Similar organisations to Shay Emma Hammer Research Foundation
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Epilepsy
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1.
Epilepsy Study Consortium Inc
Home Our Mission The Epilepsy Study Consortium TESC is a group of scientific investigators from academic medical research centers who are dedicated to accelerating the development of new therapies in epilepsy to improve patient care.
Reston
AMERICAN EPILEPSY SOCIETY
American Epilepsy Society We are a community of professionals engaged in the understanding diagnosis study prevention treatment and cure with the goal of improving outcomes for persons with epilepsy.
Chicago
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Single Organization Support
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3.
Angels4Epilepsy Inc
Angels4Epilepsy, Inc. delivers smiles to children hospitalized.
El Paso United States TX: TEXAS
Decoding Developmental Epilepsies
We serve two distinct communities. First, we serve those living with SCN8A and their families.
Washington
Kcnq2 Cure Alliance Inc
Our promise is to educate and to advance research leading to treatments or a cure for patients living with the genetic disorder KCNQ2 Raising awareness, educating, and advancing research for KCNQ2 Developmental and Epileptic Encephalopathy.
3774
Denver
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Alliance/Advocacy Organizations
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6.
Finding Nori Foundation
The Finding Nori Foundation Home About Meet the Team Finding Joy Blog Resources Publications DONATE Contact Upcoming Events More Raising research funding for PAX5 and ALG13 related neurological disordersEmpowering families with ultra rare undiagnosed diseases to find answers Our Mission Our mission is to advance scientific research through fundraising and advocacy for ultra rare undiagnosed genetic disorders.
Gilbert
Lightning and Love Foundation
Founder of Lightning and Love foundation and mom to two ultra-rare THAP12 genetic epilepsy disease daughters searching for a cure.
699
CENTENNIAL
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Specifically Named Diseases Research
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8.
SLC6A1 CONNECT
People Magazine Exclusive Milestones for Maxwell What if your child was diagnosed with a disease so rare it didnt have a name.
FRISCO
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Birth Defects, Genetic Diseases
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9.
STXBP1 FOUNDATION
Non-profit dedicated to ending STXBP1-related disorders, rare neurodevelopmental and epileptic encephalopathies, and spreading awareness of this rare disease.
3921
HOLLY SPRINGS



