Top Tweets for #lupus

Interesting editorial by Drs @Yuz6Yusof and @edvital about the need for early interventions in #lupus #SLE diagnosis and treatment. #rheumatology #calltoaction @RheumAdvisor rheumatologyadvisor.com/home/topics/sy…

Das ist es, was mein #Hausarzt befürchtet wegen der massiven Ödeme: #Lupus #Nephritis. Deshalb hab ich am 09.02.22 einen Termin zur Blutentnahme (gleich um 8) & am 15.02.22 einen Besprechungstermin. klinischeforschung.novartis.de/doctor/lupusne… @JosephusLudwig @LADAOrg @Lupuserythemato @LeslieTurn2

Lupus is a complex disease that is hard to define. It strikes without warning, affects each person differently, and has no known causes or cure. #lupus #autoimmunedisease #invisibleillness #chronicillness #chronicpain #SLE #Knowlupus

#Lupus #Science and #Medicine is a global-peer reviewed-open access that provides a central point for publication of basic, #clinical, #translational, and #epidemiological studies of all aspects of lupus and related #diseases. Submit you #manuscripts at bit.ly/3FK6TgN

This week on LSM: @ZahiTouma and this group analyze the #prevalence and #incidence of #herpes zoster (HZ) events and describe its associated factors in a study of #patients with #SLE. #Lupus bit.ly/3nEpqoJ

When my #Hydroxychloroquine disappeared because #antivaxxers took it all, I had two mini heart attacks. I have #Lupus, no immune system, and I’m a teacher. I have NO tolerance for “I’m so over Covid.”

If you’re disabled and need a reusable FFP2 mask, @CambridgeMaskCo have a 25% discount on their PRO range. The code: MASKUPGRADE Please RT! #Disabled #LongCovid #MECFS #PoTS #Lyme #Lupus #InvisibleIllness #mentalhealth #fibrofigher #spoonie #chronicpain #autoimmunedisease /1

[ Sobrevivir con enfermedades raras ] . Así como el #lupus, la #fibromialgia o el #Hashimoto, la de #Kawasaki es una afección crónico degenerativa que trastoca la vida de quien la sufre. Olga y Sergio, amigos queridos y padres de Emanuel, invitan 👉 facebook.com/12797248125861…

This is great news for all #Lupus patients and clinicians. #SLE disease activity scores are useful in guiding treatment and Easy-BILAG is brilliant @RheumatologyUK @eular_org @ACRheum @LUPUSUKtwitter.com/RheumJnl/statu…

Awareness about lupus among Americans of all ages is extremely low, with 61 percent of Americans reporting they have never heard of lupus or know little or nothing about the disease beyond the name. #lupus #lupusawareness

In Pregnant Women with Lupus, Low Blood Levels of Hydroxychloroquine Linked to Preterm Birth. Read More linktr.ee/lupuslonestar #LFALS #lupuslonestar #lupus #hydroxychloroquine #HCQ #lupusstrong #lupuswarrior #lupuslife #lupusmedication #preterm

Only one drug has ever been developed and approved specifically to treat lupus. #lupus #lupusawareness #autoimmunedisease #chronicillness #ChronicPain #invisibleillness

This episode of the #RHT features Natasha Bowles, founder and CEO of Natasha Bowles Professional Services, a virtual assistant staffing firm. #lupus #staffing #va #virtualassistant virtualexecutivedirector.libsyn.com/rht-187-natash…

DYK people with #lupus have a higher risk of bone loss (osteoporosis) and bone breaks? Women’s risk goes up further after menopause. Now, a new study suggests hormone replacement therapy may be an effective treatment. Read the study. #lupusResearch

Despite the widespread prevalence of lupus, research on the disease has remained underfunded, relative to its scope and devastation. #lupus #lupusawareness #autoimmunedisease #invisibleillness #chronicillness #ChronicPain

Lupus usually develops between ages 15 and 44, and lasts a lifetime. #lupus #lupusawareness #autoimmunedisease #invisibleillness #chronicillness #ChronicPain #lupusWarrior #lupusadvocate

Join us TONIGHT from 7-8 pm for Living Well With Lupus: A Holistic Approach. AAIDA will host Tanya Freirich, MS, RD, CDN, CDCES to kick off our webinar series for 2022! #Lupus godoaaida.org/webinars/

Join us on Feb. 8 at the virtual Chronic Disease at Work conference to hear Leanne Mielczarek, executive director of @LupusCanada , discuss the impact of lupus on the workplace. This session has been made possible by @AstraZeneca . Register: bit.ly/35gJzup #Lupus

#Lupus neurological symptoms: depression, seizures, cognitive dysfunction, mood disorder, cerebrovascular disease, polyneuropathy, anxiety

It was amazing to present on genomics in Juvenile SLE at #AdolRheum22 alongside so many other incredible speakers on important topics in Adolescent rheumatology 🧬🔬🩺 #Rheumatology #lupus #SLE #JSLE @UCL_RheumAYA

Lupus can strike anyone at any time, but 90 percent of the people living with lupus are women. Women of color are at especially high risk. #lupus #lupusawareness #autoimmunedisease #invisibleillness #chronicillness #ChronicPain

Visit our testimonial page & type in lupus, to see how many people have gotten amazing positive results by using our all natural health products. mystory.xoomaworldwide.com (type the specific condition in to the search ) #lupus #lupusWarrior

For some w/ "mild" COVID, their bodies are producing a type of antibody that attacks healthy cells, tissues, and organs in the body. The same type can be found in more than 100 autoimmune conditions, like #type1diabetes, #RA, and #lupus. ow.ly/ztsf50HAgvk?ap…

We are excited to introduce our new online lupus #SELF-management program Strategies to Embrace Living w/ Lupus Fearlessly. #SELF is free & full of tools, tips & support to help adults w/ #lupus better manage their disease. lupus.org/resources/self…

Lupus is one of the cruelest, most mysterious diseases on earth-an unpredictable and misunderstood autoimmune disease that ravages different parts of the body. It is difficult to diagnose, hard to live with, and a challenge to treat. #lupus #chronicillness #invisibleillness

Welp. I diagnosed my #lupus with the help of Google, a doctor who listened to me and didn't think I was nuts, and my 3rd round of labs which finally showed the proof we needed for the official diagnosis.

While lupus can be disabling and potentially fatal, in many cases the most serious health effects can be managed through aggressive medical treatment and lifestyle changes. #lupus #lupusawareness #autoimmunedisease #chronicllness #chronicpain #invisbleillness

Living with lupus can be baffling and isolating, as symptoms mimic other illnesses and often do not cause people to look sick. #lupus #autoimmunedisease #invisibleillness #chronicillness #chronicpain #lupusawareness

Important information about '#Lupus #erythematosus': an asymptomatic disease that destroys the body

@kjsmithofficial #TuesdayThoughts #Lupus "Lupus Loves Me So Much. Lol!" All I Can Do Is Laugh and Uplift Strangers."

Hi, I'm Karen. I'm a #teacher. I also have #lupus that puts me at an increased risk for serious complications from covid. #IHaveAPreexistingCondition ... twitter.com/sbernsteinmd/s…

Lupus symptoms can be severe and highly unpredictable and can damage any organ or tissue, from the skin or joints to the heart or kidneys. #lupus #autoimmune #invisibleillness #chronicillness #ChronicPain #lupusawareness

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