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Could it be lupus? What to know BEFORE you see a doctor
You’ve been tired for way too long. Your joints hurt. You feel off. You’ve gone to the doctor… and left with no real answers. Here’s the thing: Lupus can be sneaky. It mimics other conditions and hides behind vague symptoms. And many people (especially women) go years without a diagnosis.
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This is Lupus 💜🦋
This one is a hard one to post each time. I’m not the same person I was before my symptoms started! 💜🦋 #lupus #lupuswarrior #lupusawareness #lupusjourney #lupuscommunity Memphis
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Custom designs to inspire my Lupus Warriors💜🥰🫶🏾
#gettoknowme @Lupus Warrior Lil Trina
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This is Lupus 🥹💜🦋
It’s been almost 6 years since I was diagnosed with lupus! Everyday has been a battle ever since 🥹 trying to be more holistic has helped with my symptoms and improved my spirit substantially! My mental health tends to take a hit from the stress of having lupus and how it impacts my life in so many
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My Lupus Diagnosis Story💜
Last year around this time I was diagnosed with a chronic autoimmune disease. I began feeling sick 2023 spring semester but I thought it was due to the stress of college as well as the sickness that runs its course on campus. I noticed a problem once I can home and was not able to workout, eat, or
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Understanding Lupus and Anxiety 💜
Hey Sunshine’s Living with lupus can be challenging, especially when it comes with anxiety. The unpredictability of flares and ongoing symptoms can create a lot of stress. Remember, it’s important to take care of both your physical and mental health. Find what helps you relax, whether it’s min
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Lupus Soldier Behind The Strive
#lupus #interview #realtalk #sahnhova #lupuswarrior Jacksonville
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Lupus Warrior 💜
I'm just a girl fighting a battle that I didn't ask for. But asking for it, or not. I'm going to win at all means. Lupus messed with the wrong girl cuz I don't give up. #warriorqueen #lupus #lupuswarrior
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✨Living with lupus 🌸
So this happened today. So I have lupus and it is an autoimmune disease. This disease has a mind of its own and flares up randomly. So today I was sitting outside in the sun drinking my morning coffee, and watching YouTube videos. I then got up and went to use the ladies room and notice r
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Losing Weight With Lupus 💜
If you’ve been here for beauty finds, home projects, and everyday life… don’t worry, that’s not going anywhere. But I’m adding something new. For years, I’ve battled autoimmune diseases, including lupus. Some days my body cooperates. Some days it doesn’t. Steroids, inflammation, chronic pain,
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To my lupus warriors we got this 🫶🌸
#lupuswarrior🦋💜 #lupuscommunity #lupusjourney
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World Lupus Day
World Lupus Day #lupusawareness #lupus #chronicillness #chronicpain #autoimmune #autoimmunedisease #lupusstruggles #lupuswarriors #lupusjourney #marsblends #lupuswarrior🦋 #kidneyfailure #kidneydisease #kidneywarrior #SLE #slelupus #worldlupusday
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Lupus Emergency Pouch
New Medical Card shipment. I will now be offering an emergency kit for Fibromyalgia and Lupus. If you have Lupus, what are the must haves to include in a rescue pouch?? #lupusawareness #lupuswarrior #emergency kit #emergencybag #chronicillness
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Essential Palace Fibroid & Lupus Tonic 8oz
#herbal supplements #tonic Brand: Essential Palace Product: Fibroid & Lupus Botanical Balance Care Tonic Ingredients: This Tonic is a blend of natural Ingredients, such as French Tarragon, Linseed, Green Tea, Chives Extract, Fenugreek, gymnema, ginseng, psyllium, Cinnamon, Aloe Ver
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Lupus cheat sheet✨✨
🩸 Lupus Cheat Sheet (Save This Soft Girl Survival Guide) ✨ Lupus is more than joint pain. It’s body betrayal. It’s brain fog. It’s invisible suffering. And most days… it’s misunderstood. This cheat sheet is your daily reminder that your pain is real, your healing is sacred, and your softness
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Lupus Warrior 🐺🦋
On my personal page, I share my journey battling lupus, a relentless condition that impacts me on multiple fronts - mentally, emotionally, and physically. Each day feels like a new chapter in a never-ending battle, where the challenges persistently resurface, testing my resilience and determination
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Lupus warrior 🌸🌸🌸🌸🌸
This is for every lupus warrior... Who have fought lupus day in and day out for the rights to their body! Who have cried in the shower so no one else would see their pain. Who mourn their old self while they try to learn how to live in their new body. Who were told they were faking it when
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Lupus Unfiltered
Lupus doesn’t play by the rules—and neither does the symptoms. From brain fog to burning skin to random mouth & nose ulcers to chest pain so bad it feels like your having a heart attack. These are just a few sneaky signs no one tells you about. So, if you ever thought “Is this in my head, or is
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Lupus
It gets old quickly dealing with lupus. #lupus #lupusawareness #lupuswarrior
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The Reality of Living with Lupus.
I’ve come to realize the reality of living with Lupus means learning what the word Chronic means. The chronic fatigue has been a battle I end up losing on a daily basis. #lupus #lupuswarrior #lupussymptoms #lupusearlysymptoms #chronicpain Memphis
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Lupus Emergency Pouch
https://www.just-in-case-kits.com/ #emergencypouch #lupus #lupusawareness #lupuswarrior
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Prayers needed! Fighting Lupus 🙏🏾💜✝️
Please pray for me in this holiday season. I am battling Lupus. It affects my organs with inflammation. There is no cure #unfiltered #prayer #lupuswarrior
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Lupus Warrior
Lupus has me sitting out today. I went hard yeasterday- spent more spoons than I had. Today is a rest day. Lupus fatigue is debilitating. #lupuswarrior #lupus #lupuswarrior🦋💜
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Lupus Diagnosis Timeline
Here’s how my journey went, from starting to show symptoms in 2018, to getting diagnosed in 2024 with SLE Lupus #lupus #lupuswarrior🦋💜 #sle #lupuswarrior #autoimmunedisease
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LupusWarrior 🦋🦋💜💜
#lupuswarrior🦋💜 #lupusjourney #lupusawareness #lupusnephritis #lupuslife
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Living with Lupus & Anxiety 💜
Living with Lupus & Anxiety My Journey Hey everyone, I wanted to take a moment to open up about something personal. I have lupus, an autoimmune disease that affects my body in ways I never expected. Along with that, I also experience anxiety, which sometimes makes navigating day-to-day li
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Lupus warrior here yall
#lupuswarrior #embracevulnerability y’all ALLNforLN.com check it out I have lupus syjouren and I suffer these ppl care!!! And lupus.org y’all
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Life with Lupus
The validation when you finally get labs back that show how you’ve been feeling for years! It wasn’t “just anxiety” after all. #lupuswarrior #autoimmunedisease #chronicillnesswarrior @Ashley Lou
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#lupuswarrior
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Waking up with Lupus
How I feel when I wake up... #chronicillness #mentalhealthmatters #hidradenitissuppurativawarrior #autoimmunedisease #lupusawareness
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LUPUS 🌸🌸🌸🌸
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Lupus Girlies!
I am going to make my page a safe space for lupus sufferers! our condition does not define who we are. #lupus #lupusillness #lupuswarrior🦋💜 #lupuswarrior #lupusrealities
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Lupus affects everyone differently
Getting diagnosed with lupus was just the start of my journey. Luckily I responded well to medicine which helped with my initial symptoms but little did I know that random symptoms would pop up as I started living my life with lupus. It was difficult to feel pretty when I constantly had new symptom
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Lupus Baddie 💜
#lupuswarrior🦋💜 #lupusawareness #medicated #fyp
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My Sun Struggle with Lupus & Sjögren’s ☀️💔
I love sunny days… but my body doesn’t. Living with Lupus and Sjögren’s means sunshine isn’t always sweet. After just a little time outside, I get skin rashes, itching, redness, and full-body flare-ups that leave me completely wiped out,physically and emotionally. Hot days trigger my joint pa
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#1 question I get about Lupus
Living with lupus doesn't mean giving up on your dreams! 💜 When I first got diagnosed, I felt scared and overwhelmed. But I'm here to tell you - lupus is NOT a death sentence. With the right approach to nutrition and lifestyle, you can reclaim your energy, reduce flares, and live a vibr
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Lupus Warriors
Lupus Warriors will relate to this fun t-shirt that I designed with my purple butterfly illustration. It’s available in my Zazzle shop now! Link in bio https://www.zazzle.com/feeling_cute_might_flare_up_later_purple_butterfly_t_shirt-256874852462170685 #lupus #lupuswarrior #autoimmunediseas
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Lupus makes your immune system go haywire
Any little infection I get, goes wild. A small bump got infected somehow and just kept spreading and spreading. Now I’m on 500 mg of Keflex FOUR times a day to get it under control #lupus #lupuswarrior #lupuswarrior🦋💜 #autoimmunedisease #sle
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LupusWarrior 💜💜🦋🦋
#lupuswarrior🦋💜 #lupusjourney #lupusawareness #lupusnephritis #lupusSLE
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Lupus WARRIOR 💜🦋💜
#lupuswarrior #im spiritual New to Lemon8! Something I love：reading, politics, makeup, diy’s
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Moving forward with Lupus 💜
Healing with lupus doesn’t mean going back to who you were before. It means becoming someone new. Someone who has had to slow down. Someone who has had to listen to their body in ways they never had to before. Someone who has had to let go of certain expectations… and rebuild new ones. A
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