From family to framework: how SLC6A1 Connect UK-AQ is reshaping collaboration in rare epilepsy
When Lindsay Randall’s son Arthur was diagnosed in 2018 with SLC6A1 Developmental and Epileptic Encephalopathy, there were[…]
Metabolic Support UK: Expert Interview on Supporting Rare Disease Communities
Earlier this year swii.ch were delighted to have the opportunity to collaborate with Metabolic Support UK and[…]