The Philippine hemophilia community seeks public
support. In celebration of the World Hemophilia Day this April 17, the
Hemophilia Association of the Philippines for Love and & Service (HAPLOS)
spearheaded a national gathering of different Hemophilia groups and support
organization at the Glorietta Mall in Makati City last April 11 and 12.
Dubbed “Count Me in”, the two day activity seeks to
raise awareness and understanding about hemophilia and related bleeding
disorders. The event gathered around 300 persons with these conditions, along
with their families and friends.
Hemophilia, von Willebrand disease, inherited platelet disorders, and other factor deficiencies are lifelong bleeding disorders that prevent blood from clotting properly.
People with bleeding disorders do not have enough of a particular clotting factor, a protein in blood that controls bleeding. The severity of a person’s bleeding disorder usually depends on the amount of clotting factor that is missing or not functioning. People with hemophilia can experience uncontrolled bleeding that can result from a seemingly minor injury. Bleeding into joints and muscles causes severe pain and disability while bleeding into major organs, such as the brain, can cause death.
According to the World Hemophilia Federation, about
10,000 Filipinos have hemophilia. On the other hand about 1 million Filipinos
affected with von Willebrand disease and other bleeding disorders. However,
only 1,200 have been identified
Despite being considered as a serious and lifelong condition, awareness for hemophilia, von Willebrand Disease and inherited bleeding disorders has not gained momentum in most countries including the Philippines. As a result, significant disparities in treatment still exist, with about 75 percent receiving very inadequate treatment or no treatment at all.
Through the event in Glorietta Mall, HAPLOS hopes to educate more people with the help of PWH themselves, and create a call to action in order to close the gap in care and treatment.
“Unlike other conditions, Hemophilia, von Willebrand Disease and other bleeding disorders receive little public awareness and attention. The World Hemophilia Day, celebrated by countries all over the globe, is an opportunity for the bleeding disorder community to come together, speak out, and focus on the need to improve and maintain treatment, as well as help those with the condition to live as normally as possible,” said HAPLOS President Ric Felipe.
“Count Me In” lead campaigner Andrea Echavez said the event serves as a call to action to those with hemophilia, von Willebrand Disease and other bleeding disorders to be more active and be included in the National Hemophilia Registry.
Mr. Echavez encouraged people with Hemophilia, von
Willebrand Disease and other bleeding disorders that even though the condition
is life long, people can be productive as members of society. Mr. Echavez has
von Willebranad Disease as well
A former Inquirer reporter and now a communication consultation of an international organization, she said many patients feel overwhelmed with their condition especially when they experience bleeds.
“Our quality of life is definitely different from those without disorders. And we are not dismissing what our fellow patients feel. Many times bleeds can be overwhelming. But it should not stop us from striving to lead normal lives,” Echavez said.
Count Me In campaign also calls for volunteers from outside the Hemophilia community, public support for the Hemophilia community, and for government to look into the plight of persons with hemophilia.
The two day event feature psycho-social activities
for children and youth by Kythe Foundation, fundraising activities such as sale
of art work and products by persons with Hemophilia and their families,
testimonials of persons with Hemophilia, medical lectures on hemophilia and
other bleeding disorders, video loops in between programs, as well as
entertainment by children and adults with hemophilia and other bleeding
disorders
There will also be a blood donation campaign with the assistance of the Philippine Red Cross.
The activity is co-organized by HAPLOS and the
Philippine Children’s Medical Center (PCMC). It is supported by Glorietta Mall,
BusinessMirror Group of Publications, Novo Nordisk Hemophilia Foundation,
Philippine Red Cross and Kythe Foundation
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