Entries by Christine Kelly

First Lafora Disease Research Roundtable

Please join us for our first Lafora Disease Research Roundtable! When? It will be Thursday, April 27th, 10:30 am – 12:00 pm EST. Where? The Roundtable will be virtual. You can register to attend via Zoom! We’ll bring together Lafora Disease and Adult Polyglucosan Body Disease researchers around a common goal: reducing glycogen aggregation in […]

Update on Myozyme and Lumizyme drugs from Sanofi for Lafora Disease treatment

Chelsea’s Hope continues to champion the development of effective Lafora disease (LD) therapeutics in both the research community and with interested companies. One recurring question is whether currently used therapeutics for other glycogen storage diseases could be used in LD. As you know, this would greatly benefit our community, allowing rapid therapeutic adoption. Because of […]