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

River's Gift (AU, 30165280541) Browse events

Established in 2011 by two devastated, yet focused and determined parents searching for answers surrounding the death of their 4 month old son, River Jak Adam. River's Gift has evolved into a global movement, with thousands of supporters across the world and the formation of a dedicated research partnership that is committed to finding a cure for Sudden Infant Death Syndrome (SIDS)

The Board Meeting (AU, 87362165844) Browse events

The board meeting is a dedicated group of volunteers who run surf related events to raise much needed funds for severely disabled local children and their families. The group has been running since 2005 and has helped many families who have fallen through the cracks and those that have high needs. All the funds raised through our everyday hero account for the Sunshine Coast Marathon will be donated directly to See Banjo Run Fundraising for Stem Cell Treatment and his ongoing physical Therapy needs.

Queensland Centre for Gynaecological Cancer (AU, 53013165829) Browse events

  QCGC works in partnership with Queensland Health for the State's gynaecological cancer services. QCGC is lead by a Director and seven gynaecological oncologists providing services to major hospitals in Brisbane, including The Wesley Hospital, Mater Misericordiae and Greenslopes Private Hospital. The team also travels regularly to regional Queensland, particularly Gold Coast, Sunshine Coast, Toowoomba and Darling Downs, Far North Queensland and the Northern Territory. QCGC Research is the research branch of QCGC and is an academic (non-profit) institution situated at the Royal Brisbane and Women’s Hospital (Herston, Brisbane). Its research funds are administered through The University of Queensland, School of Medicine and the Gynaecological Cancer Society. The Director of  QCGC Research's mission is to develop the best standard of care for women experiencing gynaecological cancer. This may include finding causes for and preventing gynaecological cancer or finding better treatment options to cure women affected by gynaecological cancer. We closely work with gynaecological oncology groups nationally (The Queensland University of Technology, The Queensland Institute of Medical Research, and the Australian and New Zealand Gynaecological Oncology Group (ANZGOG)) and internationally (MD Anderson Cancer Centre, Houston, TX; Johns Hopkins Medical Centres, Baltimore, PA; Memorial Sloan Kettering Cancer Centre, New York). The topics of our research are listed on  Our research is funded partly by competitive research grants (NHMRC project grants, smart state research grants, Cancer Australia) and by support from individual and corporate donors.

Lions Cancer Institute (AU, 26521960054) Browse events

Hazel Hawke Alzheimer's Research and Care Fund (AU, 50420515821) Browse events

The Hazel Hawke Alzheimer's Research and Care Fund was established to support research  to investigate  treatments, therapies and models of care for people with dementia.  Research has the capacity to deliver the strategies and treatments to delay, reduce or minimise the impact of dementia in the future. Your donation to this fund honours the legacy of Hazel Hawke who publicly revealed her diagnosis of Alzheimer's disease in 2003 and continued to work tirelessly to raise awareness of what it was like to live with the disease.    

Australasian Lymphology Association (AU, 27091290505) Browse events

Lymphoedema is a life-long distressing condition affecting people from birth to old age.  There is no cure.  This progressive, chronic disorder of the lymphatic system can have ongoing effects on physical and emotional wellbeing of people impacting their quality of life.  With community support, we’ll build understanding of lymphoedema and contribute funds for vital research. The Australasian Lymphology Association (ALA) is committed to promoting the development of lymphology in Australasia. The Association will strive to improve the management of those with, or at risk of developing lymphoedema and enhance communication between health professionals, educators, relevant authorities and government in regard to oedemas and lymphoedema.   There are two types of Lymphoedema, Primary and Secondary - it affects people of all ages - there is no cure Lymphoedema occurs when the lymphatic circulation fails to function correctly, causing persistent swelling of the limb(s) and other areas of the body Early diagnosis can reduce the impact of the disorder for sufferers Keeping cool can help manage lymphoedema Around 100,000 Australians have Primary Lymphoedema and other lymphoedema conditions Cancer patients or survivors are at greater risk of developing Secondary Lymphoedema Around 300,000 Australians have cancer related lymphoedema 20% of Australian cancer survivors will experience secondary lymphoedema - more than 8000 new cases annually If you have unexplained swelling, seek an assessment by a medical practitioner Learn the symptoms and locate an ALA accredited practitioner today at

Southern Fleurieu Cancer Support Group (AU, 39098838042) Browse events

We offer emotional and practical support to all who experience cancer, their partners, carers, families and friends.   Liaison with the general Cancer Nurse provided by the Government for the area.   Liaison with the Breast Cancer Nurse provided by the McGrath Foundation for the area.   Our own people who are cancer survivors or ex-nurses make themselves available to support cancer patients and their families who are going through rigorous and aggressive cancer teatment.  These carers regularly are in contact/direct liaison with other suitable health professionals and departments.   Door to door transport service for people needing to attend cancer related appointments in Adelaide.   We aim to provide a comfortable, stress free journey.   Initial contact by our Care Team Coordinator within 24 hours for initial assistance and then regular contact if needed.   These are distributed quarterly to all our contacts with "goings on" of our group.

ASK-Y (Against The Silent Killer of the Young) (AU, 66190552805) Browse events

ASK Y was founded 2 years after the sudden death of our son and the realisation that so many families have been affected by the loss of loved ones due to cardiac arrhythmias. It was increasingly apparent that in likeness to ourselves, the shock and incomprehension of why and how a young life could be taken without warning signs or symptoms of disease, has compounded the grief with helplessness, emptiness and continual questioning.   So many of us are left without answers. We are not advantaged to have a specific cardiac arrhythmic condition responsible, we have no diagnosis, our loved ones deaths are “unascertained”.   ASK-Y offers support and information for families and friends of all loved ones’ lost to sudden cardiac arrhythmia syndromes and is dedicated to the many who are yet to find answers.

ausEE Inc (AU, 24162709444) Browse events

ausEE Inc. is an Australian charity providing support and information to anyone diagnosed with or caring for someone with an Eosinophilic Gastrointestinal Disorder (EGID) including Eosinophilic oEsophagitis (EE or EoE), Eosinophilic Gastritis, Eosinophilic Enteritis, Eosinophilic Colitis and Eosinophilic Gastroenteritis. We are committed to raising public awareness and supporting the medical community for further research into eosinophilic disorders in Australia. EGID’s occur when eosinophils (pronounced ee-oh-sin-oh-fills), a type of white blood cell, are found in above-normal amounts within the gastrointestinal tract. The eosinophils can accumulate in the gut in response to food and/or airborne allergens and can cause inflammation and tissue damage.