAwareness #lupus #lupusawareness #lupuswarrior #lupuseducation #lupussupport
While there are numerous symptoms, these are some of the most common! #lupus #lupusfacts #lupusawarenessmonth #lupusawareness #lupuseducation #autoimmune #autoimmunedisease #autoimmuneawareness
I'm so grateful that my hometown proclaimed May as Lupus Awareness Month! The State of West Virginia granted my proclamation and now my city. Keep pushing! Lupus voices are getting louder!💜🦋 #lupus #lupusawareness #lupusfoundationofamerica #lupusadvocate #lupuseducation #lupusvoice #lupussucks #lupuswarrior #knowlupus #livingwithlupus #lupuslife #lupusstrong #lupusawarenessmonth #lupussupport #lupusfighter
Lupus Awareness Month blog articles continue ... The Epstein-Barr virus (EBV) that causes mononucleosis, has long been implicated in also triggering lupus, especially in children. Find out more about the relationship between EBV and SLE in our article, "Epstein-Barr Virus and Lupus" by following this link! http://ow.ly/ryaC50IzmKh #kaleidoscopefightinglupus #lupus #sle #spoonie #lupusfighter #lupuslife #spoonielife #lupuscommunity #invisibleillness #butyoudontlooksick #autoimmunediseases #chronicillness #autoimmunedisease #lupusawareness #lupuseducation #lupusblogs #lifewithlupus #lupuslife #livingwithlupus #autoimmune #lupusstrong #lupustruth #livingwithlupus #lupusarticles #lupusinformation
Lupus Awareness Month, fact of the day, May 8th! #LSILupusAwareness #lupus #lupusawareness #lupuswarrior #lupuseducation #lupussupport
You can now watch our May 4th Lupus Health Conference with Dr. C Michael Neuwelt! He shared a lot of great information on lupus and treatments updates in 2024. Go to lfnc.org/lupus-videos to watch it! #rheumatologist #lupusawarenessmonth2024 #lupuseducation
Lupus Awareness Month, fact of the day, May 7th! #LSILupusAwareness #lupus #lupusawareness #lupuswarrior #lupuseducation #lupussupport
Lupus Awareness Month, fact of the day, May 6th! #LSILupusAwareness #lupus #lupusawareness #lupuswarrior #lupuseducation #lupussupport
May is Lupus Awareness Month!!! (Day 6) Did you know that it may take YEARS before you’re diagnosed with Lupus? It took 2 years and 7 doctors for my diagnosis. They pumped me up with steroids, in the meantime… 😔😔 #iHateLupus #33YearLupusConqueror #DiagnosedWithSLEIn1993 #LupusSucks #LupusAwareness #LupusEducation #TheMoreYouKnow #PurpleIs4Lupus 💜💜💜 #iAmJLaTrina www.JLaTrina.com
Another Lupus Awareness Month in full effect this May. TEN YEARS 👀 I remember my life feeling brighter before you, perhaps, because I could handle the sun exposure. Thank you for reminding me to stay in the present moment, to focus on what I can do and for not killing my vibe. Still me! A bit slower and fluffier, but still as fun, dope and in love with who I show up as in this world. 🟪🦄 #lupusawarenessmonth #lupuseducation #lupuswarrior @lupusorg donate if you can to further research, education and HOPE for others and/or wear purple on May 10th for World Lupus Day and tag me 🤘🏽💟
May is Lupus Awareness Month!!! Lupus (Our Daily Struggle) If I screamed, “I don’t feel like being strong today!” would it even matter? Because I’ve been running around here trying to be Wonder Woman, but I really feel like the Mad Hatter... And now all of my thoughts are just simply... scattered... I’m trying to accomplish a lot of things, and I don’t want them to look like a circus, or become a disaster... I’m trying to work while it’s day, because I don’t know what’s coming after... This Lupus flare up is trying to take me out, but you’d never know that I have Lupus, because I know how to mask her... My body and soul are sooo tired right now, and it’s YOU Lord that I wanna seek after... But I don’t have the strength right now, and I wanna scream, “stop the world and let me off,” but it would only go… FASTER!!! I’m trying to find out, if I fall, would somebody say, “grab her?” I know that it’s my fault that no one knows about my daily struggle with Lupus, because I refuse to complain... and remember... I know how to mask her... But for those that do know about it, and others that have Lupus like I do, do you take the time to stop, and ask her...? How are you feeling today....? Or do we even matter...? Written 2.19.2020 Allowing my pen to bleed..🩸 I am J La Trina and writing is my therapy… ✍🏽 #iHateLupus #33YearLupusConqueror #itTook2YearsForDoctors2DiagnosIt #DiagnosedWithSLEIn1993 #LupusSucks #LupusAwareness #PurpleIs4Lupus 💜💜💜 #LupusEducation #imNotAsking4Sympathy #imAlreadyValidated www.JLaTrina.com
Lupus Awareness Month, fact of the day, May 5th! #LSILupusAwareness #lupus #lupusawareness #lupuswarrior #lupuseducation #lupussupport
Today is the premier of KFL’s latest video, “CAR T Cell Therapy and Lupus!”� Dr. Donald Thomas, clinical rheumatologist and author of The Lupus Encyclopedia, shares his expertise and experience treating this challenging condition – from diagnosis to successful treatment options. You can also view this video on our YouTube channel by following this link: Special thanks to our Title Sponsor, Amgen, for their generous support in making this video possible! We also thank DeuxNorth, Tin Rocket, Blue-eyed Crow Studio, and 7-Minute Cinemas! #kaleidoscopefightinglupus #lupus #lupuswarrior #lupusawareness #chronicillness #autoimmunedisease #chronicpain #spoonie #invisibleillness #sle #autoimmune #lupuslife #lupusproblems #spoonielife #butyoudontlooksick #lupussupport #chronicillnesswarrior #lupuscommunity #autoimmunity #lupuseducation #womenshealth #lupustreatments #lupustherapies #lupusmanagement #discoidlupus
Lupus Awareness Month, fact of the day, May 4th! #LSILupusAwareness #lupus #lupusawareness #lupuswarrior #lupuseducation #lupussupport
(May is Lupus Awareness Month) I Have Lupus... My weight goes up and down... I used to hide when I gained weight and wore an awful frown... Sometimes I’ll cancel on you at the last minute, because I’m tired and that used to weigh me down... If you’re not understanding of this, I don’t need you around... There are those that love and understand and in prayer, they hold me down... God has been gracious to me and now I wear a smile... #iHateLupus #33YearLupusConqueror 👊🏽 #LupusSucks #LupusEducation #imNotAsking4Sympathy #imAlreadyValidated
Last Chance to Register for tomorrow's Health Confernce! "A 2024 Update in Lupus" find out what's happening with lupus this year!! We are thrilled to welcome back Dr. C Michael Neuwelt and also host our first Patient Panel of the year! The patient panel will not be recorded so be sure to attend in order to hear from our lupus warriors! To register go to: lfnc.org/2024_may_-lupushealth-conference #lupuswarrior #lupuseducation #lupus #LupusAwarenessMonth
🌟✨ A huge thank you to everyone who joined us at last night's seminar! Special shoutout to our sponsor, @Aurinia Pharmaceuticals Inc for their support and to our incredible Rhode Island Ambassadors, Aida Crosson and Rob Williams, for making it all happen. 🙌💜 #LupusFoundationNE #LupusAwareness #Aurinia #HealthEducation #LupusSupport #ThankYouSponsors #RhodeIslandAmbassadors #AidaCrosson #RobWilliams #LupusWarriors #CommunitySupport #LupusEducation #FightLupus #LupusAdvocacy #ChronicIllnessSupport #AutoimmuneAwareness #HealthSeminar #LupusCommunity #TogetherWeFight #LupusResearch #RaiseAwareness #SupportOurSponsors #HealthAndWellness #LupusLife #NonProfitEvent #CommunityImpact
Lupus Awareness Month, fact of the day, May 3rd! #LSILupusAwareness #lupus #lupusawareness #lupuswarrior #lupuseducation #lupussupport
Lupus Awareness Month, fact of the day, May 2nd! #LSILupusAwareness #lupus #lupusawareness #lupuswarrior #lupuseducation #lupussupport
MAY IS LUPUS AWARENESS MONTH, ALTHOUGH AWARENESS AND EDUCATION SHOULD BE A DAILY THING, THIS MONTH WE FOCUS ON AMPLIFYING OUR VOICES. WE'RE DOING IT FOR ALL THE WARRIORS, DEAD OR ALIVE, IT IS A COLLECTIVE FIGHT AND EFFORT. #LupusAwarenssmonth #lupuseducation #LupusAdvocacy #rarediseaseawareness #chronicconditions #LifeBeyondLupus 💜💜💜💜💜💜💜🦋🦋🦋🦋🦋🦋🦋
Lupus Awareness Month, fact of the day, May 1st! #LSILupusAwareness #lupus #lupusawareness #lupuswarrior #lupuseducation #lupussupport
Lupus Awareness Month, fact of the day, May 1st! #LSILupusAwareness #lupus #lupusawareness #lupuswarrior #lupuseducation #lupussupport
Don't miss out on this great topic- "A 2024 Update in Lupus" find out what's happening with lupus this year!! We are thrilled to welcome back Dr. C Michael Neuwelt and also host our first Patient Panel of the year! The patient panel will not be recorded so be sure to attend in order to hear from our lupus warriors! To register go to: lfnc.org/2024_may_-lupushealth-conference #lupuswarrior #lupuseducation #lupus #LupusAwarenessMonth
Welcome to May, foodie fam! 🌟 May is Lupus Awareness Month, so as an “experienced” lupus warrior, I’m excited to kick off this month with a special focus on sharing lupus-friendly recipes and some insights into what it’s like to live and cook with a chronic illness. 💜🍽️ Throughout May, I'll be sharing some mouthwatering dishes designed to support a lupus-friendly diet, sharing info on how certain ingredients can help manage symptoms and benefit the overall well-being, and we’ll also dig into the ins and outs of living with lupus, sharing some insights, tips, and stories as inspiration and motivation. 🥗💪 So let's roll up our sleeves, sharpen our knives, and get cooking! Here's to a month filled with knowledge, compassion, and plenty of good eats! 🌟📖 (еј, има и на македонски 😊) Гурманска фамилијо, добре дојдовте во мај! 🌟 Мај е месец за подигнување на свеста за лупус, па како „искусен“ лупус-борец, едвај чекам да го започнам месецов со нешто посебно. Овој месец ќе ставам посебен акцент на споделување рецепти кои му годат на лупусот и ќе споделам неколку „инсајдерски“ информации за тоа како е да се живее и да се готви со хронична болест. 💜🍽️ Ќе споделам неколку јадења од кои ќе ви потечат лиги. Јадења кои се дел од исхраната која му одговара на лупусот. Ќе има информации за одредени состојки кои можат да помогнат за справување со симптомите и да го подобрат целокупното здравје, и неколку кратки приказни за животот со лупус, како и совети и насоки за инспирација и мотивација. 🥗💪 Па, да ги засукаме ракавите, да ги наостриме ножевите и да се фатиме за готвење! За (ја кревам шолјата со кафе) месец исполнет со знаење, разбирање и куп вкусни јадења! 🌟📖 #LupusEducation #CommunitySupport #CookingAndLearning #LupusAwareness #lupusmkd #Mayislupusawarenessmonth #lupuswarriors #LupusFriendlyRecipes #CookingWithLove #tasijagotvi #лупусмкд #лупусборци #тасијаготви
Don't miss out on this great topic- "A 2024 Update in Lupus" find out what's happening with lupus this year!! We are thrilled to welcome back Dr. C Michael Neuwelt and also host our first Patient Panel of the year! The patient panel will not be recorded so be sure to attend in order to hear from our lupus warriors! To register go to: lfnc.org/2024_may_-lupushealth-conference #lupuswarrior #lupuseducation #lupus #LupusAwarenessMonth
Don't forget to register for our May Lupus Health Conference! We are thrilled to welcome back Dr. C Michael Neuwelt and also host our first Patient Panel of the year! The patient panel will not be recorded so be sure to attend in order to hear from our lupus warriors! To register go to: lfnc.org/2024_may_-lupushealth-conference #lupuswarrior #lupuseducation #lupus #LupusAwarenessMonth
We can’t believe Lupus Awareness Month is right around the corner. We are excited to share some other wonderful events that are being held in honor of Lupus Awareness Month 2024. These community programs are all free of charge and registration is available directly from the flyer. Check their events out at https://www.hss.edu/lupus-awareness-month.asp #lupusawareness #lupuseducation
Last chance to sign up!!!! Don't miss this FREE, VIRTUAL lupus health conference! Our first session welcomes, Dr. Tania Rivera who will discuss lupus symptoms and diagnosis. In our second session, Registered Dietitian Nutritionist, Tanya Fredrick will discuss "Does diet make a difference in lupus?" Each presentation will be followed by a 15 minute Q & A session. This program is FREE to lupus patients, family members, health professionals and other interested parties. To register go to: www.lfnc.org/events #lupuseducation #lupus #nutritiontips
#kaleidoscopefightinglupus #lupus #sle #spoonie #lupusfighter #lupuslife #spoonielife #lupuscommunity #invisibleillness #butyoudontlooksick #autoimmune #autoimmunediseases #chronicillness #autoimmunedisease #lupusfact #lupusfacts #lupuseducation #lupusproblems #lupusstrong #lupustruth #livingwithlupus #lupuseducation #lupusinformation #lupusinfo #pulmonarylupus #lupuslungs #lungsandlupus