RT @RAIRDA_org: Research results show the importance of COVID vaccination and a personalised approach for RAIRD patients 👉.

Nominate LUPUS UK (Charity No 1200671) for a chance to win £1,000 in the #MovementforGoodAwards.The first draw of 2025 will take place on Monday, so please vote by midnight on Sunday 26th Jan: �. As a small charity, this grant will make a huge difference💜

Join us in March for our Virtual Dog Walk, an exciting new fundraising challenge for 2025!! . For more information and to sign up, visit: #Lupus #SLE #VirtualDogWalk #Fundraising

RT @LUPUSUK: The University of the West of England (UWE), Bristol, is looking for individuals of ethnic minorities diagnosed with Systemic….

RT @LUPUSUK: The University of the West of England (UWE), Bristol, is looking for men diagnosed with Systemic Lupus for a survey study. You….

RT @EATC4Children: Amongst friends for lunch and an information sharing discussion today, thanks so much to @LUPUSUK for braving this chill….

The National Office is now closed for the holidays and will re open on 02/01/25. THANK YOU to our incredible fundraisers, volunteers, trustees, ambassadors, donors, and all who supported the charity throughout 2024 in helping us make a difference for people living with #lupus 💜

The University of the West of England (UWE), Bristol, is looking for men diagnosed with Systemic Lupus for a survey study. Your survey response will help develop appropriate support for SLE patients in the UK. Take part here:

The University of the West of England (UWE), Bristol, is looking for individuals of ethnic minorities diagnosed with Systemic Lupus for a survey study. Your participation will help in developing suitable support for SLE patients in the UK. Take part here:

Join over 9,000 people who have already spared 60 secs to take @WeAreSRUK's online symptom test. #BePartOfTheAnswer by helping to unlock potential breakthroughs in diagnosis and treatment for debilitating autoimmune conditions.

Spare 60 seconds to take @WeAreSRUK's online Raynaud's symptom test. See if you could have Raynaud's and #BePartOfTheAnswer in helping unlock potential breakthroughs in diagnosis and treatment for debilitating autoimmune conditions like scleroderma.

What does good care & treatment for rare disease mean to you?.The Rare Disease Quality Statement Project need your input to develop a set of quality statements for rare disease. Complete the survey on their site: Or read our FAQs:

What is CAR-T cell therapy and what does it mean for people with lupus?.You may have seen news articles about a new treatment called CAR-T. It's still in the research phase, with more trials starting soon. You can find out more in our FAQs post:

RT @dalilatm: 🤩 Since our 1st meeting in 2019, time has flown by! Fast forward to today’s meeting with 2️��� wonderful guest speakers helping….

It’s #BoneAndJointWeek and we’re calling for integrated care that supports people with MSK conditions. Living with chronic pain alongside mental health struggles like anxiety & depression is all too common. We need accessible, holistic care to improve wellbeing.#JoinedUpForJoints

Musculoskeletal (MSK) health is essential for a healthy, productive life. On World Arthritis Day, we are advocating for more collaboration health and social care to prevent and manage MSK conditions more effectively. #WAD #JoinedUpForJoints #WorldArthritisDay @WeAreARMA

RT @Yuz6Yusof: It’s #Lupus Awareness Month in the UK 🦋. What a better way to celebrate and increase awareness by exchanging knowledge and e….

RT @birdbathcharity: October is #LupusAwarenessMonth Visit @LUPUSUK for advice and support. BIRD also has a series of #Lupus podcasts recor….

Today marks the start of #LupusAwarenessMonth 💜. This important month takes place during October every year in the UK and gives us the opportunity to raise awareness of #lupus amongst the public and medical profession. Get involved here:

We have one filming slot available for our upcoming clinical trial video, aimed to help people better understand what’s involved in them. Please share with anyone who may be interested! . For more information, contact Nakita@LupusUk.org.uk. #ClinicalTrial #Lupus #Research #SLE.