Similar organisations to Plasminogen Deficiency Foundation
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Public Foundations
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451.
CARE FOR A CURE
We are a non-profit 501c(3) organization working to find cures for Alzeheimer's and Breast Cancer https://t.
910
Burgettstown
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Birth Defects, Genetic Diseases
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452.
Southeastern Rett Syndrome Alliance
TO DEVELOP UNDERSTANDING AND AWARENESS OF RETT SYNDROME; TO PROMOTE THE GENERAL WELFARE OF THOSE WITH RETT SYNDROME; TO ASSIST IN IDENTIFYING PERSONS WITH RETT SYNDROME; TO SUPPORT FAMILIES IN COPING WITH THE DISORDER, AND CONDUCT ACTIVITIES AIMED AT PREVENTION, TREATMENT AND ERADICATION OF RETT SYNDROME Be sure to grab some Awareness Items in the Research Dr.
Trussville
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Educational Services and Schools - Other
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453.
Green Foundation
Community health education with hand-holding support to learn how you are able to navigation health care system.
537
Santa Ana
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Ambulatory Health Center, Community Clinic
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454.
2435 KINWEST MEDICAL CLINIC, Inc.
We are a free and charitable medical clinic only to those without medical insurance or financial means to pay for basic healthcare services.
56
Irving
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Private Grantmaking Foundations
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455.
Wallace Beeson Foundation Inc
A 501(c) founded in 2017 to raise money for research in rare Neurogastrointestinal & Motility Disease Home About Research Our Team More JOIN OUR FIGHT TOMAKE RARE KNOWN Funding Research for Rare Neurogastrointestinal Motility disorders YOUR DONATION FUNDS A DESPERATE NEED IN RESEARCH HOW WE STARTED From being a healthy 15yearold competitive swimmer to having to fight for herlife almost overnight Wallacesaw first hand the effect a rare condition has on someone.
176
Southern Pines
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Specifically Named Diseases Research
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456.
Recurrent Meningitis Association Inc
To support those affected by Recurrent Meningitis and help fund research to find a cure.
Hayden
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Other Philanthropy, Voluntarism, and Grantmaking Foundations N.E.C.
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457.
A Chance for Therapy, Inc.
We provide funding to children with neurological disabilities and/or genetic disorders for vital therapies, allowing them to reach their highest potential Act4Me's mission is to provide financial assistance for children with special needs to be able to ac Our mission is to provide funding to children with neurological and/or genetic disorders and developmental delays for vital therapies, allowing them to reach their highest potential.
1162
KEY BISCAYNE
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Fund Raising and/or Fund Distribution
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458.
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.
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New York
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Alliance/Advocacy Organizations
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459.
Sickle Forward
Sickle Forward is dedicated to transforming the lives of individuals affected by Sickle Cell Disease (SCD) in low- and middle-income countries by championing access to timely diagnosis and basic treatment.
Greenville






