#lovealupie

MOST RECENT

So unfortunate. This is why I educate my followers on what is Lupus . #lovealupie πŸ’œ

Today is your birthday.
You are so loved + missed angel.
Happy Birthday Jaeda Rae πŸ’œ
#heavencouldntwaitforyou #lovealupie #butterfly #restinparadise

We stand in the fight against Lupus! πŸ’œπŸ’œπŸ’œ #LoveALupie #LupusAwarenessMonth #ThisIsWhyWeHope

We stand in the fight against Lupus! πŸ’œπŸ’œπŸ’œ #LoveALupie #LupusAwarenessMonth #ThisIsWhyWeHope

May is Lupus Awareness Month and I am posting this for my dear friend @ipoopedtoday1983 Because of her I have taken the time to learn a little about this disease. Just know Michelle, that you have our support and friendship for life! πŸ’œπŸ’œπŸ’œ #yepthatsapurpleshirt #lovealupie

#LupusWalk2018 team tees
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#PrintedApparelShop
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PrintedApparelShop@gmail.com
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#awarenesswalks #lupusawareness #lovealupie #squadgoals #printedshirts #customshirts #printingshop #customteesnyc #Customteesnj

Its World Lupus Day!

I was scared to share my story last year but I'm glad I did. There's nothing to hide or be ashamed of. Having a chronic illness doesn't make me different, Im still Nancy regardless.

On a side note, have you guys seen any purple lights tonight?

#lovealupie #chronicillness #lupusawareness #putonpurple #chronicwarrior #bclupussociety #spoonie #worldlupusday

Long post Alert!!
Transparent Moment!!πŸ’œπŸ’œ
TAG A LUPUS WARRIOR πŸ’ͺπŸΎπŸ™ŒπŸΎ Everyone knows the strong, confident laBria but i don’t think to many know the Labria who about 2 years ago was nearly fighting for her life, the Labria who has insecurities, but today In honor of LUPUS awareness month i want my sisters and brothers that may be dealing with this invisible disease to know that no matter what we may lose while fighting Lupus,as long as we are still alive we are winning!! I was diagnosed with lupus in 2011!! Literally lost for words, down and i truly spend months crying asking God why me! Today i stand lupus free!! Medication Free and Treatment free for 2 years now!! During my fight of lupus i lost a great deal of my hair!! Taking 8 different medications a week, doctor visits monthly, emergency room visits weekly. I was emotionally, and physically drained, but i knew it was a purpose for all of this!! Even though sometimes i asked God why. I knew why!! He knew i was strong enough to handle it, and it literally made me who i am today!! In honor or Lupus awareness month i will share with the world the only thing lupus took from me, and that was my hair! I have bald spots in the middle of my hair. It took my edges on both sides, and I’m still in the process of building my joints back up!! Lupus took my hair but it didn’t take my life and I’m grateful!!! To all my sisters and brothers that are still fighting!!! Keep fighting, keep praying, and keep trusting God because you are going to make it!! To my sisters and brothers who have lost their lives fighting may you rest in heaven!!! If i could say anything to anyone today i would say trust God with everything you have in you, and I WON!! LUPUS DIDN’T CONTROL MY LIFE I CONTROLLED IT!!! #LupusAwarenessMonth #LoveALupie #IStandWithMySistersandBrothers #WeWillWin #GodIsGood #LupusFree #2yearsStrong #IMadeitandYouWillToo #PrayerWork

Long post Alert!!
Transparent Moment!!πŸ’œπŸ’œ
TAG A LUPUS WARRIOR πŸ’ͺπŸΎπŸ™ŒπŸΎ Everyone knows the strong, confident laBria but i don’t think to many know the Labria who about 2 years ago was nearly fighting for her life, the Labria who has insecurities, but today In honor of LUPUS awareness month i want my sisters and brothers that may be dealing with this invisible disease to know that no matter what we may lose while fighting Lupus,as long as we are still alive we are winning!! I was diagnosed with lupus in 2011!! Literally lost for words, down and i truly spend months crying asking God why me! Today i stand lupus free!! Medication Free and Treatment free for 2 years now!! During my fight of lupus i lost a great deal of my hair!! Taking 8 different medications a week, doctor visits monthly, emergency room visits weekly. I was emotionally, and physically drained, but i knew it was a purpose for all of this!! Even though sometimes i asked God why. I knew why!! He knew i was strong enough to handle it, and it literally made me who i am today!! In honor or Lupus awareness month i will share with the world the only thing lupus took from me, and that was my hair! I have bald spots in the middle of my hair. It took my edges on both sides, and I’m still in the process of building my joints back up!! Lupus took my hair but it didn’t take my life and I’m grateful!!! To all my sisters and brothers that are still fighting!!! Keep fighting, keep praying, and keep trusting God because you are going to make it!! To my sisters and brothers who have lost their lives fighting may you rest in heaven!!! If i could say anything to anyone today i would say trust God with everything you have in you, and I WON!! LUPUS DIDN’T CONTROL MY LIFE I CONTROLLED IT!!! #LupusAwarenessMonth #LoveALupie #IStandWithMySistersandBrothers #WeWillWin #GodIsGood #LupusFree #2yearsStrong #IMadeitandYouWillToo #PrayerWork

πŸ’œMay is Lupus Awareness month. I still struggle w/this disease & that picture is my routine monthly. Support those who are dealing w/lupus w/compassion, love, & understanding! We may not β€œlook” sick but we have a constant internal battle.πŸ’œ
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#lupus #lupusawarenessmonth #lovealupie #lupuswarrior #purpleforlupus #wearpurple

In honor of my sister-in-law who passed away fighting Lupus in 2010. Her daughter, my niece @samarisbaby who now fight this awful desease I wear this pin on my Fedora for the month of May!
To my coworker @cherrybomb84 thank you for the pin!
πŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œ
#bandtogetherforlupusawareness #jointhefight #loveAlupie #knowlupus
#lupus #lupuswarrior #lupusawareness #lupusfighter #lupussucks #lupuslife #chronicillness #lupussurvivor #lupusflare #lupuschick #autoimmunedisease #family #familytime #love #familyfun #familyfirst #familyday

Lupus has given me every reason to have faithπŸ’ͺπŸΎπŸ™ŒπŸΎπŸ’œπŸ’œ
#lovealupie #lupusawarenessmonth #lupuswarrior #lupussucksπŸ’œ

Lupus really decreases my quality of life... It’s hard to explain to people who don’t go through it just how tired you can really be on a daily basis... Because my symptoms aren’t always visible... I use all my energy for the day just getting myself up and ready for work... After that, I’m running off of a deficit of energy for the remainder of the day... I have to take naps before I leave and go anywhere so that I don’t fall asleep at the wheel... Sometimes have to cancel plans last minute because my body shuts down and I can’t get up... My joints fail me sometimes in the middle of the day without warning... Or my body becomes inflamed unannounced out of nowhere when I could’ve just been moving around carelessly... I get migraines that are so bad I can’t stand light or sound... Nausea is unreal and comes and goes as it pleases for no reason... And if I get too much sun, my skin hurts so badly that the pressure of water hitting it while I shower is too much to bear... A lot of people have no idea what we lupies go through on a day to day basis... And MANY of them, question if we’re over exaggerating our disease or what we feel... But we don’t get any pass on life... There is no disability for lupus and no acknowledgement of it for jobs or school... We have to get up early and work hard the same way anyone else would that doesn’t deal with a chronic illness... We have to take care of our families, and often times we don’t have anything left to take care of ourselves... If you’re unfamiliar with lupus, I ask you to educate yourself this May and try to better understand how hard it can be for someone to live with lupus... We may look fine on the outside, but the pain and craziness that goes on in the inside can be indescribable at times #Surviving #FuckLupus #Breathe #BeGrateful #InnerPeace #LivingLight #GoddessVibes #GoddessTribe #LoveALupie #LupieLiberal #LupusLife #Warrior #YourFavoriteLupie #CureLupus #FindACure #LupusAwarenessMonth #Peace #Love #iAmDivine πŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œ

#Repost @kiiroilashbar (@get_repost)
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May is Lupus Awareness Month πŸ¦‹, and in honor of that I will be donating 30% of my month's earnings to BC Lupus Society. It may not be much since I'm doing this part time, but I want to give back to the community when I can. You can also donate directly through bclupus.org in my description.

The first time I had my lashes done was last year by @lashartistry. It was a tough time in my life since I was recently diagnosed with Lupus. My hair was thinning and my face was bloated. I know it sounds superficial but adding lashes to my life made me feel "pretty" again. Which inspired me to start my lash journey in hopes that other ladies in similar scenarios can feel a boost in confidence again. Everyone is beautiful inside and out but sometimes you don't see it that way.

Once again, thank you to everyone that's inspired and supported me on this venture! πŸ’• #lovealupie #chronicwarrior #lupusawareness

May is Lupus Awareness Month πŸ¦‹, and in honor of that I will be donating 30% of my month's earnings to BC Lupus Society. It may not be much since I'm doing this part time, but I want to give back to the community when I can. You can also donate directly through bclupus.org in my description.

The first time I had my lashes done was last year by @lashartistry. It was a tough time in my life since I was recently diagnosed with Lupus. My hair was thinning and my face was bloated. I know it sounds superficial but adding lashes to my life made me feel "pretty" again. Which inspired me to start my lash journey in hopes that other ladies in similar scenarios can feel a boost in confidence again. Everyone is beautiful inside and out but sometimes you don't see it that way.

Once again, thank you to everyone that's inspired and supported me on this venture! πŸ’• #lovealupie #chronicwarrior #lupusawareness

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