#CureLupus

Instagram photos and videos

#curelupus#lupuswarrior#lupusawareness#chronicillness#chronicpain#lupus#baldbeauty#rheumatoidarthiritis#fibromyalgia#inspirational#motivational#spoonies#autoimmunedisease#lupussurvivor#knowlupusnolupus#supportlupusresearch#mytruth#livingwithlupus#treatlupus#autoimmune#preventlupus#SLE#lupusresearch#informationalpost

Hashtags #CureLupus for Instagram

Antinuclear antibodies (ANA) are present in several immunologic diseases, including systemic lupus erythematosus, progressive systemic sclerosis, Sjรถgren syndrome, scleroderma, polymyositis, and dermatomyositis. #LupusFactFriday
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#lupus #lupusfact #factfriday #lupusresearch #breakingthrough #SLE #autoimmune #preventlupus #treatlupus #curelupus #ANA #chronicillness


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My Lupus story: How I came to know of IT;
In 2013, I started getting rashes on my hand and all of a sudden blood clots started appearing on my palm and the pain was unbearable. I went to a general physician and she said that this might be because of my work pressure and stress. I was in my last year of graduation, and I had lot of academic works and also had some education and career related stress. I visited an well known Ayurvedic hospital and was on medication for few months. Medicine were given to increase blood flow and purification of blood. Everything went well for 2 years
In 2015, the symptoms started repeating. I started getting rashes on my leg, blood clots on my feet with swelling and extreme pain. I was in my final year of post graduation and also was working for a organisation. With each passing day my condition worsened and I started having difficulty even to walk. I was taken to multiple hospitals, but things just got worse. Symptoms started spreading to my hands and palm.
In November 2015, with the help of one of the directors of my organisation, I was introduced to a rheumatologist. He conducted multiple blood test, ultrasound on my limb and xray of lung. And finally I was diagnosed of SLE with Vasculitis.
From then till now it has been a long journey for me and my family. But in Nov 2015 I was happy that alteast now I know why I am having these symptoms.
#mylupusstory #mylupuslife #mylupusjourney #lupus #lupusawareness #lupusdiagnosis #lupuswarrior #lifewithlupus #sle #ANA #lupustests #autoimmune #curelupus #lupusresearch #treatlupus


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Have you experienced thinning hair or balding? Share your experience with other #lupuswarriors using our community forum! There is already a discussion started asking for your advice! Get started at lupusresearch.org/community #ThursdayThoughts #CommunityTalks
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#lupus #lupuscommunity #SLEcommunity #community #SLE #autoimmune #preventlupus #treatlupus #curelupus #LupusResearchAlliance #joinus #forum #communityforum #lupusforum


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A yummy, yummy recipe for a summer meal! What are YOU cooking? #yummyforyourtummy #curelupus


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#throwbackthursday of last years #walkforlupus ๐Ÿšถ๐Ÿพโ€โ™€๏ธ if you havenโ€™t already click the link in my bio and register and/or donate to #whitbys Lupus Walk! See you all there ๐Ÿ™Œ๐Ÿพ BONUS: @vividd416 will be performing live, donโ€™t miss out! #lupusontario #lupuswalk2018 #lupuswarrior #curelupus #fundraiser #torontofundraiser #charity #charityevent #whitbyevents #whitbyfundraiser #eventplanner


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In this #AskTheDoctor segment, Dr. Alana Levine, NYC rheumatologist with a particular expertise in treating people with lupus, explains how lupus is diagnosed.
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#lupus #lupusvideo #lupusresearch #lupusdiagnosis #SLE #autoimmune #preventlupus #treatlupus #curelupus #breakingthrough #drlevine #rheumatology #rheumatologist


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When treatment works, it makes all the difference in the world. Photo on left was before treatment. On right, during treatment with Enbrel. Both photos are old. But, knees are looking a lot like the left photo these days. I had to stop Enbrel in February since S.L.E. symptoms worsening. Now taking Plaquenil and scheduled for my first Rituxan infusion tomorrow. Crossing my very sore fingers it helps.
#rhupus #lupus #rheumatoidarthritis #sle #chronicillness #chroniclife #spoonie #spoons #rituxan #rituximab #autoimmune #lupusawareness #awareness #treatment #curelupus #cureRA #strongerthanRA #cruelmystery #lupussucks #chronicpain #strongAF


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Every Dollar helps RepostBy @lupusresearchalliance: "The Lupus Research Alliance is on a mission to free the world from lupus. Because lupus is such a complex disease, we believe that science holds the key to achieving our goal.
We focus on inspiring, supporting and extending innovative research along paths that will dramatically improve the lives of people affected by lupus. We are the worldโ€™s largest private funder of lupus research, having committed $182M to date.
Learn more about the organization by visiting our website: lupusresearch.org
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#lupus #lupusresearch #hope #breakthingthrough #breakingthrough #preventlupus #treatlupus #curelupus #SLE #autoimmune" """"The @beardedvillains_ny_nj is proud to announce that we are taking part in the 15th Annual New York City Walk with Us to Cure Lupus! @lupusresearchalliance
SATURDAY, OCTOBER 13, 2018 if youโ€™d like to Donate or if youโ€™re in the NYC area and would like to join please go to http://support.lupusresearch.org and click on walk with us hit the NYC LINK and search for team name LUPUSH and you can Donate by clicking on any individual team member. all Donations go to the team . Thank you in advance. @bvcharity โš”๏ธBEARDED VILLAINS NY/NJโš”๏ธ
__________________________________________ โš”๏ธBadassโš”๏ธHonestyโš”๏ธFamilyโš”๏ธ โš”๏ธHonorโš”๏ธProudโš”๏ธRespectโš”๏ธ
โš”๏ธDiversityโš”๏ธLoveโš”๏ธCharityโš”๏ธ โš”๏ธLoyaltyโš”๏ธWorldwideโš”๏ธcourageโš”๏ธ โš”๏ธUnityโš”๏ธKindnessโš”๏ธSupportโš”๏ธ
โš”๏ธOur family is strongโš”๏ธ
โš”๏ธOur hearts are kindnessโš”๏ธ
โš”๏ธWe are the Bearded Villains NY/NJโš”๏ธ
__________________________________________

#loyalmakesyoufamily #beardedvillains
#beardedvillainsbrotherhood #family
#gentlemen #oneflag #onefamily
#badassfamily #beardedfamily #villainfamily
#igotyoulikeyougotmelikewegotus
#villainchangetheworld ๐ŸŽฉ๐Ÿ”ช๐Ÿป ๐Ÿ‘Š
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@von_knox @beardedvillains @beardedvillainscharity
@beardedvillains_charitywork
@beardedvillains_ny_nj
Stay loyal, Stay bearded, Stay villain ๐Ÿ™
villain saluteโš”๏ธ๐Ÿ‘Š๐Ÿป๐Ÿป๐Ÿ”ช๐ŸŽฉโ™ ๏ธ13๐Ÿ—ฝโš”๏ธ"


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Happy #WorldEmojiDay! ๐Ÿ˜Š๐Ÿ˜Ž๐Ÿ™ƒ๐Ÿ˜The Lupus Research Alliance is always keepinโ€™ it ๐Ÿ’ฏ (which is why this is one of our favorite emojis!) What emojis are your favorites?
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#lupus #SLE #autoimmune #lupusresearch #preventlupus #treatlupus #curelupus


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The effects of the sun on my skin even after using 100 spf sunscreen. Cutaneous lupus has always attacked my skin and scalp leaving burn like scaring. Being exposed to direct sunlight due to my employment has worsened it, but what do you do...๐Ÿคท๐Ÿฝโ€โ™€๏ธ๐Ÿ’œ๐Ÿ’œ๐Ÿ’œ #lupusrash
#livingwithlupus #mytruth #informationalpost #workingspoonie #knowlupusnolupus #lupusawarenessโœ‹๐Ÿฝ #lupussurvivor #lupuswarrior #curelupus #autoimmunedisease #chronicillness #spoonies #motivational #inspirational #fibromyalgia #rheumatoidarthiritis #baldbeauty #chronicpain #supportlupusresearch #divorcee๐Ÿ˜‰


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Support the Lupus Research Alliance while you shop on #PrimeDay! Amazon's fourth-annual Prime Day is TODAY and is one of the biggest shopping days of the year. Your shopping makes a difference. When you shop through Amazon Smile, Amazon will make a donation to the Lupus Research Alliance.
Get started by typing this link in your browser: ๐Ÿ”—bit.ly/LRAAmSmile (link is case-sensitive). Or go to smile.amazon.com and choose โ€˜Lupus Research Allianceโ€™ as your organization to support. #StartWithaSmile ๐Ÿ˜
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#lupus #lupusresearch #autoimmune #SLE #breakingthrough #preventlupus #treatlupus #curelupus #amazon #amazonsmile #charity


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Thank You Papa Murphy's for supporting people living with lupus & for your sponsorship of our upcoming Walk to End Lupus Now - Madison on Sept. 22, 2018. #Lovepapamurphys #curelupus


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Composed of numerous and varied cellsโ€”each with a specific taskโ€”the immune system is the bodyโ€™s defense mechanism. Watch this video with #MacktheMolecule to learn more!
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#lupus #lupusvideo #SLE #autoimmune #preventlupus #treatlupus #curelupus #immunesystem #knowlupus #chronic


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Letโ€™s all raise money for #lupus research. August 19th we will have entertainment for the whole family, raffles, BBQ and a live performance from @jesseakameeks ๐ŸŽค register using link in bio๐Ÿ‘†๐Ÿพ #lupusontario #lupuswarrior #curelupus #fundraiser #lupuswalk2018 #events #ontario #whitby #whitbyevents


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Shop Amazon Prime Day but first sign up for AmazonSmile & select The Lupus Foundation, Wisconsin Chapter as your charity! #curelupus


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The Lupus Research Alliance provides valuable resources to both patients and researchers. See them all at: ๐Ÿ”—bit.ly/lupusresources
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#lupus #SLE #autoimmune #lupusresearch #preventlupus #treatlupus #curelupus #lupusresources #resources #resourcesforlupus #lupusdownloads #lupuslinks


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Got Mama out for a drink at B-17 Bombers
#fightlupus #curelupus


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The Lupus Research Alliance is on a mission to free the world from lupus. Because lupus is such a complex disease, we believe that science holds the key to achieving our goal.
We focus on inspiring, supporting and extending innovative research along paths that will dramatically improve the lives of people affected by lupus. We are the worldโ€™s largest private funder of lupus research, having committed $182M to date.
Learn more about the organization by visiting our website: lupusresearch.org
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#lupus #lupusresearch #hope #breakthingthrough #breakingthrough #preventlupus #treatlupus #curelupus #SLE #autoimmune


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For patients with a positive ANA, more tests are usually performed to check for other antibodies that can help confirm the diagnosis. This series of tests, commonly called an ANA panel, checks for the following antibodies: anti-double-stranded DNA, anti-Smith, anti-U1RNP, anti-Ro/SSA, and anti-La/SSB. Learn more at lupusresearch.org. #LupusFactFriday
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#lupus #lupusfact #factfriday #lupusresearch #breakingthrough #SLE #autoimmune #preventlupus #treatlupus #curelupus #ANA #chronicillness


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I just signed up to receive this series of information! I have been in this lupus battle for over 16 years but there is always more to know. And the more we know and learn about lupus, the more we can share that knowledge with others. And the more we share, the more awareness we create. The more awareness we create, the greater hope we have for a cure! If you want to learn more please sign up!
#lupus #knowlupus #takecharge #lupusfl #tallylupie #curelupus #lupustallahassee #tallahasseelupus #localforlupus
@lupusorg @lupusfl

#Repost @lupusorg with @get_repost
ใƒปใƒปใƒป
Whether youโ€™re newly diagnosed or have been living with lupus for years, our new 8-week TAKE CHARGE email series can help you reach your health goals and live well with lupus. Subscribe to TAKE CHARGE today and start building your lupus knowledge! [visit lupus.org/TakeCharge or use the ink in our bio]


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Tough times donโ€™t last...tough people DO!!! Praying for all the Lupus fighters out there!!! Peace, Love & Strength. #CureLupus #LupusAwarenessEveryday


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Have you ever felt guilty for having such a great support system while others with lupus may not be so lucky? Share your support for the entire lupus community on our lupus community forum! Visit lupusresearch.org/community to join the conversation! #ThursdayThoughts #CommunityTalks
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#lupus #lupuscommunity #SLEcommunity #community #SLE #autoimmune #preventlupus #treatlupus #curelupus #LupusResearchAlliance #joinus #forum #communityforum #lupusforum


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#WalkwithUs this fall to raise critical funds that will help advance lupus research and bring hope to those affected. Visit support.lupusresearch.org to register for a Walk near you!
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#lupus #lupuswalk #lupusresearch #walktocurelupus #breakingthrough #preventlupus #treatlupus #curelupus #SLEwalk


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FYI...If you are taking any amount of Prednisone on a daily basis then you absolutely need to be increasing your calcium intake, either through diet or with a supplement.
#livingwithlupus #mytruth #informationalpost
#knowlupusnolupus #lupusawarenessโœ‹๐Ÿฝ #lupussurvivor #lupuswarrior #curelupus #autoimmunedisease #chronicillness #spoonies #motivational #inspirational #fibromyalgia #rheumatoidarthiritis #baldbeauty #chronicpain #supportlupusresearch #raynaudsdisease


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In this #AsktheDoctor segment, Dr. Alana Levine, NYC rheumatologist with a particular expertise in treating people with lupus, discusses how flares can affect each person with lupus differently.
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#lupus #lupusvideo #lupusresearch #breakingthrough #drlevine #rheumatology #rheumatologist #preventlupus #treatlupus #curelupus #SLE #autoimmune #lupusflare #whatislupus


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Here at Raising Artists colour theory is kind of a big deal...
For example did you know purple is the official colour for Lupus Awareness? ๐Ÿ’œโ˜ฎ๏ธ๐Ÿ”ฎ๐Ÿฆ„
Mark it down in your calendars and please join us in collaboration with @tanyamahadeo + @lupusontario in creating awareness, and raising funds for this important cause, that lies close to our hearts. ๐Ÿ’œ

Date: Sunday, July 22nd
Time: 5 pm
Location: @nathanphillipssquare
๐Ÿ’Ÿ: Bring the littles for a โœจCOMPLEMENTARYโœจ painting workshop๐ŸŽ—๏ธ๐ŸŽจ


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Be sure to follow us on Twitter & Facebook and tag us in your pictures from Walks and other events! ๐Ÿ–ฅ๏ธ๐Ÿ“ฑ๐Ÿ’ป
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#lupus #lupusresearch #breakingthrough #preventlupus #treatlupus #curelupus #socialmedia #lupuscommunity


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We all want a cure for lupus! Help us raise awareness and funding for vital lupus research. Visit lupusresearch.org.
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#wanted #lupus #lupusresearch #SLE #autoimmune #breakingthrough #preventlupus #treatlupus #curelupus #MacktheMolecule


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Ulcers can be caused by inflammation or infection. Autoimmune diseases, such as lupus, cause inflammation to many parts of the body. #LupusGlossary
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#lupus #lupusresearch #SLE #autoimmune #preventlupus #treatlupus #curelupus #educatelupus #glossaryterms #lupusterms #ulcers


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B cells are a type of white blood cell that help the body fight infection. Learn more about B cells from #MacktheMolecule in this video.
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#bcells #lupus #lupusvideo #SLE #autoimmune #breakingthrough #preventlupus #treatlupus #curelupus #immunesystem


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Be powerful. Be the reason we find the cause & cure for this mysterious and sometimes devastating disease. Donate today at www.lupuswi.org #curelupus


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Swipe left...
It's so easy for others to give their opinions and/or advice, but you've never lived a chronic illness such as SYSTEMIC LUPUS which can attack ANY SYSTEM WITHIN ONE'S BODY. Just to name a few severe complications caused by lupus..chronic pain and skin rashes throughout the body, hair loss, memory loss, depression/anxiety, joint deformities, bone deterioration, infections, blindness, teeth decay, heart attacks, strokes, seizures, rheumatoid arthritis, fibromyalgia, diabetes, hypertension, and organ failure. All of our bodies are different and may not experience all of the abovementioned, however, we have all and continuously suffer one way or another. Please keep your comments to yourself! #lifewithlupus๐Ÿ’œ #mytruth
#knowlupusnolupus #lupusawarenessโœ‹๐Ÿฝ #lupussurvivor #lupuswarrior #curelupus #autoimmunedisease #chronicillness #spoonies #motivational #inspirational #fibromyalgia #rheumatoidarthiritis #baldbeauty #chronicpain #supportlupusresearch


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Like/Share this graphic if youโ€™re a #LupusWarrior!
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#lupus #lupusresearch #autoimmune #SLE #breakingthrough #preventlupus #treatlupus #curelupus


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Itโ€™s okay to rest...those who love you will understand ๐ŸŒธ๐Ÿ’– #chronicpain #chronicillness #invisibleillness #curelupus #autoimmune ~Atlanta


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RepostBy @lupusresearchalliance: "Lupus affects African American women three times more than Caucasian women. Learn more at lupusresearch.org. #LupusFactFriday
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#lupus #lupusresearch #lupusfact #factfriday #breakingthrough #SLE #autoimmune #preventlupus #treatlupus #curelupus" """"The @beardedvillains_ny_nj is proud to announce that we are taking part in the 15th Annual New York City Walk with Us to Cure Lupus! @lupusresearchalliance
SATURDAY, OCTOBER 13, 2018 if youโ€™d like to Donate or if youโ€™re in the NYC area and would like to join please go to http://support.lupusresearch.org and click on walk with us hit the NYC LINK and search for team name LUPUSH and you can Donate by clicking on any individual team member. all Donations go to the team . Thank you in advance. @bvcharity โš”๏ธBEARDED VILLAINS NY/NJโš”๏ธ
__________________________________________ โš”๏ธBadassโš”๏ธHonestyโš”๏ธFamilyโš”๏ธ โš”๏ธHonorโš”๏ธProudโš”๏ธRespectโš”๏ธ
โš”๏ธDiversityโš”๏ธLoveโš”๏ธCharityโš”๏ธ โš”๏ธLoyaltyโš”๏ธWorldwideโš”๏ธcourageโš”๏ธ โš”๏ธUnityโš”๏ธKindnessโš”๏ธSupportโš”๏ธ
โš”๏ธOur family is strongโš”๏ธ
โš”๏ธOur hearts are kindnessโš”๏ธ
โš”๏ธWe are the Bearded Villains NY/NJโš”๏ธ
__________________________________________

#loyalmakesyoufamily #beardedvillains
#beardedvillainsbrotherhood #family
#gentlemen #oneflag #onefamily
#badassfamily #beardedfamily #villainfamily
#igotyoulikeyougotmelikewegotus
#villainchangetheworld ๐ŸŽฉ๐Ÿ”ช๐Ÿป ๐Ÿ‘Š
__________________________________________

@von_knox @beardedvillains @beardedvillainscharity
@beardedvillains_charitywork
@beardedvillains_ny_nj
Stay loyal, Stay bearded, Stay villain ๐Ÿ™
villain saluteโš”๏ธ๐Ÿ‘Š๐Ÿป๐Ÿป๐Ÿ”ช๐ŸŽฉโ™ ๏ธ13๐Ÿ—ฝโš”๏ธ"


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Be careful in the sun if you have #lupus ๐Ÿ’œ
Graphic by @lupus_uk #lupusawareness #curelupus #fightlupus ๐Ÿ’œ
~Atlanta


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Lupus affects African American women three times more than Caucasian women. Learn more at lupusresearch.org. #LupusFactFriday
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#lupus #lupusresearch #lupusfact #factfriday #breakingthrough #SLE #autoimmune #preventlupus #treatlupus #curelupus


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