Hi,
My baby has refractory epilepsy and recent genetic tests show that she is somewhere on the Dravet syndrome spectrum. She is on a cocktail of 4 meds currently, and we have approval from the MCC for her to use Stiripental (Diacomit), which is aimed at her condition but needs to be imported. Our medical aid though only will pay for 50% of the monthly cost, and we can’t afford the R2,000+ shortfall as I’ve had to stop working to look after her. Can Epilepsy SA assist us in lobbying Discovery? I know that there are NGOs assisting breast cancer patients with such issues, and hope that you are able to assist us in this case.