The Monaro Committee for Cancer Research was formed in 1996 by the daughter of a young Monaro mother who after a 5 year struggle lost her battle with cancer.Since its inception the MCCR has supported cancer outreach services on the Monaro. In 2007 after much lobbying, a local oncology service was introduced to the Cooma Hospital. Local support raised in excess of $100,000 towards this project and to-day we have a successful outreach oncology service.MCCR is a local voluntary group of dedicated women working towards further cancer support and services for the Monaro Region.Your support for our next fundraiser Dancing with the Cooma Stars will enable MCCR to continue assisting cancer sufferers on the Monaro.
The Mission Massimo Foundation is a non-profit organisation that promotes the prevention, diagnosis and treatment of childhood Leukodystrophies. These are a group of life-threatening genetic conditions that affect the formation of myelin, a complex fatty substance that acts as an insulator around nerve fibres in the brain. Unfortunately, more than 50% of variants remain genetically unclassified offering families little hope of treatment and a usually tragic outcome. Whilst individually rare, collectively these disorders are not altogether uncommon and may affect up to 1 in 2,000 births yet their existence remains almost unknown. Our mission is to accelerate the discovery of genetic causes for these disorders and to translate these into clinical treatments.
AFE is a life-threatening, acute, and unexpected birth complication that affects both mother and baby. It is a leading cause of maternal death and suffering across the globe and is estimated to affect 1 in every 40,000 births. The AFE Foundation, a non-profit organization established in 2008 by an AFE survivor, is a unique coalition of affected families, respected clinicians, world-renowned researchers, and engaged advocates working together to accomplish 3 key initiatives: Advancing research to better understand, treat, diagnose, and someday prevent AFE. In 2013, the AFE Foundation joined into a formal collaboration with Baylor College of Medicine in Houston, Texas in the United States and established the international Amniotic Fluid Embolism Registry ™ . Promoting awareness and education for the medical community through participation at various clinical meetings, grand rounds, and CME events. The foundation also provides access to safety bundles and published literature to aid in the management and diagnosis of AFE. Offering support to the patients, families, and care providers affected through access to accurate and timely information, outcome specific resources, and connecting them to our community forums.
for more information on MND . The MND Research Institute of Australia promotes MND research and encourages projects in both basic science (to understand the causes and find effective treatments and a cure) and applied research (to provide the best possible care for people living with MND). Funding is provided for MND research in Institutes throughout Australia. Reports on the funded projects are published in a bi-annual newsletter which is distributed nationally. The MND Research Institute of Australia aims to provide $2,000,000 for MND research each year and your help is needed to achieve this goal.
The Australian Mitochondrial Disease Foundation (AMDF) funds essential research into the diagnosis, treatment and cure of mitochondrial disorders, and supports sufferers and their families. AMDF also works to educate the general public and the medical profession about mitochondrial disease. One Australian child born each week will develop a severe or life-threatening form of mitochondrial disease. There is currently no cure and few effective treatments.
Shake It Up Australia has a clear mission: To find the cure for Parkinson’s. Our partnership with The Michael J. Fox Foundation funds world’s best research in Australia, targeted at finding better treatments and ultimately a cure. 100% OF YOUR DONATION GOES DIRECTLY TO RESEARCH.
The list of ailments and conditions that can affect our bones is as long as the longest bone in your body, and any one of those ailments can affect you for life and sometimes with life-threatening consequences. Since 1991, the Bone Health Foundation (formerly the Bone Growth Foundation) has funded research to identify treatments and cures for musculoskeletal conditions that include scoliosis, hip dysplasia, fragile bones and bone cancer. These conditions affect more than 6 million men, women and children in Australia.
Diabetes Australia Research Limited supports and develops the field of diabetes research in Australia. We do this by funding research towards the prevention and management of diabetes or the cure of diabetes.
Our mission is to support, inform, educate, network, and advocate for families with a child with Angelman Syndrome and to establish support systems for people with Angelman Syndrome and their families.We aim to foster scientific research activities on the diagnosis, treatment, management and prevention of Angelman Syndrome and to raise funds for the promotion and attainment of these objectives.
The Children’s Tumour Foundation of Australia (NF Australia) provides care and support to those impacted by Neurofibromatosis (NF), the umbrella term for three genetic conditions (NF1, NF2, Schwannomatosis) that cause tumours to grow on nerves throughout the body. The most common form of NF is Neurofibromatosis Type 1 (NF1). Although usually diagnosed in children, NF is a lifelong medical condition and can affect many organs in the body, including the skin, eyes, bones, and nervous system. The Foundation is dedicated to providing information and support, public awareness, and raising funds to develop effective treatments and find a cure for NF.
PlusLife is a not-for-profit organisation and one of the premier tissue banks in Australia. We collect, screen, store and distribute donated human bone and tissue graft materials for surgical procedures. Thanks to generous bone and tissue donors and their families, these transplants help children and adolescents with spinal deformity and bone cancers; adults with bone cancers and people with joint problems caused by debilitating arthritis.
We are a local charity which provides financial assistance in the form of pharmacy and chemotherapy medication, dietitian prescribed food/drink supplements, partial payment of electricity/gas accounts and food/fuel vouchers to cancer patients living in Canberra, Queanbeyan & surrounds. We provide assistance to all ages and all types of cancer which makes us unique for cancer support. Our administration costs are covered by a grant which allows us to make sure all proceeds from fundraisers and donations go directly to the cancer patients we support. Right now we are spending $35,000 per month supporting over 700 cancer patients.
The RMH Neuroscience Foundation is a world-renowned neuroscience research centre and one of the leading organisations investigating the causes, complications, treatment and prevention of brain diseases such as brain tumours, stroke, multiple sclerosis, epilepsy and movement disorders, including Parkinson’s diseases.
The E.J.Whitten Foundation is a leading men’s health not-for-profit charity organisation, aiming to increase awareness of prostate cancer and raise funds for research. Our vision is to decrease the prostate cancer fatality rate through increased education and awareness. As we receive no government funding we do this via annual fundraising events and public donations.
Down Syndrome NSW aims for everyone with Down syndrome to reach their potential and lead full, active lives in the community. We support children and adults with Down syndrome, their parents and families, sharing our experiences, expertise, resources and networks. We provide guidance, social networks, education, camps and other services.
The Mission of the Australian Spinal Research Foundation is to facilitate research and disseminate knowledge that furthers the understanding, development and effectiveness of chiropractic care.
The Craniofacial Foundation (Australian Cranio-Maxillo Facial Foundation) raises finance for needy patients suffering from craniofacial disorders or those who have suffer through accident or disease. The Craniofacial Unit is recognised world-wide as a Centre of Excellence in bringing a new face and a new future to thousands of people - 90% of whom are Australians.
The Bronchiectasis Foundation is the only charity in the UK especially for people with Bronchiectasis. We are committed to helping improve the lives of people with Bronchiectasis. Bronchiectasis is an underdiagnosed disease -- with the potential to cause devastating lung damage.
The Ladybird Foundation supports breast and gynaecologic cancer research in Western Australia. It is a registered charity in Western Australia. We raise and grant funds for excellent Western Australian researchers who are striving to improve cancer outcomes in these fields. By supporting excellent local researchers we increase our community's access to the benefits of the latest research breakthroughs. Thank you for your help!
To promote a healthier community by reducing the incidence and impact of cancer in the Canberra area through research, information, education and supportive care.
In partnership with families, other providers and the community to improve the linguistic, educational and social outcomes of deaf children by promoting innovative early intervention services, research and advocacy.
Our organization is dedicated to supporting patients and families with Alport Syndrome, a genetic kidney disease, to funding Australian research and in raising awareness. Alport Syndrome is an inherited disease leading to early kidney failure, and also affecting the inner ear and eyes.
The Gut Foundation is the only Australian not-for-profit organisation dedicated to conducting research and providing public education regarding the treatment and prevention of a range of gastrointestinal diseases and conditions. These conditions include but are not limited to bowel cancer, coeliac disease, irritable bowel syndrome, malnutrition, indigestion, reflux, diarrhoea and stomach ache.
The Spinal Cord Injury Network (Australian Spinal Cord Injury Network Ltd) is an alliance of leading researchers, frontline clinicians and people with spinal cord injury. We are working together to promote recovery from spinal cord injury by helping to develop research and facilitate clinical trials. A key goal is to work towards a cure for spinal cord injury.