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Initially the Society comprised only of the parents of the thalassaemic children and some medical advisors. Its principal function is to serve as a network of information and support group for the parents and families. In 1995 the Society's membership expanded to include well-wishers who have no other association with thalassaemia. In the past few years, we have received overwhelming support given by our friends and well wishers of the Thalassaemic patients. Through this homepage, we hope to generate more public awareness on Thalassaemia, to keep our members and friends informed of our activities as well as to link up with the other Thalassaemia societies out there in cyberspace. To those visiting this website for the first time, we wish you a warm welcome and for the ones returning, it is pleasure to have you back. We hope that you find the content of this website interesting and helpful. |
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We are very grateful to CDC INTERNET for hosting our homepage. Best viewed at resolution 800x600 |
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Updated on November 2006 |
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LICENSE NO. 26/RBK/1999 |
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Disclaimer: The Sarawak Thalassaemia Society will not be liable for any direct or indirect damage, loss, expense, compensation, or legal liability as a result from any information contained within this website. |
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Copyright 1998-2004, Sarawak Thalassaemia Society email : sarawakthalassaemiasociety@yahoo.com |