Megan Adediran: The Power of Global Collaboration in Hemophilia Care
Megan Adediran, Executive Director at Hemophilia Foundation of Nigeria, shared a post LinkedIn:
“Attending the last World Federation of Hemophilia Congress was a deeply inspiring experience for me.
It was powerful to be in a space where advocates, healthcare professionals, researchers, caregivers, and people living with bleeding disorders from across the world came together with one shared goal — improving care and quality of life for our community.
Beyond the sessions and discussions, what stayed with me the most were the stories.
Stories of resilience, innovation, advocacy, and hope. It reminded me that while the challenges in low-resource settings like Nigeria are real, we are not alone in this journey.
The Congress strengthened my passion for advocacy and reinforced the importance of awareness, early diagnosis, access to treatment, and stronger health systems.
I returned even more determined to continue pushing for better support and visibility for people living with bleeding disorders, especially women and girls whose experiences are often overlooked.
Moments like this remind me that change is possible when voices, knowledge, and purpose come together.”
Other posts featuring Megan Adediran on Hemostasis Today.
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Sep 11, 2026, 03:10Chris Oung: Anticoagulation for Atrial Fibrillation with Intermediate Stroke Risk
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Sep 10, 2026, 21:33J. Meireles-Brandao: Lp(a)HORIZON and the Role of Inflammation in ASCVD
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Sep 10, 2026, 21:31Alejandro González Veliz: Pregnancy is a Cardiovascular Stress Test
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Sep 10, 2026, 21:30Tareq Abadl: Did You Know That the Type of Hemoglobin in Our Blood Changes Throughout Life?
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Sep 10, 2026, 21:30Sumyea Kabir: Apheresis Awareness Day – One Donor, One Procedure, One Therapeutic Difference
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Sep 10, 2026, 21:30Suhasini Sil: Excited to Share Our New Publication on HLA Beyond Histocompatibility
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Sep 10, 2026, 21:29Michael Meneghini: Your Calves Are Not Just for Walking
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Sep 10, 2026, 21:27One month until International Plasma Awareness Week – PPTA Europe
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Sep 10, 2026, 21:26John Strouse: Supporting Research to Improve Lives in Sickle Cell Disease