Rare Diseases SA

Family struggles to cover R 3.6 medical bill for rare disease

Patients are being left in limbo by a 'grey area' in the law For two years, Knysna resident Irene Sabbat has known which medication could...

Rare Diseases SA

In-depth: What happens to people in SA who have rare diseases?

Little is known about the number of people in South Africa who are living with rare diseases. In fact, there is no recognised definition...

Rare Diseases SA

Legal battle to approve Zach's treatment

Read online at Alberton Record

Rare Diseases SA

Jacques and Michaney de Wet will continue to fight for their son

Jacques and Michaney de Wet from Brackenhurst are battling to get their medical aid to pay for their son Zachary’s treatment despite this...

Radio Interviews

LotusFM - Interview with Kelly du Plessis - 03 Aug 2022Fighting For Zach

00:00 / 04:16

Radio Interviews

Channel Africa - Interview with Kelly du Plessis - 02 Aug 2022Treatment Approval For Zach

00:00 / 09:38

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