Michelle Holder

Sweet's Syndrome UK - HealthUnlocked. Join our community. It's free! 🐝🐝🌻🌻healthunlocked.com/sweetsyndrome #SweetsSyndrome #HealthUnlocked

Wishing you a Happy Easter!🌷🌷🌷

Differentiation Syndrome and Sweet Syndrome‐Like Overlap Following Venetoclax–Azacytidine and G‐CSF Therapy - Grafanaki - JEADV Clinical Practice - Wiley Online Library onlinelibrary.wiley.com/doi/full/10.10…

Happy St. David's Day! 🏴󠁧󠁢󠁷󠁬󠁳󠁿🏴󠁧󠁢󠁷󠁬󠁳󠁿🌼🌼

🌍 It’s #RareDiseaseDay 2026! 💜 Today we stand with the 300 million people living with a rare disease. Together, we’re showing our colours, raising awareness, and inspiring change by talking about what equity means to us. 👉 Read more: go.rarediseaseday.org/NEWS

Rare Disease Day is Sat.2/28th! We're Showing our Stripes to raise awareness for rare #autoinflammatory and immunedysregulatory diseases w/ advocacy efforts this week. Share, download or print this show your support, &share your story to raise awareness. #RareDiseaseDay

The latest Action Plan to implement the UK Rare Diseases Framework in England has just been published. Find out more geneticalliance.org.uk/news/latest-en…

Giant cellulitis‐like Sweet's syndrome induced by gilteritinib - de Luque‐Fernández - JDDG: Journal der Deutschen Dermatologischen Gesellschaft - Wiley Online Library onlinelibrary.wiley.com/doi/10.1111/dd… #SweetsSyndrome #GiantCellulitis #AML #Gilteritinib #FLT3Inhibitor

This time next week it’s #RareDiseaseDay! Let’s amplify the voices of the rare community and their experiences of inequity. Raise awareness NOW with our advocacy pack and use your voice to build an equitable future 👉 ow.ly/XXU450Yi4Ti #RareDiseaseDay2026 #Rarequity #RDD

From Aortitis to Sweet’s: The Immune Spectrum of G-CSF Adverse Events sciencedirect.com/science/articl… #SweetsSyndrome #DrugInduced #GCSF

"...distinguishing PNF from inflammatory mimics such as #SweetsSyndrome is critical..." Periocular #NecrotizingFasciitis, JAN 2026 frontiersin.org/journals/ophth… #NecrotizingSweets

This valentine’s day, show your love and care for #rare ❤️ For #RareDiseaseDay 2026 we’ll be sharing info sheets and a new policy report informed by lived rare experience, highlighting what drives inequity and what needs to change 👉 ow.ly/P1kY50Yek6U

🌍 Rare diseases affect over 300 million people, yet access to diagnosis & treatment still depends on where you live. 💜 Equity for rare diseases means is access to suitable care, regardless of where you live. Learn more 👉 go.rarediseaseday.org/equity #RareDiseaseDay #EquityForRare

#Behçets Disease: A Comprehensive Overview of Symptoms, Pathology, Genetics, and Treatment pmc.ncbi.nlm.nih.gov/articles/PMC12… #MVK #CIAS1

3 weeks to go until #RareDiseaseDay2026! 3.5 million people in the UK live with a rare condition. Our #advocacy pack shares practical tips on how to use your voice to build an #equitable future for everyone in the rare conditions community 👉 ow.ly/rpVF50Y9p27 #RareEquity

#SweetsSyndrome: A Case of Fever and Painful Erythematous Nodules Following a #Viral-Like Illness pmc.ncbi.nlm.nih.gov/articles/PMC12… #JointPain #Mobility #RareDiseaseDay

Time to #ShowYourStripes! 🦓 #RareDiseaseDay is Feb 28. A shirt or sweater can start conversations and demonstrate support for people living with #RareDiseases. It also funds our work to improve the health and lives of everyone with a #RareDisease. Shop: rarediseases.org/rare-disease-d…

Rare Disease Day 2026 Official Video youtu.be/7J1oTfoIOGw?si… via @YouTube

🧬 People living with a rare disease often wait years for answers. 💜 Equity means every person deserves the same chance to benefit from a treatment for their condition. 👉 Learn more: go.rarediseaseday.org/equity #RareDiseaseDay #EquityForRare#TreatmentAccess