#LupusStrong

All about balance in your life....making time to do the things you love πŸ’ͺ#loveyourself #fitmomgoals#lupusstrong#iowaliving

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My brother and dad went to P.E.I this past weekend and picked me up a can of Sweet Weather Balms Sore Joints Relief Rub. My knees are very sore as always and I'm going to try it out for the first time tonight! I really hope it works. The website that you can order the product on is ilovemoonsnail.com if anyone is interested. After a while of using it, I'll post how I think it's working for me.

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"Your goals don't care about your problems" - Ebonne Davis
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The days are hard and the nights are long. Fighting a chronic illness with chronic pain and fatigue daily the struggle of keeping my promise to myself to be great is a difficult task one I sometimes question am I winning....
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YOU BEAT LUPUS HOW YOU LIVE. WHY YOU LIVE. AND IN THE MANNER IN WHICH YOU LIVE.
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#dreams #goals #studying #futurern #nursetobe #studylikesomeslifeisinyourhands #notes #fitness #anotherdegreecomingsoon #backtocollege #college #lupuswarrior #lupusstrong #lupuswillnotdefineme #immorethanaconqueror #nerd #cutewithbrains #fit #lupus #stayfocused #godgotme #nutrition #strength #courage #ifighteveryday #mysundayfunday #believeinyourself #lupusisjustapartofmytestimony #homework #studyflow

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I'd be lying if I said life is perfect because it's far from that but I'm truly #Thankful and #blessed for the man I have in my life. #christmastree #thanksgiving #relationships #riders #lupusstrong #chemotherapy #warriors #datenight #fighter #downtown #Truelove #pictureperfect

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today my eyes were swollen again. I went to the gym, some people joked my eyes were swollen because I cried all night. They thought I was crying all night because I was sad or broken heartedπŸ˜‹πŸ˜‚. for me, no problem. they do not know the truth. I do not want to tell them about my illness either. I see it makes no difference whether they know it or not. their jokes still cheer me up. I still smile at their jokes.
if they knew, a broken heart would not make me cry all night. LUPUS CAN! People with lupus and reumathoid artistic must cry every night fighting against the pain. crying in pain all over joints, crying over all the fatigue that never went away from body.

Crying when what i want, Just a good night's sleep. But don't know when I’m going to have itπŸ˜‹ Do you know how it feels? I bet you know it so well my Lupus n RA friends.

#sle #lupus #lupusindonesia #lupusawareness #lupusstrong #lupustruth #lupussupport #supportlupus #isupportlupus #supportodapus #isupportodapus
#lupuslife #lifewithlupus #lupusstories #lupusbattle #vitddeficient #vitamind3deficiency
#lupuswarrior #lupusfighter #lupussuvivor
#lupusmom #momwithlupus #odapusindonesia
#autoimunedisease #ladyodapus #staystrongπŸ’•

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Hey gorgeous! Yep, I've been in hiding lol! So sorry that I've been missing so much! This round of medical junk has been the worst yet I do believe. #lupussucks Anyway, I should be headed home in a little bit. Then I'll be blowing up your instagram!! So much needs to be posted, I just haven't had the energy to post all of the research and details. This has gotten the best of me. But.. I'm #lupusstrong and I'll be back at it in a few hours after get back home and most importantly, I get tons of hugs from my munchkins!! Love y'all!! See you very very soon.
#urbandecay #nakedskin #tarteshapetape #sydneygrace #clayplaypalette #dirtyglamcosmetics #blush #kristenleighcosmetics #sirennoire #highlights #eyeshadow #bitebeauty #katvond #coverfx #beauryblogger #beautynews #makeupaddiction #makeuptalk #makeupjunkie #makeupjunkiesunitednotdivided #lupussucks #lupusstrong #reviews #firstimpressions #bbblogers #wakeupandmakeup #loveyallπŸ’• #sicknotbrokenbeauty

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So many people don't understand what i go through having Lupus. This picture is after working three busy & late nights in a row, i get swollen with hot rashes all over my legs. It's not easy but i do it with a smile and have plenty of other bullshit thrown my way but still do my best πŸ’œsometimes you don't understand someone's silent struggles so be kind to everyone #lupusstrong #purpleribbon

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Ready for the holidays! Scarf on βœ”οΈ Mittens on βœ”οΈ My hands were turning white, blue because of my Lupus. I need to have my mittens on. It's been getting cold in Hawaii & it will get colder in December. It really sucks to have this disease. Wearing my mittens in Hawaii, people looks at me weird. I'm like, my hands are freaking cold. I tell them, "Feel my hands!"
I really need them on or else it will cause numbness on my fingers or an amputation on one of them from what my doctor told me. One of his patient had an amputation on one her finger due to cold wheather, the reason why, it turned black. Scary shit! I need my fingers. #lupussucks #icantliveanormallife
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#lupuswarrior #livingwithlupus808 #ihavelupusandimatter #lupusstrong #lupuslife #happyholidays #snapchatfilter

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Making it matter on a gorgeous Texas Saturday afternoon. Day 77. Life is so good right now and I am so happy and Blessed. #makeitmatterfitness #goals #chestdayΒ  #pushthrough #gym #healthylifestyle #lupusStrong #teamFit #teamSupa #smilesarecontagious #liveLife #believeinyourself #health #supersetΒ  #reps #greatness

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Why am I doing the "Captain Morgan" pose on a seated walker you may ask while taking a selfie? If you don't laugh and have fun during the misfortunes they will consume you.
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My doctor and I decided on me getting this for the days during and after bad flares when I need to go out to appointments or run errands and I am very weak, so I can stay mobile while gaining my strength up. Usually it takes a couple days after a bad flare. Also for when my Dysautonomia is really bad. This thankfully is not a all the time thing. It is as needed!
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I am still not giving up on my journey and I will continue to fight to do the things I love. I will be in a fashion show next weekend that I will post details about this weekend. It is important to keep doing things we love or finding something we are passionate about to distract us from the hardships many of us face day-to-day.
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I still have a lot of unanswered struggles with regards to my health and it is another waiting game. I found myself this past week consumed in defeat. It is when I look back at all that I have accomplished this past year and a half with my passions in spite of it that I start to pick myself back up and shake off the self pity.
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I may have hardships, we all do but I am truly blessed and I need to believe it and receive it every single day I am blessed with life on this Earth to keep living! God is the reason I am able to do all that I do and accomplish and I am thankful for that.
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Bless you all and have an amazing weekend!
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#lupuswarior #lupusfighter #SLE #lupus #lupusflare #lupussucks #lupusstrong #spoonielife #spoonies #fibromyalgia #fighter #mediport #bladderproblems #bladderpacemaker #walker #autoimmunedisease #neurocardiogenicsyncope #neurocardiogenicsycopesucks #dysautonomia #dysautonomiaawareness #anemic #anemia #osteoporosis #onedayatatime #ig_photooftheday #positivepeople #godisgoodallthetime #godislove #strongertogether #gratitude

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Are you working towards obtaining something valuable or are you wasting valuable time? #goodmorning #Saturday #morning #work #workout #exercise #weights #muscle #gains #gainz #gym #gymlife #fit #fitness #lupus #lupusstrong #health #healthy

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Lawd. Spoke to my soul. I WILL NOT BE ON THE STRUGGLE BUS next year. Once December slides by and I have time to grind like I'm used to... no more of this for sure. I just need to grasp a little bit more patience because I KNOW God is setting me up. No more Lupus. No more bullshit. πŸ˜€πŸ’œ #lupusstrong #lupuswarrior #lupus #lupie #lupusstrong #repost

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For my Detroit Lupus ladies! πŸ˜ƒ if you're interested in meeting a supportive group of ladies who can relate! Come out and chat! πŸ’œ #Lupus #lupusdetroit #lupuswarrior #lupie #lupusstrong #lupussurvivor

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Lupus can affect anyone! I personally have lived with this for about 17 years and just this year it struck me the hardest. Having an autoimmune disease is unfortunately a chronic disease. It affects each person differently. So important to support anyone dealing with any kind of health challenge. Bringing awareness and education will help patients, family & friends understand more about Lupus. Just because you can’t see it doesn’t mean someone isn’t sick. Thank you to our Lupus heroes @official_nick_cannon_ @tonibraxton @selenagomez #lupus #lupusfacts #lupusstrong #lupuschick #educate #lupusflares #lupuswarrior

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Hi Mommy I just wanted to say I love you. Thank you being the most amazing mom EVER #lupusstrong

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πŸ‘€ I'm very excited to link with the Zeta's of Grand Valley State University to spread awareness about Lupus! 😊 I'll be sharing my journey, positivity tips, and some new products that have improved my progress! πŸ’œ #lupusisreal #lupus #lupie #lupuswarrior #lupusstrong #lupusawareness

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Lupus sucks especially when it’s raining 🌧️ outside.... I feel so old right now.. #mmjgirls #lupuschick #lupuswarrior #lupusstrong #prop215

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Believe you can accomplish the impossible. I keep pushing because it's something I'm doing for me. Don't better yourself for anyone else be you and comfortable in who you are. Day 74 and still going strong #makeitmatterfitness #goals #AbDayΒ  #pushthrough #gym #healthylifestyle #lupusStrong #teamFit #teamSupa #smilesarecontagious #liveLife #believeinyourself #health #supersetΒ  #reps #greatness #flexagram

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When being strong is your only option πŸ’œπŸ’ͺ🏾 #LupusWarrior #PhuckLupus #LupusStrong

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I’m so excited that I got to attend this Healthy Churches 2020 Conference AND I get to sit at the booth and tell people about Lupus and the Lupus Research Alliance πŸ’œπŸ’œπŸ’œ #lupusadvocate #lupusstrong #lupie #nativebutterfly

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I know this photo looks blurry. then why did I post it? because this photo really reflects myself and my current conditionπŸ’•. From the outside I am like a healthy person. But in fact I have a deadly disease that can not heal and can kill me anytime. I can be healthy in one, two days, then fall ill tomorrow for days or weeks or even months. Who would have suspected I had a very unstable health?

what I want to say is there are still many people around me who do not know I'm sick, they do not know my circumstances and my real condition, because I do not tell my illness to them. I keep my illness not because I do not trust them. I just want to be treated as a healthy friend without pity.

Honestly, There is a story behind every person, and there is a reason why they are the way they are, you never truly know the daily struggles of others. β€œBecause what you see is not always the truth. Its BLURRY!”. But if you curious About the BLURRY in me, if you want to know the truth, ask me. I will explain. as long as you promise stay the same and will not pity me😊

#sle #lupus #lupusindonesia #lupusawareness #lupusstrong #lupustruth #lupussupport #supportlupus #isupportlupus #supportodapus #isupportodapus
#lupuslife #lifewithlupus #lupusstories #lupusbattle #vitddeficient #vitamind3deficiency
#lupuswarrior #lupusfighter #lupussuvivor
#lupusmom #momwithlupus #odapusindonesia
#autoimunedisease #ladyodapus #staystrongπŸ’•

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