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.

Neil Sachse Foundation (AU, 30624423759) Browse events

Today they will never walk again. Neil Sachse lives for the day that people with spinal cord injury will walk again. He established the Neil Sachse Foundation as a first step to curing spinal cord injury. Thanks to vital community support, we have established the Neil Sachse Foundation Spinal Cord Injury Research Centre, to provide a dedicated laboratory for researchers and students. As an integral part of the University of Adelaide's Neuroscience Research Insitute, the Centre will also become an international centre-of-excellence aimed at making a significant difference to the lives of people who suffer a spinal cord injury. Research will focus on protection of nerves in the spinal cord immediately following damage caused by accidents or falls (neuroprotection) and to nerve regrowth (reconnection). Your support will help these people take their first step to a better quality of life.

Bendat Family Comprehensive Cancer Centre (AU, 84140233790) Browse events

  The Bendat Family Comprehensive Cancer Centre has brought together most of the elements involved in cancer care and combined them on one campus, with clinicians from a full range of disciplines associated with cancer treatment including oncology, haematology and palliative care.   The Centre not only makes Western Australia a national leader in providing comprehensive cancer programs but ensures Western Australians have access to the very best cancer treatment. An important component of the Bendat Family Comprehensive Cancer Centre is the complementary therapy services provided by SolarisCare.   The Centre is also committed to ongoing research of cancer treatment and outcomes - ensuring our patients are receiving the most advanced, contemporary treatment as well as contributing to the wider body of knowledge in relation to cancer. Integral to the success of the Centre is providing coordinated care. Multi disciplinary teams ensure optimal standards of clinical care are achieved.   The Bendat Family Comprehensive Cancer Centre includes: Ground floor - Ivy Suite and specialist rooms Harry Perkins Ward (3rd floor) - 30 bed ward including 5 palliative care rooms Rhinehart Family Floor (4th floor) - Endoscopy Unit The Hancock Family Medical Foundation (Inc) - St John of God Pathology   For further information, please contact the Bendat Family Comprehensive Cancer Centre on 9382 9562.  

Bolt Blower Invitational (AU, 81998938403) Browse events

IRT Research Foundation (AU, 52000726536) Browse events

Our population of older people is on the rise, and we are living longer than ever before.  Our health and wellbeing is the key to ageing well and keeping us active within our communities.  We might have friends, relatives or be caring for people who are starting to feel the effects of mature age.  Chronic pain, dementia, stroke, falls and mental health can have a major impact on quality of life. The IRT Research Foundation supports research that can positively influence the ageing experience.  The findings from the research we have funded can be shared with the community, other researchers, policy makers, carers, health professionals and service providers to make an impact.   Research has the ability to throw light on important issues like disability, poverty, social exclusion, nutrition, mental health and risk factors in dementia. Research is essential to help policy makers and organisations representing older people to plan better and more efficient services.   Research helps older people to lead full and meaningful lives and participate in their communities, living independently with dignity and the ability to make their own decisions.   When you donate to the IRT Research Foundation you are supporting positive ageing – for the people you care for, your friends, family and future generations.  Your donation is backed by the funds of the IRT Group, so you can ensure 100% of your donation will go directly to fund important research.   Your donations are completely tax deductible and you will receive a tax invoice immediately via e-mail upon completing your donation.   IRT Research Foundation: a division of the IRT Group.

Solaris Care (AU, 29933725490) Browse events

SolarisCare aims to improve the quality of life of cancer patients and carers by giving them the support they require to cope with the emotional and physical side effects of cancer diagnosis, treatment and recovery. A purpose built drop-in centre provides a safe place to reflect and have time-out. Trained volunteers provide information, links to other support groups, a 'listening ear' and complementary therapies. The SolarisCare Foundation Research Team brings together representatives from health care services, accredited complementary therapists and universities across the Perth metropolitan area with the vision of promoting and supporting research into patient centred cancer care.  SolarisCare Foundation is completely self funded and relies on the generosity of people from local business and the community who share the vision and recognize the importance of providing supportive care to cancer patients and carers.

All Mixed Up (AU, 97204841349) Browse events

  To Help Tasmanian Families and Individuals struggling with Terminal Cancer by helping them financially, whether it be by paying bills, airfares or the necessaries of life.   ALL MIXED UP came together when a very close friend was diagnosed with terminal secondary liver cancer. The group of friends wanted to help out the family financially and to help there friend live out his life long dream of travelling Australia with his family.   All Committee members have volunteered there time an energy into all details of this orgasnisation and fundraisers we personally as an organisation have run, no wages are paid to any member from any of the funds that we raise.                        Living with a chronic illness, such as cancer, can be a disrupting force in your life. Besides the physical aspects of the illness, from coping with treatment side effects to being limited in your abilities or independence, there are also numerous social complexities that can make managing difficult and everyday life more stressful.          Your illness may make working an impossibility, which may cause financial problems or add to the stress of paying for treatment. For some patients and families, the financial burden is apparent at diagnosis, while for others, it builds up over the course of years of treatment.          The financial burden for cancer patients is the cause of many missing doctor appointments, failing to take medication, or cutting back on necessities. Out-of-pocket expenses for cancer patients continue to be on the rise, leaving many with a huge financial burden that can be almost impossible to overcome.                                     You may also feel alone while dealing with the hurdles of treatment, testing and doctor visits. Experience has taught you that your body post-treatment is different than you were prior to The diagnosis, but nobody said anything about that. Right now, feeling overwhelmed might be described as an understatement.           Still, matters of the pocketbook are often the most stressful, and it is not unusual for patients and family to feel embarrassed to discuss financial issues. However it is important to reach out before The illness becomes a tremendous financial crisis, but where do you look for help?                     This is where we can help, we run Fundraisers to help patients and families in their time of need, whether it be car registration, rates payment, medical equipment, air fares, new washing machine or other household item, school clothes/excursions, the list is endless.                               Just remember you are not alone, we are here to help.    

Hereditary Spastic Paraplegia (HSP) Research Foundation (AU, Hereditary Spastic Paraplegia (HSP) Research Foundation - N/A) Browse events

The HSP Research Foundation is an Australian organisation formed in 2005. It is both an Incorporated Association and a Registered Charity. It is 100% run by volunteers. There are no paid workers. The focus is on research, support and education. Over 95% of all funds raised (ie. over 95c in every dollar) go directly to fund HSP research in our Towards a Cure for HSP research program. Our website is the hub of our widely dispersed community. We are part of an HSP global community and actively collaborate with similar organisations worldwide. The Hereditary Spastic Paraplegia (HSP) Research Foundation was created in 2005 with the purpose of finding a cure for HSP – an inherited, degenerative disease affecting mainly the legs, causing spasticity and severely impairing walking.  Many HSPers need canes, walkers or wheelchairs to get around.  The HSP Research Foundation is an incorporated, registered Australian charity, which has successfully funded research into genetic testing to identify specifically which of numerous possible gene mutations is causing the disease in each case. We are now funding a research program Towards a Cure for HSP using adult stem cells, and are at the stage of initiating a project to discover therapeutic drug candidates to compensate for impaired cell functioning caused by HSP gene mutations.   An early focus of the Foundation was to facilitate the establishment of a reliable, fast, affordable, nationally-available, genetic testing service for HSP.  One of the immediate benefits is to vastly improve diagnosis, so eliminating the uncertainty regarding family members’ disease status and the negative impact that has on the wellbeing of both individuals and families.  By far and away our main focus now is our research program Towards a Cure for HSP. The Foundation is also the community hub for HSPers in Australia, providing support, awareness and education – including this website and annual Workshops in different cities.   Over a period of 2 years the HSPRF collaborated with the ANZAC Research Institute of the University of Sydney to develop tests for the most common HSP genes and funded the research in the amount of $84,000.   The Foundation then turned its attention to stem cell research, raising $100,000 to fund a Pilot Study conducted by the National Centre for Adult Stem Cell Research (NCASCR) at the Griffith University-based Eskitis Institute for Cell and Molecular Therapies in Queensland, in association with the Kolling Institute of Medical Research of the University of Sydney.   Because of the scope and promise of this research, and the local availability of world-class people and facilities, the Foundation initiated this project and fostered it to the stage of implementation. It is now complete, yielding promising results and lending confidence to pursue a new research project for 2010/11 to discover therapeutic drug candidates to compensate for cell functioning impaired by HSP gene mutations.   The Foundation is pursuing funding from Australian philanthropic organisations, and from the Australian HSP community by direct fundraising and encouraging people to hold events and fundraise on our behalf.   Paramount in the Constitution is the purpose statement. Objects and purposes of the association are: As its principal activity, to promote the prevention and/or control of Hereditary Spastic Paraplegia (HSP) in human beings and without limiting the foregoing. To promote research into the detection and prevention of the disease of HSP. To advance genetic detection, control, prevention and alleviation of suffering for people with HSP. For the above purposes to maintain a gift fund into which gifts and any money received will be paid.