RT @AnnaGaddy: Had a great time talking with the @LupusOrg Lupus Foundation of America about Lupus Nephritis tonight with @nkfwi @nkf. Than….

RT @Lupus_SM: 🎙️ Our podcasts give you the latest insights and developments in #lupus & related diseases. Hosted Dr. Anna Wolska, they pres….

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It's #NationalEyeExamMonth, and eye health is incredibly important for people with #lupus. 👀 Listen to our The Expert Series podcast episode with Dr. Michelle Petri as she discusses eye health and what to look out for:

Big life changes can be exciting but stressful. For those with #lupus, stress may trigger flares, so planning and self-care are key. Our guide offers tips to protect your health during major events. 👉 Explore the full resource:

Meet Erich 💜 He completed his first Half-Ironman in honor of his mom, a #lupus warrior whose memory continues to inspire him. Through Choose Your Own Race, you too can race and dedicate your miles to end lupus through any race you'd like. Learn more:

Fatigue is a common symptom of #lupus, but there are many steps you can use to help manage it. 💤 Check out this resource with some great tips to ensure you get the rest you need, and share how you manage your fatigue in the comments below:

Could preload deficiency be a cause of fatigue and exercise in people with #lupus? A new study finds a potential connection, biomarker and treatment for the condition. Read the study:

🥗💜 There’s no one-size-fits-all #lupus diet, but the foods you eat can still have a big impact. From easing symptoms like fatigue and joint pain to supporting your health. 🍽️ Get tips on healthy choices, what to avoid, and how to build a balanced plate:

💜🎉 It's #NationalNonprofitDay! Let's spread the word about the vital work we do together! Share why you’re proud to be part of the community and how it supports people with #lupus and their loved ones:

RT @bodybyboddie: @LupusOrg @cvspharmacy

August is Make-A-Will Month! 💜 Create or update your will in just 20 minutes with our free, secure tool from Free Will. Care for loved ones & leave a legacy for those with #lupus. Every gift helps bring us closer to a world without lupus. ➡️ Start today:

RT @Lupus_SM: Want to stay up to date with #basic, #clinical, #translational, and #epidemiological #studies of all aspects of #lupus and re….

📸 Whether it’s a photo of a symptom, a hospital moment, or a smile at an LFA event, your story matters. Share what your life with lupus really looks like:

Meet Alexandra. 💜 Diagnosed with #lupus nephritis at 16. At times, the pain and exhaustion felt isolating — but finding the Lupus Foundation of America changed that. Through stories from others and events like #WalktoEndLupusNow, she found strength, connection, and support.

It's #NationalRelaxationDay! How are you planning to relax and take care of yourself? If you need some ideas, check out our resource on mindfulness meditation, and how it can help with chronic pain:

A new study links systemic #lupus erythematosus-specific risk factors with increased risk for #osteoporosis. Read the study:

Managing finances can be a significant concern when living with #lupus. This National Financial Awareness Day, we're highlighting our resource for financial assistance. Understanding available options can allow you to focus on well-being. Learn more:

📚 For kids with #lupus, managing your health at school is key to having an enjoyable year. 🌟 Read our essential tips to help you navigate school life while staying on top of your lupus management and get ready for a successful school year! . Learn more:

RT @PosLupusLiving: The LFA has partnered w/SNOOPDOG in honor of his daughter Cori Broadus who is living with lupus.The Broadus Collection….