Similar organisations to Eleanor Kaplan Foundation Inc
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Patient Services�Entertainment, Recreation
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334.
ANGELS AMONG US
Helping families of children battling cancer by reducing the amount of stress in their lives so that they can focus more of their attention on their children.
5044
Omaha
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Birth Defects, Genetic Diseases
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335.
Tennessee Prader-Willi Association, Inc.
We provide support and information for people with PWS & their families.
640
Nashville
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Alliance/Advocacy Organizations
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336.
Stargardtians Inc
Our mission is to raise awareness of Stargardt’s Disease and to create opportunities for people living with Stargardt’s to further their education and develop their own business.
Falmouth
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Fund Raising and/or Fund Distribution
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337.
The Telomere Project
The Telomere Project is dedicated to funding lifesaving efforts for those affected by telomere syndromes, in particular, idiopathic pulmonary fibrosis IPF The Telomere Project is dedicated to funding lifesaving efforts for those affected by telomere syndromes TS in particular those which result in shortened telomeres or low telomere promotion.
206
Austin
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Birth Defects, Genetic Diseases
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338.
The PolG Foundation
The mission of The POLG Foundation is to support and accelerate research to find effective treatments and a cure for PolG mitochondrial disorders.
New York
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Specifically Named Diseases
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339.
Watch 4 Wegeners
It could save a life. Home Sarahx27s Story About Our Board Contact Us Run To Raise Testimonials More Watch 4 Wegeners It Could Save a Life Our daughter Sarah River Whitmire was a college student in pharmacy school when she died suddenly at age 20 from complications of undiagnosed Granulomatosis with Polyangiitis GPA also known as Wegener39s Disease a rare autoimmune disease that no one knew she had.
Nazareth
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Fund Raising and/or Fund Distribution
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340.
Undiagnosed Diseases Network Foundation (UDNF)
Improving access to diagnosis, research, and care for all with undiagnosed and ultra-rare conditions.
3469
Washington
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Cultural/Ethnic Awareness
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341.
May5Foundation
The May5Foundation and founder Dr. Alexia Mays are committed to supporting the communities of sickle cell, grief & loss, thru research ,advocacy &awareness The May5Foundation is centered in the values of dedication to education,community and service WE DO AMAYSING THINGS Programs and Events Support Our Efforts Who We Are More Community Events 2024 Warrior of The Year .
493
New Orleans
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Cancer Research
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342.
THE NEUROBLASTOMA CHILDRENS CANCER
Copyright NCCS 2024 The Neuroblastoma Children039s Cancer Society Home New Hope for More Tomorrowsfor Children with Neuroblastoma An advocate for the children who suffer from neuroblastoma and their families Raising money to assist local research in neuroblastoma cancer Raising national awareness to focus additional research and funding for a cure Our Mission The mission of the Neuroblastoma Childrens Cancer Society is to cure neuroblastoma and its related childhood cancers as well as to improve the quality of life for patients survivors and their families.
SCHAUMBURG