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
#lupusstrong
#lupus
2025/5/4 Edited to
1/2
Related posts
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
912 likes
Chronic Illness - Lupus
#gettoknowme #lupus #lupuswarrior🦋💜 #chronicillness #autoimmune
54 likes
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
2 likes
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.
107 likes
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
19 likes
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
1 like
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
48 likes
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
289 likes
Lupus
#chronicillness #chronicillnessjourney #lupusawareness #lupusjourney
4 likes
Newly diagnosed with lupus?
Let me say this first: You are not alone. When I was first diagnosed, I felt overwhelmed, confused, and honestly—scared. There was so much no one warned me about. So I created this post to share what I wish someone had told me back then. Here are a few do’s and don’ts I’ve learned the hard
40 likes
Lupus
Surprising this that Lupus and Rheumatoid Arthritis do. They make your nails all wonky! I use to have beautiful hands🥺 #arthritis #lLupus sucks
124 likes
Lupus crash
#lupus #embracevulnerability #unfiltered
8 likes
World Lupus Day
World Lupus Day #lupusawareness #lupus #chronicillness #chronicpain #autoimmune #autoimmunedisease #lupusstruggles #lupuswarriors #lupusjourney #marsblends #lupuswarrior🦋 #kidneyfailure #kidneydisease #kidneywarrior #SLE #slelupus #worldlupusday
26 likes
What you see v what you don’t see👀 life w lupus edition
you see: a cute leopard set + iced coffee vibes you don’t see: brain fog, chest pain, cement limbs, nap countdowns, swollen tongue, muffled hearing, and a body that feels like it’s working against me. Chronic illness isn’t always visible. But here’s the truth: illness will take your energy, b
4 likes
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
46 likes
Custom designs to inspire my Lupus Warriors💜🥰🫶🏾
#gettoknowme @Lupus Warrior Lil Trina
11 likes
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
19 likes
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
0 likes
🌿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
68 likes
lupus & Hormones
Hormones, particularly estrogen, act as powerful chemical messengers that can significantly influence the immune system. This is a primary reason why lupus (Systemic Lupus Erythematosus) is much more common in women, especially during their childbearing years when hormone levels are at their peak.
85 likes
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
106 likes
#IHaveLupus 🫶🫶🫶🫶
40 likes
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
104 likes
Warning ⚠️ Living with lupus and EDS+co
#lupus #ehlersdanlossyndrome #chronicillness #terminallyill #esblcolonized
7 likes
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
7 likes
My workout split with Lupus!
#gettoknowme #workouts #workoutroutine I wanna first start with I always do about 5-10 mins of stretching before & after my workout & these are just ideas for the week… sets and reps are up to you. Typically I do 4-5 sets 8-10 of each exercise. Day 1 - Glutes & Hamstrings - Bu
11 likes
Managing Lupus
#lupusawareness #lupus #systemiclupus #chronicillness #embracevulnerability
31 likes
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
0 likes
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
5 likes
My Lupus Diagnosis Timeline
I’ve been asked a lot how my Lupus story went, and this is it. After pregnancy in 2018, I started getting rashes on my face and hands in the sun. I also would get frequent joint pain and was exhausted all the time. I chalked it all up to being a new mom, roseacea and eczema. This continued until my
3 likes
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
5 likes
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
25 likes
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💜
3 likes
Lupus 💜💜💜
Hi, my name is Chasity . I have lupus I’ve been having lupus ever since I was pregnant with my first child and it’s been 11 years. I have been dealing with lupus and it’s a pain I went to I went to the rheumatologist trying to see what a lot of things I can alleviate my pain, and I am just trying t
8 likes
✨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
50 likes
Lupus And Fibromyalgia Are NO Joke
10 likes
Defeating lupus 💪🏽
Lupus is my worst enemy but I won’t let it win
9 likes
What is lupus
#lupus #lupusspeaks #lupusillness #lupuscommunity #lupusjourney
5 likes
Lupus support
Lupus and other chronic conditions can feel so isolating but it doesn’t have to be that way! I am building my TikTok support group here on Lemon 8! #chronicillness #lupuswarrior
7 likes
Lupus is hard to live with
Does anyone else suffer from lupus or any other autoimmune #lupus #autoimmunedisease #lupuswarrior🦋💜
5 likes
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
9 likes
🌸🌸LUPUS 🌸🌸
6 likes
Lupus
We look normal but our inside of our bodies are deteriorating. We need a cure. We suffer more than people realize and trust me the pain is extreme. I have been dealing with lupus for 47 years. My heart goes out to her family. Fly high my lupus warrior sister 💜🙏🦋 #gonetoosoon #lupus #chronic
27 likes
💜 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
66 likes
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
1 like
Lupus Emergency Pouch
https://www.just-in-case-kits.com/ #emergencypouch #lupus #lupusawareness #lupuswarrior
38 likes
Go to Lupus Warrior Princess 1 for more
#lupuswarrior #lupusfacts #lupusawareness #spoonies #spooniesoftiktok
4 likes
Systematic Lupus 💜💜
Having a chronic illness is hard. I never know when I'll have a good day,and at any moment, my symptoms can arrive. That makes it hard for me to plan things or even have a regular schedule. If I cancel plans with you,don't take it personally. I'm not shady, I'm sick. No one talks
17 likes
Lupus Fact Friday
Slide each picture brings a new fact and the last picture is Me! #lupusfacts #lupusfactfriday #lupus #spoonies
1 like
See more