Similar organisations to Dion Foundation for Children with Rare Diseases Inc
PHEO ALLIANCE
Advocacy, awareness and support for those affected by #pheochromocytoma/ #paraganglioma The mission of the Pheo Para Alliance is to invest in research to accelerate treatments and cures while empowering patients, their families, and medical professionals through advocacy, education and a global community of support.
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Surgery
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281.
American Association of Neurosurgeons Inc
NREF, the philanthropic arm of @AANSNeuro, advances patient care by supporting neurosurgical research, education and innovation.
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Birth Defects, Genetic Diseases
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282.
Gene Spotlight Inc
We are a nonprofit medical research and advocacy organization committed to spark breakthroughs in treatments and cures for rare genetic disorders, including lysosomal storage diseases, uncommon cancers and other orphan diseases.
MIAMI
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Specifically Named Diseases
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283.
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.
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Private Grantmaking Foundations
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D Jones Family Charitable Foundation Inc
WPlook is a creative Web Studio that creates professional and attractive Premium WordPress Themes.
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Health Support Services
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Kinera Foundation
Pediatric Physical therapy, Occupational therapy, Speech therapy, resources & parent navigation and support Mission: to enhance the quality of life for children with special healthcare needs & disabilities Kinera Foundation will enhance the quality of life for children with special needs and their families.
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Connective Tissue Coalition, Inc
Empowering Progress; Inspiring Hope Our Mission: The Connective Tissue Coalition (CTC) drives research, raises awareness, and provides resources for individuals affected by Ehlers-Danlos, Marfan, and Loeys-Dietz Syndromes.
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Specifically Named Diseases
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Project CASK
An innovative rare disease non-profit driving breakthroughs in treatments and a cure for CASK gene disorders.
502
New York City
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Public Foundations
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288.
The Mathew Forbes Romer Foundation Inc
Education & Research of Children's Genetic Diseases of the Brain MFRF was founded in South Florida in 1998 with a mission to prevent and eventually cure fatal children's genetic diseases of the brain.
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Boca Raton







