🗓️ Tuesday, February 24 at 9:30am 📍 Big Night Live, Boston | Virtual options also available Through discussions and stories, Rare Disease Summit will spotlight innovation across drug development, diagnostics, funding, and policy – while centering the voices of patients and caregivers driving change alongside industry and research leaders. Speakers include: ✅ Dr. Wendy Chung, Chief of Pediatrics, Boston Children's Hospital ✅ Kristen DeAndrade, Founder and Executive Director, Little Legs Big Hea

17K views · 60 reactions | Stars bravely sharing rare disease stories in 2025! #CelebHealth #OliviaNewtonJohn #SelenaGomez #LadyGaga #Awareness2025 | Star Moment | Facebook

Today is #RareDiseaseDay 2019! Watch and share the official Rare Disease Day 2019 video to see Lorena's story of living with Phelan-McDermid syndrome. Help raise awareness to break isolation for people living with a rare disease! #ShowYourRare National Organization for Rare Disorders, Inc. (NORD) Rare Diseases South Africa Rare Disease UK Rare Voices Australia Canadian Organization for Rare Disorders BBC News The Mighty BBC Stories | Rare Disease Day

On Rare Disease Day, discover Zuzia's story. Get inspired by her positivity and learn how the EU is working to improve awareness, diagnosis and treatment of rare diseases. #ICountonEurope | European Parliament

Like to help me raise awareness for rare diseases 😁 #raredisease #raiseawareness#607 | Lukas Caldwell

Join #LightUpforRare and raise awareness for 300 million people living with a rare disease | Rare Disease Day