sahabatthalassaemiamalaysia blogspot.com

SAHABAT THALASSAEMIA MALAYSIA

Thalassaemia is the most common genetic disorder in the world, with around 250 million people, 4.5 percent of the world population, affected by the fatal disease. As 2010, Malaysia registered 4,768 people as Thalassaemic which required regular blood transfusion. And 5 of its population are carrier. SAHABAT THALASSAEMIA MALAYSIA, created by Thalas for Thalas. Leaving the LEGACY of PEACE and LOVE. THALAS, IMPIAN, HARAPAN DAN LEGASI. AKU THALAS MENONGKAH ARUS. BAPAK MALANG BUKIT JALIL. Ramai di antara pesa.

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KELAB TALASEMIA HOSPITAL AMPANG

We Share, We Care, Leaving the Legacy of Peace and Love. Saturday, July 13, 2013. BERBUKA PUASA BERSAMA KELUARGA THALAS 2013. Majlis berbuka puasa bersama keluarga thalas KTHA telah diadakan di Zarlith Events and Catering, bertempat di Kampung Batu Muda, Kuala Lumpur pada 13hb Julai yang lepas. Thursday, July 26, 2012.

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SAHABAT THALASSAEMIA MALAYSIA

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Thalassaemia is the most common genetic disorder in the world, with around 250 million people, 4.5 percent of the world population, affected by the fatal disease. As 2010, Malaysia registered 4,768 people as Thalassaemic which required regular blood transfusion. And 5 of its population are carrier. SAHABAT THALASSAEMIA MALAYSIA, created by Thalas for Thalas. Leaving the LEGACY of PEACE and LOVE. THALAS, IMPIAN, HARAPAN DAN LEGASI. AKU THALAS MENONGKAH ARUS. BAPAK MALANG BUKIT JALIL. Ramai di antara pesa.

CONTENT

This web page sahabatthalassaemiamalaysia.blogspot.com states the following, "Thalassaemia is the most common genetic disorder in the world, with around 250 million people, 4." We saw that the webpage said "5 percent of the world population, affected by the fatal disease." It also said " As 2010, Malaysia registered 4,768 people as Thalassaemic which required regular blood transfusion. And 5 of its population are carrier. SAHABAT THALASSAEMIA MALAYSIA, created by Thalas for Thalas. Leaving the LEGACY of PEACE and LOVE. THALAS, IMPIAN, HARAPAN DAN LEGASI."

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