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 non-profit organization. EIN: 27-1008382
Chelsea’s Hope, Post Office Box 348626, Sacramento, CA 95834
Update on 2021 LD Meeting
/by Alan BarterDue to continued COVID restrictions, the July 2021 LD meeting has been rescheduled for September 20th – 21st, 2021 at the Sanford Consortium for Regenerative Medicine in La Jolla, CA. The meeting will be both in person and available on-line. Presentations will begin in the early afternoon on September 20th with an update regarding current research and efforts to move therapies into the clinic. This update will be followed by scientific talks, time for Q&A, and the evening will conclude with a meal to promote discussion and interactions. September 21st will be a full day of scientific talks focused on LD research with a poster session and meals provided.
Researchers Have Discovered the Cause of Neurodegeneration in Lafora Patients
/by Frank HarrisOne of the more horrifying impacts of Lafora Disease is the neurodegeneration that these children suffer. Families bear witness as their children suffer in frustration from their own cognitive decline. Researchers now understand the cause of this degeneration. As Dr. Jordi Duran explains in this article, “For years it was believed that the disease was caused by the accumulation of Lafora bodies only in neurons, but now we have shown that neurodegeneration is caused by accumulations in glial cells.”
Chelsea’s Hope is thrilled to thank Dr. Guinovart, Dr. Duran, and their entire staff of researchers for this great discovery. We also offer our sincere thanks to Dr. Matt Gentry and Dr. Jose Antonio del Rio for their important support and contributions to this discovery.
Chelsea’s Hope and all the Lafora families desperately hope for a cure for Lafora. Drs. Guinovart and Duran have gotten us a step closer.
Calling all People and Caregivers in the Lafora Disease Community: We need your help!
/by Alan BarterTake a survey to help better understand what it’s like living with Lafora disease (LD) and to help guide development of new potential LD therapies.
Learn more here: Calling All People and Caregivers
A Special Song for Angelina
/by Alan BarterJust Like A Butterfly by Niki Markou
“Just Like A Butterfly” Audio Release Date: February 10th, 2021, available on multiple digital music platforms like Spotify, Apple Music & TikTok. We ask that you stream the song and also make a donation! Help save our children.
“This journey has been extremely difficult and devastating and we do not want to lose our beautiful girl. I have written a song that is about how she bounces back from her seizures and what I wish for her ” – Mother, Niki Markou
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