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rare disease

Showing 27 of 27

‘Smells like rotten fish, feels like a curse’: Pain, odour and isolation for people with rare skin disease

22/07/2023

Commentary: Singapore cannot rely only on crowdfunding to help those with rare diseases

24/05/2023

On The Red Dot: Undiagnosed - Part 4 Of 4

26/03/2023 23 mins

On The Red Dot: Undiagnosed - Part 3 Of 4

19/03/2023 23 mins

On The Red Dot: Undiagnosed - Part 2 Of 4

12/03/2023 23 mins

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On The Red Dot: Undiagnosed - Part 1 Of 4

05/03/2023 23 mins

Gen Y Speaks: My child is the only one in Singapore with this disease. Every day he is alive is a blessing to us

29/01/2023

Paralysed former journalist co-writes book on rare degenerative disease ALS to show he 'still can give back to society'

27/12/2022

Commentary: Having a rare disease has helped me to be super in my own way, even without superpowers

02/12/2022

Strides made towards an inclusive S'pore but more can be done, say disabled community and experts

26/08/2022

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Baby in NUH ICU with severe disease, parents hope to raise S$3 million for 'world's most expensive drug'

23/08/2022

A rare disease diagnosis came too late for this boy, who says he’s not ‘poor thing’

05/03/2022

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