Lupus Fact #2; Day 2

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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The front label of Essential Palace Botanical Fibroid & Lupus Care Tonic, highlighting key ingredients like French Tarragon, Linseed, Green Tea, and Chives Extract. It also states "NEW 5 IN 1 ULTIMATE BLADDER & SEXUAL SUPPORT" and claims to be 100% organic.

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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🌿Herbal Support for Lupus🌿

Hey friends! I wanted to hop on here and talk about herbal support for lupus. My sister has lupus, and these natural remedies have really helped improve her health and keep flare-ups at bay, alongside exercise, a balanced diet, and healthy lifestyle changes. 💚 Flax, Reishi, and Turkey Tail are po

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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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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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Symptoms of Lupus

I spent a year trying to figure out what was wrong with me. My functional medicine doctor tested me for autoimmune disorders and it was lupus. #lupusawareness #lupus #autoimmunedisease #autoimmunehealing

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A white background with purple text asking about chronic tiredness, lifelong medication, depression, and mood swings, all related to an invisible illness. Purple butterflies and ribbons are also present.

A purple background with text stating, 'Lupus Fact Change of weather can trigger a flare' and 'Lupus Butterflies and more...'. A purple ribbon with 'LUPUS' is in the top right corner.

A pink and purple background with text explaining that chronic fatigue is not just being tired and cannot be cured by sleep or coffee, describing it as total physical, mental, and emotional exhaustion.

#IHaveLupus 🫶🫶🫶🫶

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Be the bad ass that you are! Be the Lupus warrior

Lupus Warriors don’t give in We push through the pain and hide behind the mask

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Lupus summer saving products

#beautyhaul #lemon8challenge @FabFitFun @CVS Pharmacy @L’Oreal Paris @elfcosmetics @Aquaphor @Neutrogena @Lemon8 Beauty these are the products I would save if I were to be on a deserted island. The @Neutrogena spf 60 blends in beautifully under my makeup. I live in Phoenix an

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Lupus Supplement ✨🌸🫶

BENEFITS: Reduces Inflammation Enhances Immune Function Provides Relief for Muscle, Joint and Chest Pain Improves Mental Health and Well-Being Ingredients Filtered Water, Papaya Leaf*, Marshmallow Root*, Moringa*, Seamoss*, Kola Nut*, Barberry*, Goldenseal Root*, Slippery Elm*, Cardamom

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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 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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Lupus

It gets old quickly dealing with lupus. #lupus #lupusawareness #lupuswarrior

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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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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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This image defines Fibromyalgia (FMS) as a neurological condition where inappropriate nerve signals cause various symptoms. It states sufferers experience up to five times the pain level of non-sufferers, set against a background with butterflies.

This image, titled 'THE THIEF THAT IS FIBROMYALGIA,' lists various aspects that fibromyalgia 'steals,' such as body, energy, health, mind, sleep, friends, family, happiness, fun, special moments, careers, and the person you used to be, with a purple ribbon and butterfly.

This image describes Vulvodynia in Fibromyalgia, a chronic pain condition affecting the vulva. It details symptoms like burning, stinging, rawness, itching, throbbing, and soreness, and its impact on daily life, with a small anatomical illustration.

Fibromyalgia And Lupus Life 🫶✨🫶✨

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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 Awareness

https://bit.ly/FightingtheInvisibleHC #lupusawarenessmonth #lupusawareness #lupuswarrior #lupusfighter #lupusstrong #lupus

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LUPUS 🌸🌸🌸🌸

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LupusWarrior 🦋🦋💜💜

#lupuswarrior🦋💜 #lupusjourney #lupusawareness #lupusnephritis #lupuslife

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Go to Lupus Warrior Princess 1 for more

#lupuswarrior #lupusfacts #lupusawareness #spoonies #spooniesoftiktok

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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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Managing Lupus

#lupusawareness #lupus #systemiclupus #chronicillness #embracevulnerability

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Lupus And Fibromyalgia 🫶🫶🫶🫶🫶

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Lupus Fact #4 : Day 4

You can read my story with Lupus if you like in my book: “Fighting the Invisible: My Life with Lupus” Click link for book: https://bit.ly/FightingtheInvisibleHC #lupusawarenessmonth #lupusawareness #lupuswarrior #lupusfighter #lupusstrong #lupus

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Anyone here with Lupus?

So I have Lupus. Which is an autoimmune disease this where the body fights against it self, instead off the infection in your body. Doctors are still unaware of the infection that’s is in the body. There are different ways of getting lupus. Rather it is generic or environmental. When I found out th

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Lupus

Surprising this that Lupus and Rheumatoid Arthritis do. They make your nails all wonky! I use to have beautiful hands🥺 #arthritis #lLupus sucks

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Lupus 🍋🍋🍋🍋🍋

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What doctor don’t tell us about lupus .

🩸 Part 1: What Doctors Don’t Tell You About Lupus ✨ What doctors don’t always say… we need to start saying out loud. Lupus doesn’t just affect your joints. It shifts your life. From misdiagnosis to emotional breakdowns, this is the real story of autoimmune survival. Save this post for when yo

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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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World Lupus Day 2025

You don’t have to see my battle to believe it’s real. This is what living with lupus feels like. It’s painful, exhausting, invisible — and still, every day, we rise. To everyone fighting lupus: You are not alone. You are not invisible. You are powerful beyond measure. Today we honor you. To

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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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As a girl with Lupus, I love:

All the comfort items, providers that listen, and awareness/advocacy for Lupus 🦋 #lupuswarrior🦋💜 #sle #autoimmunedisease #lupus

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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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Lupus sucks

#lupusjourney #autoimmuneawareness

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LupusWarrior 💜💜🦋🦋

#lupuswarrior🦋💜 #lupusjourney #lupusawareness #lupusnephritis #lupusSLE

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Lupus 🤍

My most viral video on TikTok! #medicalstudent #learnonlemon8

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A close-up selfie of a woman with text overlays "I am the face of Lupus" and "fyp#foryou #explorepage". The image is decorated with purple hearts and butterflies, emphasizing Lupus awareness. The TikTok handle @angiebaby0215 is visible at the bottom.

#LupusWarrior💜🦋 #IamTheFaceOfLupus #ButGotGod♥️🙌🏾

#gettoknowme

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A person with neck tattoos, sunglasses, and a red hat smiles, showing medical tubing on their chest. Text overlay reads: "You can have 1000 problems in life.."

A person with facial tattoos cries, with tears visible on their cheeks, and a medical dressing on their chest. Text overlay states: "Until you have a health problem.. then you only have 1 problem.."

A medical drainage bag filled with dark red liquid, possibly blood, with measurement markings and a connected tube, rests on a tiled floor.

Warning ⚠️ Living with lupus and EDS+co

#lupus #ehlersdanlossyndrome #chronicillness #terminallyill #esblcolonized

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Custom designs to inspire my Lupus Warriors💜🥰🫶🏾

#gettoknowme @Lupus Warrior Lil Trina

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A woman wearing sunglasses smiles on a cruise ship deck, with text overlay indicating she is sharing items she packs for a cruise with Lupus.

A screenshot of travel insurance benefits, highlighting coverage for emergency care, evacuation, and other travel-related incidents, emphasizing its importance for a cruise.

A hand holds a tube of broad-spectrum sunscreen, emphasizing the need for ample sun protection, especially for individuals with Lupus.

Things I pack to go on a cruise with Lupus

Sunscreen, heating pads, meds… oh my! Here’s all the big things I always remember to bring with me on a cruise #lupus #lupuswarrior #sle #autoimmunedisease

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Lupus Sucks 🫶🫶🫶🫶

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Lupus sucks!

Currently freezing cold even though it's 70° outside, but my toes feel like Alaska! Heated blanket and heated whatever this beanbag think you heat up in the microwave. #lupuswarrior #alwayscold #pain

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To my lupus warriors we got this 🫶🌸

#lupuswarrior🦋💜 #lupuscommunity #lupusjourney

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Lupus Baddie 💟

#selfie #selflove #me #pretty #newtolemon8 #cuteglasses #loveme #lovemesomeme

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💜 Lupus: What You Should Know 💜

🦋Lupus What You Should Know 🐺 So many people have heard of lupus but don’t really know what it is. Here’s a quick breakdown: 💜 It’s an autoimmune disease 💜 It can affect your joints, skin, and organs 💜 Fatigue, pain, and rashes are common 💜 It’s not contag

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