29 November 2019 Letter One Step Forward By Ministry Of Health For SMA Patients One Step Forward by the Ministry of Health with the National Framework for Rare Disease. Patients and families with Spinal Muscular Atrophy (SMA) in Malaysia are encouraged.
13 November 2019 Malaysia MOH Forms National Framework For Rare Diseases The committee will look at procuring orphan drugs for Malaysia.
8 October 2019 Malaysia Budget 2020: Patients Want New Cancer Drugs, Rare Disease Funds Increase allocations for public university hospitals, as most cancer patients there suffer financial catastrophe.
12 July 2019 Letter Happy Birthday Branden! – Edmund Lim The 9 years of lessons gained growing up with a rare disease called Spinal Muscular Atrophy (SMA).