Leah Schust from the FamilieSCN2A Foundation presents her parent and foundation perspective - Life with a child suffering from a rare genetic disease https://www.scn2a.org
Watch video Life with a child suffering from a rare genetic disease - SCN2A online without registration, duration hours minute second in high quality. This video was added by user Dr. Dennis Lal 02 March 2018, don't forget to share it with your friends and acquaintances, it has been viewed on our site 1,059 once and liked it 13 people.