#lupusstrong | Explore Tumblr Posts and Blogs

digicontact · 1 year

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World Lupus Day !

May this World Lupus Day bring us one step closer to finding a cure for this chronic illness. Let's continue to raise awareness, funds, and support for lupus research. …

https://www.facebook.com/DigiContactOfficial

#WorldLupusDay #LupusAwareness #LupusWarrior #LupusStrong #FightLupus #HopeForLupus #SupportLupusResearch #LupusAdvocacy #LupusCommunity #LupusAwarenessMonth #digicontact

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heatherjpp13 · 2 years

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After it all I am stronger from it💪💪💪🙏🙏🙏💜💜💜 #lupusanemia #lupusstrong #lupusnephritis #lupusfoundationofamerica #lupusawareness #lupuseritematososistemico #lupuswarrior #lupusmom #lupusfacts #lupusadvocate #lupusdoesntdefineme #fuckyoulupus https://www.instagram.com/p/CgXh3lmgcgo/?igshid=NGJjMDIxMWI=

#lupusanemia #lupusstrong #lupusnephritis #lupusfoundationofamerica #lupusawareness #lupuseritematososistemico #lupuswarrior #lupusmom #lupusfacts #lupusadvocate #lupusdoesntdefineme #fuckyoulupus

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spooniestrong · 3 months

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Thank you, Selena, for making ME not feel so alone and for sharing the feeling that if I can keep going, someone else can too.

That's why I created #SpoonieStrong 💙🥄

#spooniestrong #spoonie #personal #lupus #disability #chronic illness #chronic pain #selena gomez

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debbiesuesviews · 3 years

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#lupusawarenessmonth #lupusawareness #lupus #lupuswarrior #lupuslife #lupusstrong #togetherforever #supportingeachother #warriors

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cherrykisses78 · 3 years

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#tattoos #love yourself #believe #lupusstrong

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msbotalley · 4 years

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💜ANNOUNCEMENT 💜 . TOMORROW SUNDAY MAY 17, 2020 Our nonprofit organization @ballingforlupusluvs will present its 1st Balling For Lupus Luvs Foundations VIRTUAL Insta-A-Thon, a digital event to help raise funds and awareness for families impacted by Lupus . This SUNDAY MAY 17, 2020 . 12noon- 8pm est . Please TUNE IN on this IG page @iammsbotalley. I WILL BE STREAMING LIVE from 12n-8pm est . Come meet some favorite celebrities Coaches, Players, Host and entertainment from the previous years . They will be coming on and helping us continue to spread lupus awareness . Please be sure to set your reminders because you don’t want to miss the first ever Balling for Lupus Luvs Charity Basketball Game virtual Insta-A-Thon . 💜💜 . #Lupus #LupusStrong #WeareInThisTogether #LupusMatters #LupusAwareness #lupuswarrior #lupusadvocate #b4LL #Ballingforlupusluvsfoundation #ballingforlupus #botalley #Wnba #Nba #Nfl #nhl #Atlanta #Dallas #losangeles (at Balling For Lupus Luvs Foundation) https://www.instagram.com/p/CAQ7y60n7FD/?igshid=1f3fzpd9bqvyl

#lupus #lupusstrong #weareinthistogether #lupusmatters #lupusawareness #lupuswarrior #lupusadvocate #b4ll #ballingforlupusluvsfoundation #ballingforlupus #botalley #wnba #nba #nfl #nhl #atlanta #dallas #losangeles

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smith0507 · 6 years

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What’s Your Source of Energy?

No matter how many hours I sleep per night, when my alarm goes off in the morning I still feel restless. What’s a girl to do? I take vitamins. I even give myself prescribed B12 injections biweekly. Regardless of the remedy, my level of energy is only changed temporarily. There is only a week of relief. I recently started drinking coffee regularly, however, when the coffee wears off I crash. Then, the vicious cycle continues. What’s the key to boosting my energy level? EXERCISE!!!! I know what you’re thinking. If I’m already fatigued & have no energy, how will I gain energy to go exercise. Listen, I get it. I have the same thoughts on most days. The exercise doesn’t have to be strenuous. Try bike riding, yoga, Zumba, or even walk around the neighborhood. Take one day at a time. Eventually, your level of energy will increase drastically.

#LupusStrong #PurplePress #EnergyBoosters #BeActive

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godsspokenspeaker · 3 years

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Long overdue post 🚨 I’m Back in the 📍239, not sure for how long but I’m here!! Why? Over the past few months my health hasn’t been great I mean there were days I couldn’t walk, I couldn’t dress myself, nor let alone get out of bed! (SN: S/O to the best roommate ever @keera_doee, I appreciate you so much, THANK YOU! 💙) Long story short on June 9th, 2021 I was diagnosed with (SLE) Systemic Lupus Erythematosus and (RA) Rheumatoid Arthritis. Most of y’all already know my sister @monicatobeautiful was diagnosed with the same disorders in 2016. 🦋🦋🦋💜💜💜💜 How am I doing? Some days are better than others. Since finally being on medication that suppress the pain, I’ve been okay. Thank you to supportive family and friends. Please do not get offended if you are just now finding out. I’m still trying to settle in. Understand that I needed time! Everything happened so fast, in a nutshell all in one month: I got diagnosed, lost my job in Lakeland, then got a job offer in Marco Island and I moved back to Naples the following week! 🤷🏾‍♀️ It was all on Gods timing so I can’t complain. All Glory To God! #LupusStrong #HealingIsHerName #SLE #SystemicLupusErythematosus #RheumatoidArthritis #LupusWarriors #PurpleButterflies (at Naples, Florida) https://www.instagram.com/p/CS7M1-enP1D/?utm_medium=tumblr

#lupusstrong #healingishername #sle #systemiclupuserythematosus #rheumatoidarthritis #lupuswarriors #purplebutterflies

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becausethefamilymatters · 4 years

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Fighting Lupus like a couple on a mission and a husband fighting to save his wife who hasn’t slept or rested in days. We are making a kale, white turkey, veggie soup filled with anti-inflammatory fighting nutrients that Dave went out to scavenger for early this morning. I’m gonna beat the heck out of this flare up. My weapons are all AIP and Paleo, the armor of God and a whole lotta garlic 🧄 😊. Oh and a husband who hasn’t slept because the battle I fight, he fights. #Lupusstrong 💪 💜🙏🏽 Whoa the neighbors at the corner can smell the garlic 🧄 . Lord Jesus let the inflammation just dissolve. Let my body rehydrate through my dehydration episodes. As Olivia would say “Mam need more aider gators 🐊 “ Lord Jesus bring back all our local therapists to working full time again so we can all share the burdens of our community. Lord Jesus find a vaccine for COVID-19 and help our leaders make right decisions. Lord Jesus bless our Pastors who minister daily to families. Give us all continued strength to honor You and serve, bringing peace and comfort to families during this time. In Jesus name -Amen https://www.instagram.com/p/B_AyiFMj0p9/?igshid=1u9bmh1ay08vc

#lupusstrong

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angela-johnson-me · 4 years

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Such a mantra to have I have been feeling actually very warn down. Haven't gotten out of bed in two days every thing hurts. Sometimes this illness just wreaks havoc. I however keep going. #lupus #lupuslife #lupusproblems #lupusstrong https://www.instagram.com/p/B7tQrFTlA7R/?igshid=efh28ai3hnmf

#lupus #lupuslife #lupusproblems #lupusstrong

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heatherjpp13 · 2 years

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Do I complain? NO! Do I ever tell you when I feel my worse? NO! I love my life & I live it to the best I can. My son is the reason I fight daily. My other prognosis' are just that. So I bleed...& I know because sometimes it won't stop...Anemia...I have COPD & Asthma, I have Kidney issues, yet I push through with my brain having issues from Lupus. I don't give up & I fucking live my life. I try to record daily because it's all I have for Tristan to remember. Life is short...love, live, & enjoy💜💜💜💜💜💜my cousin died from this disease & I miss her every fucking day!!! #lupuswarrior #lupusawareness #loinpainhematuriasyndromeawarenessday #sickpost #lupus #sle #lupusfighter #lupussucks #lupusflare #lupusawarenessmonth #lupuslife #lupusadvocate #lupusstrong #edsawareness #lupusproblems #lupussurvivor #ankylosingspondylitis #lupussupport #chronicillnessmemes #lupuswarriors #knowlupus #rheumatoidarthritis #lupusfoundation #crps #lupusfacts #chronsdisease #lupie #lupusnephritis #gastroparesis #fibrowarrior https://www.instagram.com/p/CfmuoJuFwVR/?igshid=NGJjMDIxMWI=

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spooniestrong · 30 days

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Things To Avoid If You Have Lupus

#spooniestrong #spoonie #lupus #sle #systemic lupus erythematosus #flare

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iamalupuswarrior · 5 years

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Bloom. #lupuraforlupus #lupus #lupuswarrior #lupusawareness #lupussucks #lupusfighter #LupusChick #lupuslife #LupusSurvivor #lupusflare #lupusbodybuilding #lupusnephritis #lupusawarenessmonth #lupusstrong #lupusupport #lupussupportraleigh #lupusleisure #lupuscoach #LupusSupport #Lupuseven #lupusdiet #lupuseritematosus #lupuswithstyle #lupushero #lupusalphacalligraffiti #LupusAdvocate #lupuscommunity #lupuspatient #lupusawarness #lupuswillnotwin (at Duncanville, Texas) https://www.instagram.com/iamalupuswarrior/p/Bw6-qCeASu16dGvfFIPLHWJobV5pWyB3yO29Os0/?igshid=1soti0dp4igyv

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lojasdofuturo · 5 years

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Novo canal quero alcançar outras mães e pessoas com lúpus. Dar dicas de auto ajuda. É receber tbm dicas de outros portadores de Doenças auto imune compartilhem. Para que mas pessoas sejam alcançadas. https://www.youtube.com/channel/UCj2vpkx0UFePnN1z8WFOCGg Link do canal tbm na bio... #lupus #lupuswarrior #lupusawareness #lupusfighter #lupussucks #lupuslife #chronicillness #lupussurvivor #lupusflare #lupuschick #autoimmunedisease #lupuswalk #lupusstrong #spoonie #lupusawarenessmonth #invisibleillness #lupuswarriors #sle #purpleforlupus #chronicpain #lupusproblems #fibromyalgia #lupusadvocate #lupie #lupusfacts #atlanta #lupustruth #selenagomez #lupusrash #lúpus https://www.instagram.com/p/Bv2wNrzhsTX/?utm_source=ig_tumblr_share&igshid=1ltzj0q13zuij

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msbotalley · 4 years

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Lupus Awareness Month . We’ve announced this already. I just want to make sure everyone knows that our Annual charity event has been postponed . Please follow our @ballingforlupusluvs and website www.Ballingforlupusluvs.com for updates . You can still donate and help us in our donations to a family in need during this world crisis . THANK YOU . #Lupus #LupusStrong #WeareInThisTogether #LupusMatters #LupusAwareness #lupuswarrior #lupusadvocate #b4LL #Ballingforlupusluvsfoundation #botalley #Wnba #Nba #Nfl #nhl #Atlanta #Dallas #losangeles #Basketballwife #RealHousewife #CoachesWives #BlackGirlsRock #botalleywilliamssaidit https://www.instagram.com/p/B_1b2SeHleV/?igshid=2gpg36yvytrx

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eyeologyinc-blog · 5 years

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Reposted from @yahminahmcintosh_ - Oftentimes I'm asked how does Lupus affect my life and depending on what stage of life I'm in, my answer will be short or loaded. Today I see it differently although the pain can sometimes be more severe during Flare ups or on not so amazing days, but Im alive and that is the blessing that keeps on giving. This picture is an accurate depiction of the type of discomfort that many of us with Lupus experience. I remember the last time I was training for a Trio of Marathons that were coming up in 2015 that I wanted to do. That was such an exciting time for me but it would also be the moment that I heard my body loud and clear and realized that it was time to step away and rest. My kidneys were in distress, I had a minor stroke and a host of other issues began to manifest. The road was bumpy, hard and a blessing all at the same time because I learned to listen to my body and started paying attention to the little things. Fast forward 3.5 years and I feel better than I have in a very long time although I still have some rough days. I take each of beautiful day as it comes and take excellent care of myself. I am a Lupus Warrior. Reposted from @lupus.fighters - #lupusawareness #lupuswarrior #livingwithlupus #lupuschick #lupusproblems #knowlupus #lupussupport #lupusfighter #lupusnephritis #lupusfacts #lupusflare #lupussurvivor #nolupus #lupus #lupustruth #lupusstrong #lupusincolor #lupuslife #lupuswarriors - #regrann #yahminahmcintosh #inspiretogohigher #soulfruitexpressed #systemiclupus - #regrann https://www.instagram.com/p/BtJDnZ-nZpk/?utm_source=ig_tumblr_share&igshid=lgo22gyhhgzc

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