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

31K views · 431 reactions | 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 | Facebook

41 reactions · 6 comments | Support Milaap Rare Disease Fund: https://milaap.org/stories/support-milaap-rare-disease-fund-yogita-sm Yogita stayed on ventilator support for more than 50 days. She had lost all movement in her body, from the neck down. But your support saved her. However, there are many who need a helping hand to overcome rare diseases. | Milaap | Facebook

22 reactions | Today is Rare Disease Day. There are an estimated...

Rare Disease Day is next week! Rare diseases are life-long and at least 80% are known to have a genetic basis. Not sure what to expect at a genetic counseling appointment? Intake Coordinator Donna Farren-Chavez, MS, provides an overview. To learn more about the Department of Medical Genetics and Genomic Medicine at Saint Peter’s University Hospital, please visit https://hubs.ly/H0mC2xs0 | Saint Peter's University Hospital | Facebook

1.2M views · 10K reactions | 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 | Facebook

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

February 29 is Rare Disease Day, raising awareness for rare diseases...