Join us for #WorldLupusDay Luncheon on 20 May 2018 @ celebrity #MasterChef’s George Calombaris’s new restaurant, Hellenic Republic in Brighton

Day 2! Alternating lunges: Stand with your feet together and hands on hips. Take a big step forward with the right foot and bend your knees (see below). Rise up as you step back to the starting position. Now step forward with the left foot, then return to the starting position.

"#Lupus is such an ugly diagnosis, and I truly think people who are not experiencing it only think in terms of PHYSICAL." Read more:

Releasing a piano version of the ‘Joanne’ title track along with an accompanying music video, making a donation to the Lupus Research Alliance and possibly performing the new version at the #GRAMMYs this Sunday is a perfect way for Gaga to honour her late aunt and end this era.

Immunologic markers (C3/4 levels) and demographic factors (age and race) are strongly predictive of risk for incident #proteinuria in patients with #lupus , https://t.co/5ctFJQODvy according to the results of a recent cohort analysis published in @Lupus_SM

Sonia Walmsley who has #lupus (along with a number of other diagnoses) was recently the subject of discrimination and abuse because she has an invisible illness. Have you experienced anything like this because of your condition? https://t.co/nXXi4UN5Ic

Each person with #lupus has slightly different symptoms that can range from mild to severe and may come & go over time.

Most people with lupus don’t look sick. SHARE 4 #lupusawareness #lupussurvivors https://t.co/TClwcK0izG

To every #spoonie out there, please know how wonderful you are, you make all the days bearable. Finally, we're never alone anymore and that one action makes life not so terrible. #SLDquote #Lupus #Fibro #MS #ME #CRPS #endo #PTSD #PsA #Lyme #behcets #migraine #AS #sjogrens #POTS

Pain relief is being restricted/denied to pts suffering with conditions like: #Lupus #MultipleSclerosis #Fibromyalgia #endometriosis #InterstitialCystitis #mecfs #rheumatoidarthritis #spondylosis & many others painful conditions. Share your story! #shareourpain

Model shares photos of her #lupus blisters to inspire others to feel confident in their skin - Metro https://t.co/Lq7HGjpPvX

New research has identified a simple blood test that could be a good predictor of #lupus nephritis relapses. https://t.co/CU0GfVPja6

Want general information about #lupus to share with family & friends? Mack the Molecule is here to help!

Common symptoms of #lupus include painful or swollen joints, unexplained fever, & fatigue. Learn more here:

#lupus research: Endothelial dysfunction in early systemic lupus erythematosus patients and controls without previous cardiovascular events. - To assess the prevalence and risk factors for endothelial dysfunction detected by peripheral artery tonometr...

Peggy's Story - Living with #Lupus by @mountaingrace1 #LOU

Spreading awareness of invisible illnesses because you don’t need to look sick to feel sick. #lupus #POTS #invisibleillnes #Dysautonomia #eds #chronicillness #Spoonies #EDS #spoonie #autoimmune #blogger #potsie #sisters #posturalorthostatictachycardiasyndrome #HealthyLiving

Do you have travel plans this season? #lupus https://t.co/Gsea3pC54q