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#WorldLupusDay
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
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baeleaf1606 · 1 year
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it’s world lupus day 💜
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A lupus flare causes your immune system to attack and damage your tissues and organs.
The inflammation caused by lupus affects joints, skin, kidneys, blood cells, the brain, heart, and lungs, leading to severe pain and fatigue.
Lupus flares can be unpredictable and last for days, weeks, or months. Treatment is vital to reduce inflammation and manage symptoms.
On this #WorldLupusAwarenessDay, let us spread awareness and support for Lupus warriors. Together, we can fight for a lupus cure.
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ricardodahcor · 2 years
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World Lupus Day was created by Lupus Canada in 2004 to raise awareness of this little-known disease that can have devastating effects on sufferers and their families. Ultimately, it was organized by lupus organizations from thirteen different countries, who called for their governments to increase funding for research, provide better patient services, increase epidemiological data and raise awareness. In the years since then, the day has been observed in an increasing number of countries in most of the continents all over the world, in Africa, Asia, Australia, North & South Americas, and Europe. In short, lupus causes the immune system to become overactive, creating antibodies that attack healthy tissue causing pain, inflammation and damage in a given part of the body. Although lupus can be fatal, there is currently no known cure. Sadly, a large majority of people have little to no idea about lupus, often confusing it with arthritis, a much less serious disease. One high profile supporter of World Lupus Day is musician and philanthropist Julian Lennon who is a Global Ambassador (and also the son of John Lennon, of Beatles fame). Other celebrities who have made sizable contributions to the Lupus Association of America are Daniel Radcliffe, Lady Gaga and Ian Harding. #WorldLupusDay #RacketOfTheDay #CustomMade #TennisRacket #BreakTheTie #breaktothefuture (em Lupus Canada) https://www.instagram.com/p/CdXkffhgjln/?igshid=NGJjMDIxMWI=
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etymologyrules · 1 year
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#etymologyrules #etymology #lupus #worldlupusday
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#WorldLupusDay
#10MAY #2023
#motivationalgurujee
#SLOGAN #OM #SHORT @motivationalgurujee जीवन में उत्साह भरने के लिए हमारे सभी वीडियो को देखें ! जिससे आपको मोटिवेशन मिलेगा #सुविचार #प्रेरणा #हिंदी #इंग्लिश #भाषा
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testiwol · 1 year
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Make Lupus Visible
How can we increase public awareness about lupus diagnosis
and its psychological, social, and economic consequences?
#Lupus #worldlupusday #lupusawareness
##Anantnag #testiwol #yourlabatyourdoorstep
#facts #testiwol #Health #healthylifestyle #Healthykashmir @testiwol @srlcare @redcliffelabs @who @noor__khann01 @corediagnostics @atulayahealthcare @1mgofficialpage @sofidiagnostics
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capitallaparoscopy · 2 years
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Having #Lupus #Disease doesn’t mean it is the ending, have the authority and fight your way out with a big bright smile and warrior’s Heart. #WorldLupusDay #capitallaparoscopy #laparoscopy #Bbsrlaparoscopy #drsambitmohanty #drgsmishra #bbsrgynicdoctor #bbsrgastrosurgeon https://instagr.am/p/CdYaWzBotec/
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pncrealty · 3 years
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Did you know that May 10 was World Lupus Day? #WorldLupusDay #Lupus #LiteUpPurple #Butterfly #2Sisters2Lupus #Charity #MakeLupusVisible www.2sisters2Lupus.org https://www.instagram.com/p/CPCEf5ShQPH/?utm_medium=tumblr
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Today is world lupus day. One of the most important days in my life. I have had lupus for 15 years now and there is still not any awareness about the disease. Not as much as there should be despite celebrities like @selenagomez talking about it. This year I was asked to talk at gangaram hospital about my experience of how I dealt with the disease and how important a support system is for us to have a positive mindset through the journey. I was surprised to see how many young people still suffered from ignorant teachers and bullies. Let's make one thing clear. Lupus is real. No, I am not imagining my pain. Yes, I don't look sick but my body is fighting a battle against itself with every single breath I take. No, it's not easy but yes, I make it work because I don't really have an option. On this world lupus day I would ask everyone to talk about this disease as much as you can. It's not your fault. Don't be ashamed rather be proud for fighting the fight most people can't. Lastly, you are not alone. Don't hesitate to ask for help. It doesn't make you weak. Asking for help is one of the bravest thing you will ever do so don't be afraid! #worldlupusday #spoonies #lupus #sle #selenagomez #butterfly #purple
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wsnaturalproducts · 3 years
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5/10 World Lupus Day.... 🚨LONG POST🚨 3 1/2 years ago I found out I have lupus. Phone: Hello Doctor: Hey Cherisse, how are you? Me: I’m ok. Doctor: It’s no easy way to tell you, you strongly test positive for Lupus. Me: Nah Doc. You sure it said Cherisse? Doctor:Yes. we need to get you in to see a kidney doctor ASAP. you have stage 3 kidney failure & your CRP is very high. C-Reactive protein test. Me: Shiiiiiiddddd..... you lying!😳 I hung up on the doctor & called Ras. 😩😂 Me: you know what them mf’rs said I have?!! Ras: what? Me: Lupus & it’s affecting my kidneys. I’m sure I had the ugly cry. Lol Ras: We will get through it! (forever grateful for my honey) 💚Fast forward..... Now I have to go through genetic testing. I contact the man I believed to be my dad & explained what was going on. Started testing including a dna test. Email came in w/results/ Mr. X is NOT your father 😱 HUH❓ Fast Forward again... I contacted everyone I knew & ask who my dad was. NOBODY would tell me the truth. (a few ppl did tell me the truth & pointed me in the right direction) I was devastated‼️😢 2 days later I sent my brother Mark the dna results. He said I’m sorry sis. I asked who is my dad Mark?... Idk. 20 mins later, Mark: Somebody is going to contact you soon. Fast Forward... Michael McQueen is 99.9% the biological father of Cherisse. 😳 Me: WTF IS GOING ON? Still stuck on why nobody ever told me the truth about ME‼️ (mind you I’m still going on with genetic testing to find out what type of lupus I have) BOOM results are in: Cherisse you have Systemic lupus erythematosus & skin lupus. 😩🤦🏽‍♀️ I also found out my dad carries the lupus gene. My journey with lupus has been a roller coaster ride with lots of tears & pain. 5/4/2021 I found out my kidneys are doing good!! 🙌🏽 5/24/2021 I will be having surgery to correct another issue lupus has caused. But GOD‼️ I’m not sad! I’m not worried! I’m not scared!! I am a Warrior who will overcome any obstacles thrown my way‼️💪🏽 WS Natural Products helps keep my lupus scars under control. (lupus scars are hard to get rid of) Our products WORKS WONDERS 💪🏽 Look at my skin!! #worldlupusday https://www.instagram.com/p/COu5ny7nSnC/?igshid=i2tdte1vubm6
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[World Lupus Day 2021] Memperingati Hari Lupus Sedunia (10 Mei 2021) yang dipersembahkan untuk seluruh penyandang AUTOIMUN di seluruh Indonesia. Lupus adalah penyakit Autoimun yang disebabkan sistem kekebalan tubuh menyerang sel-sel sehat seseorang. 90% penyandang LUPUS adalah Perempuan dengan usia 15-45 tahun. Hingga saat ini belum ada obat serta belum diketahui penyebabnya. AUTOIMUN sulit didiagnosa. Ribuan orang mungkin tidak terdiagnosa dan tidak mendapatkan pengobatan yang tepat. Jadi, YUK bareng aku, #BERSAMAODAPUS, kita sama-sama kenali Penyakit AUTOIMUN/Lupus, juga dukung Penyandang Autoimun - Odapus (Orang dengan Lupus) untuk mendapatkan akses serta fasilitas pengobatan yang baik. #BERSAMAODAPUS #WORLDLUPUSDAY #WORLDLUPUSDAY2021 #MAKELUPUSVISIBLE #BERSAMAODAMUN #CEMPLUKFIGHTING #UNDERSTANDLUPUS @sahabatcempluk #ChaconneAmongRaindrops (at Special Region of Yogyakarta) https://www.instagram.com/p/COtWo56LAaH/?igshid=g7vj6zz2lxh4
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#WorldLupusDay is observed every year on the 10th of May to create awareness of the devastating effects of Lupus and encourage people who are battling the disease. We Hetero Healthcare would like to raise awareness of the physical and emotional impact of Lupus patients.
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kidneystories2013 · 3 years
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National Kidney Foundation @nkf “Today we observe #WorldLupusDay to shine a bright light on lupus nephritis, how autoimmune diseases impact the body, and the importance of understanding your kidney health,” shared @CEOatNKF https://www.kidney.org/news/national-kidney-foundation-observes-world-lupus-day . (at Hammond, Indiana) https://www.instagram.com/p/COtBiUdjOGK/?igshid=iz463o7zx6c1
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Happy first birthday to this adorable pile of puppies!!!!! It has been one year since you came into this world and we have been overjoyed with ever minute of the experience. Ginger & Hank we see every day. Griffy & Snoopy we see from time to time. And Henry, we know, is loved so deeply! Today is also
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SELAMAT MALAM SOBAT PURBA 💜 setiap tahunnya di tanggal 10 Mei, seluruh masyarakat di dunia memperingati Hari lupus Sedunia. Adanya peringatan Hari Lupus bertujuan untuk meningkatkan kepedulian masyarakat terkait penyakit  yang cukup mematikan ini. 💜 Lupus sendiri merupakan penyakit autoimun kronis yang menyerang sistem kekebalan tubuh manusia. Akibatnya, tubuh yang seharusnya melindungi organisme asing seperti virus dan bakteri justru menyerang sel-sel, jaringan, serta organ tubuh lainnya yang sehat. 💜 Semenjak ditemukannya penyakit ini, belum ada satu pun obat yang bisa menyembuhkan. Bahkan pengobatan yang dilakukan orang dengan lupus (odapus) hanya bertujuan untuk meringankan gejala saja dan meminimalisir terjadinya kerusakan pada organ yang terkena lupus. 💜 Oleh karena itu, lupus dapat digolongkan sebagai penyakit kronis yang bisa kapan saja membahayakan pengidapnya. Sebab, dalam beberapa kasus, odapus tidak bisa menebak kapan kondisinya mengalami penurunan drastis dan kapan ia akan terlihat sehat. #BergerakBersamaMasyarakatMenujuPurwosariBermart #PurwosariBermartabat #worldlupusday #worldlupusday2021 #makelupusvisible (di Purwosari) https://www.instagram.com/p/COsWVE5pstx/?igshid=10atipnk2kyls
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