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MLDA
   Home » In the News » General News » 
  In the News
  MLDA Launch - October 9th 2011
  ‘Every Life Counts’ Solidarity Campaign
  General News
 
 
 
 
A father’s fight for awareness

Lee Yee Seng is on a mission to ensure every child suffering from lysosomal storage diseases gets the medical treatment they need and rightly deserve, writes Chandra Devi Renganayar.
» Read more..
 
 
A hard, lonely road

IN THE not-too-distant past, it was common for parents to pray for boys to carry on the family line. Nowadays, most parents just hope that their newborn child will be healthy, with all their fingers, toes and everything else in the right place.
» Read more..
 
 
Articles about MLDA in Chinese Language

Articles from the Newspaper Segment "Mingguan Kesihatan"
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Association hopes to create public awareness on rare metabolic disease

The event, organised by the Malaysian Lysosomal Diseases Association (MLDA) and Tenaga Nasional Berhad (TNB) was aimed at creating awareness on the a group of little-known metabolic disorders.
» Read more..
 
 
MPS Awareness Day at Wisma TNB Seremban

State Exco Datuk Hashim Rusdi said he would recommend to the state government to set up special unit to deal with treatment for lysosomal storage diseases.
» Read more..
 
 
Articles about MLDA in China Press Newspaper

Articles from China Press Newspaper
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Articles about MLDA in Nan Yang Newspaper

Articles from Nan Yang Newspaper
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Articles about MLDA in Sin Chew Newspaper

Articles from Sin Chew Newspaper
» Read more..
 

 
   
 


 
 
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© Copyright Malaysia Lysosomal Diseases Association (Pertubuhan Penyakit Lisosomal Malaysia) 2011    All rights reserved.
Registration No: 2621-NSE
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