Fair Trade is about better prices, decent working conditions, local sustainability, and fair terms of trade for farmers and workers in the developing world. By requiring companies to pay sustainable prices, Fair Trade addresses the injustices of conventional trade, which traditionally discriminates against the poorest, weakest producers. It enables them to improve their position and have more control over their lives. The Fair Trade Association engages with and supports local fair trade network groups and our growing network of Fair Trade Communities: councils, universities, workplaces, faith groups and schools who have made a commitment to fair trade. We recognise and promote the Fairtrade Mark, the World Fair Trade Organisation, and our own system Fair Traders of Australia as credible fair trade systems, which meet international fair trade standards. For more information on the Fair Trade Association please visit
The Australian Missing Persons Register was created more than seven years ago to bring awareness of missing persons to the public. Its aim is to provide information about missing persons from every State and Territory in Australia, no matter how long they have been missing, and the ultimate aim of course is to find these people and bring peace to, and possibly reunite the families. We provide emotional support and practical help wherever possible to the friends and families of the Missing. There is absolutely NO charge or fee to anyone for publication of missing persons details or messages. The work I have done is entirely voluntary. All missing persons are listed, from decades ago to people reported missing today. If you have any information about any of the cases listed on the site please call Crimestoppers on 1800 333 000 - going missing is NOT a crime but the Crimestoppers number puts you through to Police who are ready to help locate the person and make sure they are safe and well.
Pallister-Killian Syndrome is a rare chromosomal disorder. PKS Foundation of Australia is a not for profit organisation aimed at generating awareness about the disorder within the general community and medical professionals; supporting kids and families of those affected by PKS achieve a better quality of life, through therapy and equipment support and generating sufficient resources to fund research into many of unknown facets of this disorder. Pallister-Killian Syndrome is a relatively rare syndrome. As a result, very little information and support has been available to families in the past. Most medical professionals have never heard of PKS. PKSFA has been established to provide help and support to individuals diagnosed with PKS and their families as well as raising awareness and providing information to the medical community. To maximise the quality of life of individuals who are diagnosed with Pallister-Killian Syndrome by: Providing equipment and services for those with PKS; Supporting parents and family; Promoting research into PKS; Raising community awareness of PKS.