Lupus Trust @lupustrust
The Lupus Trust was set up as a registered charity in 1991. Its aim is to support lupus research at Guys Hospital & raise lupus awareness. lupus.org.uk London Joined March 2012-
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Very true! 🙄 #chronicpain #autominnunedisease #invisibleillness #lupusSucks #lupusfighter #chronicillness #lupusLife #lupuswarrior #lupus #lupustrust #lupusawareness #lupustruth #lupusfact
This happened to me recently and I reacted exactly the same way 😁 #chronicpain #autominnunedisease #invisibleillness #lupusfighter #lupusSucks #chronicillness #lupusLife #lupuswarrior #lupus #lupustrust #lupusawareness #lupustruth #lupusfacts
I find myself trying to negotiate with my body saying 'I know there has to be some pain, but could it be a bit less than this?' #chronicpain #autominnunedisease #invisibleillness #lupusSucks #chronicillness #lupusLife #lupuswarrior #lupus #lupustrust #lupusawareness
And so they should! #chronicpain #autominnunedisease #invisibleillness #lupusfighter #lupusSucks #chronicillness #lupusLife #lupuswarrior #lupus #lupustrust #lupusawareness #lupustruth #lupusfacts
Very true, it's exhausting explaining over and over why you aren't 'better yet' or how 'yes, you're still in pain'. #chronicpain #autominnunedisease #invisibleillness #lupusfighter #lupusSucks #chronicillness #lupusLife #lupuswarrior #lupus #lupustrust #lupusawareness
I start a story, lupus brain fog kicks in and I can't remember where the heck I was going with it, so I just keep going in the hope I'll eventually remember. 😆 #lupus #lupustrust #lupusawareness #brainfog #lupusbrainfog #chronicillness #autoimmunedisease #chronicpain
We all do this. It saves continually complaining or explaining how lupus makes you feel. 🙄 #chronicpain #autominnunedisease #invisibleillness #lupusfighter #lupusSucks #chronicillness #lupusLife #lupuswarrior #lupus #lupustrust #lupusawareness #lupustruth #lupusfacts
Sadly true. 🫤 #chronicpain #autominnunedisease #invisibleillness #lupusfighter #lupusSucks #chronicillness #lupusLife #lupuswarrior #lupus #lupustrust #lupusawareness #lupustruth #lupusfacts
Accurate! 🙄 #lupus #lupustrust #lupusawareness #lupuslife #chronicillness #chronicpain #invisibleillness #autoimmunedisease
Another very accurate description. 🫤 #chronicpain #autominnunedisease #invisibleillness #lupusfighter #lupusSucks #chronicillness #lupusLife #lupuswarrior #lupus #lupustrust #lupusawareness #lupustruth #lupusfacts
These are all things we try to explain to others but they often just don't understand. 🫤 #chronicpain #autominnunedisease #invisibleillness #lupusfighter #lupusSucks #chronicillness #lupusLife #lupuswarrior #lupus #lupustrust #lupusawareness #lupustruth #lupusfact
A sadly accurate description. As you get older more aches and pains come along so I can't remember when I last had a completely pain free day, something others take for granted. #chronicpain #autominnunedisease #invisibleillness #lupus #lupustrust #lupusawareness
Exactly! 😊👍 #chronicpain #autominnunedisease #invisibleillness #lupusfighter #lupusSucks #chronicillness #lupusLife #lupuswarrior #lupus #lupustrust #lupusawareness #lupustruth #lupusfacts
🫤🙄 #chronicpain #autominnunedisease #invisibleillness #lupusfighter #lupusSucks #chronicillness #lupusLife #lupuswarrior #lupus #lupustrust #lupusawareness #lupustruth #lupusfacts
I'm quite sure you know what I mean! 🙂 #chronicpain #autominnunedisease #invisibleillness #lupusfighter #lupusSucks #chronicillness #lupusLife #lupuswarrior #lupus #lupustrust #lupusawareness #lupustruth #lupusfacts #flare #flareup
This is really accurate, of course we'd like a cure but 'manageable' would be great. At least then we'd be able to do more, plan things in advance and have some sort of 'normal' life. #lupus #lupustrust #lupusawareness #lupuslife #lupuswarrior #chronicillness #chronicpain
The fact that we know we are going to pay later for any activity we decide to do is a really sad state of affairs, most people have no idea what that's like. We're constantly asking ourselves 'is it worth doing it'? #lupus #lupustrust #lupusawareness #chronicillness
The Lupus Trust is funding a study looking at how menopause and HRT affect women with lupus. It is being led by Melanie Sloan at Cambridge University. The team are looking to recruit a researcher to help with this study, either full time or part time: jobs.cam.ac.uk/job/45849/
Laurent ARNAUD @Lupusreference
17K Followers 595 Following MD, PhD | Professor of #Rheumatology | #Lupus #SLE | #Digitalhealth | President of @SLEuroSociety | @ERN_ReCONNET Disease Coordinator for Lupus & RP 🇪🇺LUPUSUK 💙 @LUPUSUK
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@lupustrust I got one for you that gets under my skin. “Why do you have to go to so many doctor appointments?” REALLY?🤨😡
For #LupusAwarenessMonth, we hear from one of our Consultant Rheumatologists, Chris Wincup, about upcoming research at @KingsCollegeNHS. He said: "It is a very exciting time to be researching Lupus and we intend to share some of these advances ..." Read➡️bit.ly/3Fmr1bf
Visit lupus.org.uk for helpful resources, the latest news on research and donation links if you'd like to offer your support. 💜 @lupustrust #lupusawareness #livingwithlupus #lupustrustuk
What is #Lupus? Around 50,000 people in the UK are thought to have Lupus. October is #LupusAwarenessMonth. Please read our post, learn about the symptoms of Lupus and the organisations that offer support to people with the disease. @LUPUSUK @HibbsLupusTrust @lupustrust
Thank you sincerely to everyone who voted . I literally never. Especially with such a beautiful line up of nominee's. #winner #TV personality excellence award. ✨️ Thanks to @RB_Official @leemorgan_mgnt @paulinebriscoe @lorraindublin My next next door neighbour and my mum 🥰
Wow, this is spot on! It's how I ended up pretty much completely isolated. I have one friend who regularly checks in with me. Everyone else pretty much buggered off - this is why I started Spoonie on a Mission! We need to support one another!!
🙁 #lupusfighter #lupusSucks #chronicillness #lupusLife #lupuswarrior #lupus #lupustrust #lupusawareness #lupustruth #lupusfacts #chronicpain #sickofbeingsick
@lupustrust It's bloody well true! Spent Sunday with a friend, having lunch and sitting, talking quietly, in a bookstore for a few hours. Seemed fine - we had a good time. Been suffering with less sleep, more tiredness, and higher levels of pain since Monday morning. Can't. Fecking. Win.
Grateful to @MedResFdn for supporting this exciting neuroinflammation academic meeting in Edinburgh on 7th & 8th Nov. Registration & abstract submissions open – book now! edin.ac/3Zno6If #lupus @HuntLabEdin @LupusResearch @lupustrust @LupusEurope @LUPUSUK @NHSEngland
Please everyone get your COVID XBB subvariant vaccine... FDA approved today! Yay! If you have #Lupus , #SLE, #sjogrens or immunocompromised in any way, especially get it! Anti-vaxers, just ignore my Tweet (but I would love some of you to change your mindsets)... Donald Thomas, MD
Today, we took action approving & authorizing for emergency use updated COVID-19 vaccines formulated to more closely target currently circulating variants & to provide better protection against serious consequences of COVID. Here’s what you need to know: fda.gov/news-events/pr…
@Volsicle @lupustrust My immune system is apparently the equivalent of an under-enriched Jack Russel terrier. It will chew through **anything**.
Follow me guys. @lupustrust #lupus #chemotherapy