Eve smith
@evemdsmith_evePaediatric rheumatologist, University of Liverpool, EATC4Children, Alder Hey. Interested in everything lupus, & raising awareness of paed rheum @WORDDay_org
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📢 Postdoc position available @crow_lab @InstitutImagine to study lung inflammation seen in interferonopathies #SAVI #COPAsyndrome #RareDiseases Do not hesitate to apply! welcometothejungle.com/fr/companies/i…
Very honoured and delighted that my LUNG-in project has been funded by the @ANR #ANRJCJC Looking forward to better understanding the lung inflammation seen in interferonopathies @crow_lab @InstitutImagine! #RareDiseases
The dates are in for Ten Topics in Rheumatology 2025 Save the 3rd and 4th July 2025! tentopics.com
There’s less than two weeks left to submit your abstract for #LUPUS2025! Present your groundbreaking research and be part of advancing #lupus care and treatment. 💜 Submit your abstract by 18 November 2024 at 23:59 EST: bit.ly/3UN5FvG #Rheumatology #Rheum #LupusResearch
Congratulations to our research teams who have successfully secured £1.1m from the @NIHRresearch to improve the delivery of research across Liverpool 👏 @CRFalderhey @AlderHeyRes
🎯New paediatric targets show promise in lowering damage, healthcare costs & improving quality of life. Looking forward to future results, including the NEPHROTARGET study🔎 & innovative tools to make this approach accessible. #T2T #cSLE #lupus #RareRheumatology @evemdsmith_eve
Interested in a PhD in Neuroimmunology? Keen to find the answers to important questions in Neuroimmunology? Looking for a challenging programme?
PhD studentship alert (Neurobiology)!!!!- Jan 6th, 25last date. We offer a fully funded PhD project through the Northwest Bio- DTP partnership in collaboration with Prof Julia Edgar (Glasgow) @JuliaEdgar1, Dr Cheryl Hawkes, Dr Neil Dawson @neilneuro and Prof. Gourine (UCL)-
Glad you enjoyed it and likewise thank you @JARProject for all that you do!
Always a pleasure to hear @evemdsmith_eve speak. Speaking at @UCD_CAR #RareRheumatology Conference. Fantastic developments in the world of Lupus. Thank you for all you do Dr Eve and the team at @AlderHey
🔥🔥VERY IMPORTANT #SLE #lupus article: journals.sagepub.com/doi/10.1177/09… Similar to adult studies: 26% of well-treated pediatric SLE patients were ANA negative at two years. LESSON TO LEARN BY ALL HEALTHCARE PROVIDERS: When you get a new patient previously diagnosed with SLE by another…
⏳ Time is running out! Have groundbreaking research on pediatric SLE? Share it at #LUPUS2025 to drive advancements in the diagnosis, care, and treatment for young patients. Submission deadline: November 5: bit.ly/4hlfaf7 Let’s shape the future of pediatric #lupus care!
🗓️Coming up! Join "Rare Rheumatology," organised by UCD Dublin, on Nov 6th. Our chair, Dr. Eve Smith, will present: "Patient Centred Target Drive: Working to Improve Outcomes for Childhood Systemic Lupus Erythematosus Patients." 🚨Don't miss it #cSLE #Pediatric #lupus
We are delighted to announce the full programme for our online conference taking place next week November 6th: Rare Rheumatology, Niche Conditions and Future Directions. Registration is still open via the link below: forms.gle/ESaZCqRTDJJQMc…
🌟Meet Trinity Beesley, an 11-year-old girl from the UK, living with Juvenile Idiopathic Arthritis (JIA). Watch her inspiring story here👉 pulse.ly/oaamz1r9yr @thebeesleybuzz @jarproject
✅ Vaccines don't worsen lupus symptoms. In fact, they help protect against infections, which could be more severe in #lupus patients. Always consult with your doctor for personalised advice. They will tell you which vaccination schedule is safe & effective for you #KickLupus
Our new Systemic JIA / Still's disease resource is now on it's way to rheumatology hospitals. #ThinkJIA #StillsDisease #sJIA #SystemicJIA #PaedRheum #arthritis #rheumatology #PaediatricRheumatology @rheumatologyuk @NICEComms @pscommissioner
Project CHANGE was developed in collaboration with individuals with lupus, community organizations, healthcare providers, and researchers to get to the root of healthcare inequities and ensure that every person living with lupus has access to the best possible care. Hear from…
🆕Latest study from Hanif M et al. @evemdsmith_eve shows that disease activity (AMS/PGA) and factors like methylpred exposure and baseline damage are KEY predictors of damage in cSLE #lupus 💡Highlights the need for practical strategies to reduce disease activity & Tx toxicity ⬇️
✅ Are you taking care of patients with #Cogan's syndrome? Check the French #Recommendations for the #diagnosis and #treatment of this very rare inflammatory disease, including a detailed list of differential diagnosis 👍 Open-access DOWNLOAD at: authors.elsevier.com/sd/article/S02…
**job vacancy** Calling all data scientists Come work with us 👇🏼👇🏼👇🏼👇🏼 Be part of the UK Kidney Ecosystem- an exciting transformation of research & bring our ‘science pipeline’ to life
📢We are seeking to recruit a Data Scientist to support a wide range of research projects within the newly funded LifeArc-Kidney Research UK Translational #Research centre for rare #kidney diseases led by Dr Louise Oni. Apply ➡️ tinyurl.com/yc2ytutt @LivuniILCaMS @LivUniHLS
A huge thanks to all the amazing #pedsrheum, pediatric nephrologists, other experts, patients and caregivers who worked with us to make this dataset. @angela_migowa @PedsLupusRenal @TamarPedsRheum @elissa_weitzman and so many others!
🚨Landmark study describing the FIRST standard dataset for childhood lupus registry research!!! -Many registries collect cSLE data -Differences in data collection is a major barrier to collaborative research -This effort will pave the way for advancing cSLE research 🤝🔬🩺
🗣️Excited to share our paper defining a standard dataset for cSLE registry research! 🩺Our team developed a core dataset to harmonize cSLE data collection and promote international collaboration to advance cSLE research! ard.bmj.com/content/annrhe… @evemdsmith_eve @AlexandreBelot
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