Hemophilia Philippines - Haplos Community

🎉 A Fresh Look. The Same HAPLOS Heart. 💚

Welcome to Hemophilia Philippines – HAPLOS Community!

You may have noticed that we've refreshed our page name and banner. While our look has evolved, our heart and mission remain the same.

For over 30 years, HAPLOS has been dedicated to supporting Filipinos with hemophilia and other inherited bleeding disorders, together with their families, caregivers, healthcare professionals, volunteers, and partners across the country.

Our new page name makes it easier for people searching for hemophilia in the Philippines to find us, while proudly retaining the name that has united and inspired our community for generations—HAPLOS.

Our new banner reflects what HAPLOS stands for:
🩸 Advocacy for better access to comprehensive care
🤝 Community built on families supporting families
🎓 Education that empowers patients and caregivers
💚 Support through every stage of life's journey
🌏 Partnerships that strengthen our impact locally and globally

As we embrace this refreshed identity, our commitment remains unwavering: to empower, care for, and serve the Filipino bleeding disorders community.

Thank you for being part of our journey. We look forward to continuing this mission with all of you as we build a stronger, more connected, and more empowered HAPLOS family.

💚 Stronger Together. HAPLOS Family Forever.

Send a message to learn more

💚 HAPLOS at the 2026 Conference on Hemophilia Exchange and Development 💚

Hemophilia Philippines (HAPLOS Community) Foundation, Inc. was proud to be represented by our President, Dr. Flerida G. Hernandez, at the 2026 Conference on Hemophilia Exchange and Development held in Tianjin, China on 13–14 June 2026.

The conference brought together healthcare professionals, researchers, patient organization leaders, and representatives from the World Federation of Hemophilia (WFH), China, ASEAN countries, and India to exchange knowledge and experiences on the latest advances in hemophilia care, innovative therapies, healthcare financing, and patient advocacy.

Beyond the scientific sessions, the conference provided meaningful opportunities to strengthen friendships, share experiences, and build partnerships with colleagues across the region who share the same commitment to improving the lives of persons with hemophilia and other inherited bleeding disorders.

We extend our heartfelt appreciation to the organizers for their warm hospitality and for creating a memorable and enriching experience that fostered learning, collaboration, and international friendship.

💚 Together, we continue to learn, connect, and advocate for a better future for the bleeding disorders community.