Are you a young person aged 18-30 years old living with #lupus or in the middle of receiving a diagnosis? Come along to our next Virtual Young People Lupus Group, in collaboration with The Wren Project. Register here: https://bit.ly/3LQNlAE 💜

This month is #RaynaudsAwarenessMonth, which raises awareness for Raynaud's phenomenon, a condition affecting blood circulation in fingers and toes in many people living with #lupus. (1/2)

Our Virtual Dog Walk is officially underway! 🐾 Walk, donate, or cheer us on! Every step helps raise vital funds, awareness, and hope for the #lupus community. 💜 There’s still time to sign up! Join us any time this month by setting up your JustGiving page: https://bit.ly/3NyVPg9  #VirtualDogWalk 🐶

This month is #NationalHeartMonth. #Lupus can impact heart health and it is important to know more about its effects. You can find out more about how lupus affects the heart through our publication here: https://bit.ly/4bkGMk6 #LupusAwareness #LupusSupport #LupusCommunity #SLE

Chelsea, our Young People and Family Support Officer, has shared their experience of living with cutaneous lupus. You can watch their presentation on our YouTube Channel (@LupusUkOfficial) or by clicking the link below. 🔗https://youtu.be/KTGtjo8tFq8 #Lupus #SLE #LupusCommunity #CutaneousLupus

Skilled at explaining complex information clearly and engagingly, with strong knowledge of the UK healthcare system? Join us as a Policy and Communications Officer and play a key role in shaping Lupus UK’s policy work. Apply by 12th February: https://bit.ly/3ZlCEsZ

Our Virtual Dog Walk is back for 2026! Have you signed up yet? 🐾 For more info and to create your JustGiving page, visit https://bit.ly/3NyVPg9 By joining in, donating, or cheering us on, you’re helping to provide support, awareness and hope for the #lupus community. 💜 #LupusAwareness #SLE #Dog

NICE have recommended that a new treatment, obinutuzumab, can be used in combination with mycophenolate mofetil (MMF) to treat some patients with lupus nephritis in the NHS in England and Wales.  👉 Learn more at https://lupusuk.org.uk/latest-news/ #Lupus #LupusNephritis #Obinutuzumab

The ADAPT trial is now recruiting! Researchers from the University of Cambridge and UEA are inviting people with autoimmune diseases who experience daily fatigue to take part in an online research study investigating Pilates and Tai Chi classes! 🔗 Visit tinyurl.com/ADAPTweb for further information.

Today is #InternationalDayOfAcceptance which promotes social acceptance and inclusion for individuals with #disabilities. Living with a disability like #lupus can be difficult to accept and it's okay if you don't. Here are some things that can help with self acceptance:

Join our email community! ✨ From January 2026, our E-Newsletter will be sent monthly, bringing you the latest news and events, research updates, blog articles, volunteer updates and more. Sign up today to stay in the loop! 📩 🔗https://lupusuk.org.uk/newsletter-sign-up/ #Lupus #SLE #LupusCommunity

We're hosting virtual events for Parents/Carers & Young People! 💻 You can find all upcoming events for 2026 at https://lupusuk.org.uk/youth-events/. You'll also be able to sign up to our mailing lists. 📅 Our next Parents / Carers meeting will take place on January 29th. We hope to see you there! 💜

Did you know that we created a 3-part series on lupus, and CAR T-Cell Therapy? If you want to learn more about how CAR T-Cell Therapy is being explored as a potential lupus treatment and clinical trials involving it, scan the QR code for more information or visit https://bit.ly/4rgNRrv

Wishing everyone a very #HappyNewYear from all of us at Lupus UK! ✨💜

Thank you to our wonderful community and everyone who supported us in 2025! Your kindness has made a real difference for people living with #lupus.💜 We wish you a safe & happy holiday! 💜

The General Pharmaceutical Council (GPhC) makes sure pharmacy is safe and effective for patients and the public. They are inviting patients, carers, and members of the public to share their views on pharmacy services across Great Britain. There are two ways to get involved:

Are you passionate about creating high-quality, trustworthy, and up-to-date health resources for the #lupus community? Applications are now open to join the Lupus UK staff team as a Health Information Officer! 🔗Apply now: https://bit.ly/456zTie 🗓️ Closing 4th January 2026.

Chelsea, our Young People and Family Support Officer, has shared their experience on what it's like to live with lupus as a young person. You can watch their presentation on our YouTube Channel (@LupusUkOfficial) or by clicking the link below. 🔗https://youtu.be/StdzyINaI8M

If you're a Lupus UK member, you'll receive your membership renewal letter soon (if you haven't already)! Alternatively, you can renew your membership online at https://lupusuk.org.uk/join-lupus-uk/ 📱💻

One Mission, 5 aims & 10 Year Goals. Read about your new Lupus UK Strategy at https://lupusuk.org.uk/strategy/

Looking to purchase from our shop? Please place any orders by Thursday 18th December. Orders placed after 2pm on this date will be sent out on Friday 2nd January 2026. Our mystery pack of 5 Christmas Cards are still available for purchase! Visit https://lupusuk.org.uk/store/ for more Thank you 💜

Lupus UK Head Office will be closed from 24th December - 2nd January 2026. Helpline and support services will resume from 5th January. You can still find information at www.lupusuk.org.uk, or please contact 111 or 999 If you require immediate support during this time. Enjoy the festive period! 💜

This #InternationalVolunteerDay, we would like to say a massive THANK YOU to all our amazing volunteers who dedicate their time to help our work supporting people with #lupus. 💜

Did you know, we provide ReciteMe accessibility and language support online?  You can access a customisable toolbar on our website to read and understand content in a way that suits your needs.

Have you seen our birthday video celebrating 35 Years of Lupus UK? 💜 Watch the full video on our YouTube channel here: https://youtu.be/F432b3u4Ju8?si=fKukFsNYrusg6Rz9

Thank you to the wonderful team at Guy's Hospital for holding an awareness stand during Lupus Awareness Month last month! 💜

During the colder months, viruses like flu, COVID-19, and respiratory syncytial virus (RSV) circulate more widely. The NHS is offering free vaccines this winter to help protect those most at risk. For more information on winter vaccinations, read our article at: https://bit.ly/4impV1O

The 2026 Edgar Stene Essay Prize is open now! Participate to share your story of family life with lupus. You can find the competition theme, rules, and how to enter on our website here: https://lupusuk.org.uk/2025/11/20/edgar-stene-prize/

Aged 11-18 years and in full-time mainstream education? Living with a long-term health condition like Lupus? Complete the INSCHOOL Needs Assessment survey to help improve the school lives of other young people with health conditions - and be entered to win a £50 GiftPay voucher!

This year for our 35th Birthday, we are asking you to Pick & Mix our fundraising campaigns and support us by raising vital funds for EVERYONE in our community living with lupus or waiting for a diagnosis. 💜

35 Years of Lupus UK 💜 Full video out on our YouTube channel now: bit.ly/4qZW3Mv 🎥 #lupus #LupusUK

Dr Yuzaiful Yusof, Associate Professor and Consultant Rheumatologist, is taking on the ultimate challenge of The Great World Race (7 Marathons, 7 Continents, 7 days) to raise vital funds for Lupus UK and Sjögren’s UK! 🌍 Support Dr Yusof here: https://gvwhl.com/VZWJS 💜

For one year only, you can purchase 5 mystery packs of #Christmas cards for £10 over on our shop! Get yours now at https://lupusuk.org.uk/store/Mystery-Pack-of-5-Christmas-Cards-p779456958 💜 Order before December 12th to receive your packs on time and avoid disappointment! ✉️ #ChristmasCards

Come and join the Leeds Lupus Group for our next Coffee and Chat meeting on Saturday 8th November from 12:00pm to 2:00pm. We are meeting at Starbucks (Leeds City Point), 9-11 St Pauls Street, King Street, Leeds, LS1 2HL. Everyone is welcome to join! 💜

Celebrating 35 Years of Lupus UK. 💜 Full video out 14.11.25

Today marks the final day of #LupusAwarenessMonth Thank you to everyone who took part, whether by learning about #lupus, fundraising, resharing content or showing support, your involvement has made a real difference. 💜

You may have seen “CAR-T cell therapy” in the news recently as a potential new treatment for lupus. Want to learn more? Watch our 3-part series over on YouTube! - What is lupus?  - What Is CAR T-Cell Therapy? - Clinical Trials with CAR T-Cell Therapy Watch here: http://bit.ly/3Wh6rRX #Lupus #CarT

Invisible disabilities are conditions not immediately obvious to others and can often go unnoticed. Even though you might not see them, they can significantly impact a person's life.

Did you know that 35% of people with #lupus report symptoms of hairloss? For more information on symptoms of lupus, visit www.lupusuk.org.uk/the-symptoms/ Do you experience hairloss? #LupusAwarenessMonth #KnowLupus #MakeLupusVisible #SLE #Hairloss

Come and join the Leeds Lupus Group for our next Coffee and Chat meeting on Saturday 8th November from 12:00pm to 2:00pm. We are meeting at Starbucks (Leeds City Point), 9-11 St Pauls Street, King Street, Leeds, LS1 2HL. Everyone is welcome to join! 💜

ENCA, the Global foundation for Children, and families, with Juvenile rheumatic diseases, is hosting a free online event on important topics for patients and families affected by juvenile rheumatic conditions.  For more information and to sign up, visit www.encanetwork.org/event

#Musculoskeletal (MSK) conditions like #lupus affect people at every age and hit hardest in the most deprived communities. (1/3)

Come and join the Leeds Lupus Group for our next Coffee and Chat meeting on Saturday 8th November from 12:00pm to 2:00pm. We are meeting at Starbucks (Leeds City Point), 9-11 St Pauls Street, King Street, Leeds, LS1 2HL. Everyone is welcome to join! 💜

#Lupus is an unpredictable condition that can turn everyday life into a challenge, but together, we can make sure nobody faces it alone.  Every donation to Lupus UK helps fund research, provide support, and brings hope to thousands of families. 💜

Did you know that 50% of people with #lupus report symptoms of headaches or migraines? For more information on symptoms of lupus, visit www.lupusuk.org.uk/the-symptoms/ Do you experience headaches or migraines?   #LupusAwarenessMonth #KnowLupus #MakeLupusVisible #SLE #Headaches #Migraines

From Wales to Australia! 🌍 We were thrilled to have Chloe Bayliss join our group meeting and share her inspiring #lupus journey 💜 Her story featured in our report for @lupusuk.bsky.social’s magazine — and now she has a copy all the way in Australia! 🇦🇺 So exciting! #Cardiff

“While I wouldn’t wish this experience on anyone, lupus taught me a powerful lesson: even on my weakest days, I am stronger than I ever imagined." This #LupusAwarenessMonth, Steph has shared her #lupus story, expressing the difficulty she experienced receiving a lupus diagnosis.

Come and join the Dorset Lupus Group for our next Coffee and Chat meeting on Saturday 11th October from 10:30am to 12:00pm. We are meeting at Haskins Garden Centre, Longham, Ferndown BH22 9DG Everyone is welcome to join! 💜

We’ve only gone and done it!? We’ve raised over £1000 in just 5 streams for @lupusuk.bsky.social with 14 more streams to go! Thank you @strakerplays.bsky.social for collab streaming with me today. I appreciate you so much! www.justgiving.com/page/lupusaw...

Today is #WorldMentalHealthDay, which raises awareness about mental health and considers how, together, we can help improve everyone's #MentalHealth.