People with bleeding disorders need your help.

MONTHLY FEATURE


Big Dreams to the Big Ben: The Inspirational Journey of Peter John Tetangco

Peter John “PJ” Tetangco, 27, has turned a life of challenges into a tale of triumph. Living with severe hemophilia A, PJ grew up with many limitations on physical activities and experienced several life-threatening bleeds. His is a story of resilience, determination, and the power of community support.

Hemophilia Community Updates

 

What is HAP?

We are registered with the Securities and Exchange Commission as non-stock, non-profit organization. Our main objective is to provide immediate assistance to our members who are experiencing life-threatening bleeds.

We receive humanitarian donation of anti-hemophilic Factor concentrates from non-profit organizations abroad and we distribute these for free to patients with life-threatening and limb-threatening bleeds.

Hemophilia in The Philippines

Majority of Filipinos with bleeding disorders live below poverty line (Around US$233/month income or less). Many of them either have limited or no access at all to medicines mainly because of poverty and lack of education (or lack of awareness on their condition)

Very few hospitals have the capability to handle patients with bleeding disorders. Hospitals that are properly equipped to treat people with bleeding disorders are mostly based in urban centers like Metro Manila, Cebu and Davao. Worse, they are mostly private hospitals that are not affordable to majority of the patients.

1M

1million Filipinos are estimated to have bleeding disorders

10k

Ten thousand of them are estimated to have Hemophilia

1.7k

but only less than 1,700 have been registered in the Philippines

these numbers need to change

PEOPLE WITH BLEEDING DISORDERS NEED YOUR HELP

HAP is generously supported by

OUR MEDIA PARTNERS