The Malaysia Lysosomal Diseases Association (MLDA) is a non-for-profit patient support organisation dedicated to improving the lives of all patients afflicted by Lysosomal Storage Diseases by:

  • Advocating for the establishment of a sustainable healthcare system for all LSD patients
  • Creating greater awareness of the 50 Lysosomal Storage Diseases
  • Supporting research for a cure and treatment that will improve the quality of life of the patients
  • Developing and sustaining an effective patient community network that provides comprehensive support for the ever-increasing needs of individuals and families affected by Lysosomal Storage Diseases.
The first Annual Grand Meeting (AGM) in 2011.