hemophiliaphilippines.info@gmail.com

Start

April 11, 2026 • 9:00 AM (GMT+8)

Organizer

Venue

Virtual Event (Online)

Programs

Empowering the Community: 3-Part Hemophilia Lay Forum Series

In celebration of National Hemophilia Awareness Month, the Hemophilia Philippines (HAPLOS Community) Foundation, Inc., in partnership with the UST Hospital Section of Pediatric Hematology-Oncology and the National Children’s Hospital – Blood and Cancer Care Center, launched its 3-part Virtual Hemophilia Lay Forum Series.

Theme: Stronger Together: Awareness, Care, and Community

Forum Schedule

Session 1: April 11, 2026
Session 2: April 25, 2026
Session 3: May 9, 2026

Session 1 Highlights

Opening the Conversation

Ms. Herminia C. Palacio, President of HAPLOS Community, delivered the opening remarks, emphasizing awareness, early diagnosis, and community support.

Guided by Lived Experience

Mr. Jose Antonio G. Perez facilitated the session and ensured an engaging and meaningful discussion.

Expert Lecture: Hemophilia 101

Dr. Paula Bianca E. Nuqui delivered a patient-friendly discussion on hemophilia, covering causes, symptoms, and the importance of early diagnosis.

Patient Perspective

Mr. John Francis G. Sarmenta shared his journey, highlighting resilience and the importance of strong support systems.

Nationwide Participation

Participants from across the Philippines joined the virtual forum, showing strong nationwide engagement.

Closing Message

Mr. Reynaldo R. Sarmenta delivered the closing remarks, reinforcing HAPLOS’ commitment to advocacy and patient empowerment.

Key Takeaways

Hemophilia is a lifelong genetic bleeding disorder
Early signs such as easy bruising and prolonged bleeding should not be ignored
Early diagnosis helps prevent complications
Patient stories highlight resilience and support systems
Education improves outcomes and reduces stigma

Upcoming Sessions

April 25, 2026: Living Well with Hemophilia – Preventing Bleeds and Disability
May 9, 2026: Living Fully and Getting the Right Help

Join Us

Be part of the next sessions and help build a stronger, more informed hemophilia community. Together, we are stronger.

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