Muscular Dystrophy Foundation of Australia is the national body supporting people with neuromuscular conditions. This event will raise much needed funds to continue vital research into treatments and cure and provide essential services. State Muscular Dystrophy programs provide camps for kids, respite for carers, home support, medical seminars and Childfamilycare programs. Muscular Dystrophy Foundation is committed to: • More understanding today through awareness and education • The best available support through best practise service delivery • A better future through vital research and essential advocacy Join us in supporting our fellow Australians who are living with these serious life-threatening neuromuscular conditions.
Our school is a very harmonious place, where the total development of the child is the focus. We feel that the social and emotional development of the children enhances their development in key curriculum areas. We aim to assist all children to become worthwhile, productive citizens.
OvaCare's mission is to: “Improve diagnosis and education of ovarian cancer within Ireland, through sharing global research and best practice, and providing support and advocacy through OvaCare’s dedicated support network” Follow us here:twitter.com/OvaCare like us on:facebook.com/OvaCare
HelpArgentina is a nonprofit organization that has been promoting social investment in Argentina since 2003. Our goals are to strengthen the nonprofits working to create social change in Argentina, to increase confidence in the Argentine nonprofit sector and to promote the culture of giving among Argentines. We work with organizations that meet our criteria of transparency and best practice, providing a safe and efficient infrastructure for them to receive support. HelpArgentina is registered in New York as a nonprofit under article 501(c.3) of the U.S. tax code - making donations made by US taxpayers tax deductible.
Myalgic Encephalomyelitis/CFS Australia (Vic,Tas, NT) is the PEAK body and only charitable organisation in Vic,Tas, NT dedicated to providing information, support and services specifically to people with Myalgic Encephalomyelitis (commonly called Chronic Fatigue Syndrome), their families and the community at large. It is estimated 42,000 adults, teens and children live with Myalgic Encephalomyelitis in Vic,Tas,NT. ME/CFS Australia (Vic,Tas, NT) works with all governments, communities, researchers and professionals to help educate and raise awareness about this complex, chronic and highly debilitating neuro-immune condition. We provide support, care, early intervention, education and conferences. We are fighting hard for awareness, biomedical treatments, biomedical research and a cure. Our services, support, advocacy and education can be accessed by people located anywhere in Australia. Myalgic Encephalomyelitis like any chronic illness can be mild, moderate or severe. Some will recover, however 25% of people who contract Myalgic Encephalomyelitis remain highly bedbound or housebound and unable to work. ME destroys lives.
The Josh Carrick Foundation aims to fund research into the prevention, diagnosis and treatment of testicular cancer for the advancement of health and to also provide funds for technological advancement in cancer research. The Foundation also wishes to help raise awareness of testicular cancer.
Helping to make North-east Scotland's cancer and haematology care the best it can be