Similar organisations to Smashsmard, Inc.
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Neurology, Neuroscience
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64.
JB'S KEYS TO DMD INC
Giving boys affected by DMD the opportunity of a lifetime.
1100
Dover
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Other Philanthropy, Voluntarism, and Grantmaking Foundations N.E.C.
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65.
INTERNATIONAL CHILDRENS ANOPHTHALMIA NETWORK INC
ICAN a voluntary not for profit organization, is a group of families and professionals dedicated to lending support to individuals who want to learn more about microphthalmia and anopthalmia and associated genetic counseling.
Philadelphia
Coming Together For A Cure, Inc
A 501c3 nonprofit dedicated to advancing stem cell therapy for Duchenne MD and other rare diseases.
2400
Wichita
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Nerve, Muscle, and Bone Research
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67.
FSHD Society
World’s largest research-focused patient organization for facioscapulohumeral muscular dystrophy (FSHD).
8717
Randolph
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Specifically Named Diseases Research
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68.
Cure Szt2
Cure SZT2 is a non-profit organization dedicated to families affected by the genetic mutation SZT2.
113
Woodland Hills
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Fund Raising and/or Fund Distribution
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69.
COALITION TO CURE CALPAIN 3
Coalition to Cure Calpain 3 (C3) has a pinpoint focus: to drive research towards a cure for limb-girdle muscular dystrophy type 2A (LGMD2A/R1, a form of Calpainopathy).
Westport
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Fund Raising and/or Fund Distribution
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70.
The Children's Rare Disorders Fund
Dedicated to curing rare genetic disorders Founded in July 2022 by parents of a toddler affected by FOXG1, The CRD Fund focuses on under served communities in the rare disorder space.
32
New York
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Birth Defects, Genetic Diseases
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71.
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
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Specifically Named Diseases
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72.
FOUNDATION FOR PRADER-WILLI
Foundation for Prader-Willi Research focused on treatments & cure for PWS Our Research FPWRs research programs aim to develop new therapies that will improve the health and wellbeing of those with PWS.
2031
COVINA







