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We are a worldwide team of Lafora Disease family and friends dedicated to finding a cure. We have been where you are now, and we understand the emotions you are experiencing.
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Update on Myozyme and Lumizyme drugs from Sanofi for Lafora Disease treatment/0 Comments/in News, What's New /by Christine Kelly
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 […]