#lupuswarriors

Instagram photos and videos

#lupuswarriors#lupus#lupusawareness#chronicillness#lupuslife#lupusproblems#lupussucks#lupuswarrior#LupusWarriors#lupusfacts#lupusflare#lupusstrong#invisibleillness#livingwithlupus#lupuschick#lupussupport#lupusfighter#purpleforlupus#lupusincolor#lupusawarenessmonth#lupusnephritis#canislupus#lupustruth

Hashtags #lupuswarriors for Instagram

Are you a person living with lupus or taking care of a lupus warrior? I wanted to let you know about an exciting event happening in Atlanta on December 6, 2018. If you're a person living with lupus, come out to Night of Beauty, an experience created just for you and your village of supporters. Join Us in Lupus for mini makeovers, self-care tips, a panel discussion, lupus education, and photo sharing! RSVP today and read more event details at NightofBeautyATL.com #UsinLupus #UsinLupusNOB #UsinLupusATL #LupusWarriors


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This disease (Lupus) is seriously fucking nuts. Yesterday I was stuck in bed flaring with a low grade fever, butterfly face rash, extreme hypoglycemia (low blood sugar), muscle aches, joint pain, nausea, headaches on and off, sore throat, and a cough. 😷🤢🤕🤒🤧😴 Today all those symptoms are gone (including my face rash) and all that remains is some nausea, joint pain, and low blood sugar issues. I’m not complaining and I’m not going to question it lol 🤷🏻‍♀️
I’ve spent 15 years battling this disease and I’m still amazed at how we can go from one extreme to another overnight. Today I feel better than I have in weeks so I will be taking full advantage and getting outside today! AND I just got a fresh haircut so stay off the roads everyone because there’s a #lupieontheloose this Tuesday! 😂😂😎🦋💜💜💜


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Celebrate the holidays with your lupus community at our #WalkToEndLupusNow holiday potluck party in Seattle on December 8th! Bring your family and friends, a dish to share, and copies of your recipe for other attendees to take home! We can't wait to see you there! RSVP: Link in bio!


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#GivingTuesday is a week away! See how your donation can make an impact on our community (and of course, no amount is too small!). Visit supportlupustristate.org to make a donation next week.


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Are you a person living with lupus or taking care of a lupus warrior? I wanted to let you know about an exciting event happening in Atlanta on December 6! If you're a person living with lupus, come out to Night of Beauty, an experience created just for you and your village of supporters. Join Us in Lupus for mini makeovers, self-care tips, a panel discussion, lupus education, and photo sharing! RSVP today and read more event details at NightofBeautyATL.com #UsinLupus #UsinLupusNOB #UsinLupusATL #LupusWarriors


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#lupuslife is full of surprises. You never know when your next #lupusflare is coming, canceling plans is a new “normal” and you can look good on the outside but on the inside your #lupusproblems are trying to kill you... P.S. I’d like to let you know that a reputable supplements company is giving FREE supplements that can be very helpful for people with #lupus . These 2 #supplements provide nutrients that are often lacking in people with lupus and #autoimmunediseases It’s truly free, no strings attached. You can get it via my website http://lupusselfhelp.com/free or just click the link in my instagram profile @lupusselfhelp <<<===clickable link


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"Fairy tales are more than true: not because they tell us that dragons exist, but because they tell us that dragons can be beaten" #neilgaiman and my fav #quote -
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FAIRYTALES WITH LUPUS IS WAKE UP WITHOUT BIG PAIN ,SO 🍸I hope it will stay all #today . -
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"Mom, I don't think you should wait that he will come back to you, coz life is not a #fairytale , you know? -
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I have to, coz if I stop believe , if I stop believe that LOVE IS STRONGER THAN DEATH, kindness more than hate ..
If I stop be a #believer and #dreamer if I stop believe in humanity, in small things, which are big miracles, babe, I will rather be death. -
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Coz #allwhatyouhaveisyoursoul
So I WILL BE A COMÉTE 🌌
LOVE, HUGS n 🍫🍫🍫💜 #meandcinderella🎠 MAY GOD BLESS ALL.
#lupuschick #lupies #lupuswarriors #alopecia #dělámsvěthezčím #invisibleillness #invisiblepain #spoonie #life stay alive #blessed #blessings#goodday #dakujemeterezkezamikcu! #weloveflowers and #teddy #cutemorehateless #chooselove #now #for_ever #anabaheback #okay ? OKAY. #tilltheend


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Me and the younger sister.... She's probably awake like me. I'm a night owl and she has Lupus... Sleeplessness 👀is one of the light effects of the illness. She has insomnia all the time. This was my birthday last year , I turned 45. The hat she's wearing helps hide her hair loss, another effect of having Lupus. She has beautiful Locs, but they fall out sometimes too ☹️😔 . I'm just thinking about her right now. Not familiar with Lupus, learn more. She joins so many others as Lupus Warriors! 💜💜. Research matters. Get a Cure. @lupusresearchalliance @lupusorg @kazytauginas #southerngirl #lupussucks #curelupus #ilovemysister #nashvillesisters #tnchicks #BlackQueensWithLupus #blackqueens #lupuswarriors


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Lupus is a terrible disease that effects everyone differently...it is hard not to worry about what other people think about you...it is hard not to judge yourself. But you need to focus your energy on things that are important like getting through each day, your family, your own health & not worry about the little thoughts of people who aren't even going to be in your life when you really need them. It has taken me a long time to learn that & I still worry from time to time...but at the end of the day...I know what & who is important & who will really be there for me when I need someone. And I can literally count those people on one hand! I am okay with that. Because those people are so very special. 💕💫🦋 #slesucks #lupus #lupusnephritiswarrior #LupusWarriors #lupusnephritiswarrior #lupie #slewarrior #lupusflare #chronicpain #chronicpainwarrior #invisibleillness


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30 minutes is only 2% of your day.

I hear working out and eating healthy is too expensive but so is being sick!
Are you ready to make some changes?
#chopwoodcarrywater #gethealthy #tiredofbeingtired


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I'm grateful for finding out that such a large community of #lupuswarriors exists here on Instagram!


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Generalidades del lupus, enfermedad autoinmune que ataca las células y tejidos sanos por error.

#lupuslife #lupuseducation #lupusawareness #lupusfacts #lupuswarriors #lupiesaroundtheworld #lupiegirl #chronicwarrior #chronicillness


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This ✨


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FPM has been producing videos for Making Lupus Look Good since 2015. Check out our latest promo and please like and share! #fpmvideo #weddingsandmore #lupus #lupusawareness #lupuswarriors
https://youtu.be/ZdJzK93aDi4


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Make the decision to make today ❗️great❗️ ... or make it a lifestyle.

February ➡️ November

Consistency isn’t easy.
BUT
Perfection isn’t possible.

Greatness isn’t sexy, it’s DIRTY, HARD, WORK.
what do you want to achieve?

Im inviting you to join our virtual fitness community as we work on consistency together!! 🏆🧘🏻‍♀️ #chopwoodcarrywater #strongerthanyesterday #lupusproblems


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A message of #hope from the priest's sermon today. In 1998, we were told that there's no cure but I never believed. After 2 decades, I was introduced to a #healing nun who helped me find the answer 😇😍💝 Now, I know there is cure, there is hope
Let's stay positive no matter what we're going through in life so we can be a sparkle of hope to others 🌻💞👼 #naturopathicmedicine #naturopathicdoctor #wellnessjourney #holistichealing #worklifebalance #autoimmunediseases #autoimmune #chronicillness #chronicpain #overfatigue #chronicfatiguesyndrome #empoweredwomen #womenempowerment #natureheals #naturehealing #meditation #spiritualhealing #spiritualawakening #holisticwellness #rheumatoidarthritis #diabetes #henochschonleinpurpura #lupuswarriors #fibromyalgia


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There are so many things people don't see inside of my life. They assume that because I'm up and about, smiling and laughing, I'm automatically healthy and fine. But I'm not. I'm surviving. If I completely shut down and give up then what kind of life would I live. People don't see the injections, medication, bruises, hours of time I spend crying or vomiting. They don't see the internal struggle I face. Because I don't want to be seen as the sick girl. I am more than my illness. I'm Leah, the history major, crazy aunt, who spends her time acting goofy, taking pictures, dancing and playing piano. The girl who loves impromptu dance parties in the kitchen and solo karaoke alone in my dorm. I'm more than my illness. It's only a piece of me not me entirely. I wish people could see me for me instead of a simple piece of me. But I can't control people's opinion but I can control the way I see myself. And I choice to see myself as a goofy warrior who never gives up. And I know each and everyone of you are warriors too. Don't let others get you down because you are remarkably strong.
Alway,
The goofy warrior

#lupuswarriors #chronicpain #spoonie #lupus #warrior #chronicloveclub #pain #chronicillness #lupuswarrior


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Together we can bring Lupus Awareness out of the darkness and into the light! #lupus #lupusawareness #invisibleillness #chronicillness #lupuswarriors


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Happy Saturday peeps 😀


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