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Gray Foundation to Cure Batten Disease | Improving the lives of children and families affected by Batten
The Charlotte & Gwenyth Gray Foundation to Cure Batten Disease was founded to save the lives of all children impacted by Batten Disease by accelerating the research for a cure and providing support to patients and their families.
Batten Disease Support & Research Association
ABOUT US BDSRA is dedicated to funding research for treatments and cures, providing family support services, advancing education, raising awareness, and advocating for legislative action. Founded in 1987, by parents seeking to build a network for those diagnosed with Batten disease, BDSRA
Author: Tom Evans
Funding Research for Shone's Syndrome
The Christina Capozzi Foundation is a non-profit foundation which was formed to raise funds for research on heart disease at Childrens Hospital in Boston, MA.
Funding the Best Minds in Cancer Research
The Cancer Research Foundation is a non-profit organization that funds early-career scientists and researchers to ignite their careers to help find a cure for cancer.
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.
Children’s Liver Disease Foundation | Liver Disease Research and Support
Children’s Liver Disease Foundation. Fighting childhood liver disease by providing information, emotional support, research.
Niemann- Pick Disease - Ara Parseghian Medical Research Foundation - Lysosomal Disease
The Ara Parseghian Medical Research Foundation's goal is to find a cure for the devastating Niemann-Pick Type C disease.
Help Cure PD - Donations, research, information on finding a cure for Parkinson Disease.
Help Cure PD - Donations, research, information on finding a cure for Parkinson Disease.
Awareness for Motor Neurone Disease - Racing For MNDi
A foundation established to race against time in helping find a cure for Motor Neuron Disease (MND) by focusing on the research. We welcome your support.
Author: Dev
Jack McGovern Coats' Disease - Rare Eye Disease - Home Page
Jack McGovern Coats' Disease - Funds research to find a cure for Coats’ Disease and pediatric retinal Disease - We serve as a hub for the Coats’ Disease community
Mito Foundation - Hope for mitochondrial disease
The Mito Foundation drives mitochondrial disease research to find a cure. It also provides support to patients and their families until such time as a cure is found.
Polycystic kidney disease | PKD treatment research | PKD Foundation
PKD Foundation — We give hope. We fund research, advocate for patients, and build a community for all impacted by polycystic kidney disease. #endPKD
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MyLymeData is a Lyme disease research project. It lets Lyme disease patients provide data that can help drive research to find a cure for Lyme disease
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NEHI Research Foundation is working to improve the diagnostic process, find treatments, and ultimately cure all forms of Children's Interstitial Lung Disease through the support of research.
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How We Will Cure Brain Disease The United Brain Association’s mission is to empower every individual living with brain disease and to support innovative research for a cure. Finding a cure is about courage, willpower, endurance, and acceptance. It’s about belonging to a community of compassionate listeners. It’s about sharing your hopes and supporting
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The Michael J. Fox Foundation for Parkinson's Research
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MND Scotland | Motor Neurone Disease
MND Scotland is the leading charity in Scotland providing care and support to people affected by Motor Neurone Disease (MND), as well as funding vital research into finding a cure.
Perry Cross Spinal Research Foundation | To Cure Paralysis for All
The Perry Cross Spinal Research Foundation funds key medical research that aims to find a cure for paralysis caused by spinal injuries. You can help cure paralysis. Contact Us.
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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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Jeff Gordon Children’s Foundation is a pediatric cancer foundation benefiting families and kids with cancer. We fund children’s cancer research to help find a cure and develop better treatments. Did you know that only 4% of federal cancer research dollars go to pediatric cancer? Learn more about how we’re making an impact.
JDRF - Type 1 Diabetes Research Funding and Advocacy
JDRF leads the global type 1 diabetes research effort to keep people healthy and safe until we find a cure for the disease. Help create a world without T1D.
Auckland Medical Research Foundation
AMRF funds world-class health and medical research to save lives. Our donors support work in infectious diseases, neuroscience (like Parkinsons, dementia, Alzheimer's disease), paediatrics, cancer, tinnitus, and more. Get in touch to find out how you can help | Auckland Medical Research Foundation
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Thrasher Research
The Thrasher Research Fund provides grants for pediatric medical research. The Fund seeks to foster an environment of creativity and discovery aimed at finding solutions to children's health problems. The Fund awards grants for research that offers substantial promise for meaningful advances in prevention and treatment of children's diseases, particularly research that offers broad-based applications.
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We at Project Sebastian gives support, funding and hope to families affected by a child with a rare disease. Provide education, therapies, and counseling.
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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AIM Youth Mental Health is a nonprofit organization devoted to the mental health of youth. We fund clinical research to find treatments and cures.
Best Children’s Charities to Donate to | Stand By ELI Foundation
Want to Donate to a Children's Charity? The Stand By ELI Foundation was created to provide needed research funds to help, ultimately, treat and cure children affected with mutations on the IRF2BPL gene. Donate today and help a child have the healthy future he or she deserves.
There is HOPE in your HELP!!! MAKE A DONATION
The Cure Tay-Sachs Foundation is dedicated to funding the on-going research needed to find treatments and a cure for Tay-Sachs Disease. Once the cure for Tay-Sachs has been found - and we will find it! - we will dedicate our efforts to promoting carrier-testing and Tay-Sachs awareness initiatives.
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.
Fragile X Syndrome Research & Treatment • FRAXA Research Foundation - Finding a Cure for Fragile X
FRAXA Research Foundation’s mission is to find effective treatments and ultimately a cure for Fragile X syndrome. Fragile X syndrome is the most common inherited cause of autism and intellectual disabilities We directly fund research grants and fellowships at top universities around the world. We partner with biomedical and pharmaceutical companies, large and small, to bridge the gap between research discoveries and actual treatments.
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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.
The Children's Neuroblastoma Cancer Foundation - CNCF
The Children's Neuroblastoma Cancer Foundation (CNCF) is the premier source for neuroblastoma information and resources. Comprised of families just like yours, we are committed to finding a cure for neuroblastoma through research, education, awareness and advocacy.
AVRF: American Vitiligo Research Foundation
American Vitiligo Research Foundation Inc. (AVRF) provides public awareness about vitiligo through dedicated work, education and counseling. We seek to make a difference worldwide to those afflicted by the disease, focusing on children and their families.
It's time to talk about mito - The Lily Foundation
The Lily Foundation is a UK charity dedicated to fighting mitochondrial disease. We work in partnership with the NHS and leading mitochondrial clinics to support those affected by the condition, raise awareness, and fund research into effective treatments and therapies. Our long-term goal is to find a cure for mitochondrial disease.
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Neuroblastoma UK
We are a national charity, dedicated to finding a cure for neuroblastoma, an aggressive childhood cancer. We fund leading research to develop new, effective and kinder treatment for children with neuroblastoma. Donate today to help save more young lives.
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Foundation Fighting Blindness — Foundation Fighting Blindness
The urgent mission of the Foundation Fighting Blindness is to drive the research that will provide preventions, treatments and cures for people affected by retinitis pigmentosa, age-related macular degeneration, Usher syndrome and the entire spectrum of retinal degenerative diseases. The Foundation is a beacon of hope for those affected by these blinding diseases. Join the fight and help us accelerate our mission.
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.
Saoirse Foundation – Making Positive Life Impacts for Sick Children
Welcome to The Saoirse Foundation Making positive life impacts for sick children We are a registered Irish not-for-profit charity dedicated to making positive life impacts for critically and seriously ill children throughout the island of Ireland. We raise funds to deliver services and supports to these sick children. We help fund vital research and provide guidance
Author: Admin
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Toby's Foundation is a non-profit organization dedicated to providing resources and support to aid in the fight against canine epilepsy. Established in 2004, Toby's Foundation seeks to increase awareness of canine epilepsy and to help eliminate it by supporting the research to find a gene marker and develop a screening test for this disease.
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Candle in the dark
Candle in the Dark is a charitable organisation funding research into gene therapy for inherited eye disorders causing blindness in young children. Its aim is to help develop effective treatments, ultimately providing a cure for blindness and visual impairment. Visit our pages to find out more and see how you can help.
Candle in the dark
Candle in the Dark is a charitable organisation funding research into gene therapy for inherited eye disorders causing blindness in young children. Its aim is to help develop effective treatments, ultimately providing a cure for blindness and visual impairment. Visit our pages to find out more and see how you can help.
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Find a cure for Lichen Sclerosus (lichen sclerosis). Research and Providers listed. Lichen Sclerosus treatment (especially vulvar lichen sclerosus treatment) is under diagnosed, under treated, and under funded. We are trying to end the pain. Dr. Charles Runels (inventor of the O-Shot (R) procedure) spear headed the funding and organization of this research which will feature principal investigator Andrew Goldstein, MD.
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We need your help to find a cure for dystonia. Dystonia is a movement disorder that affects several hundred thousand children and adults. There are multiple forms of dystonia, and dozens of diseases and conditions may include dystonia as a symptom. Dystonia may affect a single body area or be generalized throughout multiple muscle groups.
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Together let's bring hope for generations of healthy families
Connecting patient care communities with specialized clinical studies. We are a clinical site network embedding research studies in the comfort and convenience of patient communities. By providing easy access to care, we help patients suffering from debilitating diseases now, while bringing hope for a cure to future generations.
Home :: Connecticut Brain Tumor Alliance
The Connecticut Brain Tumor Alliance is a non-profit organization dedicated to offering support and compassion. Our mission is to raise awareness of the disease, provide hope and support for others living with brain tumors in Connecticut and raise money to support and advocate the cutting-edge research we all know someday will find a cure.
DKMS Africa | non-profit organisation | stem cell donors | blood disease
The Sunflower Fund is a non-profit organisation that fights blood diseases like Leukaemia through the recruitment of stem cell donors and maintaining a registry of potential donors committed to helping anyone in need of a life-saving stem cell transplant. We fundraise to cover the cost of education and awareness about the need for and the process to become a blood stem cell donor as well as to cover the cost of the HLA tissue-typing test involved in the recruitment of donors. Together we can fight life-threatening blood diseases. Be somebody’s hope for life by registering to be a stem cell donor, donating money or volunteering.
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Brisbane and Beyond is the result of our extensive travels in Australia. We spent many hours researching for this website and would like to share our experiences and travel tips with you. We hope it will provide you with plenty of information to help you plan your next holiday downunder. During our time in Australia …
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The Draper Richards Kaplan Foundation finds, funds and supports early stage, high impact social enterprises that are tackling some of the world’s most challenging problems. Borrowed from our venture capital legacy we find exceptional entrepreneurs, provide them with 3 years of unrestricted capital and provide rigorous on-going support by joining their board of directors for the 3 years of the grant and partnering with the leader to help them to build capacity in their organization and scale their impact.
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Beyond Batten Disease Foundation
Batten disease is a fatal neurodegenerative disorder that takes away childhood, and then takes away the child.
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