Similar organisations to L-CMD RESEARCH FOUNDATION
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Fund Raising and/or Fund Distribution
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64.
TODD CRAWFORD FOUNDATION TO CURE PARALYSIS INCORPORATED
Our goal is to raise money to support spinal cord injury research and bring awareness to the progress being made in this field.
prospect
Hereditary Disease Foundation
The official Twitter feed of the Hereditary Disease Foundation.
2417
New York
THE PARENT PROJECT FOR MUSCULAR DYSTROPHY RESEARCH INC
Let's advance the research evolution. #EndDuchenne Our mission is to end Duchenne.
33616
Washington
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Brain Disorders
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67.
VANISHING WHITE MATTER FOUNDATION
Our mission is to raise funds to support VWM Leukodystrophy specific research to help treat and cure this rare disease.
Salt Lake City
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Birth Defects, Genetic Diseases
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68.
Curefa Foundation Inc
CUREFA FOUNDATION FUNDS CAPITAL INTENSIVE PROJECTS GATED WITH SUCCESS MILESTONES, LEVERAGING NOVEL TOOLS OF SCIENTIFIC RESEARCH FOR THE TREATMENT AND CURE OF FRIEDREICH'S ATAXIA.
Port Washington
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Specifically Named Diseases
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69.
Pmd Foundation A New Jersey Non Profit Corporation
#Research #Awareness #Advocacy & #FamilySupport for those with #PelizaeusMerzbacherDisease #PMD #newbornscreening #raredisease #leukodystrophy #myelin The PMD Foundation is a 501(c)3 non-profit organization formed to serve three distinct interest groups as they relate to Pelizaeus-Merzbacher Disease: The Children and Families, the General Public, the Researchers and Clinicians.
1616
Marlton
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Fund Raising and/or Fund Distribution
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70.
COALITION TO CURE CHD2 INC
Fighting for our kiddos, and others, with CHD2-related neurodevelopmental disorders.
586
Dallas
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Single Organization Support
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71.
Beck S Helping Hands Inc
Helping Families of Kids with Duchenne Muscular Dystrophy DMD What is Duchenne.
Gainesville
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Specifically Named Diseases
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72.
LUPUS LA
Lupus Foundation of America is the only national force devoted to solving the mystery of lupus while giving support to those who suffer from its brutal impact.
331036
ENCINO





