#lupuswarrior

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Im not super woman but im super warrior 💜💜💪💪 . Wear purple and show the world how strong you are 🔥🔥🔥💪💪 . Comment «yes» if you want one 💜💜 . Get your now 💜, Link in my bio 🔥🔥🔥 . #lupus #lupuswarrior #survivor #lupussurvivor #lupussupport #lupusfamily #motivation #support #awareness #lupusawarenessmonth #lupusfighter #lupussucks #invisibleillness #chronicillness #mentalillnessrecovery #invisibleillnessawareness #mentalillnessawareness #invisableillness
News on my liver: The doctor called and they found a 7 mm lesion, but felt it was no cause for concern. 🙌🏻. My pancreas and kidneys look good too. They’re going to recheck my liver enzymes in two weeks to see what levels are. We think The high enzymes are most likely due to the large use of Tylenol and ibuprofen over the last nine years for my achey joints, migraines, etc... God is good and always provides! I’ve been very fortunate over the years to test negative for a lot of complications docs felt lupus was causing. I am grateful for the health I do have and will continue to strive for better health. Thank you EVERYONE for your prayers! I love you ALL! #lupuswarrior #lupie #lymewarrior #fibrowarrior #findacure #raiseawareness
Nothing wrong with a touch of warmth, cozy, and simmer from the @tartecosmetics toasted palette on the eyes for a fall day like this❤🍁🍂#orlandomua #blackgirlsrock #beautyguru #fall #autumn #beauty #lupuswarrior #myblackisbeautiful #cozy #tartecosmetics #naturalhair #youtube #blackmua
Today I want to share with you all a modified burpee. We all know every fitness instructor loves to use burpees against their clients will! Truth is, they are great at increasing muscular endurance. If you decide to try the modified version, take it slow and one step at a time. To make the modified version a little easier, you can elevate your upper body by using a step or sturdy piece of furniture. • • • #burpees #fitness #personaltraining #modifiedburpee #modifiedversion #trythisathome #fitspo #homeworkouts #lupuswarrior #chronicillness
Sighs. It's been a rough one. I couldn’t even deal with tying a scarf or anything else today after this morning; a cap and wig it had to be. They want to cut into my Mom's Brain but I just couldn't consent to that. SMH. Though life throws you blows, you still have to keep moving and pushing until you can’t any longer. #DustYourselfOffAndTryAgain #InfusionNumber2 #Again #AndAfterThisIStillHaveToGoHandleMyMomsSituation #YouFightBecauseYouHaveTo #LupusFighter #LupusWarrior #LupusSLE #DiscoidLupus #BullousLupus #LupusCerebritis #Survivor #ThatsMyMiddleName #NoExcuses #NeverGiveUp #PrayersUp #SuckItUp #JustDoIt 💪🏾🤷🏾‍♀️
LISTEN LINDA!! I cant make this ish up🤷🏾‍♀️ #staywoke you are what you eat. I just wanna heal, and spread knowledge its necessary! #VeganLyfe 🌱 #VeganChef #DMVegan #Drsebi #Fresh #VeganBaltimore #LupusWarrior #Createinspirerize #EatToHeal #MakeTheSwitch #Alkaline #LetMeLIVE
It’s been a season. I can feel the light at the end of the tunnel, but I can’t seem to get their soon enough. Life has been rough during this season. Dealing with medication changes, a new therapist, working on my eating disorder, working on me, gaining weight due to medications, depression, anxiety, death of a loved fur baby, school, and worse of all I am currently in a lupus flare. I’m tired 99.9% of the time. I smile even though my muscles and joints are screaming and I am in pain. But- I wouldn’t change this horrific season for anything in the world. I have had so many accomplishments and growth amidst the chaos of this season in life. Pain changes you. It’s just the beginning of the winter, so I know it’s going to be a difficult one. But I will get through this because I have faith. #lupus #lupuswarrior #lupussucks #chronicillness #invisibleillness #autoimmunedisease #stormseason #fighter #chaos #life #spoonie
I have a million things I should be getting done today. Some of the list includes house cleaning, laundry, grocery shopping... but I decided I needed to do a little something for me. My hands aren’t what they used to be and sometimes that makes me sad.. I wonder if they’ll ever go back to how they used to be or if the RA has changed them forever. It’s something I was ashamed of and wanted to hide in the beginning, now I just see it as one more sign of resilience. I won’t be held down, I won’t give up and I won’t let anything stop me! Remember, your mess can turn into your message and your test can turn into your testimony🙏🏽 #rastinks #lupuswarrior #gravesdiseasefighter #selfcare #manicure
One week post #IVIG . Still dealing with my headache, but feeling well enough to shop until I drop while my hubby is in Boston for meetings! Hope all my fellow warriors are doing great! #primaryimmunodeficiency #lupus #lupussurvivor #lupuswarrior #spoonie #spoonlife #cantkeepagoodwomandown #whenthecatsaway
"Often the people who succeed, in spite of the difficulties they face, have one thing in common. They read... They have hope because they know once upon a time there was a boy or a girl, a woman or a man, who managed to survive." Alice Hoffman . . I just finished reading The Red Garden by Alice Hoffman and I was completely moved. I cant wait to read more of her work. I love the mysticism, themes of hope and survival, and relationships between nature, family, and fate. 🌟🌟🌟🌟🌟/5 . . #hope #inspiration #theredgarden #bookstagram #lupuswarrior
My babies, Cheetah & Jynx are resting with me today, they never leave my side when I’m not feeling well. That’s love. #PuppyDaughters #MySidekicks #UnconditionalLove #Love #Chihuahuas #ChihuahuasOfInstagram #Lupie 💜#Spoonie 🥄 #LupusWarrior #AutoimmuneDisease #InvisibleIllness #ChronicPain #ChronicFatigue #WithPainComesStrength #IWillNotGiveUpThisFight 💪🏾
My life in a nutshell... Thanks @thelupustrainer for summing it up so eloquently 🥄SPOON THEORY 101: “Spoonie” is a name we use to describe those who suffer with a chronic illness/autoimmune disease. The term was derived from Christine Miserandino’s famous “Spoon Theory” article. Her article went viral and revolutionized the way we talk about our illnesses to our friends and family. It’s a great read and very informative and helpful if you are trying to understand someone who lives with a chronic illness/autoimmune disease. 🥄🥄🥄 To give you a brief summary of the Spoon Theory I want you to view “spoons” as our units of energy. 🥄🥄🥄 Healthy people have lots and lots of spoons to use up each day but for those who are chronically ill many of our spoons (energy) are used up just to keep us functioning on a basic level. Our bodies are under attack and fighting illness 24/7/365 so just that takes up a tremendous amount of energy each day. All that’s left is about 12 spoons per day (if you’re chronically ill). Most people don’t need to rest up before taking a shower or lay down to recover afterwards so they don’t even think twice about putting their energy towards basic tasks like showering, brushing their teeth, getting dressed, etc. But we do- we have to because a shower uses up 1 spoon (2 spoons if you’re shaving and washing your hair) and that only leaves us 10 for the rest of our day. Getting dressed and getting ready/making a meal uses 2-3 spoons so by the time we leave our house we only have 7-8 spoons left for that day (not much energy to do stuff). This usually means I’m out of spoons (read: completely exhausted and usually starting to not feel well) by 3pm. So what happens if it’s 3pm, you’re all out of spoons but you must go on because you have a family to make dinner for that night, a spouse that needs attention, and a house that needs to be cleaned ? We push through it and borrow spoons from tomorrow. But this usually means triggering a flare and spending a day (or longer) in bed just to recharge our spoons. 🛌🥄🥄 And because I said I feel good today, don't mistake that for me being able to climb mountains...my feel good and yours, are not the same
This happens to me ALL THE TIME! Warriors, Anyone else? I know I’m not alone here 😋 #pills #meds #toomanypills #lifeofalupie #chronicillness #lupusawareness #lupusfighter #lupuswarrior #livinglupie
I don’t straighten my hair often...but when I do I take lots of pictures 😜
#SejaGentil #Conscientização 🦋🍀🐺 #Repost @vidacomlupus • • • • • Essa frase poderia ser tatuada pelos portadores de doenças invisíveis, não é? 😁 . Tudo bem você achar que alguém com lúpus não parece doente. Mas há formas gentis de falar isso, e duvidar dos sintomas não é uma delas. . Quem nunca acordou gripado, com dor ou deprimido e teve que engolir isso para seguir o dia e suas obrigações? É isso que os portadores de doenças crônicas fazem, só que diariamente. . E é justamente o fato de ser uma luta diária que faz com que os lúpicos se acostumem e se tornem mais resilientes a ela. Mas cada dia é um dia. Há dias em que é fácil se manter ativo apesar da dor. E há dias em que ela é mais forte. E uma coisa é certa: lidar com dores todos os dias pode esgotar a mente. . Portanto, se você conhece alguém com uma doença invisível, seja gentil. 💜 #vidacomlupus #lupusandme #lupuswarrior #lupusawareness #lupusbrasil #lupus #lupusfighter #lupusrj #lupusquestaodefoco #autoimune #chronicillness #doencacronica #doencainvisivel #invisibleillness #resiliencia #bekind #fucklupus
A little peek into last night 💜 ...and now sleep. 💤💤💤💤 #eveningofhope
I ran for 20 minutes and did 80 squats. Byron says I may not be squatting correctly. He thinks I drop it like it’s hot too low. Is there such a thing as squatting too low?? 🤔🧐🤨. What y’all think?? And 😒side eye to the scale for weighing me in at 149 lbs. @billiusmaximus929 @soldierdozier @allencoachb #lupus #lupuswarrior #goldielocs #armpitsweatissexy #dropitlowgirl #workoutatwork
R2 LIIFT4 👉🏻 SHOULDERS/ARMS Circuit ✅ oh my word!!! Arms are J-E-L-L-O 😭 #hurtsogood #liift4 #applewatch #armworkout #thursdayworkout #november
That time i went to the club with a Lupus Flare.... face messed up and all lmfaooo long before mommy life #lupuswarrior #tbt
Ok y’all what is this white crap falling on me in November? I’m not ready for a snowstorm yet!! But nevertheless it’s gonna happen so I made the Turkey butternut squash chili! Perfect day for it!! Anyway got our mile walk in , did the dms, 7 minute Hiit and mega arms and abs with @studiotoneitupstefanie and then did gorgeous core and stretch!! And thank you @karenadawn for all the love lately!! Makes me 😊!! Now I’m just gonna take it easy for the remainder of the day! Still feeling a bit under the weather with my BP up... woke with a very red face again too! Hoping my med will help otherwise back to my Doc! Well have a good one #tiuteam #tiucheckin #tiugirl #tiucommunity #lupuswarrior #tiuover50 #tiu50plus @toneitup @katrinaascott 💪💪🦋🦋😁💕💕❄️☃️❄️☃️
4) The biggest adjustment I've had to make since my diagnosis. 💜💜💜 Since being diagnosed with #Lupus and #SjogrensSyndrome , I've had to realize that there are some things I won't be able to do as much as I would want to. I used to work at @curves and I used to dance, now I can't do both as much as I would want. Some days I can't even get out of bed. It's really hard to be so young and full of life and not be able to do something as take a shower without being in a world of pain. I remember after my first round of #chemotherapy ... I was such a mess. It was terrible. I can't really get into this without getting really sad. . . . . #LivingAndThrivingwithSLE #Lupus #LupusWarrior #lupusfighter #lupuschick #lupusstrong #lupusawareness #chronicpain #chronicillnesswarrior #chronicfatiguesyndrome #sjogrenssyndrome #sjogrenswarrior
Some of you may have noticed that I have been absent from social media lately... 💜 Due to stress my fibromyalgia flared up and of course when it rains it pours, my Lupus flared slightly... 💜 I tend to become an Ostrich when I'm not feeling well lol...I I just stick my head in the sand and hide 😂... 💜 I'm so incredibly grateful for my Life Drink from @ultimatehealth.igniteyourlife which continues to pull me out of flare ups and sustains me... 💜 Now I'm back baby! World watch out here I come! 💜 I want all of my fellow invisible disease warriors to know that during these times of battle, your post and testimonies encourage me to keep going...to never give up! Thank You!😃 💜 #lupus #fibromyalgia #lupuswarrior #fibrowarrior #iwillwin #notdefeated #uh #ultimatehealth #lifedrinkplus #mygojuice #cantlivewithout #ontheroad #invisabledisease #neveralone #ihavemylifeback #readytowin #watchoutworld #holdingeachotherup #purpleribbon #lupusawareness #fibromyalgiawarrior #fibromyalgiasupport #nomorepain
Every day above ground is a really good day! There's so much to be thankful for and happy about. Focusing on the positive side of things can literally change your mindset and life in the blink of an eye. May all that IS beautiful, fruitful and good be upon us all. #yahminahmcintosh #soulfruitexpressed #thinkpositive #thinkboxer #healthymindset #womanhood #wisdom #loveyourself #mindfulness #bepresent   #beautifullyhuman  #selfcare #relaxation   #positivemindset #Lifestrategy #Lifestrategist #survivor #empowerment #wisdom #speaklife #lupuswarrior #healthylifestyle #insight #enlightenment #lifecoach #encouragement #businesswoman
Good morning! 🌟💫✨ Dear Lord, written words have lasting power. May what I write bring solace and joy! #liftothers #praypowerfully #meditationspace #lupuswarrior #prayerwarrior
#TBT This was not too long ago but my besties and I had the opportunity to be guest on @lifeincouture podcast I was not feeling well this evening, my lungs were inflamed due to a Lupus flare up. It was hard to breath let alone talk. I remember texting my besties during the interview telling them I couldn’t breathe and I couldn’t get through the interview. They told me “We got you”. I love my besties for all the encouragement and support they always provide on days were my chronic illness is trying to take me out the game • Special thanks to Terrace Sherman on The @lifeincouture Podcast for being patient and kind as I struggled to get through this interview. • Check it out It was a good one • Pre-Order your copy of The Bestie Code today! • Link in bio • • • #besties #bestiegoals #thebestiecode #thebestiecodebook #bestfriends #friendsinbusiness #businesspartners #bestfriendsforever #authorsofinstagram #lifeincouture #podcast #blackgirlswrite #blackgirlmagic #friendsinthefight #spoonie #spoonielife #chronicillness #chronicillnesswarrior #lupuswarrior #support @thebestiecode
Lupus nephritis is inflammation of the kidney that is caused by Lupus. Lupus is an autoimmune disease that causes the body's immune system to target its own body tissues. Lupus nephritis often develops within first five years after Lupus symptoms starts. It usually affects people between the ages of 20 and 40. . Credit: @lupusorg #lupusawareness #lupus #warrior #lupies #lupusupdate #lupusnews #lupusresearch #lupusfacts #lupuslife #lupusadvocate #lupuschick #purpleforlupus #lupuscommunity #lupusresearchnews #lupusawareness #lupusfighter #lupuswarrior #lupussurvivor #lupusinspiration #lupusmotivation #mylifewithlupus #autoimmune #autoimmunedisease #health #instagram
🥄SPOON THEORY 101: “Spoonie” is a name we use to describe those who suffer with a chronic illness/autoimmune disease. The term was derived from Christine Miserandino’s famous “Spoon Theory” article. Her article went viral and revolutionized the way we talk about our illnesses to our friends and family. It’s a great read and very informative and helpful if you are trying to understand someone who lives with a chronic illness/autoimmune disease. 🥄🥄🥄 To give you a brief summary of the Spoon Theory I want you to view “spoons” as our units of energy. 🥄🥄🥄 Healthy people have lots and lots of spoons to use up each day but for those who are chronically ill many of our spoons (energy) are used up just to keep us functioning on a basic level. Our bodies are under attack and fighting illness 24/7/365 so just that takes up a tremendous amount of energy each day. All that’s left is about 12 spoons per day (if you’re chronically ill). Most people don’t need to rest up before taking a shower or lay down to recover afterwards so they don’t even think twice about putting their energy towards basic tasks like showering, brushing their teeth, getting dressed, etc. But we do- we have to because a shower uses up 1 spoon (2 spoons if you’re shaving and washing your hair) and that only leaves us 10 for the rest of our day. Getting dressed and getting ready/making a meal uses 2-3 spoons so by the time we leave our house we only have 7-8 spoons left for that day (not much energy to do stuff). This usually means I’m out of spoons (read: completely exhausted and usually starting to not feel well) by 3pm. So what happens if it’s 3pm, you’re all out of spoons but you must go on because you have a family to make dinner for that night, a spouse that needs attention, and a house that needs to be cleaned ? We push through it and borrow spoons from tomorrow. But this usually means triggering a flare and spending a day (or longer) in bed just to recharge our spoons. 🛌🥄🥄🥄 So it is not uncommon to hear one of my friends or family members ask me how many spoons I have left and for my response to be “I’m all out of spoons today”. That’s how they know where I’m at that day. 🦋💜🥄
Happy Friday Eve!!! I’m on a mission to get all my adulting done early so I can just relax and enjoy the second half of my day 🙌🏻 #fridayeve #almostfriday #thursdaymorning #adultingishard #november
{ Diet Tracker } Okay. Couple things. 1. I suck at eating. I forget to make myself eat and by the time I do, I binge. I need to eat more regularly. 2. I'm eating too much junk. My meals are always very healthy but I've been known to indulge in the #canadiancrack known as @mccains Deep 'n Delicious too often....and WAY too large of servings. And chips. Omg regular chips. And Barq's root beer lol! I gotta get this under control! I'm hoping this tracker will make me see just how poorly I'm doing and my hope is that it will encourage me to start eating more regularly and cut down the junk! This tracker is in my beautiful purple butterfly #dreamdori along with my lupus tracker. #bulletjournaldailylog #bulletjournaljunkies #bulletjournalcommunity #bulletjournallove #healthtracker #tninserts #travelersnotebook #travelersnotebookinserts #diettracker #mealtracking #mealtracker #lupus #lupusawareness #lupuswarrior #lupussucks #lupusfighter #lupie #lupiechick #lupielife #spoonielife #spoonie #spoonies #wellnessjourney #wellnesswarrior #healthylifestyles #habittracker #bujoinatn #bujojunkies
Feeling the autumnal vibes today with this make up look 🖤 • • The live tutorial is up on my Business page on Facebook Natalie Lovejoy- The Make Up Maven. There is a direct link in my bio to watch. • • • • • • #stylediaries #influencerstyle #dreamersanddoers #dreambig #lifestylebloggers #personalblog #themakeupmaven #primania #fashionbloggerstyle #younique #youniquemakeup #younique_corporate #mentalhealthadvocate #makeuptutorial #followformore #nofiltersneeded #shoplinkinbio #ootdinspo #fallfashion #lupuswarrior #lupusawareness #whatiwear #notyourtypicalblogger #beyourownicon #inspireothers
My eldest baby @mrs.cheetahprint and I! #lupuswarrior I may have lupus, but it doesn’t have me! #survivor #winning #livingmybestlife #notbothered #joyous #happy #livinginthemoment
Coconuts milk & miso soup🥥 ココナッツミルクとお味噌のゴマスープ🍲 Ingredients: -1/2 cup Broccoli ブロッコリー -1/4 tofu豆腐 -1/4 cup belle pepper ベルペッパー -1/2 bamboo shoots たけのこ -1/4 maitakeまいたけ -1/4 shimeji しめじ -2 shiitake しいたけ -handful of spinach ほうれん草 -8 leaves basilバジル -5 silk sheath絹さや -1 canned coconut milk ココナッツミルク -150 ml water 水 -1/4 tbs cayenne pepper カイエンペッパー -1/3 tbs onion powder オニオンパウダー -1/4 tbs garlic powder ガーリックパウダー -1/3 tbs salt塩 -dash of black pepper 黒コショウ -1/4 paprika powder パプリカパウダー -1 tbsp Kombu stock powder昆布だし -1 tbsp misoみそ -2 tbsp grinding sesames すりごま Instructions: -sauté maitake, shimeji, and shiitake, broccoli, belle pepper and bamboo shootまいたけ、しめじ、しいたけ、ブロッコリー、ベルペッパー、たけのこを炒める -add coconut milk and waterココナッツミルクと水を加える -add Kombu stock powder, cayenne pepper, onion powder, garlic powder, paprika powder, salt, and black pepper 昆布だし、カイエンペッパー、オニオンパウダー、ガーリックパウダー、パプリカパウダー、塩、黒コショウを入れる - cook with middle heat for 10 mins中火で10分ほど煮る -add spinach, silk sheath and basilほうれん草、絹さや、バジルを加える -add sesame and misoすりごまとみそを加えて味が馴染んだら出来上がり! #vegan #veganglutenfree #glutenfree #veganrecipes #veganglutenfreerecipes #veganlife #glutenfreelife #plantbased #plantbasedrecipes #vegetarian #vegetarianrecipes #lupus #lupuswarrior #autoimmunedisease #ビーガン #ビーガンレシピ #ビーガン料理 #グルテンフリー #ビーガングルテンフリー #ビーガングルテンフリーレシピ #グルテンフリー生活 #プラントベース #健康的な食事 #全身性エリテマトーデス #膠原病 #味噌 #miso #ココナッツミルク #coconutmilk
Plants are kind of amazing 🌱 Nature can help our bodies with so many things and messages like this make my heart happy 🌱 And this happened in less than 12 hours 💕 #SaveYourself . . . . #lupus #lupuswarrior #lupusawareness #autoimmune #chronicillness #autoimmunedisease #support #autoimmunewarrior #nontoxic #nontoxicliving #essentialoils #wellness #plantbased #cleanliving #allnatural #natural #wellpreneur #wellnessjourney #plants #nature #giftsfromgod #drugfree #natureisamazing
I swear they test me in the morning, but to see those smiles and creativity makes it worth it! Check out SelleyBellys outfit! OMG! I love it!😂😂❤️❤️😂😂❤️❤️ #mindyourbodymindyoursoul #avabadayva #giselleybelly #giselleybellyandavabadava #beautifulblackbabies #strongmom #strongwilledchildren #locjourney #locs #personaltrainerariel #personaltrainermom #lupuswarrior #lupusmom #strongmoms #fitness #fitmom #alwaysbeaworkinprogres #giselleandavasmom
Swipe left ⬅️ Lupus Foundation of America's Evening of Hope!! It was absolutely beautiful & inspiring! Hanging with my ladies @karenmiller97 @vashtiv Let's come together and End lupus Now!! #lupus #ambassador #gala #event #eveningofhope with my booski. Thank you so much for being my date 💜💜💜💜💜💜💜💜💜💜💜💜💜💜💜💜 #candid #shots Heart of Giving's 2nd annual lupus Gala coming soon. #nyc #ny #lupuswarriors #lupuswarrior #praying & #working for a #cure #love #message #heartteller
"Realness, is something you cant shake. And I don't know how to be any other way"-Lp Da Artist. #TBT 😏 Grand Rising Kings and Queens! Even in the snow, Go be GREAT! Just safely🤗🔮🌠 #LupusWarrior #LupusWontBeatMe #LetMeLIVE #LetMeLiveWarriors #Love #peace #Light #IWillInspire 💪🏾
PUT ON YOUR POSITIVE PANTS... I get asked A LOT how I stay so positive. Straight up, there is no easy answer to this. I do not have some kind of magic or shortcut. It is not always easy & being positive is not something that just happens. But I'm not faking it either. It really is a decision that I make. And I don't mean a one off type of deal... I mean daily. It is a constant choice that I consciously make over & over again. Yes I have bad days. Yes I have negative days. Yes, sometimes I feel sorry for myself. Yes I get frustrated, angry & sad. But when I finally pop my head out from under my Blanket Fortress of Despair™ & emerge back into the world... I dust myself off & I CHOOSE to go forward with a positive perspective. I fully acknowledge that you, I & the rest of the chronic illness community have EVERY reason to feel down on life sometimes. I would NEVER take that validation that from you... nor should anyone else. But have a bit of a think about the following: "Would you rather to be right, or would you rather to be happy?" This saying has always resonated with me, mainly because I'm a stubborn bitch from hell & can be my own worst enemy... I blame the red hair. Case in point: "Living with a chronic illness is soooo shitty." Fuck yes, you're RIGHT, it is. "Chronic pain is the absolute worst." Fuck yes, you're RIGHT, it is. "No one in my life understands what it's like." Fuck yes, you're RIGHT, they probably don't. You are right & all of those things are true. There, I concede. Now, has focusing on that made you feel any better? Ok, maybe a little... it's totally natural, however... it's entirely momentary. But focusing on it long term, day in, day out? Um. Fuck. No. It doesn't. It really, really doesn't. It can make you feel like you've been sucked into a dark vortex of grumpy faces & scary clowns. A positive outlook is not the same thing as denying your experience & being all... CONTINUED IN COMMENTS BELOW 👇 📷: @amberibarreche
. You can't judge something you've never experienced. It's easy to be on the outside looking in. But to live through the fight. To battle with defeat day after day. And still rise. Yes bruised and scarred. But strong and fierce. 💜💪👑 #lupus #support #awareness #forlupuswarriors #lupie #lupusapparel #putonpurple #lupusawareness #lupuswarrior #spoonie #wearpurple #flareday #flaring #invisibleillness #chronicillness #fightlikeagirl #autoimmunedisease #lupusawarenessmonth #like #followme #poem #poetry #poet #literature #relatable #quotes #sayings #life #quoteoftheday #writer
Today’s workout has been overcame by illness. #lupuswarrior #goingbacktobed
When you really get down to it things like fear, hopelessness, anger, disappointment, most likely came from an event outside of our control. Focus on what you can control and those negative emotions will appear less. Tap into your power within. Have a beautiful day😊 #ificanyoucan #strength #courage #lupus #invisibleillness #lupussucks #lupuswarrior #lupusawareness #healthylifestyle #chronicillness #thickfit #weightloss
When you forget it's your BDay then starbucks remind you with a free drink. Thanks starbucks 🌟#ilovestarbucks #starbucksisbae #birthdaytreat #starbucks #pumpkinspice #37 #clockisticking #lupiechick #lupusnephritis #lupuswarrior
But Without Darkness, We would Never See the Stars 🌟 ~ Unknown You may have noticed I have been MIA for the past week... I have been in the battle of my life. Last week, I was given the official Lupus Diagnosis, followed immediately by the Worst Flare Up I could have imagined. Trips to the hospital, Uncontrollable Tears of Pain of Defeat, and week of Sleeping and not getting out of bed (which is NOT like me at all). I am Beyond thankful for my knight and shining armor @robbiecaud. He truly is my Prince Charming and has jumped in fighting this Disease as if he has it himself. Also, I have the Most amazing supportive friends 👭 sending countless texts of encouragement, offering their time, and also just letting me vent and say “this sucks.” Today I wake up with slight relief, but an overwhelming hope. This battle will not defeat me. I have learn there are days that I have to choose myself. There are days I will have 0 Spoons 🥄 and that’s okay. Lupus does not define me. It is just a chapter in my story. #lupuswarrior #ameliajames #girlboss #spoonie #chic414 #femalepreneur #fashioninspo #boutiquefashion #boutiqueshopping #beyourownboss #dreamjob #goaldigger #fallfashion #fasiongram #bossbabe #fashion #fashiondirector #charlottenc #charlottestylist #fortmillsc #fashionblogger #styleblogger #thatsdarling #thedarlingmovement #clicktoshop #fallfashion2018 #instastyles #onlineshopping #shopoholics #lupusawareness
Created this for a hoodie for me. Let me know if you want a hoodie, tee, or your own graphic designed. I'll send my website link.
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