Rare Disease Day/LinkedIn
Feb 3, 2026, 14:54
300 Million People, One Global Community – Rare Disease Day
Rare Disease Day shared a post on LinkedIn։
՛՛300 million people. One global community.
Rare diseases affect millions, yet research and funding is limited. Funding rare disease research is not only a moral imperative, it’s a smart, forward-looking investment. Discoveries in rare disease science often pave the way for treatments in cancer, neurology, and beyond, sparking progress across all of healthcare.
- Equality gives every disease the same level of funding.
- Equity for rare diseases means investing more where it’s needed most.՛
Stay updated with Hemostasis Today.
-
Nov 9, 2026, 13:48PF4-ELISA–Negative HIT: Are We Missing a New Class of Anti-PF4 Immunothrombotic Disease?
-
Nov 9, 2026, 13:07Nandini Sadasivam: Gene Therapy for Sickle Cell Disease and Thalassaemia
-
Nov 9, 2026, 13:04Raising Awareness of Bleeding Disorders in Women and Girls – EHC
-
Nov 9, 2026, 12:59Rahul Bohra: Exploring the Complex Mechanisms of Sickle Cell Disease
-
Nov 9, 2026, 12:53Three Years of Movement and Thrombosis Awareness in the Czech Republic – World Thrombosis day
-
Nov 9, 2026, 12:51Octavio Marques Pontes-Neto: Intensive Blood-Pressure Control Reduces Cardiovascular Events After Ischemic Stroke
-
Nov 9, 2026, 12:49Irma Bagdoniene: What Really Makes Us Live Longer
-
Nov 9, 2026, 12:47Imo Akpan: Announcing the 2027 Women’s Hematology Summit
-
Nov 9, 2026, 12:45Shadi Yaghi: Rethinking Antithrombotic Therapy After Stroke