lindasulzer posted a contribut | Gallery posted by lindasulzer

Custom designs to inspire my Lupus Warriors💜🥰🫶🏾

#gettoknowme @Lupus Warrior Lil Trina

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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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Lupus Warrior

Something that most people don't know is getting up to walk when you have swollen ankles is a daily struggle #lupuswarrior #embracevulnerability #godlovesyou #survivor #thestruggleisreal #poetry

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To my lupus warriors we got this 🫶🌸

#lupuswarrior🦋💜 #lupuscommunity #lupusjourney

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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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Text on a white background introducing 10 obscure signs of lupus, beyond common symptoms like fatigue and joint pain, including random fevers, chest pain, headaches, and burning skin.

Text on a white background describing '1. Lupus Headaches (aka "Lupus Migraine")' as throbbing, relentless headaches that may not respond to regular medication, potentially linked to brain inflammation.

Text on a white background describing '2. Unexplained Fevers' as low-grade fevers (99-101°F) without infection, where the body spontaneously overheats.

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 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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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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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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Lupus and Seasonal Allergies?

My eyes swell, get so red and watery, lymph nodes swell, can’t stop sneezing…my body goes bananas when it happens. Anyone else? #autoimmunedisease #lupuswarrior🦋💜 #lupus #lupuswarrior

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Lupus Soldier Behind The Strive

#lupus #interview #realtalk #sahnhova #lupuswarrior Jacksonville

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Lupus

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

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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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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 Baddie 💜

#lupuswarrior🦋💜 #lupusawareness #medicated #fyp

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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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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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Waking up with Lupus

How I feel when I wake up... #chronicillness #mentalhealthmatters #hidradenitissuppurativawarrior #autoimmunedisease #lupusawareness

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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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LupusWarrior 🦋🦋💜💜

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

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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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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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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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A person with curly hair wears a black t-shirt featuring the text "FEELING CUTE MIGHT FLARE UP LATER." with purple butterfly illustrations and "Lupus Awareness." They also wear a flower crown with yellow flowers and blue butterflies.

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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LupusWarrior 🦋🦋💜💜

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

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LupusWarrior 💜💜🦋🦋

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

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My Lupus Journey 💜🦋🙏

#lupuswarrior #rheumatoidarthritiswarrior #sjrogrensdyndromewarrior #chronicpainwarrior 🙏🦋💜💘

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Lupus and fibromyalgia

Literally no fun at all but i am learning how to adapt an change things to make a better quality of life ❤️ #lupus #lupuswarrior🦋💜 #fibromyalgia #fibromyalgiafighter💜

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A close-up image of skin showing a reddish, raised, irregular ring-shaped mark. The accompanying text describes it as a rapidly growing infection on a leg, requiring antibiotics, and related to Lupus.

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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Sending love to my Lupus Fighters 🫶🏽

Starting the new year with healing and hope 🙌🏾✨ My flareup on my arms is 70% better, and I’m claiming 2025 as a year of fresh starts and growth. 🥂Cheers to progress and all the good things ahead! Happy New Year! #HealingJourney #Lupus #LupusWarrior #discoidlupus #skincare

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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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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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The image displays various 'URGENT MEDICAL ALERT CARD's for different conditions. These include cards for Lupus Flare, Fibromyalgia Flare, Mast Cell Activation Syndrome, Type 2 Diabetes, Migraine, PCOS Flare, Dysautonomia, and POTS, all laid out on a patterned surface.

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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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 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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✨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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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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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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Life with Lupus

#lupus #lupuswarrior #chronicillness #Lemon8 #unfiltered #Lemon8Diary #healthylifestyle2024 #autoimmunedisease #journaling

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Warning ⚠️ Living with lupus and EDS+co

#lupus #ehlersdanlossyndrome #chronicillness #terminallyill #esblcolonized

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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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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 awereness day

hello everybody i want to take a moment to dedicate this post to all who's are fighting with this autoinmune disease i know it aint easy i don't have lupus before you ask but i know someone dear to me that has it and I know how hard it is. soo i want to tell you all are warrios dont gi