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Scleroderma: autoimmune disease, research chair, funding Scleroderma BC
Scleroderma Association of B.C. provides moral and medical support for systemic sclerosis patients, and information tools for patients and health professionals.
Scleroderma India - Patient Support Group
Scleroderma India is a patient support group in India for Scleroderma, Sclerosis, Systemic Sclerosis. which is commited to promote public awareness and support
Author: Scleroderma India - Patient Support Group
Scleroderma Clinical Trials Consortium - SCTC - representing researchers & clinicians systemic sclerosis
The SCTC (Scleroderma Clinical Trials Consortium) is an international consortium representing the vast majority of researchers and clinicians who have particular interest and expertise in the care of, and research in, scleroderma (systemic sclerosis).
Raynauds Scleroderma Global Patients
In 1997 I was diagnosed with scleroderma and given a 15month prognosis. In 1998 I became a patient at the Scleroderma Unit. The cause and cure to both Scleroderma and Raynaud's remain unknown. Please donate to help fund medical research where 100% of your donation will be used for research purposes only. The Royal Free Hospital has the largest centre specialising in scleroderma in the UK led by Professor Chris Denton. #SclerodermaFreeWorld #RaynaudsFreeWorld #Research
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Welcome to the SynGAP Research Fund
Help us help #Syngap Patients today. The SynGAP Research Fund was incorporated in 2018 in California to improve the quality of life of SynGAP1 patients through the research and development of treatments, therapies and support systems
Royal Adelaide Hospital Research Fund | Home
The Royal Adelaide Hospital Research Fund is simple: to raise funds for life-saving medical research at the iconic hospital.
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SarcoidosisUK provide information and support to anyone affected by sarcoidosis. We also raise awareness and fund research into a cure for sarcoidosis.
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The Mesothelioma Applied Research Foundation is a nonprofit organization providing funding for research; and treatment support for mesothelioma patients.
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The Myeloma Crowd Research Initiative (MCRI) is a new approach to funding cancer research; combining the skill and knowledge of leading myeloma specialists with the patient perspective and supportive patient social communities to select and fund promising research projects in multiple myeloma world wide.
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The Colorectal Cancer Alliance raises awareness, provides support, and inspires the efforts that fund critical research to end colorectal cancer.
Research, Scholarships, Funding Agencies, Certifications
A web source to facilitate students, faculty and research personals providing latest scholarships, research funding, certifications information etc
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A Breath of Hope Lung Foundation fights lung cancer through funding research, raising awareness, and providing patient support.
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Eliminating death and suffering from prostate cancer through providing support, raising awareness, funding research and advocating on behalf of patients.
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The Will Herndon Fund for Juvenile Batten Disease Research
The Will Herndon Fund for Juvenile Batten Disease Research has partnered with the Beyond Batten Disease Foundation to find a cure for Juvenile Batten Disease. With your HELP, we will provide HOPE to Will and the hundreds of children like Will.
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Rare Disease Foundation
The Rare Disease Foundation is on a mission to find cures and treatments through its innovative patient-centric approach to research. The Foundation also funds and operates programs that provide resources through community and clinical support channels.
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Children’s Liver Disease Foundation. Fighting childhood liver disease by providing information, emotional support, research.
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Our nonprofit supports Arizona’s public teaching health care system by raising funds for research, facilities and patient services. Make an impact. Donate today!
Tyrosinemia Type 1: information, fundraising and research
The Tyrosinemia Foundation raises funds for research into the rare metabolic disease Tyrosinemia Type 1. We provide information about the disease and give insights in available researches.
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CCSVI Alliance is dedicated to educating patients with research-based information, providing tools for patients to advocate for themselves, and supporting medical professionals\' exploration of Chronic Cerebrospinal Venous Insufficiency (CCSVI)
Alzheimer's Disease: A Current Perspective on Research and Treatment
MEDIVISION provides information on Alzheimer's symptoms, diagnosis and treatment as well as reports on current research, clinical trials and other educational resources for patients and physicians.
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An Atlanta-based NPO funding academic medical research of Congenital Diaphragmatic Hernia (CDH), supporting CDH families, and raising awareness. Forever hopeful. 100% transparent. Let's Go!
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Canadian MPS Society for Mucopolysaccharide & Related Diseases – We believe in a brighter future for all Canadians affected by and with MPS
Support for families. Research for a cure. Our support and education programs assist those affected in managing the diagnosis and progression of these rare, often devastating, disorders. Funds raised through donations and special events help fund research that provides hope for a brighter future for all children born with lysosomal
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CO Research Funding UK | Formerly Gas Safety Trust | CO Research
CO Research (formerly known as Gas Safety Trust) was set up to reduce the incidents of death and serious injury from carbon monoxide (CO) poisoning. The Trust provides grant funding, advice and support to organisations wishing to carry out research and evidence gathering relating to safety.
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Meningitis and septicaemia are dangerous diseases which can **** in hours. We provide life-saving information and fund vital medical research into the diseases.
Home | Rare Diseases Clinical Research Network
The Rare Diseases Clinical Research Network (RDCRN), an initiative of the Office of Rare Diseases Research, NCATS, is made up of 21 disease research groups (consortia) and a Data Management and Coordinating Center that work together to improve availability of rare disease information, treatment, clinical studies, and general awareness for both patients and the medical community.
Kure It Cancer Research
Kure It Cancer Research is a nonprofit dedicated to providing direct funding to support the brightest minds in translational research for underfunded cancers at leading cancer centers. Founded in 2007 by Barry Hoeven after battling kidney cancer for 9 years, he realized there was disparity in funding for rare cancers. Kure It started funding kidney cancers and grew to support other underfunded cancers. Today, Kure It has raised over $9 million for cancer research and has worked with the dedicated researchers in the nation's top cancer centers.
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Melanoma Focus commissions and funds innovative melanoma research, while providing support & information for patients, carers and healthcare professionals.
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CHSG is dedicated to improving the lives of those patients with cluster headache by providing patient-directed support and education, collaborating with health care systems to drive research, and empower patients to advocate for and raise awareness of cluster headache.Read More →
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Research | Disease | Sickle Cell Warriors Inc.
Sickle Cell Warriors Inc. provides education, awareness, research access & support for those living with sickle cell disease. We are the largest patient-run sickle cell disease advocacy nonprofit firm in the world, with over 24,000 members. Join the movement to end sickle cell disease. Contact us.
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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.
The Wiskott-Aldrich Foundation
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Welcome to CurePSP | Neurodegeneration | Support | Assistance | Research
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Neonatology: Research, Treatment and Education
Neonatology is a subspecialty of pediatrics that focuses on the medical care of newborn infants. The principal patients of neonatologists are newborn infants who are ill or require special medical care due to prematurity, low birth weight, intrauterine growth retardation, congenital malformations (birth defects), sepsis, or birth asphyxias. Neonatology-info is a Medivision Healthcare web portal designed to provide current information on neonatal care research, education and treatment.
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HOME | United Leukodystrophy Foundation
September 14, 2021 “Unlock CTX” Partipate in a Patient-FocusedDrug Development Meeting Learn More Previous Next WHO WE ARE The United Leukodystrophy Foundation (ULF), incorporated in 1982, is a non-profit, voluntary health organization dedicated to funding cutting-edge research and to providing patients and their families with disease information and medical referrals. The Foundation is located in … HOME Read More »
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We work on issues that families and individuals with genetic conditions face. We provide information, support families and influence the services needed by these patients. Our work includes: reproductive techniques, diagnosis, medical research, healthcare and delivery, access to treatments and living and education.
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David Collins Leukaemia Foundation of Tasmania Inc.
David Collins Leukaemia Foundation of Tasmania Inc. is a Tasmanian organisation dedicated solely to the care and cure of Tasmanians living with leukaemia, lymphoma and related blood disorders. Since 1980, the Foundation has provided hundreds of patients and their families with care and support through their leukaemia journey, funded research for improvements to treatment and awarded scholarships for professional development of medical staff in Tasmania.
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