Labuan General Hospital-NBS Facility

16/07/2026

🎉 EXCITING NEWS! 🎉

We are delighted to share a proud milestone with everyone! The official logo and visual identity of the Labuan General Hospital Newborn Screening Facility have been officially approved!

More than just a logo, it symbolizes our shared commitment to protecting every newborn through early detection, timely intervention, and quality newborn screening services. It reflects our dedication, compassion, and vision of giving every child the healthiest possible start in life.

This marks the beginning of a stronger and more unified identity for our Newborn Screening Facility as we continue to advocate for healthier generations and promote awareness of the life-saving impact of newborn screening.

A heartfelt thank you to everyone whose support, dedication, and hard work made this milestone possible. Together, we will continue to make a difference—one baby, one family, and one healthy future at a time.

💙 Labuan General Hospital-NBS Facility Labuan General Hospital Zamboanga City
Screen Early. Save Lives. Build Brighter Futures. 👣🩸

16/07/2026

03/07/2026

📌

14/05/2026

📢 NOTICE TO ALL PARENTS

Good day!

The Newborn Screening (NBS) Results of your baby are now available for release.

Parents or authorized guardians may claim the result at the Labuan General Hospital-NBS Facility Labuan General Hospital

Newborn Screening helps detect certain health conditions early to ensure your baby receives proper care and treatment if needed. Our healthcare staff will be available to assist and guide you regarding the results.

📸 Photos taken during the release are with proper consent from parents or authorized guardians.

Thank you for your cooperation in keeping your baby healthy and safe.

27/02/2026

📢 NOTICE TO ALL PARENTS

Good day!

The Newborn Screening (NBS) Results of your baby are now available for release.

Parents or authorized guardians may claim the result at the Labuan General Hospital-NBS Facility Labuan General Hospital.

Newborn Screening helps detect certain health conditions early to ensure your baby receives proper care and treatment if needed. Our healthcare staff will be available to assist and guide you regarding the results.

📸 Photos taken during the release are with proper consent from parents or authorized guardians.

Thank you for your cooperation in keeping your baby healthy and safe.

27/02/2026

🩸

Equity for rare diseases means MORE OPPORTUNITIES than you can imagine.

Meet Prince, 12, from Pasig City. He is living with Congenital Adrenal Hyperplasia (CAH), a rare condition that, without newborn screening and confirmatory testing, could have gone undetected and become life-threatening.

Because he was screened at birth, Prince was diagnosed early and guided by medical professionals who helped him and his family understand and manage his condition. Today, he continues to grow, study, and play, with the right care and support behind him.

This is what more opportunities look like.

Opportunities to access timely diagnosis.
Opportunities to receive proper treatment and follow-up care.
Opportunities to go to school, play sports, and dream big.
Opportunities not just to survive but to thrive.

Rare diseases may affect not more than 1 in 20,000 individuals in the Philippines, but collectively, they impact millions worldwide. Most patients are children. Many families still face delayed diagnosis, limited treatment options, and barriers to care.

This 17th National Rare Disease Week (February 22–28, 2026), with the theme “More Than You Can Imagine,” you can help move the conversation forward:
💙 Share verified information about rare diseases
💙 Start conversations in your schools and workplaces
💙 Wear blue denim to show solidarity
💙 Raise your hand and tag National Rare Disease Week Philippines and Philippine Society for Orphan Disorders Incorporated

When awareness grows, policies strengthen.
When communities unite, systems improve.
When opportunities expand, children thrive.
Let’s imagine and build a Philippines where rare disease patients are fully seen, supported, and empowered.

Together, let’s create a future where no one is left behind, more than we can imagine.

27/02/2026

🩸

In celebration of the National Rare Disease Week, join us for an informative and timely discussion on rare diseases and newborn screening.

HEALTH UPDATES WEBINAR #275
Rare Disease: Safe ba ang Anak Ko?
Featuring insights on Maple Syrup Urine Disease (MSUD), Pompe Disease, and Osteogenesis Imperfecta

February 27, 2026 (Friday)
12:00 NN – 1:00 PM

Our featured speaker, Dr. Ebner Bon Maceda, Director of the Institute of Human Genetics, National Institutes of Health, UP Manila, will help us better understand these rare conditions, the importance of early detection, and how families can be supported through proper care and newborn screening.

Together, let’s raise awareness, promote early diagnosis, and strengthen support for individuals and families affected by rare diseases.

Register now: bit.ly/HealthUpdatesWebinar275

Let’s continue working toward equity, awareness, and hope for every Filipino family. 💙💛

27/02/2026

🩸

Equity for rare diseases means MORE COMMUNITY.

Meet Ziah, 7, from Rizal. She is living with 6-PTPS Deficiency, a rare condition detected through newborn screening.

Because she was screened at birth, Ziah was diagnosed early and closely monitored, helping prevent serious complications such as brain damage and repeated seizures. Today, she continues to grow and thrive with the support of her family and healthcare team.

Rare diseases are individually uncommon, but collectively they affect millions. In the Philippines, a disease is considered rare if it affects not more than 1 in 20,000 individuals, and most patients are children.

Behind every diagnosis is a family, a healthcare team, and a community working together.

This National Rare Disease Week (February 22–28, 2026), let’s build more community than you can imagine, where awareness leads to understanding, and understanding leads to action.

💙 Stand with Filipino families living with rare diseases.
💙 Support newborn screening.
💙 Be part of a stronger, more connected rare disease community.

27/02/2026

🩸

Equity for rare diseases means MORE HOPE.

Meet Dana, 17, from Batangas, Philippines. She is living with Phenylketonuria (PKU), one of the rare diseases included in the Philippine Newborn Screening panel.

Because of newborn screening, Dana was diagnosed early. With proper medical care, regular follow-ups, and support from healthcare providers and her family, she continues to grow, learn, and pursue her dreams, even sharing her music with the world.

Without early detection, PKU can lead to intellectual disability, behavioral problems, and poor growth. But through timely screening and lifelong care, children like Dana are given a chance at a healthier future.

This is why equity matters.
Equity means access to screening.
Equity means access to treatment and follow-up care.
Equity means no Filipino child is left behind.

This National Rare Disease Week, February 22–28, 2026, we stand with over 300 million people worldwide living with rare diseases.

RARE IS STRONG.
RARE IS MANY.
RARE IS PROUD.

Join us in raising awareness, sharing stories, and calling for more opportunities, more action, and more hope for the rare disease community. Be part of the movement:
✔ Wear blue denim
✔ Raise your hand for Rare
✔ Share this post
✔ Use the hashtags below:

27/02/2026

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