Haemophilia Foundation of Nigeria

19/06/2026

Today we honor the strength and resilience of everyone living with sickle cell disease. On this World Sickle Cell Day, let’s raise awareness, support affected families, and advocate for better care and brighter futures. Together, we are stronger. Together, we build hope.

HFN StrongerTogether

14/06/2026

🩸 World Blood Donor Day 2026

As an advocate for people living with bleeding disorders, I celebrate and thank every blood donor today.

Many people do not realize that blood and plasma donations play a vital role in the production of life-saving treatments used by people with haemophilia and other bleeding disorders. Your donation helps make treatment possible, prevents complications, and improves quality of life.

Behind every blood donation is a chance for someone to live healthier, dream bigger, and thrive.

This World Blood Donor Day, I encourage all eligible individuals to become regular blood donors. Your generosity can save lives and bring hope to countless families.

Donate blood. Give hope. Save lives. ❤️🩸

SaveLives HFN OneDropOfHumanity

18/04/2026

MINISTERIAL PRESS BRIEFING BY THE COORDINATING MINISTER OF HEALTH & SOCIAL WELFARE

PROF. MUHAMMAD ALI PATE
To Commemorate the 2026 World Haemophilia Day
Theme:
DIAGNOSIS – The First Step to Care

& OFFICIAL FLAG-OFF OF THE ROAD TO CLOT INITIATIVE

& LAUNCH OF THE NATIONAL BLEEDING DISORDER REGISTRY IN NIGERIA

April 17, 2026

12/03/2026

The treatment landscape for haemophilia is changing rapidly, bringing new possibilities for improved care and quality of life.

Join us for an upcoming webinar hosted by the Haemophilia Foundation of Nigeria (HFN) – Medical and Scientific Advisory Committee (MaSAC):

New Treatment Options in Haemophilia: Extended Half-Life, Mimics, and Rebalancing Therapies

🎤 Speaker: Prof. T**i Adeyemo
📅 Date: 28 March 2026
⏰ Time: 10:00 AM
📍 Venue: Zoom - https://us06web.zoom.us/j/81006227625?pwd=lUHdUZkYOv9DuZ0EQrMIc6KOr5QAW4.1

This session will explore emerging therapies that are reshaping haemophilia treatment and what they mean for care in our setting.

Healthcare professionals, researchers, and advocates are warmly invited to join the conversation.

HFN

01/03/2026

23/02/2026

We need to speak more on this topic

Are you a woman or girl with a thinking about a future pregnancy?

Join the WFH webinar on March 6 to learn why preparation before, during, and after pregnancy matters. Hear from healthcare professionals and women from our community as they discuss postpartum hemorrhage, risk factors, and how to advocate for the care you deserve.

📅March 6 | 8:00 a.m. to 9:30 a.m. EST
Learn more and register now: https://bit.ly/4ape3tt

23/02/2026

What you are watching is not just a van being built. It is hope being welded together. It is access being created for persons who bleed silently. It is answers traveling toward families who have waited too long. From an empty shell to a moving lifeline, every screw, every fitting, every detail carries a promise. Road to Clot is coming. And it is carrying hope with it.

23/02/2026

A diagnosis can change everything. But awareness can change outcomes.
When people understand haemophilia, they recognize symptoms earlier and seek help sooner. This will help prevent complications. ROAD TO CLOT is initiated to make the invisible visible. Because awareness is not just information. It is protection.

19/02/2026

Behind every person with haemophilia is a family learning, adapting, and hoping. Parents who stay awake at night. Siblings who learn to be careful.
Families who become stronger through challenges they never expected.

HFN honors not just the patient, but the entire family journey. Because haemophilia affects more than one person. It shapes entire lives.

19/02/2026

For most people, bleeding stops. For someone with haemophilia, bleeding can continue silently inside the body, especially in joints and muscles. This is not just bleeding.
It is pain, fear and uncertainty.

We want you to know. As understanding leads to compassion.Compassion leads to action.