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Register for Symposium!

August 26, 2022/by Christine Kelly

Chelsea’s Hope Lafora Children Research Fund and the Lafora Epilepsy Cure Initiative are happy to announce the return of our in-person Annual Lafora Disease Science Symposium.

The deadline to register to attend in person has passed, but virtual registration will remain open!

Click here for more details and the registration form

This conference is ideal for families affected by Lafora, researchers, healthcare professionals, and our industry partners.

You will hear from caregivers, clinicians, researchers, and pharmaceutical representatives on therapeutic development and diagnosis progress. We will also have an optional session for caregivers.

Date: September 26th – 27th, 2022.

Details: Attend virtually from anywhere in the world!

Check out our agenda outline for the event!

Virtual attendees must also register online.

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https://chelseashope.org/wp-content/uploads/2022/02/ChelseasHope1.png 0 0 Christine Kelly https://chelseashope.org/wp-content/uploads/2022/02/ChelseasHope1.png Christine Kelly2022-08-26 11:00:192022-08-26 10:39:58Register for Symposium!
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About Chelsea’s Hope

Chelsea’s Hope began as a website in the fall of 2007 to share Chelsea Gerber’s story with family and friends. A 501(c)(3) organization since 2009, we have made an impact by raising awareness, connecting families worldwide, funding research, and maintaining hope.

Our mission is to improve the lives of those affected by Lafora disease and help accelerate the development of treatments. [Read More]

View Chelsea’s Hope Newsletter Archive 

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Latest News

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The mission of Chelsea’s Hope is to improve the lives of those affected by Lafora disease and help accelerate the development of treatments.

Chelsea’s Hope Lafora Children Research Fund is an IRS 501(c)3 nonprofit organization. EIN: 27-1008382

Location imageChelsea’s Hope c/o Dr. Donohue

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info@chelseashope.org

Use ICD-10 code G40.C for Lafora.

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