What I wouldn't give to feel those feels...
*in a whispered voice*
Tell me.. What's it like? 🥺
#rarediseaseawareness #chronicillnessbabe
#BehcetsDisease #behcetsbaddie
Behçet’s disease is rare, systemic, and often dismissed—until it isn’t. It can affect the mouth, eyes, skin, joints, blood vessels, and brain, with unpredictable and serious flares. Awareness matters. Early recognition saves lives. 🔗 zurl.co/F50Gz
#BehcetsDisease #RareDisease #AiArthritis
"I know how you feel..."
Really? Do you??
#behcets #behcetsdisease
www.behcets.org/reference/sy...
This report describes a rare case of a patient who presented with unilateral necrotizing scleritis as the main ocular manifestation of Behcet’s disease.
bit.ly/cjo_necrotiz...
#Ophthalmology #BehcetsDisease #Scleritis #NecrotizingScleritis #EyeDisease
FYI: LucidQuest Views >>> Rare Diseases Weekly News – August 7th 2025 #News #Behcetsdisease #DMD #drugdevelopment #EMA Comment below!
ICYMI: LucidQuest Views >>> Rare Diseases Weekly News – August 7th 2025 #News #Behcetsdisease #DMD #drugdevelopment #EMA Comment below!
LucidQuest Views >>> Rare Diseases Weekly News – August 7th 2025 #News #Behcetsdisease #DMD #drugdevelopment #EMA Comment below!
Recognizing clinical and genetic clusters in pediatric Behçet’s disease can guide earlier diagnosis and personalized treatment approaches.
#Meded #SoMe4PedSurg #Pediatrics #PediatricRheumatology #BehcetsDisease #AutoimmuneDisease #PrecisionMedicine
link.springer.com/article/10.1...