#putonpurple

MOST RECENT

A cause that is dear to my heart. Because I am a #Warrior join me and #PutOnPurple on #May18 for #lupusawareness #savethedate #std

Got my old port removed and a new one placed today. This port’s name is Danielle (I name my IVs after nurses who are able to get one started, because I’m a hard stick). My surgeon was super sweet and even cut my dressings into a heart :)

Some people are too amazing to put into words. πŸ’œ
Check out these awesome tees One In A Million Inc. made for my golf outing! I’m so thankful for the Port Authority Police Officers who came up with the idea of making tees and polos for the golf outing, and for @oiaminc for making these shirts. I can NOT wait to rock mine and even more, can’t wait to see others in them 😊. If you’re having an event or want team shirts for the walk contact @oiaminc , they’re great πŸ’œ. #nicoleslinksforlupus ⛳️

We did it guys!! We hit our goal! πŸ¦‹πŸ’ͺπŸ’œ Oh, and the Lupus Foundation called me... *turn sound up* #lupusawareness #lupiewarriorsproject THANK YOU for all your support and generous donations!! πŸ’œπŸ’œπŸ’œ
Thank you for the voicemail @lupusorg @lupusfl #walktoendlupusnow #knowlupus #walkforlupus #lupuswarriors #lupus #lupiewarriors #thelupustrainer #lupusfundraiser #teamlupustrainer #lupusfoundation #lupusorg #lupusfl

What is lupus? Lupus is a cruel disease. Lupus not only hurts patients, but also hurts their families and love ones. Lupus is detrimental to the lives of so many. Lupus is a disease with not nearly enough awareness or funding. Lupus is a disease that needs a cure.
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Someone you know has lupus. Someone you know needs a cure. May is Lupus awareness month. It's almost here! I would like to ask you all, to once again help me to raise awareness for this cruel disease by rocking your purple every Friday of May. Your support in raising awareness over the past few years has been nothing short of amazing! Please pass this on to get as many participants as possible this year. Please share your pictures in May with the hashtags: #PurpleForErin & #LupusAwareness
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Each Friday in May, I will be selecting at random, one person who rocks their purple and their hashtags, and will send that person a $5 Starbucks gift card!
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Share! Share! Share!
Let's raise awareness together, and work towards finding a cure! πŸ’œ
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#mayislupusawarenessmonth #lupussucks #fucklupus #lupuswarrior #spoonie #awarenessiskey #findacure #knowlupus #mycause #cantstopwontstop #nevernevergiveup #autoimmunedisease #chronicallyawesome #chronicillness #putonpurple #itsanerinthing #purpleforlupus #purpleforlupusawareness #onfridayswewearpurple #freecoffee #yourchancetowin

A look back to last years Walk to End Lupus! I’m SO excited for this year and can’t wait to see everyone 😊. I changed my team name to β€œIn The Loop” so keep an eye out! For more info on the NYC walk on May 5th, please click the link in my bio. πŸ’œ #tbt

πŸ’œ Today 10 years ago I got the official diagnosis of lupus. They suspected for years then bam, that's what I have. Crazy thing is I'm having a #ihatelupus day. But grateful because I know a few people who didn't make it to today with lupus. So, counting my blessing and making through the day. Good morning.
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#lupus #lupusawareness #putonpurple #pop #fightahardbattle

This cause means a great deal to us.
We walk for our fallen and our fighting.
We walk in hopes of a cure and to spread awareness of this mysterious illness.
This year we will be sending out token of our gratitude to all of our donors.
Please help support our team and this cause. Link is in my bio, read our story and donate. Thank you #lupusawareness #walktoendlupusnow #teamradiantroses #wewalk #forourfallen #forourfighting #donate #support #pop #putonpurple

Our Walk To End Lupus Now - Saint Louis is just around the corner! Register to walk today and experience firsthand the power of the movement to end lupus: http://chapters.lupus.org/site/TR/WTELN/LFAHeartlandChapter?px=1013146&pg=personal&fr_id=1540

#lupus #lupusawareness #fundraiser #putonpurple #findacure #bandtogether #takesavillage

πŸ’–You Were Born A Warrior You Can Do This! πŸ‘ŠπŸΌ Autoimmune Diseases are not for the Weak... Let me Tell You πŸ™ŒπŸ½, In order to Deal with these Diseases You Must Get Tough (You Really have No Other Choice) & You must Fight Everyday! But Always Remember to Pat Yourself on the Back πŸ‘πŸ»πŸ™πŸΌπŸ˜˜ Because You Are Braver, Stronger & Smarter than You Think. πŸ‘ŠπŸΌπŸŒΊπŸ€“ #LiveWithGuts #Preach #WeekendVibes #Blessed #Sunday #SundayFunday #Autoimmune #Warrior #AutoimmuneWarrior #AutoimmuneDisease #AutoimmuneIllness #AutoimmuneDisorder #AutoimmuneAwareness #ChronicIllness #Spoonie #chronicillnesswarrior #Spoonies #Spoonielife #YouDontLookSick #Latina #PutOnPurple #Blogger #Chronicillness #Wellness #chronicdisease #Health #Awareness #invisibleillness #invisibledisease #invisibleillnessawareness πŸ“·: @livewithguts1 πŸ’– www.LiveWithGuts.com

Final week to submit your purple related cosplays and stories. Can't wait to share you all next month. Be sure to attach photographers as well so they can get credit as well. #lupuscharity #lupus #lupusawareness #fibromyalgia #fibromyalgiaawareness #cosplay #cosplayer #cosplayforacause #cosplayersforlupus #lupuswarriors #putonpurple

Final week to submit your purple related cosplays and stories. Can't wait to share you all next month. Be sure to attach photographers as well so they can get credit as well. #lupuscharity #lupus #lupusawareness #fibromyalgia #fibromyalgiaawareness #cosplay #cosplayer #cosplayforacause #cosplayersforlupus #lupuswarriors #putonpurple

I miss driving him to school every morning. My body insisted I give it up and that he start riding the bus in the mornings, too. (Not just evenings) My feet are the main reason β€” neuropathy caused by lupus as well as very painful joints due to RA. They hurt so badly I can’t even wear socks. It’s been this way for 5 years now... Someday, it will all be better...right?
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#lupus #sle #systemiclupus #mylupuslife #lupielife #advocateforlupus #putonpurple #anewnormal #chronicpain #chronicillness #chronicallyawesome #lupussucks #teamlupus #cruelmystery #LFA #iwearpurpleforme #spoonie #butyoudontlooksick #spoontheory #invisibleillness #spreadawareness #advocate #lupiechick #painsomnia
#jointpain #weneedacure #lupuswarrior #autoimmune #disease #autoimmunity

πŸ’πŸ»β€β™€οΈToday while working, I Meet another Warrior!πŸ‘ŠπŸΌ Her Autoimmune Battle was with #LymeDisease πŸ’œ, we talked, shared similar stories on the struggles of dealing with a Chronic Illness & ended up both in tears by the end of our conversation. 😭 We bonded over Autoimmune Diseases, over similar experiences & struggles and so Much in Common. When she Left my Office, I Sat for a Moment & Realized Us Warriors are Made Tough, She also had that Fighting Spirit πŸ’ͺ🏼, that Drive that Keeps You Just Wanting to Feel Normal, & In that Moment I made a Friend πŸ™πŸΌπŸ€“πŸ‘ŠπŸΌ. #LiveWithGuts #MotivationMonday #MondayVibes #Warrior #Work #Latina #Autoimmune #AutoimmuneWarrior #AutoimmuneDisease #AutoimmuneAwareness #Chronicillness #Chronicdisesse #crohnswarrior #hswarrior #lupuswarrior #psoriasiswarrior #invisibleillness #Autoimmunedisorder #youdontlooksick #Spoonie #Spoonies #Awareness #Spoonielife #putonpurple #KeepFighting #Blessed #Blog #Blogger www.LiveWithGuts.com πŸ‘ŠπŸΌ πŸ“·: @livewithguts1

Share by Cathy Tice Fleming

βšͺοΈπŸ’œβš«οΈ
Lokai wearin since day 1...this is my favorite one yet.
Last month’s Lokai was made for Alzheimer’s Awareness, and this particular bracelet is made to represent those living with alzheimers as well as those caring for them. Purple is also the color for lupus (and fibromyalgia) so voila! My brother and I have gotten all of the Lokais but this one holds a special meaning because of how much he’s done for me. I’d never be where I am today without my amazing support system. #livelokai

5️⃣ weeks until the Walk to End Lupus Now in NYC!!!!
Check out my team at the link in my bio...but the fun doesn’t stop there! My golf outing will be 6/11 and I also am in the middle of planning TWO other fun events!!! Stay tuned! πŸ’œ
OH! And send me a message if you’ll be there. I’d love to meet up!!!!

πŸŽ‰To Celebrate My Birth Week πŸ˜‹ & Autoimmune Disease Awareness MonthπŸ’œ It’s GiveAway Time!!! πŸ‘ŠπŸΌπŸ‘ŠπŸΌπŸ‘ŠπŸΌπŸ‘ŠπŸΌπŸ‘ŠπŸΌπŸ‘ŠπŸΌπŸ‘ŠπŸΌπŸ‘ŠπŸΌπŸ‘ŠπŸΌπŸ‘ŠπŸΌπŸ‘ŠπŸΌ1.) Like This Photo πŸ“· 2.) Follow @livewithguts1 3.) Tag 3 Warriors (You Can Always Tag More for More Entries). πŸ’πŸ»β€β™€οΈ *GiveAway Ends March 30th, Winner Announced on my Bday, March 31st! We’ll pick 3 Winners To Win an Awareness Band & Be Featured! πŸ‘ŠπŸΌ Good Luck WarriorsπŸ’œ. #LiveWithGuts #March #GiveAway #Autoimmune #Warrior #Autoimmunewarrior #AutoimmuneDisease #autoimmunehealing #autoimmuneprotocol #AutoimmuneDisorder #AutoimmuneIllness #AutoimmuneAwareness #autoimmuneawarenessmonth #PutOnPurple #ChronicIllness #chronicdisease #invisibleillness #invisibledisease #Spoonie #Spoonies #spooniesupport #raiseawareness #Band #Bands #Contest #bdaygirl #Blog #Blogger #Etsy #AwarenessMonth www.LiveWithGuts.com

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