Lupus Empowerment Conference tomorrow night 6:30-8:30 EST. I’ll be on the panel 🫶 https://lupusfoundationofamerica.regfox.com/southeast-region-virtual-lupus-you-empowerment-conference-?_gl=1*1j3ahk2*_gcl_au*MTAxOTA2MjU2NC4xNzYyMzg5MTQ0*_ga*Mjk2NDQ4MDQzLjE3NjIzODkxNDQ.*_ga_YYDMSWHGD2*czE3NjQ4MDA5OTQkbzU0JGcwJHQxNzY0ODAwOTk0JGo2MCRsMCRoMA..#register #lupuswarrior #lupuswarrior🦋💜 #sle #autoimmunedisease

2025/12/3 Edited to

... Read moreThe Southeast Region Virtual Lupus & You Empowerment Conference is a key event for anyone affected by lupus or interested in autoimmune diseases. Taking place on December 4 at 6:30PM ET, this event offers a unique opportunity to engage with medical experts, patient advocates, and fellow lupus warriors in a supportive virtual environment. Lupus, or systemic lupus erythematosus (SLE), is a complex autoimmune disease that can affect multiple organs and systems in the body. Living with lupus involves daily challenges, including managing symptoms like fatigue, joint pain, and inflammation, and dealing with the emotional impact of chronic illness. Conferences like this empower individuals by providing educational resources, sharing the latest research updates, and highlighting strategies for self-care and advocacy. Participants can expect panel discussions featuring specialists and experienced patients who share personal stories and coping techniques. Such events foster a strong community and raise awareness about the importance of early diagnosis, treatment options, and ongoing research. If you or a loved one are navigating lupus or another autoimmune condition, signing up for events like this can provide vital support and knowledge. The conference also emphasizes the role of hope and resilience, connecting you with others who truly understand the journey of living with lupus. To register, visit the Lupus Foundation of America’s official webpage linked in the original post. Mark your calendar for December 4th at 6:30 PM Eastern Time—you don’t want to miss this empowering experience designed to lift lupus warriors and allies alike.

1 comment

beautifully_broken's images
beautifully_broken

🥰

Related posts

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
EssentialOrganicShop

EssentialOrganicShop

913 likes

Chronic Illness - Lupus
#gettoknowme #lupus #lupuswarrior🦋💜 #chronicillness #autoimmune
Karisa Lyons📚🫶🏼✝️☕️

Karisa Lyons📚🫶🏼✝️☕️

54 likes

I got invited to be a panelist for the virtual Lupus Empowerment Conference 🥹💜
Yes, I accepted! It’s completely free and you can register on their website for it https://www.lupus.org/southeast/events/southeast-region-virtual-lupus-you-empowerment-conference. I’m so beyond honored to represent the Lupus community 🥹💜🦋 #lupus #sle #lupuswarrior #autoimmunedisease #lupu
Heather - Living with Lupus 🦋

Heather - Living with Lupus 🦋

2 likes

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
Mandy Gillespie

Mandy Gillespie

48 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
Heather - Living with Lupus 🦋

Heather - Living with Lupus 🦋

2 likes

Lupus Fatigue
That lupus fatigue is something else. Cheers to days on the couch! #lupus #lupuswarrior #lupusawareness #autoimmunedisease #chronicillness Memphis
Mandy Gillespie

Mandy Gillespie

18 likes

North Florida Lupus Conference!
23 days yall! I can’t wait! I hope to meet some of you in person there 💜💜💜 #lupuswarrior🦋💜 #sle #lupus #autoimmunedisease #chronicallyill #autoimmune #lupuswarrior #lupusempowerment
Heather - Living with Lupus 🦋

Heather - Living with Lupus 🦋

1 like

🌿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
Herbswithjen

Herbswithjen

70 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
Heather - Living with Lupus 🦋

Heather - Living with Lupus 🦋

1 like

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
Mandy Gillespie

Mandy Gillespie

46 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.
Maria

Maria

108 likes

Warning ⚠️ Living with lupus and EDS+co
#lupus #ehlersdanlossyndrome #chronicillness #terminallyill #esblcolonized
Julian 🦓♿️🏳️‍⚧️🪼 (He/They)

Julian 🦓♿️🏳️‍⚧️🪼 (He/They)

7 likes

Raw Vegetable Diet•Healing LUPUS✅
Let’s try for 30 days 🎯 #healinglupus #lupuswarrior🦋💜 #lupuswarrior🦋💜 #healwithfood #lupuscommunity
Autumn Saioré 🌹

Autumn Saioré 🌹

44 likes

Custom designs to inspire my Lupus Warriors💜🥰🫶🏾
#gettoknowme @Lupus Warrior Lil Trina
XpressWitFinesse

XpressWitFinesse

11 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
Chakrabaeselfcare

Chakrabaeselfcare

295 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
Mar.In.Bloom

Mar.In.Bloom

25 likes

Lupus crash
#lupus #embracevulnerability #unfiltered
Heather♋️✨

Heather♋️✨

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
Mar.In.Bloom

Mar.In.Bloom

26 likes

Lupus won't defeat me!
Lupus is an autoimmune disorder in which the body attacks itself. Affecting organs, skin, hair, joints, and more. #lupusawareness #chronicillness #lupus #dancer #Lambda4theCure
SwanBetty

SwanBetty

3 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
Shedrica | Her Rebuild Era

Shedrica | Her Rebuild Era

43 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
Heather - Living with Lupus 🦋

Heather - Living with Lupus 🦋

5 likes

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
Auntttlg77

Auntttlg77

0 likes

Lupus
#chronicillness #chronicillnessjourney #lupusawareness #lupusjourney
Kate

Kate

4 likes

Lupus
It gets old quickly dealing with lupus. #lupus #lupusawareness #lupuswarrior
Tiffany Ingram

Tiffany Ingram

6 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
talklupustomeg

talklupustomeg

4 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
a berry

a berry

104 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
MAD

MAD

107 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
Richeel Frazier

Richeel Frazier

124 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💜
Tiffany Ingram

Tiffany Ingram

3 likes

Lupus sucks
#lupusjourney #autoimmuneawareness
Julianna🖤

Julianna🖤

8 likes

An infographic titled 'Signs & Symptoms of LUPUS' displays various symptoms including extreme fatigue, hair loss, face rash, fevers, sun sensitivity, brain fog, liver issues, migraines, kidney issues, mouth sores, anemia, and joint issues.
✨Signs of Lupus✨
This past week has been a lot, especially after being diagnosed with Lupus. But at the same time, I am so grateful to know that I was not crazy imagining my symptoms. With symptoms that come and go (due to flare ups) one day your fine and the next day your dehabilitated. One min your body hurts so
SuddenlySouthern

SuddenlySouthern

633 likes

Empowerment in Illness - Join us!
We support autoimmune diseases and chronic conditions. We support you! Allies are welcome too! Dallas #empowermentinillness #autoimmunedisease #chronicconditions
lupuschick

lupuschick

2 likes

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
Adeyummy💗

Adeyummy💗

75 likes

Lupus And Fibromyalgia 🫶🫶🫶🫶🫶
Jackie1976

Jackie1976

17 likes

Managing Lupus
#lupusawareness #lupus #systemiclupus #chronicillness #embracevulnerability
Sophia Gianotti

Sophia Gianotti

31 likes

Lupus 🤍
My most viral video on TikTok! #medicalstudent #learnonlemon8
grace the medical student

grace the medical student

35 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
GigiAlive

GigiAlive

19 likes

A person with red hair, glasses, and a medical mask lies in a hospital bed, connected to medical monitoring equipment and an IV drip.
A close-up of a person's arm with an IV line inserted, showing blood in the tubing and a hospital wristband.
An IV bag labeled 'SODIUM CHLORIDE INJECTION' hangs from a pole, with a small amount of red liquid visible inside the bag.
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
Rasheedah

Rasheedah

17 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
Maria

Maria

7 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
TONYA NOEL

TONYA NOEL

27 likes

Lupus sucks
My first hospital visit (ever) for my lupus 😬🥺my first ever hives and spreading rash that is unbelievably itchy and burning 😢 #lupus #lupuswarrior #lupusawareness
Loretta Lynn’s Store

Loretta Lynn’s Store

4 likes

To my lupus warriors we got this 🫶🌸
#lupuswarrior🦋💜 #lupuscommunity #lupusjourney
TheonlyKakeeya

TheonlyKakeeya

8 likes

Lupus - Raymond
Sharing my personal journey living with Raynaud's phenomenon, a condition often associated with Lupus and Hashimoto's. Hopefully this video helps someone realize that these "symptoms" are not normal. Push for answers. You're not alone. #RaynaudsAwareness #LupusWarrior #
Mandy Gillespie

Mandy Gillespie

13 likes

Symptoms on Lupus before I knew I had Lupus (SLE)
I’m going to be very vulnerable and show you pictures of my (SLE) Lupus journey. For three months I struggled not knowing why I was sick all the time and I had more symptoms by the day. Now that I’m diagnosed I want others to know what to look for and if you’re experiencing the same symptoms I was
Avery

Avery

155 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
Heather - Living with Lupus 🦋

Heather - Living with Lupus 🦋

5 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
Chasity

Chasity

8 likes

Lupus skin infusion therapy 💉
Alright family… gather around. 👋🏾💜🧑‍🧑‍🧒‍🧒 Ya girl is officially starting Benlysta infusions. Lupus has been getting louder lately with harder flares and skin changes, so we are stepping into a new level of treatment. After prayer and talks with my husband and doctors, we knew it was time. This
AshFightsLupus

AshFightsLupus

3 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.
Tisha Mukes

Tisha Mukes

108 likes

Lupus Emergency Pouch
https://www.just-in-case-kits.com/ #emergencypouch #lupus #lupusawareness #lupuswarrior
Just in Case

Just in Case

38 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
Heather - Living with Lupus 🦋

Heather - Living with Lupus 🦋

3 likes

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
Lisa

Lisa

63 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
Heather - Living with Lupus 🦋

Heather - Living with Lupus 🦋

7 likes

See more