World Federation of Hemophilia/LinkedIn
Mar 2, 2026, 11:06
Advancing Visibility, Research, and Equitable Care on Rare Disease Day – WFH
World Federation of Hemophilia shared a post on LinkedIn:
“Rare Disease Day
For the World Federation of Hemophilia, this is a reminder that rare bleeding disorders deserve visibility, research, and equitable access to care.
At the WFH Congress 2026 in Kuala Lumpur, dedicated sessions will spotlight rare Bleeding Disorders, from complex clinical cases and emerging therapies to lived experiences and advocacy.
Let’s advance knowledge, strengthen community, and ensure no one is overlooked.
Explore the sessions and plan your experience.”
Other posts about World Federation of Hemophilia on Hemostasis Today.
-
Jul 18, 2026, 15:49Heghine Khachatryan: ISTH 2026 – Final Day Highlights
-
Jul 18, 2026, 15:40Marc Carrier: New ISTH 2026 Data May Simplify DVT Evaluation During Pregnancy
-
Jul 18, 2026, 15:38Hermine Sayiyan: Dreams Do Come True – Often When We Least Expect Them
-
Jul 18, 2026, 15:31Alyaa Al-Mughairy: Presenting Real-World Emicizumab Data at the ISTH 2026 Middle East Summit
-
Jul 18, 2026, 15:25Rim Diab: Presenting Protein S Research as a Rebalancing Strategy at ISTH 2026
-
Jul 18, 2026, 15:22Owen McCarty: Honored to Speak at the 1st Mediterranean Platelet Symposium
-
Jul 18, 2026, 15:18Strengthening Regional Learning for Hemophilia and Sickle Cell Disease Care – Novo Nordisk
-
Jul 18, 2026, 14:54Fabien Mselati: Reflecting on 25 Years of Hemophilia Progress
-
Jul 18, 2026, 14:50Nikola Pantic: Grateful for the People Who Made ISTH 2026 Special