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Lafora Disease Biomarker Workshop August 19th - 20th Hybrid event hosted by Chelsea’s Hope at UTSW Register Now to Participate

Announcing the Hybrid Lafora Disease Biomarker Workshop

July 5, 2024/by Kit Donohue

August 19-20, 2024 at UT Southwestern

Chelsea’s Hope is proud to partner with the UT Southwestern Medical Center (UTSW) in Dallas, Texas, to host a biomarker workshop. Our goal is to provide a platform for community education about the role of biomarkers in accelerating the path to clinical trials for Lafora disease. 

Lafora Disease Biomarker Workshop Biomarker 101 for families Patient sample collections Discussion panels Register Now August 19 - 20 Hybrid at UTSW

For Families

Have you ever wondered why we collect blood serum and CSF samples for our children with Lafora? Do you have questions about why patients undergo regular MRI scans? This workshop is designed to educate about how biomarkers can accelerate the path to therapy approval in clinical trials. Also, we want to learn which biomarkers are the most promising for use in treating Lafora disease. Above all, this knowledge will lead to a brighter future for our children. Please register to attend virtually.

For the Lafora Research Network

Clinicians and researchers, we will be sponsoring several expert discussion panels during the workshop to reach a consensus on protocols for sample collection and critical markers to track. Please register to be a part of the discussion for the topics below: 

  • Metabolic Biomarkers from Serum, CSF, and MRI/FDG-PET scans
  • Epilepsy & EEG Clinical Markers
  • Cognitive Evaluation & Markers
  • Motor Skill Evaluation & Markers


Questions? Please check out our FAQs section on our webpage. 



Register to attend virtually

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https://chelseashope.org/wp-content/uploads/2024/07/Biomarkers-workshop-post-featured-image.png 628 1200 Kit Donohue https://chelseashope.org/wp-content/uploads/2022/02/ChelseasHope1.png Kit Donohue2024-07-05 07:50:102024-08-09 14:05:21Announcing the Hybrid Lafora Disease Biomarker Workshop
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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

976 Maywick Dr.

Lexington, KY 40504

info@chelseashope.org

Use ICD-10 code G40.C for Lafora.

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Link to: Empowering Lafora Disease Research: Launch of Patient Mutation and Canine Databases Link to: Empowering Lafora Disease Research: Launch of Patient Mutation and Canine Databases Empowering Lafora Disease Research: Launch of Patient Mutation and Canine D...White text says 'NEW LAFORA DATABASES' above an image of genetic mutation. It has a purple overlay. Purple text over a white block says 'Canine & Mutation.' There is a photo of a beagle to the left of the text. White and purple circles decorate the edges of the graphic, with the round Chelsea's Hope Lafora Children Research Fund logo in the bottom right-hand corner. Link to: G-Tube Tips – A Mother’s Perspective Link to: G-Tube Tips – A Mother’s Perspective Blog post G-Tube Tips for Lafora familiesG-Tube Tips – A Mother’s Perspective
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