Top 100 alternative sites to proteus-syndrome.org
Global Down Syndrome Foundation | Research, Care, Education, Advocacy
The Global Down Syndrome Foundation is dedicated to improving the lives of people with Down syndrome through research, medical care, education and advocacy.
Supporting Families who have Children and Adults with Smith-Magenis Syndrome - Smith-Magenis Syndrome Foundation UK
Help us support a fulfilling future for everyone living with Smith-Magenis syndrome We want to bring more families together, provide education and awareness training, and sponsor research into SMS. But we can’t do it without your help. We are the Smith-Magenis Syndrome (SMS) Foundation UK, and we support families who have children and adults with …
The Cute Syndrome Foundation: SCN8A Epilepsy Support, Awareness, and Research - Home - The Cute Syndrome Foundation
Learn more about The Cute Syndrome Foundation and the SCN8A Epilepsy and PCDH19 Epilepsy Research we fund
Home - SATB2 Gene Foundation
OUR MISSION The SATB2 Gene Foundation, Inc. was established to enrich the lives of individuals with SATB2-associated syndrome, including those diagnosed with the condition and their families, through support, research and education. Our mission will be met by raising awareness about the characteristics of SATB2-associated syndrome, providing support to families, and supporting research in
Author: Brett Garwood
Noonan Syndrome Foundation
The Noonan Syndrome Foundation: created to help support, educate, & advocate for and on behalf of all those who have bee affected by Noonan Syndrome.
Home - Dravet Syndrome Foundation
Your Content Goes Here More News Dravet Syndrome Foundation is a non-profit organization dedicated to aggressively raising research funds for Dravet syndrome, a rare and catastrophic form
Author: Admin
The Down Syndrome Development Trust (DSDT)
Down Syndrome Development Trust exists to improve the lives of people living with Down syndrome. Including support to individuals and their families via research-based training workshops, outreach, educational enrichment and social groups for children and young people living with Down syndrome.
Author: Dsdt Updates
International FOXG1 Foundation
The International FOXG1 Foundation’s Mission is to provide hope and support to individuals with FOXG1 and their families via any means possible, to facilitate discussion and fund research within the medical community, and to bring awareness and education to the public. Our goal is to find treatments and a cure for FOXG1. We hope this Foundation will provide support and inspiration to the many families who have been blessed with a FOXG1 miracle.
Home Page - Koolen-de Vries Syndrome Foundation | KDVS
Koolen-de Vries Syndrome Foundation's mission revolves around Awareness, Education and Research. Learn more about the syndrome, research and upcoming events
Alport Syndrome Foundation - Hope, Action, Support
Alport Syndrome Foundation is a patient-led non-profit dedicated to improving the lives of those affected by Alport Syndrome.
The George Pantziarka TP53 Trust – Li Fraumeni Syndrome – supporting families and individuals with this cancer predisposition syndrome
Li Fraumeni Syndrome - supporting families and individuals with this cancer predisposition syndrome
Homepage - Chicago Public Library Foundation
Through the generous support of corporations, foundations and individuals, the Chicago Public Library Foundation funds programs that open minds & change lives.
Home - Phelan-McDermid Syndrome Foundation
Improving lives affected by Phelan-McDermid Syndrome Join Donate Newly Diagnosed International DataHub Upcoming Events Resource Library It is the mission of the Phelan-McDermid Syndrome Foundation to improve the quality of life of those affected by Phelan-McDermid syndrome worldwide by providing family support, accelerating research, and raising awareness. Latest News & Blog Post We are Phamily […]
Reye's Syndrome | National Reye's Syndrome Foundation | United States
In 1974, the National Reye's Syndrome Foundation, a children's health advocacy organization, was incorporated as a 501(c)3 charity, with a mission to eradicate the incidence of Reye's Syndrome. The Foundation does not receive, nor seek, government funding, and relies on the generosity of donors for support of all progr
Down Syndrome Association of Wisconsin
The Down Syndrome Association of Wisconsin supports individuals with Down syndrome and their families through education, information, programs, services, and the exchange of ideas and experiences.
Home | Dravet Syndrome UK
Welcome to the Dravet Syndrome UK website. We are dedicated to improving the lives of those affected by Dravet Syndrome through support, education and medical research.
Home | Down Syndrome Limerick
We support families and individuals with Down Syndrome throughout their life, with a range of Social, Education and Development activities.
Author: Bluescope
International Mosaic Down Syndrome Association
We are The International Mosaic Down Syndrome Association. A community that supports the awareness of Mosaic Down Syndrome via content publishing, sharing of resources and annual conferences. Providing support for families and individuals whose life has been touched by Mosaic Down Syndrome. We are continuously pursuing research opportunities and increasing awareness in medical, educational and public communities throughout the world.
The Ashley G Charitable Foundation
The Ashley G Charitable Foundation was established in 2008 with the goal of educating the public about symptoms, treatment, and care of children and teens with lymphoma, to fund research for treatment, and to assist patients.
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National Public Education Support Fund
The National Public Education Support Fund (NPESF) brings together education foundations, policymakers, and leaders from around the globe to learn from each other and work together on improving our public education system.
Author: Linda Darling-Hammond
Compost Research and Education Foundation > Home
The Compost Research and Education Foundation supports initiatives that enhance the stature and practices of the composting industry by supporting scientific research, increasing awareness, and educating the public to advance environmentally and economically sustainable organics recycling.
Down Syndrome Education USA
We support scientific research and deliver evidence-based advice and information to improve educational outcomes for children with Down syndrome.
Activating Wellness - Supporting families living with chronic fatigue syndrome
Supporting families living with chronic fatigue syndrome
Author: Annette Ford
Epilepsy Foundation New England | Epilepsy Information, Support & Programs
Epilepsy Foundation New England provides information, education, support & services to individuals with epilepsy & seizures. The foundation works to build awareness & raise funds for research to accelerate therapies, stop seizures and find cures for epilepsy.
Mater Foundation - Mater Foundation - Supporting healthcare, education and medical research programs at Mater.
Mater Foundation - supporting compassionate care for our community by raising funds for healthcare and medical research programs at Mater.
Fetal Health Foundation: Hope for Families Experiencing Fetal Syndromes
The Fetal Health Foundation gives hope to families who are hearing a fetal syndrome diagnosis. We understand the scary moment when a parent hears their baby is in danger. We connect patients with world-class maternal fetal medical centers, and fund fetal syndrome-related medical research.
Patten Family Foundation: Supporting Education, Healthcare and Financial Learning
The Patten Family Foundation is committed to supporting education, healthcare and financial learning.
Angelman Syndrome - UK Support, Education and Research Trust - Angelman Syndrome
UK Support, Education and Research Trust
The Global Foundation for Peroxisomal Disorders | Tulsa Oklahoma
The mission of The Global Foundation for Peroxisomal Disorders is to fund and promote peroxisome disorder research and to assist families and professionals through educational programs and support.
The Michelle Lynn Holsey Foundation | Supporting the quest to battle cancer
The Michelle Lynn Holsey Foundation support men, women, and children in their quest to battle cancer and other debilitating diseases: while funding innovative research and supporting education.
Author: Michelle Lynn Holsey Foundation
The Wiskott-Aldrich Foundation
The Wiskott-Aldrich Foundation is a non-profit organization dedicated to funding research to find improved cures for WAS ,providing up-to-date information and support for families living with Wiskott-Aldrich Syndrome worldwide. This website provides information, resources, and support for families coping with WAS. It is intended to bring together patients, researchers, and physicians to help with early diagnosis, better ways of managing the disease, and to spur the research necessary for a better cure.
Supporting Causes to Generate Education, Work, and Culture - Steelcase Foundation
The Steelcase Foundation funds projects for accessible public education, improving equity and opportunities in the Grand Rapids, Michigan and Athens, Alabama communities.
Catholic Education Foundation – The Catholic Education Foundation aims to provide financial support to Catholic families to ensure that thei
The Catholic Education Foundation aims to provide financial support to Catholic families to ensure that their children receive the Catholic education they...
Loeys-Dietz Syndrome Foundation
Our purpose is to provide information about what Loeys-Dietz Syndrome is and give hope to those impacted by the condition. We hope that you will find medical information and personal support to assist you and your family on your journey with Loeys-Dietz Syndrome. Learn more about our foundation and
RPH Nursing Research Foundation | Supporting Perth Nursing Research
The RPH Nursing Research Foundation supports nurses to undertake research through funding, professional support, networking & mentorship.
Mesothelioma Applied Research Foundation » Research and Support
The Mesothelioma Applied Research Foundation is a nonprofit organization providing funding for research; and treatment support for mesothelioma patients.
Lynch Syndrome Hereditary Cancer Foundation | AliveAndKickn
Hereditary cancer foundation, lynch syndrome, non-profit, patient advocacy organization, colon cancer, endometrial cancer, genetic mutation, AliveAndKickn AliveAndKickn is a patient advocacy organization for individuals and families with Lynch syndrome hereditary cancer genetic mutations.
One in a Million Fund - Post Traumatic Stress Disorder, PTSD, PTSD Support, PTSD Support Group, Post Traumatic Stress Disorder Support, Post
The One in A Million Fund has been established as a Donor-Advised Fund within the Community Foundation of Ottawa. Grants will be made annually to organizations supporting Post Traumatic Stress Disorder research, education, treatment and family support.
Author: Pixelera Inc
London Down Syndrome Association – Supporting and Enriching Lives!
Established in 1983, the London Down Syndrome Association is a volunteer-run charity, raising funds to provide responsive, compassionate support services to children, youth, adults and families living with Down syndrome in London, Ontario, and surrounding areas. Providing support within the counties of Elgin, Huron, Middlesex, Oxford and Perth. LEARN ABOUT US
Author: Kristen
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Educational Foundation for Rockport - Educational Foundation for Rockport
The primary mission of the Foundation is to manage funds in support of all fields of study in the Rockport schools, including science, technology, arts and the humanities. We solicit and accept donations from individuals, corporations and foundations whether in cash or in kind.
The National CFIDS Foundation's Home Page
The Foundation's objective is to fund research to find a cause, expedite treatments and eventually a cure, as well as providing information, education, and support to people who have CFIDS (chronic fatigue and immune dysfunction syndrome also known as chronic fatigue syndrome (CFS), myalgic encephalomyelitis (ME) and many other names).
The National Fragile X Foundation | Fragile X Syndrome
The NFXF serves all those living with Fragile X, including awareness, research, and community for individuals and families at all stages of life.
DownSyndrome SA - Supporting people with Down Syndrome in SA
Down Syndrome South Australia supports people with Down syndrome, their families and carers by offering a broad range of services and support.
National Center on Shaken Baby Syndrome - Home
The National Center on Shaken Baby Syndrome (NCSBS) is a non-profit 501(c)3 public charity with a mission to “Prevent shaken baby syndrome and promote the well-being of infants generally through the development and implementation of programs, policy and research; and to support and educate families, caregivers and professionals.”
The Champ Foundation
The Champ Foundation supports research toward better treatment and a cure for Pearson Syndrome.
False Memory Syndrome Foundation
The False Memory Syndrome Foundation is a 501(c)(3) organization founded in March, 1992 to seek the reasons for the spread of the false memory syndrome, to work for ways to prevent the spread of the false memory syndrome, and to aid those who were affected by the false memory syndrome and bring their families into reconciliation.
Home | Children's Hospital Foundation -Children's Hospital Foundation
The Children’s Hospital Foundation provides entertainment, support, and funds vital research and new equipment for sick kids and their families.
Allan Frenkel Foundation
The Allan Frenkel Foundation raises funds for Leukaemia research and practical support for teenagers and their families touched by Cancer. We support the Leukaemia Foundation, Canteen and Arrow charities.
International WAGR Syndrome Association
The International WAGR Syndrome Association is a not-for-profit organization comprised of an international network of families, health care professionals and researchers, and others who care for individuals with WAGR syndrome.
Kidney Foundation of Central PA | Support & Kidney Foundation Donation %
The Kidney Foundation of Central Pennsylvania provides education, advocacy, and support to families living with CKD in 28 counties. Learn more about programs and services to support the the work of the KFCP % through donations of time and money..
Angelman Syndrome Association of WA – Providing support in Western Australia since 2007
Our mission is to support, inform, educate, network, and advocate for families with a child with Angelman Syndrome
Home - RMC Research & Education Foundation
Ready Mixed Concrete (RMC) Research & Education Foundation Science and Credibility Behind Industry Action and Education CONTRIBUTE TODAY The RMC Research & Education Foundation is a lasting resource for increasing quality, professionalism, and sustainability in the ready mixed concrete industry by funding and implementing research and education programs. JOIN OUR MAILING LIST Making a donation…
Home | Save Our Seas Foundation
The Save Our Seas Foundation funds and supports research, conservation and education projects worldwide, focusing primarily on charismatic threatened wildlife and their habitats.
Child Vikas Foundation
The Child Vikas Foundation (CVF) is a Bangalore based independent, non-profit research and advocacy organization working in extending medical support, orphanage support, educational support, rural school support and tribal support for children. CVF gets its core funding from individuals for its various projects.
Pulmocare Research & Education Foundation
Pulmocare Research & Education Foundation
Foundation for Advancement of Education and Research.
Foundation for Advancement of Education and Research.
The UB Foundation supports the University at Buffalo
The UB Foundation supports the University at Buffalo to attract top students & faculty, conduct research, & remain a premier public research university.
Jerome Lejeune Foundation USA - Down Syndrome Research, Care, and Advocacy
The Jerome Lejeune Foundation USA centers its activities on Research, Care, and Advocacy for people with Down Syndrome.
Author: JLF USA Team
Home – Li-Fraumeni Syndrome Association: LFS Patient Advocacy | Support | Research | Awareness
LFS Association provides a wide range of information, advocacy, and support services for individuals and families with Li-Fraumeni Syndrome.
Author: LFS Association
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Foundation Home
The Lloyd’s Register Foundation is a charity that helps to protect life and property and support education, engineering-related research and public engagement.
The Hartwell Foundation - Funding Biomedical Research - Benefitting Children - Hartwell Foundation - Inspiring Innovation and Achievement
The Hartwell Foundation provides funding for individual biomedical researchers eligible research institutions
Author: Paul Metheney; Paulm @ Metheney Com
Short Gut Syndrome: Parents' Support Group
A support group for families of children with short gut syndrome
Supporting Indianapolis Education | The Mind Trust
The Mind Trust contributes to equity and excellence in Indianapolis public school education by connecting communities and educators to funding and support.
Author: Indianapolis Web Design by TBH Creative
Down Syndrome Association of Toronto, DSAT Non-Profit Charity
Down Syndrome Association of Toronto, DSAT mission is to support and empower individuals with Down Syndrome and their families throughout the GTA.
Author: Dsat1
Aesthetic Surgery Education and Research Foundation - The Aesthetic Surgery Education and Research Foundation
The Aesthetic Surgery Education and Research Foundation
Gorlin Syndrome Alliance – Treatment | Symptoms | Basal Cell Carcinoma
The Gorlin Syndrome Alliance serves people with Gorlin syndrome (Gorlin Goltz syndrome) and their families with disease information, support and research.
FAST (Foundation For Angelman Syndrome Therapeutics) - Home
FAST is committed to assisting individuals living with Angelman syndrome to realize their full potential and quality of life.
Author: Gerardo Duenas
The Sherry Lansing Foundation
The Sherry Lansing Foundation is committed to making the world a better place by funding and raising awareness for cancer research, and by supporting education, art, and culture.
The Desmoid Tumor Research Foundation- DTRF
The mission of The Desmoid Tumor Research Foundation is to aggressively fund research to accelerate the development of improved therapies, and ultimately find a cure for desmoid tumors. We collaborate with dedicated researchers and clinicians worldwide to improve the lives of patients through education, awareness and support.
The TAPS Support Foundation - Supporting TAPS Research and Families
What is the TAPS Support Foundation? We are a not-for-profit foundation based in the Netherlands. We passionately support research into Twin Anemia Polycyth
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British Car Parts and Accessories. Ol Phartz Partz, formed in 2010, manufacturers and sells a unique line of performance components along with restoration parts for classic British cars. Located in Sunny Southern California .
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AITC released an app for children, which is available Now! The app can be obtained on Apple at this link AITC APP or Android select this link AITC APP and it’s free, making it...
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