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Chelsea's Hope Lafora Children Research Fund Research Roundtable Thursday, April 27th, 10:30 am - 12:00 pm EST. Register to attend via Zoom We'll hear from Lafora Disease and Adult Polyglucosan Body Disease researchers around a common goal: reducing glycogen aggregation in the brain.

First Lafora Disease Research Roundtable

April 20, 2023/by Christine Kelly

A square image announcement for the Lafora Disease Research Roundtable. The top half of the image reads: Chelsea's Hope Lafora Children Research Fund Research Roundtable The bottom half contains the event details: Thursday, April 27th, 10:30 am - 12:00 pm EST. Register to attend via Zoom We'll hear from Lafora Disease and Adult Polyglucosan Body Disease researchers around a common goal: reducing glycogen aggregation in the brain. 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 the brain. The Research Roundtable will feature several presentations, followed by time for group discussion.

The presentations will be geared toward the science community as we work to build allies toward developing treatments for Lafora disease, but everyone is welcome. Families are welcome to attend and ask questions, so we hope you will be able to join us for this event!

It’s only one week away, so register today for the Lafora Disease Research Roundtable!

Also, please register if you are interested but you are unsure if you can attend or not! We hope to send the Zoom recording of the roundtable to everyone who signed up. However, we will not make the recording available publicly.

Chelsea’s Hope is excited for our first Research Roundtable. If successful, we plan to continue the series in the future. Please contact us before the roundtable if you have any questions.

Register for the Research Roundtable
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https://chelseashope.org/wp-content/uploads/2023/04/Research-Roundtable-Announcement-04.18.png 1620 1620 Christine Kelly https://chelseashope.org/wp-content/uploads/2022/02/ChelseasHope1.png Christine Kelly2023-04-20 08:51:382023-06-22 15:23:21First Lafora Disease Research Roundtable
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June Research Roundtable Registration
Image includes a purple rectangle in the background of top third. The Chelsea's Hope Lafora Children Research Fund research roundtable logo is towards the left of the rectangle in white. It has half a bullseye to the left of the text. To the right of the logo's text is a purple line. On the other side, white text says 'Thursday, 8 February 10:30 AM - 12 PM EST.' a darket purple line separates the purple background from the white hexagons that make up the rest of the image. Below that, white text on a purple oval says 'REGISTER IN ADVANCE.' The photo on the left is a headshot of Sharmistha Mitra, Ph.D. with text beneath her name that says 'UT Southwestern Medical Center.' The photo on the right is a headshot of Jeff Milton with text beneath his name that says 'La Jolla Labs, Inc.' Announcing February Research Roundtable Speakers
A graphic with nine headshots introducing new team members; text says: Meet the team sophie stein research support intern jeremiah paul fundraising support intern samy sharif science communications intern sara gerber research support intern sally leung research support intern jhanavi kotian science communications intern kait fedor development fellow vaishali jain fundraising support intern anna gould science communications intern New Team Members Join Chelsea’s Hope for the Summer
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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]

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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

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