Welcome to SCN2A Insights. Bringing you the latest research and clinical updates onSCN2A and genetic epilepsy from around the world.
Hi I’m David Cunnington and I’m Kris Pierce. Our son Will has SCN2A. One of thehardest things we faced as parents throughout the years is not knowing. Not knowingour son’s diagnosis. Not knowing what the future holds and not knowing how we canhelp Will and others with SCN2A. As parents and caregivers we want to do everythingwe can to support researchers to find a cure for SCN2A. The best way to do this iswork in collaboration with the patient community around the globe.
That’s why we’re starting this podcast. By interviewing researchers, clinicians, industryrepresentatives and members of the patient community we hope to better informeveryone working on and impacted by SCN2A.
Keep up to date with the latest updates by subscribing to this podcast.
Get regular updates on SCN2A through SCN2A Australia’s Facebook or Twitter @SCN2AAustralia.