Browsing Charities
226 - 250 of 615 results

The Skin Hospital (AU, 23001578105) Browse events

YTD Raised: $848.00

Since 1978, we have been a not-for-profit centre of excellence in the diagnosis, treatment, research and education of skin disease, including skin cancer. We have specialist dermatology clinics and licensed day surgeries in Darlinghurst and Westmead in Sydney where each year we have over 44,000 patient visits and see some of the most serious cases of skin cancer.

Cancer Surgery Research Foundation (AU, 83089161704) Browse events

YTD Raised: $847.60

CanSur is a not-for profit charity providing donors with tax deductibility for their contributions. One in three people will get cancer. It will touch your life as it has touched many others. Please share in CanSur - your participation will make a difference in the battle.

Danii Foundation Ltd (AU, 91157880147) Browse events

YTD Raised: $835.00

Established in 2012 by parents Donna and Brian Meads-Barlow, the DANII Foundation was set up as a legacy to their 17 year old daughter Daniella following her sudden passing in 2011 as a result of a night-time hypoglycaemic episode - a diabetes complication more widely known as "Dead in Bed" syndrome. The Foundation's vision is for a world where people with type 1 diabetes live without the fear of never waking up. Our mission is to make affordable, life-saving alert technology a reality for people with type 1 diabetes, with the ultimate goal of preventing Dead in Bed syndrome.

Haemophilia Foundation Australia (AU, 89443537189) Browse events

YTD Raised: $821.21

Haemophilia Foundation Australia (HFA) represents people with inherited bleeding disorders and their families. We are committed to improving treatment and care through representation and advocacy, education, and the promotion of research.

Lung Institute of Western Australia (AU, 91052654451) Browse events

YTD Raised: $810.31

The Lung Institute of Western Australia’s objectives are to:

MND and Me Foundation (AU, 34148877141) Browse events

YTD Raised: $804.64

The MND and ME Foundation Ltd is a not for profit registered charity built on the support of volunteers. Our aim is to raise funds to assist to provide a quality of life for people living with MND which is not compromised by their diagnosis - a life with dignity and independence. The Foundation actively contributes financially towards research into finding a cure . The next stage in the Foundation's development will be to ensure those who have to live with this terrible disease and their families are supported both in financial and non-financial ways.

Tour de Rocks Ltd (AU, 50157824014) Browse events

YTD Raised: $799.00

Tour de Rocks is an organisation committed to inspiring and engaging our communities to work together to make a difference in the fight against Cancer. Our objectives include raising funds for cancer research, increasing the level of awareness in relation to Cancer prevention through education and awareness programs, training programs and nutritional information. We will also assist where we can to ease the burden for those engaged in the battle against Cancer. We work, achieve, celebrate together.

Arthritis & Osteoporosis WA (AU, 43390598024) Browse events

YTD Raised: $795.95

Arthritis & Osteoporosis WA is dedicated to reducing the incidence and disabling effects of arthritis, osteoporosis and related conditions in the people of Western Australia, through programs in care, education and research.

Centenary Institute Medical Research Foundation (AU, 85778244012) Browse events

YTD Raised: $774.79

When you support Centenary Institute, you’re helping awesome, dedicated scientists fight and beat disease to improve our health. We conduct fundamental research understanding the work of the body’s genes, cells and proteins. Through our connection to RPA and the University of Sydney, we apply all we learn directly to better treat and prevent diseases that affect so many of us. It is our dream to see people live better, longer lives. www.centenary.org.au

Clifford Craig Medical Research Trust (AU, 12058280961) Browse events

YTD Raised: $770.15

The Clifford Craig Medical Research Trust was established in 1992 by the local community with the founding vision to create a world-class medical research institution in Northern Tasmania. Clifford Craig conducts vital medical research into the health issues that affect the people within our community. Most importantly, our program funds medical research that helps attract researchers, higher degree students, and specialist doctors and physicians to work in our region.

Children's Cancer Centre Foundation (AU, 96114942415) Browse events

YTD Raised: $745.00

The Children’s Cancer Centre Foundation was established in 1992 to improve the welfare of children and adolescents with cancer by funding clinical, research and family support programs. Our funds are directed to programs at the Children's Cancer Centres of The Royal Children’s Hospital, Monash Medical Centre and Peter MacCallum Cancer Centre, and to childhood cancer clinical research at Murdoch Childrens Research Institute.

No Matter What (AU, 97598172463) Browse events

YTD Raised: $738.51

The Evie Charitable Association exists to support children and young people living with or dying of cancer.

Asthma Foundation of Victoria (AU, 16873513650) Browse events

YTD Raised: $732.00

Since 1963, the Asthma Foundation of Victoria (AFV) has worked actively in the community towards reducing the impact of asthma on the day-to-day lives of Victorians. Over the last 50 years, AFV has been the leading consumer authority on asthma and anaphylaxis education, information, research, community advocacy and support in the state. Nominated as a Federal Government health priority, Australia has amongst the world's highest rates of asthma. It is one of our most prevalent chronic health issues. Asthma is among the key reasons for childhood hospitalisation and school absenteeism but impacts across all age groups. Over 600,000 Victorians have asthma. It is a serious condition, which resulted in 378 deaths in 2011. Recently AFV has expanded its services to encompass anaphylaxis, including peanut food allergy, to inform and assist people in ways to best manage this condition. It is people like you that help make a difference. If your activity requires our support please call our office on (03) 9326 7088 or visit our website.

Victor Chang Cardiac Research Institute (AU, 61068363235) Browse events

YTD Raised: $727.25

Heart disease remains the leading cause of death and disability in our society. The Victor Chang has as its mission the relief of pain and suffering and the promotion of well-being through an understanding of the fundamental mechanisms of cardiovascular biology in health and disease.

Sanfilippo Children's Foundation (AU, 16165855470) Browse events

YTD Raised: $687.03

Sanfilippo Children's Foundation is a not for profit organisation dedicated to driving clinical research, enabling access to effective treatments and improving the quality of life for children affected by the fatal childhood disease, Sanfilippo Syndrome.

Haemophilia Foundation Western Australia Inc. (AU, 42961282521) Browse events

YTD Raised: $681.60

HFWA is a voluntary organisation dedicated to attain better treatment conditions for people with a bleeding disorder and provide support to their families (and others) by providing information about bleeding disorders, advocacy, liaising with Government and Hospitals, welfare, education support, research and development of new and improved therapies.

The Australian NPC Disease Foundation Inc (AU, 87767010514) Browse events

YTD Raised: $680.00

The Australian NPC Disease Foundation Inc supports patients and their families diagnosed with Niemann Pick Type C Disease (NPC Disease). NPC Disease is a terminal, progressive, neurological disease with a life expectancy of only 10 years from time of diagnosis. NPC Disease has a relevance of 1:150,000 births and there are only approximately 500 world wide diagnosed patients aged from new born to adulthood. Approximately only 10-15 cases of those world wide diagnosed, reside in Australia. There are different onset ages for NPC Disease, infantile (new-born to 3), Childhood (aged 3-13), Adolescent (13-20) and Adult onset (over 21 years). Each age onset still has the same prognosis... death! There is currently NO CURE for NPC disease, and symptoms are only treated accordingly with available medications. Symptoms include: - Slurred/Mumbled/Broken Speech, leading to loss of speech completely - Balance issues, mobility problems, gaits, leading to being bedridden or wheelchair bound - Swallowing problems, leading to choking and high risk of aspiration and lung infections causing pneumonia, leading to being peg fed through the stomach - Dementia, short term memory loss, Cognitive regression and behavioural issues - Limb distortion, stiffness, dystonia causing high levels of pain and inability to use limbs and digits - Seizures, varying from minor to Grand Mal uncontrolled seizures - Psychotic episodes, hallucinations, etc  - Certain death. Currently the Foundation is desperately trying to raise funds for a more appropriate and advance treatment option for NPC Disease, being conducted at the University of Melbourne. Compounds such as zinc and copper are being worked with on NPC Mice, which could potentially lead to increasing the life span and quality of NPC Patients both in Australia and around the world. The project needs urgent funds to continue to employ the Scientist and to manage and house the NPC Mice. This cost is estimated at $120,000 per year. Fundraising around Australia has began with a limited amount of diagnosed families, but extra help is desperately needed to reach this cost.

Motor Neurone Disease Association of Queensland Inc. (MND) (AU, 75990922939) Browse events

YTD Raised: $676.00

At Motor Neurone Disease Association of Queensland's (MNDAQ),we aim to provide and promote the best possible support for families living with motor neurone disease within Queensland, to support research and raise awareness in our community. Since 1983, MNDAQ has been supporting people living with MND, their families and those who care for them, through the provision of information, education, support services and specialised equipment. Today, MNDAQ is committed to supporting many Queenslanders who have been affected by MND, including their families, friends, employers, and workmates. MNDAQ receives very little recurrent funding and relies heavily on community support to help people with MND to live better for longer. MND is a neurological disorder which can affect anyone at any time. The most common period is midlife, however it is increasingly affecting younger people, and can affect both men and women. For a person being diagnosed with MND, it could mean the progressive loss of the use of their limbs, their ability to speak, to swallow and to breathe, whilst their mind and senses usually remain intact. The effects of the disease are rapid, debilitating and terminal. Currently there is no known cause or cure. Please help us support people living with MND. For more information: www.mndaq.org.au or Phone 07 3372 9004

Saba Rose Button Foundation (AU, 59188154493) Browse events

YTD Raised: $640.00

This Foundation was established to help our special little girl Saba. Saba has brain damage (CP), quadriplegia and epilepsy because of a severe reaction to the flu vaccination. This Foundation enables Saba to access all the ongoing necessary therapy, equipment and intensive care she needs 24/7. Please help support Saba. X

The Spinal Research Institute (AU, 11162207169) Browse events

YTD Raised: $602.29

The Spinal Research Institute (SRI) is mobilised by a vision: to see people with spinal cord injuries lead the most healthy, active lives possible. Our mission is to support world-class clinical research and trials. We provide means for spinal researchers to build vital international collaborations and to translate research into life changing health solutions for people living with spinal cord injuries. People with spinal cord injuries live with many health challenges which limit their independence and quality of life. They hope a cure will be discovered, but they want better health and to live well – TODAY.

Edith Cowan University (AU, 54361485361) Browse events

YTD Raised: $588.01

Edith Cowan University (ECU) is a large, multi-campus institution based in Perth, WA. We’re proud of our strong community ties and vibrant research culture - donations to ECU can support anything from student scholarships to world-class research, making a real difference in our communities.

Lung Foundation Australia (AU, 36051131901) Browse events

YTD Raised: $575.00

Lung Foundation Australia is responding to the need to reduce the significant and debilitating cost of lung disease to individuals and the community and to provide information and support to patients, their families and carers who are impacted by a lung condition. Our mission is to make lung health a priority for all in Australia and is underpinned by our goals to promote lung health; empower patients, their families and carers; influence public and corporate policy; work with clinicians to promote best practice in prevention, diagnosis and management; and encourage medical and scientific research through research Awards. Programs and initiatives of Lung Foundation Australia include: - Lung Cancer National Program - Interstitial and Orphan Lung Diseases - Chronic Obstructive Pulmonary Disease (COPD) National Program - Information and Support Centre - Lung Cancer Network - Respiratory Infectious Diseases - Chronic Cough in Infants, Children and Adults - Research Awards - Indigenous Health Lung Foundation Australia receives no on-going government funding to support our core activities and relies on funding from events, projects, bequests and donations from private and corporate donors. Lung Foundation Australia was established in 1990 by thoracic physicians concerned at the lack of research into lung diseases and support for lung disease sufferers, Lung Foundation Australia is a registered charity with its national office located in Brisbane.

Cambodian Kids Foundation Inc (AU, Cambodian Kids Foundation Inc - N/A) Browse events

YTD Raised: $573.70

The Cambodian Kids Foundation is an Australian not for profit organisation, founded in Woodend, Victoria. CKF focuses on working at ground roots level, with funds raised going directly to their education programs in Cambodia.

CMV Australia (AU, 21882833408) Browse events

YTD Raised: $571.99

Congenital Cytomegalovirus (cCMV) is the most common viral & infectious cause of disabilities to newborn babies with 1 to 2 babies being born significantly affected with disabilities in Australia every day. CMV Australia's mission is to raise awareness about CMV and the preventative strategies which can reduce a mothers risk of exposure during pregnancy. We also provide information and support to families who have been affected by congenital CMV and assist and support Australian research projects.

Whitford Catholic Primary School (AU, 84158364198) Browse events

YTD Raised: $545.82

Whitford Catholic Primary School caters for approximately 620 students in a co-educational Pre-Kindergarten - Year 6 community. The school is currently fundraising for one it's students, Nate. Here is his story, as told by his mum: Nate was diagnosed with Acute Lymphoblastic Leukaemia - B cell high risk on Wednesday 19 February 2014. Nate underwent intense chemotherapy treatment at PMH. He noticeably started to limp a few weeks after treatment and his left leg would give way on him. His pain threshold is of a true champion and he tried to walk despite the pain - we would later be told that over 3/4 of the femur growth plate had a hole in it and severely fractured. Following a biopsy results revealed on ANZAC day the fatal news that Scedosporium Prolificans Osteomyelitis, an extremely rare fungal that is worse than cancer was attacking Nate's femur. He would be permanently disabled and no one had beaten the fungus without debridement or amputation. Chemotherapy plan had to be modified to try and beat the fungus. Nate had grommets inserted to allow him to do 10 metre "dives" at Fremantle's Hyperbaric Chambers which required him to be in a clear tank for over 2 hours. This required daily routine of being transported by ambulance from PMH to Fremantle. In addition to this Nate had 10+ surgeries to his femur on "Saturdays" to ensure he could continue to go to the chambers. By early June further scans revealed that Nate now had a hole in his sphenoid bone (base of skull). Our worst fears had come true - the infection had gone to a place no one could get to. Nate's motor neurone skills started to decline and his blood count refused to rise naturally and the medicines to push them higher no longer worked. On Friday 19 June 2014, only 5 months since his original diagnosis, we made the decision to bring Nate home and surround him with love and light. It was the worst weekend of our lives and we held a vigil by his side. Something changed after that, Nate started to smile and have fun....he also turned 5. Nate started to improve and was teaching himself all sorts of new things. He was on the improve despite all the painkillers being required for his leg. Further scans were requested and the infection in Nate's head was getting smaller! He was kicking the infection through his love of life and determination! Unfortunately, Nate's leg however, had taken the brunt of the fungus and travelled further up his femur. The decision was made to amputate his leg. Nate suffered horrendous phantom pain and was one of only a few children in Australia to use an Adult drug to help with his pain. Nate continues his chemotherapy treatment to ensure his Leukaemia stays in remission while continuing to rehabilitate for his leg. Due to the chemotherapy Nate's weight and fluid retention continually changes therefore his prosthesis continues to provide challenges just to fit. He is currently being refitted for a new cast and uses his wheelchair in the meantime. He hopes to play Auskick soon and wants to get out there to play cricket on the oval with his mates at school. Once up and walking Nate would love to have the option of a "Running leg". Throughout his childhood this will continue to need to be updated. Please join our school in fundraising for Nate and his ongoing needs.

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