Similar organisations to The Shank2 Foundation
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Professional Societies & Associations
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343.
Suneel Research Foundation
Our mission is to spread awareness about Duchenne Muscular Dystrophy (DMD), raise funds to support treatments and find a cure for DMD.
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Buffalo
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Neurology, Neuroscience
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344.
Parkinsons Movement and Disorder Foundation
CONDUCTING OF EDUCATION AND RESEARCH The Parkinsons Movement Disorder Foundation PMDF Westminster Orange County CA 14772 Moran Street Westminster CA 92683 7143697426 our mission is to create a world without PARKINSONS all Movement Disorders Do you have Parkinsons Disease.
Westminster
Hope for Depression Research Foundation
Non-profit dedicated to cutting-edge research into origins, diagnosis, and treatment of depression and its related mood disorders.
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NEW YORK
The Foundation for Peripheral Neuropathy
Improving lives of those with PN via education+awareness and pursuing advocacy+lobbying+biobank growth+research for better treatments, one day, cures Our purpose: to improve the lives of patients living with peripheral neuropathy Our mission is to dramatically improve the lives of people living with peripheral neuropathy by: -Serving as the premier resource of information for patients, their families and healthcare providers -Accelerating a cure for peripheral neuropathies -Funding collaborative efforts of leading scientists -Raising awareness of peripheral neuropathy Our Purpose We strive to improve the lives of those affected by peripheral neuropathy through awareness education advocacy and research to advance the discovery of new therapies and cures.
14329
Buffalo Grove
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Epilepsy
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347.
LOGAN JETT RESEARCH FOUNDATION INC
By building connections within the epilepsy community, offering hope to families affected by this condition and raising the necessary funds, our mission is to have a positive impact on the lives of everyone who is touched by epilepsy.
Fort Mill
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Specifically Named Diseases
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348.
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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Other Philanthropy, Voluntarism, and Grantmaking Foundations N.E.C.
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349.
Liam M Kinne Foundation
Serving proudly as an avenue of mental and physical health and wellness aimed at empowering individuals, families, and communities to move together as one.
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Sherrill
Be Still Foundation Inc
To empower and uplift those with tremors, along with their families.
Mohnton
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Alliance/Advocacy Organizations
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351.
Horners Syndrome Awareness Action & Advocacy Foundation Inc
To increase awareness, education and understanding of the signs, symptoms, treatments, recovery challenges and lifestyle changes as a result of Horner’s Syndrome, in addition to facilitating access to education, medical funding and support groups.
Bradenton





