When Phua Wee Seng’s six-year-old son was diagnosed with a rare genetic disorder, his family had weeks to raise a $100,000 pledge – on top of subsidies – before the treatment could go ahead. For Warren Sheldon Humphries, the burden looks different: $200 a month in essentials and support is temporary. As a new government task force wraps up more than 30 engagement sessions, Andrea Heng and Hairianto Diman find out what real, lasting support for persons with disabilities in Singapore should look like with Phua Wee Seng, Executive Director, Rare Disorders Society & Warren Sheldon Humphries, Learning Partnerships Manager, Blended Concepts and Docent, Enabling Village
Trending
- 7 Best Alarm Clocks For ADHD, Matched To Why You Can’t Wake Up
- The Average Retiree Household Spends $65,354 a Year. Social Security Covers About Half. Here’s What Covers the Rest.
- Teaching Teenagers Emotional Regulation: Strategies for the Adolescent Brain
- Why Hustle Culture is Burning Founders Out (And What to Do Instead)
- CNA938 Rewind – Employment, care, affordability: What persons with disabilities are asking for
- New Estimate Places Social Security’s 2027 COLA at 4.7% – But Retirees Shouldn’t Celebrate Yet
- Baby ‘sloth bear’ found abandoned, given second chance by rescuers
- DS Group launches ‘Pallu Protection Equipment’ campaign for women farmers – Campaign Brief Asia

