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.”
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