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Niki Markou
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Niki Markou2022-10-01 04:00:172023-02-14 11:58:00Our second annual #LaforaBodyDiseaseDay is October 1st, 2022
Creating Awareness,
Connecting Families,
Funding Research,
Maintaining Hope.
In Memoriam
Chelsea Gerber
1990-2016
Creating Awareness,
Connecting Families,
Funding Research,
Maintaining Hope.
Lafora patient
Adela Richer
Creating Awareness,
Connecting Families,
Funding Research,
Maintaining Hope.
In Memoriam
Kelsey Anne Harris
1995-2014
Fighting the Rare
A documentary about Lafora disease that features Chelsea’s Hope.
Living with Lafora
The Merriam family tells their story after a devastating diagnosis.
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Niki Markou
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Niki Markou2022-10-01 04:00:172023-02-14 11:58:00Our second annual #LaforaBodyDiseaseDay is October 1st, 2022
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Frank Harris
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Frank Harris2019-10-11 18:07:222023-02-14 07:50:38Lafora Documentary to Be Shown at San Francisco Film Festival
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Christine Kelly
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Christine Kelly2023-02-07 08:44:162023-02-07 11:17:14Chelsea’s Hope Received CZI Grant to Advance Lafora ResearchPartners
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 c/o Dr. Donohue
976 Maywick Dr.
Lexington, KY 40504
