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Similar organisations to 24 Hours for Hank Inc

Community Rebuilding
  • Diseases, Disorders, Medical Disciplines N.E.C.

  • 64.

U R Our Hope

Non-profit serving individuals with undiagnosed & rare disorders through education, advocacy, and support in order to bring hope through knowledge, empowerment Assisting those with undiagnosed or rare disorders at any age and any stage.

Social Rank

2304

Location

AUSTIN

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Community Rebuilding
  • Mental Health Disorders

  • 65.

Bluefield Project To Cure Frontotemporal Dementia

frontal lobe of the brain and may extend back to the temporal lobe.

Location

San Francisco

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Community Rebuilding
  • Specifically Named Diseases

  • 66.

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.

Social Rank

1616

Location

Marlton

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Community Rebuilding
  • Research Institutes and/or Public Policy Analysis

  • 67.

Riaan Research Initiative Inc

501(c)(3) non-profit organization hunting for a cure for rare and life-limiting genetic diseases that hurt children, starting with Cockayne syndrome.

Social Rank

684

Location

Oakland Gardens

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Community Rebuilding
  • Fund Raising and/or Fund Distribution

  • 68.

The Stiff Person Syndrome Research Foundation

Finding a cure for Stiff Person Syndrome through RArE: Research, Awareness, and Education.

Social Rank

2749

Location

Bethesda

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Community Rebuilding

Hunters CMT4B3 Research Foundation Inc

Pioneering cutting edge scientific research to develop treatments for CMT4B3 patients and children with rare neuromuscular diseases.

Social Rank

645

Location

Scarsdale

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Community Rebuilding
  • Alliance/Advocacy Organizations

  • 70.

Jansen De Vries Syndrome Foundation

The Jansen de Vries Syndrome (JdVS) Foundation is a nonprofit, tax-exempt organization as defined in section 501(c)(3) of the Internal Revenue Code and, as such, contributions to JdVS Foundation are tax-deductible.

Location

Natick

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Community Rebuilding
  • Fund Raising and/or Fund Distribution

  • 71.

CURE RARE DISEASE INC

Nonprofit biotech leading a global collaboration to develop life-saving medicines for rare diseases Revolutionizing UltraRare Disease Treatment through Innovation and Collaboration Revolutionizing UltraRare Disease Treatment through Innovation and Collaboration What Wex27re Working Towards We envision a future where every patient has access to treatment.

Social Rank

8226

Location

WOODBRIDGE

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Community Rebuilding
  • Fund Raising and/or Fund Distribution

  • 72.

CHILDRENS PSC FOUNDATION

Help Make Treatment a Cure Donate Now What is PSC.

Location

MENLO PARK

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