Autoimmune Resource & Research Centre (AU, 77436705768) Browse events

Autoimmune Resource and Research Centre (ARRC) provides education, support , counselling and research programs to help individuals with autoimmune illnesses, in particular, lupus, scleroderma, Raynaud’s, Sjögrens and associated illness. Our mission is to improve health and quality of life of individuals with autoimmune illness through education, support & research.

Meniere's Australia (AU, 30128195371) Browse events

Meniere’s Australia is a national non-profit, non-government organisation supporting those living with Meniere’s disease and other vestibular disorders. Meniere’s disease is a currently incurable condition which affects the fluid balance of the inner ear, causing: fluctuating, progressive hearing loss; aural fullness; tinnitus; dizziness; brain fog; nausea; vertigo & drop attacks.

Peter's Project (AU, 60448395029) Browse events

Before the success and momentum of Peter's Project, those members of the Warnambool community who were faced with cancer had no other choice but to drive 3½ hours to access and undertake the stressful, frequent and time consuming cancer treatment process.    Peter's Project is working to provide a state of the art facility for cancer patients in south-west Victoria and south-east South Australia.    The formation of Peter's Project was driven by the difficulty to access cancer treatment facilities for patients living in the Warrnambool area and surrounding regions.   Peter's Project's inception was on 15th September, 2008, when local man Peter Jellie, aged 49, passed away from oesophageal cancer.   Peter was a family man living and working in Warrnambool.   During the last twenty weeks of his life he was diagnosed and treated.  For eight of these twenty weeks Peter was in Melbourne, 320km away, having treatment sessions lasting for fifteen minutes each day, meaning that Peter spent precious time away from his family, home, work and support network.   This scenario is typical for regional cancer patients. All of this time is critical in their shortened life.    After his death, Peter's wife Vicki, moved forward with a goal to bring radiotherapy to South West Victoria and South East of South Australia, so people affected by cancer could have access to vital radiotherapy treatment locally rather than spending precious weeks away from their family and support network and travelling up to 4-5 hours one way, to receive that treatment.   A recent research document into the need for Radiotherapy for South West Victoria, exhibited above average mortality rates for cancer cases in the region.   One third of those persons who need Radiotherapy, declined treatment due to tyranny of distance, financial, sickness and family social stress issues.   In March, 2009, a Board and Committee of Peter's Project were convened and in June that year, a Trust known as Peter's Project Charitable Trust, was set up and was also endorsed as a tax deductible gift recipient by the ATO.    Peter's Project is a community supported initiative committed to the facilitation of comprehensive cancer services for our region.    After a year of gathering information and initial State government lobbying, a public launch to the community was held in February, 2010.    Over the next 3 years, Peter's Project became very widely recognized by their supportive regional community.    The Committee set a solid foundation model and lobbied both State and Federal governments for a commitment and financial assistance to provide radiotherapy and an Integrated Cancer Centre, based in Warrnambool.    The community took ownership of this cause and rallied together to begin to raise funds to make this vital need a reality.    We have been heard by our Politicians ... the Peter's Project Committee and the thousands of people in our regional community have made their strongest possible representations and have now, in May 2013, had full financial commitment from the Victorian State Government, and the definite outcome of a Cancer Centre with radiotherapy to be established in Warrnambool.    The Peter's Project Committee will continue to lobby the Federal Government for a $10 million contribution toward this facility in 2013.    Peter's Project and their amazing community are ordinary people who have worked together and have achieved positive change through their committed efforts.    The region's community will continue to support Peter's Project until their goal becomes the reality of a fully operational Cancer Centre.      

HAE Australasia (AU, HAE Australasia - N/A) Browse events

HAE Australasia is a patient support network and health promotion organisation dedicated to improving the quality of life for those who suffer the rare condition Hereditary Angioedema. Patients suffer random and debilitating swelling around their bodies including life-threatening attacks in their airways. Your gift can change their life.

Paceline INC (AU, 93943434934) Browse events

Paceline is a charity that raises awareness and funds for cardiac arrhythmias (irregular heartbeats). The funds gathered through Paceline are directed to research which enhances our understanding of these debilitating disorders. With more than 400,000 Australians having one kind of cardiac arrhythmia or another, and this number constantly growing, it is essential that every effort is made to promote understanding and develop treatments. Having funding will allow us to better understand why cardiac arrhythmias occur, enabling us to develop cures whilst also producing strong rehabilitation programmes to change the lives of the people with these conditions. Please help us achieve our objective by donating funds to assist with the research of our world class research facilities, Baker IDI Heart and Diabetes Institute and the Victor Chang Cardiac Research Institute.

One Disease (AU, 57162909284) Browse events

One Disease believes that no Australian should die of a preventable disease. Our mission is to eliminate disease from remote Indigenous communities, one disease at a time. First on the hit list is scabies, which affects 7 in 10 children before they turn 1. Scabies is a mite which gets under your skin. What starts as an innocent itch can result in life threatening illnesses if left untreated, such as rheumatic heart disease and kidney failure.

Asthma Australia (AU, 47931649319) Browse events

Asthma Australia, comprising the Asthma Foundations in every state and territory, is the peak asthma charity in Australia.  For more than 50 years we have been providing education, support and resources for people with asthma and funding important research.  As an independent charitable organisation, we rely on the support of the community to fund asthma education and support programs and to fund vital research into the causes, treatments and a potential cure for asthma.

Lynne King Cancer Care Foundation (AU, 58086074962) Browse events

The Lynne King Cancer Care Foundation was established in memory of the late Lynne King, who as a nurse spent much of her life caring for those with cancer. To read more of her story go to

Hastings Cancer Trust (AU, Hastings Cancer Trust - N/A) Browse events

Cancer is the number one cause of death in Australia, with 1 in 3 men and 1 in 4 women developing cancer by the age of 75. With the Mid North Coast one of the fastest growing regions in NSW the Hastings Cancer Trust was established in 2004 to enhance the care of cancer patients and support for those who care for them. The funds are raised locally and are administered by local people, who fund local cancer projects, on the basis of their value to our community.

Redlands Community Cancer Support Inc. (AU, 52389155735) Browse events

RCCS is established to be a Not-for-profit Charity whose purpose is to advance Health by: 1)    Raising funds for the purpose of assisting individuals, children and families whom are directly impacted by cancer and cancer treatment.  2)    Connecting cancer affected families to education and research material. 3)    Raising funds to purchase cancer diagnostic and treatment equipment for hospitals and medical centres.

Sarah and Friends Foundation Ltd. (AU, 16168050548) Browse events

Sarah was born in 2007 with a suspected rare genetic Inborn Error of Metabolism (IEM). As a result, Sarah is physically disabled, has severe developmental delay, sleep apnea, uncontrolled epilepsy and is unable to speak. The Sarah and Friends Foundation is a registered not for profit charity in Australia, founded by Sarah's parents, and committed to help Sarah and other children with diagnosed or suspected rare genetic Inborn Errors of Metabolism (0-16 years of age).  Inborn Errors of Metabolism (IEM) are a group of disorders, each resulting from a specific gene defect, causing a clinically significant block in a metabolic pathway. Symptoms can include: • Intellectual Disability • Physical Disability • Neurological symptoms and deficits • Encephalopathy • Seizures • Movement Disorders • Temperature Instability • Feeding Difficulties • Deafness and Hearing Defects • Absence or Loss of Vision • Hormonal Defects The Sarah and Friends Foundation raises funds to: • Provide children with rare Inborn Errors of Metabolism with equipment and therapy. • Support research and development in the area of rare Inborn Errors of Metabolism. • Support projects and programs to help diagnose children with rare Inborn Errors of Metabolism.

Haemochromatosis Australia (AU, 79827140617) Browse events

Haemochromatosis Australia is the support, advocacy and health promotion group for people affected by haemochromatosis and their families.  We are run entirely by volunteers with no paid staff. Our vision is that no Australian will suffer harm from haemochromatosis.   We aim to raise awareness of haemochromatosis in the community so that those people at risk are diagnosed and treated early. We organise an annual Haemochromatosis Awareness Week nationally, and conduct awareness activities throughout the year.  We provide support and information through our website, INFO LINE 1300 019028, print and electronic information products, public information sessions and other activities. Haemochromatosis (inherited iron overload disorder) is the most common genetic disorder in Australia, affecting one in 200 people of European descent. If untreated, it can lead to serious, even fatal health complications. Yet is is easy to treat, and if diagnosed before harm occurs, people with haemochromatosis can look forward to a normal, healthy life.

Leukaemia Foundation - VIC (AU, 39133812745) Browse events

 

Menzies Research Institute Tasmania (AU, 95091467444) Browse events

In the late 1980s, the Menzies Foundation supported the establishment of an epidemiology research centre at the University of Tasmania in Hobart, to be named the Menzies Centre for Population Health Research.   The Foundation provided annual funding to the Institute and was successful in obtaining matching funds from the Tasmanian Government. The Menzies Centre for Population Health Research was formed in 1988 and became the Menzies Research Institute in 2004.   From modest beginnings, the Menzies Research Institute quickly gained a reputation for its ground-breaking work into the link between babies’ sleeping position and sudden infant death syndrome (SIDS).   From this work, our research expanded and epidemiological research programs were developed. In 2006, we expanded our focus on both clinical and basic science, to ensure that the depth and quality of our research was enhanced and strengthened.   Some notable successes include discovering: The link between babies' sleeping position and sudden infant death syndrome (SIDS) Platelets found in the blood kill the malaria parasite during the early stages of a malarial infection Seven genetic markers linked to men's risk of developing prostate cancer Higher vitamin D levels are associated with a lower relapse risk in multiple sclerosis Nerve cells in undamaged parts of the brain can remodel themselves in response to acquired brain injury. At the Menzies Research Institute Tasmania our aspiration is to contribute significantly to human health and wellbeing, with particular emphasis upon research that takes advantage of Tasmania’s unique population resource and other competitive advantages.   Our research efforts focus on preventing a range of diseases including cancer, multiple sclerosis, cardiovascular disease, diabetes, chronic lung disease, osteoporosis, mental health and dementia.   We are undertaking nationwide studies and collaborating with interstate and international researchers.   Menzies has a clear vision for the future. We plan to continue expanding our research to cover more disease areas, start new projects that are highly innovative, attract more world-class scientists to our shores, and increase our collaborative links throughout Australia and internationally.   Our forward thinking will bring us one step closer to our vision of preventing or curing disease and saving lives.  

Muscular Dystrophy SA (AU, 54094195356) Browse events

The Muscular Dystrophy Association Inc provides a range of specialised services to adults and children with a neuromuscular disorder, which affects around 1 in 1000 people.  That equates to roughly 1,500 South Australians. At present there is no cure for Muscular Dystrophy which causes muscles to become weaker and waste away.  Everyday tasks like walking, showering, turning over in bed and sometimes even breathing become much more difficult.  Many people with neuromuscular disorders will eventually need to use a wheel chair, although some will manage without.  Despite this, most people with Muscular Dystrophy are not affected in their ability to think, feel, hope and dream.  They, their families and carers all aspire to as full and active a life as possible.   By donating to, or raising money for, the Muscular Dystrophy Association in SA you will make a difference to the life of a child or adult with a neuromuscular disorder.  You can help them to live the full and active life they deserve. For more information visit  

RoCan (AU, 97131857719) Browse events

Rotary Against Ovarian Cancer - is a trust fund established by Rotary Club of Williamstown in 2003 with the objective of increasing community awareness of this deadly disease. Ovarian cancer is the predominant form of gynaecological cancer, claiming the lives of hundreds of women each year. By the time that most women are diagnosed with ovarian cancer, it has spread throughout the body and the survival rate is less than 30%. If ovarian cancer could be detected at an early stage, before it has left the ovary, then the survival rate would be greater than 85%. Currently there is no community-based screening test for early stage ovarian cancer. Most people mistakenly believe that the Pap cancer smear will detect all gynaecological abnormalities, but this is not the case. This year, more than 1200 women in Australia will be diagnosed with ovarian cancer. Over 700 women will die from the disease. ROCAN'S fund raising aims to provide the financial resources to find an early stage diagnostic test to increase the survival rate of women affected.   Support a group of 30 cyclists riding for a cause to help research find an early detection test for ovarian cancer March 6

Australian Centre for Blood Diseases (AU, 44074856572) Browse events

The Warwick Cancer Foundation (AU, 86605357879) Browse events

The Warwick Cancer Foundation is the first non-profit organisation in Australia focused on supporting young adults under 40 during their cancer treatment. The foundation also supports carers of those currently in treatment and survivors aged under 40. Young adults are the fastest growing demographic among over 10 million new cancer diagnoses each year worldwide. While there are many cancer related organisations in existence today for children and older adults, there are none that focus on meeting the needs of young adults past the age of 25. Young adults with cancer can experience a unique set of issues and challenges: • Feelings of anger, panic, denial, guilt, uncertainty, shock and fear • Feelings of isolation and disconnection from family and friends • Fear of mortality • Emotional distress • Loss of independence • Financial pressure and uncertainty- many young adults do not have sufficient health or life insurance to cover   expenses and time away from work • Fertility Preservation • Intimacy and Relationship changes The Warwick Cancer Foundation’s programs and services have been developed under psychosocial guidelines to   address key issues faced by young adults with cancer. • Peer to peer support programs aim to reduce isolation, destigmatise cancer and normalise side effects of cancer   treatment • Social media platforms provide a safe environment to communicate feelings of depression, anxiety and fears   related to cancer. Many young adults with cancer are unable to voice their fears to loved ones and friends for fear   of `burdening’ them • Provide a safe environment to connect with others who are currently in treatment without fear of judgement of   physical appearance • Promote psychosocial support to assist in coping skills for different stages of cancer and survivorship • Provide age appropriate information and referral • Awareness campaigns to promote prevention of cancers in young adults To learn more about The Warwick Cancer Foundation and the work we do, visit

Hunter Prostate Cancer Alliance (AU, 19231156786) Browse events

Hunter Prostate Cancer Alliance is challenged to provide primary care support for men, their partners, families and colleagues when they seek information and services relating to a diagnosis of prostate cancer.    We also work to encourage men over 40 years of age to take advantage of the simple "Little Prick" test know as a PSA test.  This test is performed by your GP and looks for Prostate Specific Antigen which can be the first indicator that something is wrong with the prostate.    Early diagnosis of prostate cancer increases the likelihood of a full cure.   The Alliance is firstly targeting men over 40 years of age as the chance of developing prostate cancer for such a man is 1 in 8 throughout his remaining life. Also, men with a family history of prostate cancer as they have a risk of at least three times greater, than those who do not have such a family history, and should be tested from the age of 40.   To assist individuals and groups of men and women with information about prostate cancer, in order to promote rational testing of men for this disease and to encourage the development of intellectual and emotional support systems for men diagnosed with prostate cancer and those supporting them.   Advocate a strong awareness within the Hunter New England region of the need for immediate initial testing and thereafter regular prostate cancer testing as frequently as available evidence dictates in order to curb this disease in its onset. Provide primary care services to newly diagnosed men, their partners, families and colleagues to understand and come to terms with the complexity of this disease along with the variety of options available for treatment.  Encourage the development of services that will promote a positive mental outlook for those affected by this disease and in those supporting them. Emphasise the importance of continued education to recognise and deal with the many far reaching effects of prostate cancer, including the fact that many low grade cancers may be safely monitored without treatment.  

MS Australia - NSW/ACT (AU, 20000049669) Browse events

Each working day five Australians are diagnosed with Multiple sclerosis (MS). MS is a chronic, often disabling disease that randomly attacks the central nervous system – the brain and spinal cord. The progress, severity and symptoms of the disease are unpredictable and symptoms may range from tingling and numbness to paralysis and blindness. MS usually strikes people in the prime of their life – the average age of diagnosis is just 30 and 87% of these people are of working age. It affects three times as many women as men. The overall cause is still unknown and there is no known cure. MS Australia raises funds to help care for people living with MS and to continue the research to find a cure. You can help us by calling 1800 CURE MS (1800 287 367).

Foundation 21 (AU, 99586790028) Browse events

Our aim is to enhance and support existing services and to raise the public's awareness of the positive contributions individuals with Down syndrome make in our community. foundation 21 is dedicated to helping ease the financial burden placed on families who have a child with Down syndrome. Without financial assistance some families may never have access to the extra services that their child requires. At present, our focus is providing funding for speech therapy. It has been widely published that to maximise communication development in children with Down syndrome they should receive early and continuing instruction. We raise funds through corporate sponsorships, donations, bequests and other fundraising initiatives, such as Buddy Walk and an annual gala dinner. All donations of $2 or more are tax deductible

Garvan Research Foundation (AU, 67107850751) Browse events

The Garvan Institute of Medical Research is a world leader in biomedical research, pioneering study into some of the most widespread diseases affecting our community today. Research at Garvan is focused on understanding the role of genes in health and disease as the basis for developing future cures. For over 45 years, significant breakthroughs have been achieved by Garvan scientists in the understanding and treatment of diseases such as: Cancer Diabetes and obesity Alzheimer’s and Parkinson’s disease Osteoporosis Arthritis, asthma, rheumatoid arthritis and other immune disorders Pituitary disorders Garvan’s ultimate goal is prevention and cure of these major diseases.

Look Good Feel Better (AU, 39010976682) Browse events

Motor Neurone Disease (MND) Tasmania (AU, 21877144292) Browse events

Casey Tutungi Future Fund (AU, 75491220191) Browse events

Casey Tutungi a local footballer was tragically involved in a football incident that has left him with debilitating spinal cord damage. The Casey Tutungi Future Fund is a trust fund that he been established for Casey's future. The fund will assist in providing Casey with support, medical equipment and essential equipment he will require during his rehabilitation and into the future.