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Refugees must be seen as an essential part of our shared humanity. Today more than 65 million people have fled their homes seeking safety wherever they can find it - nearby communities, neighbouring countries and often new continents. The global response has been a band-aid solution to a humanitarian crisis that needs long term, sustainable solutions. In countries like Malaysia, where refugees are denied legal status, offered few protections and faced with restrictions on education, work and the perpetual fear of arrest; both their lives and their plight remain in the shadows. We're here to change that. Our vision is of a single, shared humanity, where social inclusion is about dignity and choice, not dependence, not charity. Payong Organisation (which is fully supported by Liberty to Learn Berhad) champions 'Equitable Outcomes' for all refugees living in Malaysia. By championing we support refugee initiatives, leverage partnerships, increase advocacy and work towards creating and funding solutions to bring about systemic changes in the education, health and livelihoods sectors for refugees and asylum seekers in Malaysia. With an outcome that all refugees will be able to build meaningful, purpose-driven and successful lives for themselves. Because refugees are in transit in Malaysia, while waiting for resettlement we believe it is critical that we work with and support them to becoming 'transition ready'. Resettlement or repatriation can happen at any point, so all programmes aim to equip them with hard skills/soft skills and tools so that they can navigate their lives during/after transition. Essentially setting them up for success.

Many people living in remote regions of Nepal do not have access to primary healthcare, medical treatment or rehabilitation services. Medical care is not free in Nepal and poverty is widespread. Our mission is to support and work with our project partner organisation (Nepal Healthcare Equipment Development Foundation (NHEDF), an organisation that was set up after the 2015 earthquake in Nepal, to improve health outcomes and provide opportunities for people who experience life changing injuries or illness but cannot access medical and rehabilitation services due to poverty. Together we help rebuild physical and emotional health, self-reliance, dignity and confidence and change the lives of people who have no one else to turn to and nowhere else to go. We provide funding that pays the wages of three nurses and a physiotherapist, and also funds medical and surgical intervention, pharmaceutical products and medical supplies to patients at NHEDF's Shelter as funds allow. The amount of support we can give is directly related to the number of donations we receive. We also work with our clinical staff to provide ongoing professional development and educational opportunities as appropriate. We are an Australian not-for-profit organisation registered with the Australian Charities and Not-for-profits Commission (ACNC) which gives us accountability and transparency with our Government, our donors and the general public. We were established at the end of 2016. We have two projects under the umbrella of our organisation and our NHEDF Shelter project is the main part of our work. We also accept referrals for women with obstetric fistula and are working with NHEDF to introduce an initiative called Circles of Hope which will provide opportunities for skills training and possible temporary employment for NHEDF patients manufacturing washable reusable sanitary products and incontinence pads specifically made for women with fistula. NHEDF used to be a not-for-profit organisation that repaired and recycled medical technology but after the April 2015 earthquake that devastated the lives of many in Nepal, this all changed. The Director, a wonderful man called Samrat Basnet, removed all the medical technology from the premises and took in patients when they were discharged from hospital way too early to make room for more. Samrat also engaged volunteer doctors, nurses and a volunteer physiotherapist and NHEDF became a medical Shelter, housing people instead of biomedical equipment and providing free medical and nursing care and rehabilitation services to people whose lives were changed by injury as a result of the earthquake. NHEDF had tremendous support both from the local community within Nepal and internationally. Samrat never dreamed that the project would be permanent - he thought he would 'shut up shop' a few months after the quake, and he could go back to being a biomedical engineer again, but patients kept coming. To this day hospitals, community organisations, other not-for-profit organisations in Nepal and individuals, especially nursing and medical staff continue to refer more patients to NHEDF than they can accept. Today, NHEDF's patients may not have earthquake related injuries (though we still have one patient who was injured in the 2015 quake) but they all have experienced trauma, illness and injury requiring rehabilitation and cannot access medical care due to poverty. NHEDF has a Shelter - a rented house - which is located in Kathmandu and this 14 - 20 bed facility provides free accommodation, food, medical intervention, physiotherapy, rehabilitation services and around-the-clock nursing care to as many patients as it can fund in a family centred environment. Everything at the Shelter is completely free thanks to the generosity of ours and NHEDF's donors. Life in Nepal is tough and life for someone with a disability in Nepal is even tougher as people with a disability are generally not treated kindly or compassionately in Nepal. Usually patients are referred to NHEDF following a lengthy expensive hospital stay, however sometimes patients come prior to embarking on this journey of navigating the complexities of medical care in Nepal. Either way, NHEDF finds the most suitable hospital in Kathmandu for investigations, specialist appointments and further surgery as required. Should surgery be required, they are transferred back to NHEDF as soon as they are well enough. Some patients stay only a couple of weeks; others' months, and the occasional patient 1 - 3 years as individual roads to rehabilitation are often long. Our NHEDF Shelter patients have all sorts of diagnoses resulting from trauma/injury/illness. Diagnoses range from fractures, soft tissue injury, amputations, wounds, burns, burns contractures, head injuries, neurological conditions and obstetric fistula. Some of our patients may have bone cancer requiring an amputation, extensive rehabilitation and the fitting of unusual prostheses. Occasionally Samrat accepts a patient who is terminally ill who is simply kicked out of hospital because they cannot pay any more and would otherwise be simply left to die. Patients are either referred or simply picked up from hospital foyers where they are found begging for money to pay for their medical care or that of a loved one. Almost all of NHEDF's patients come from remote regions which are severely lacking in funding, health and medical care. Most larger villages have a clinic staffed by a Health Assistant who has done two years of training and can dispense 35 different medications and do basic wound care and vaccinations, but their medical knowledge is poor. There are often no hospitals for anywhere up to a 2 - 3 day walk, or over the years, dirt roads have paved the way for lengthy rough journeys on a local bus. These hospitals may only have rudimentary services - they often do not have operating theatres, anaesthetists, surgeons or anaesthetic machines, or staff who can use them. Investigative technology and ancillary services like pathology are often basic or non-existent. Many people travel to major cities like Kathmandu to access medical care, and for many varied and complex reasons (including corruption) end up paying a fortune for their medical care. Many of our patients come to NHEDF after a lengthy history with the Nepalese medical system, and some of our patients have spent as much as US$20,000 - $22,500 on medical bills. We have not made a mistake with this figure and put too many zeros in - this figure is correct despite Nepal being coming between 27th and 30th poorest countries in the world and having up to 25% of its population living below the poverty line. Some of our patients are injured working overseas usually in Malaysia or the Gulf and are sent back to Nepal after initial treatment with no compensation. Also, there is no such thing as workers compensation in Nepal. All their savings from working overseas end up going on medical bills. The Government may provide a disability allowance if certain criteria are met, but this is approximately the equivalent of US $44 a month and many hurdles are put in the way which makes it difficult to even apply. As most of our patients come from rural and remote regions they have often sold all or most of their land which has been in their family for generations in order to pay their medical bills. Other patients keep a small parcel and home is a shack or a tent. Many women with fistula live in desperate poverty having been abandoned by their families. They cannot seek medical attention because they are poor; because knowledge of fistula in Nepal is poor; their injury is often not recognised; they are marginalised, socially isolated, often living in stables or caves having been abandoned by their family and ostracised by their community. Many of our patients are in debt to family, money lenders and/or their local community and some of our patients are suicidal when they come to NHEDF. All are in desperate circumstances. Many are unable to return to their pre-injury employment because of their disability, hence the Circles of Hope initiative which will support NHEDF's efforts to help patients help themselves once their rehabilitation is complete. This pilot program will eventually provide skills training and employment opportunities for both NHEDF and fistula patients and help them help themselves. NHEDF will establish a small workshop at the Shelter, manufacturing washable, reusuable, incontinence products which will be donated to NHEDF patients and women with fistula, and also sold in medical supply shops and other outlets initially in Kathmandu and then further afield. Women with fistula, some of NHEDF's patients and many other people in Nepal need incontinence products and none are available other than expensive disposable ones which are only sold in major towns and cities and cost $0.80 - $1 per pad. Our project addresses many articles of the UN Declaration of Human Rights and we are non-discriminatory; support children, women and men of all ages, castes, religions and ethnic groups; help alleviate poverty; improve health; support people with disabilities; improve access of people with a disability to earn an income; promote dignity, independence, self-respect and advance personal, social and economic well-being.

Apadrina la Ciencia (Sponsor Science) is a new initiative to promote scientific research and public understanding of science in Spain. It stems from the conviction that scientific research is a source of wealth and prosperity, and that investment in science is an investment in the future. Apadrina la Ciencia (Sponsor Science) was launched by a group of scientists with extensive experience in several research areas, who have joined efforts to promote communication and direct collaboration among scientists and the rest of society. Unlike other initiatives, the goal is not to obtain funding for their own research, but rather to secure resources through patronage, sponsorship and micro-grants to support science research and outreach in Spain. More than 200 internationally renowned scientists from different universities and research institutions support this initiative. Apadrina la Ciencia (Sponsor Science) aims to direct people's solidarity to support research on issues related to health, the environment and new technologies, with special attention to basic research, which is the foundation of scientific progress and technological development. Through job contracts and project grants, Apadrina la Ciencia (Sponsor Science) is a means by which citizen support can have an optimum return and maximum impact on the goal of strengthening the Spanish scientific system. Scientific outreach is a priority of Apadrina la Ciencia (Sponsor Science), to inform citizens about scientific advances and help to generate critical opinion on important social issues. One of the main objectives of Apadrina la Ciencia is thus to make science more accessible, especially to young people. Apadrina la Ciencia (Sponsor Science) will be a platform for meetings, discussion and collaboration between scientists and society. In addition, Apadrina la Ciencia hopes to involve all members of society, including institutions and companies, to help make our dream come true: to achieve strong, visible scientific research in Spain that generates knowledge and increases prosperity for society.

Our mission is to protect and support women and children though prevention of, and direct support against, abuse, exploitation and human trafficking. AAT VIETNAM is a peer-based Non-Government Organization which was founded by a social worker with many years experience working in Vietnam and peer educators with a deep understanding of the Vietnamese context. We develop realistic projects to tackle the root causes of abuse, exploitation and human trafficking. AAT VIETNAM is a pioneering NGO which has established the first models of action to tackle the causes and consequences of human trafficking and sexual exploitation in Vietnam over the past fifteen years. AAT VIETNAM is unique thanks to its international task force network of local partners in fifteen countries worldwide, its direct field actions in five countries of Southeast Asia and its relationship and partnership with regional governments. AAT Vietnam's approach is to engage the Vietnamese population and Government to promote social development. Preventative actions though awareness and education are at the core of our activities, in order to achieve mindset changes in our beneficiaries, empowering them to protect themselves. Currently AAT Vietnam is mainly focused on prevention through education at schools to combat social harms and associated issues. We offer a comprehensive extra curricular course to schools with a student-interactive and comprehensive approach, which educates students about Reproductive Health, sexuality, drug use, incest, early marriage, early pregnancy, abortion, self defense, migration, human trafficking, while increasing understanding of gender differences and human rights. Our goal is to make this course adaptable to the Vietnamese National Educational curriculum in order to reach all children in Vietnam and to achieve recognition by the Ministry of Education that this is an essential activity for the well-being of new generations and social development in general. AAT Vietnam also focuses on the assistance and the protection of victims and potential victims of trafficking; offering repatriation, rehabilitation and reintegration services. We are able to offer effective services in this area when the government allows us to access to assess victims and provide support to them. The work of AAT depends on foreign aid assistance.

MISSION To eradicate extreme poverty in rural areas of southern India. To improve the living conditions of India's most disadvantaged groups, enhance their dignity and self-esteem, and help them achieve the necessary means to combat poverty. To ensure sustainable development with the active involvement and leadership of the communities. To reach as many poor people as possible and help organize them both individually and as community-based organizations, affording them strength, confidence, and the ability to lead their own development. To transform the semi-desert land through a holistic approach involving land, water, vegetation, and livestock development and to ensure the people live in harmony with natural resources. To sensitize men and women to the inherent discrimination and violence against women in both family and society, and to develop appropriate support systems and networks to fight such discrimination. To help people with disabilities gain equal rights and opportunities in every area of development, as well as access to all resources and services related to health, education, livelihood, and rehabilitation, helping them live a dignified life. To build a dynamic and creative organization that strives to participate in all development efforts and is spiritual in its motivation, based on knowledge and skills, shares the aspirations and struggles of the poor, and, though permanent in time, adapts to the changing times and needs. To raise public awareness about the living conditions of the rural and urban poor and to promote a more caring society. VISION For everyone from poor and oppressed communities to live with justice, dignity, and socioeconomic equality, and for all people to live in peace and harmony with one another. For people to live in harmony with nature, on land capable of sustaining its population. VALUES Permanence: We are a long-term project. Respect: We respect the people's culture and customs. Participation: We encourage the active participation and leadership of our stakeholders. Action: We have an action-based work philosophy. Accountability: We believe in efficient and accountable program and financial management. Humanism: We are strong believers in people and their capacity to help others. OUR PRINCIPLES RDT-Vicente Ferrer believes that people are the main actors in their development process and ensures their active involvement and leadership in the programs. The organization endorses a multi-sectoral approach with a view to enhancing people's overall progress. As a result, RDT addresses all major areas of development, including access to quality education, improved livelihoods, ecologyand the environment, equal opportunities for people with disabilities, women's development and empowerment, and access to healthcare. We organize, at a grassroots level, women, men, andpeople with disabilities into groups to enhance their strength, confidence, and ability to resolve their own issues and problems. An important RDT-Vicente Ferrer approach is the continuous sharing of knowledge, skills, and awareness about all aspects of life. Collaboration with the government and other NGOs to draw maximum benefits from development. To raise people's awareness and support their use of government schemes and resources. Though the organization has a special program forwomen's development, it believes that women's progress should be a factor in every area of work and life, including education, where emphasis is placed on young girls, and healthcare, for the overall well-being of women and girls. We believe in continuous training and orientation for staff members and people. We also have an HR department that regularly organizes internal and external training sessions for staff members of all levels and people on leadership, group building, problem solving, and gender-related matters, among others. To create an efficient human organization capable of acting regardless of where the need arises, even in emergencies. We believe that we must have a strong organization focused on community development, yet flexible and able to accommodate the changing needs of the people. RDT-Vicente Ferrer also stresses continuous dialogue with people and seeks to ensure its programs are useful and practical. An empathetic approach to helping individuals in severe distress due to chronic or acute illness, abandonment, or abuse of any kind.

KEC's mission is to create and offer innovative services and programs for people with intellectual disabilities so they may live fulfilling lives of independence and quality in their homes and communities. KEC is a civic organization that strives to meet the needs of people with disabilities in order to improve their position in society, secure a high quality of life and realize positive social change so that people with disabilities will be accepted as equal members of society. Our vision is to be a synonym for an NGO that is constantly raising the standards in the field of social welfare, improving the quality of life and degree of social inclusion for people with disabilities, realizing their human rights in the fields of employment, social welfare, health care and culture as well in the realm of raising public awareness. We aim to constantly be rethinking how and why we deliver services to our community to make sure that they are relevant and meaningful. KEC was established in 2002 in order to ensure that young adults with intellectual disabilities have the opportunity to participate in the community and that their on-going educational and social needs are met. All of KEC's programs are developed in close partnership with our beneficiaries and their parents and guardians. In response to this vital input, KEC is constantly creating innovative programs or reshaping existing ones to meet the new interests and challenges of its beneficiaries. We work with the community to build a partnership that fosters acceptance and strives for inclusion. KEC is committed to enhancing the quality of life, and realizing the potential of all people with developmental disabilities. KEC mission is fulfilled through three primary program areas: a day center, work programming and a social enterprise. The day center was KEC first program and has been running since the organization's inception in 2002. Today, KEC is fortunate enough to provide this program in a modern new facility located in the center of Belgrade.This large and well-equipped facility was made possible through the joint efforts of the City of Belgrade and the U.S. Department of Defense. Both of these institutions recognized KEC's important and unique contribution to the lives of people with special needs in Belgrade and joined forces to create this truly special facility. As a result of its high caliber program KEC's day center was accredited by the Serbian Ministry of Labor, Employment, Veterans and Social Policy. This accreditation is further evidence of KEC's distinctive work on behalf of people with developmental disabilities. In order to ensure that people with special needs are truly a part of the larger community in 2004 KEC embarked in a program to build partnerships with the business community. The program started with McDonald's and has grown to include over 30 companies, institutions and organizations across Belgrade and almost 200 beneficiaries. Based on the company's needs KEC matches its beneficiaries with work placement positions. KEC provides all the necessary forms of support, training and evaluation. Its experience in creating and implementing this program made it possible for KEC to become the licensed trainer for such programs in Serbia. Today KEC helps other organizations implement similar programs in their communities. Finally, in an effort to strive for financial self-sustainability KEC launched a small enterprise, Gardenika, to produce natural snack foods. The enterprise's fruit rolls are sold in stores and markets throughout Serbia and can be found in corporate cafeterias and in their PR packages. In addition to providing jobs for KEC beneficiaries any profit will be channeled back into the NGO. Overall, KEC aims to ensure that people with intellectual disabilities living in the community or returning to the community after a life in an institution have meaningful fulfilling lives. We shape our programs around the users needs and desires. The Serbian government is working towards closing down its massive network of institutions providing long term residential care for people with intellectual disabilities. So on the one hand it must find a way to prevent more people from entering the institutions and on the other hand work to create and support programming for those who are leaving the institutions. KEC's activities are a best practice model for achieving both of these goals. The organization supports families so they can keep their loved one with special needs at home and helps those leaving the institutions to fill their lives with interesting and meaningful programs when they rejoin the community.

The Hungarian Civil Liberties Union (HCLU) is a non-profit human rights watchdog NGO established in Budapest, Hungary in 1994. The HCLU operates independently of political parties, the state or any of its institutions. Its aim is to promote the case of fundamental rights and principles laid down by the Constitution of the Republic of Hungary and by international conventions. Generally it has the goal of building and strengthening the civil society and rule of law in Hungary and the CEE region. The HCLU strives to educate citizens about their basic human rights and freedoms, and takes stand against undue interference and misuse of power by those in positions of authority. Its main activities are: Legal advocacy: The HCLU initiates the formulation of new legislation that falls within its competence, as well as the modification of existing legislation and the changing of law enforcement practices. Strategic litigation and legal aid: The HCLU provides pro bono legal aid to citizens who suffer human rights abuses. The HCLU is also the most prominent litigator in the field of freedom of information and freedom of expression, helping journalists with legal advice and representation on a daily basis. Public education: The HCLU informs the general public of important legal cases on its website, its blogs and through the media, as well as in specifically designed informational brochures. The HCLU also organizes conferences and public debates, as well as trainings for different stakeholders. Focus of the HCLU's activities Patient rights: rights to health care, freedom of choice, informed consent, refusal of treatment, access to medical records, substituted decision making, advance directive, right to complaint, and to participate in decision making related to health care Right to self-determination: abortion, euthanasia Right to informational privacy: protection of medical data, disclosure of medical data, protection of personal data in the media, access to public information Right to freedom of expression: protection of basic information rights Right to political representation: NGO participation in the legislation Drug policy: promote alternatives to the prohibition of drugs AIDS policy: rights of people living with HIV The HCLU helps patients to freely exercise their legal rights related to medical treatment: the right to informed consent, the right to refuse treatment, the right to have access to their medical files, and the right to confidentiality in the patients' relationship with their physicians. The organization is governed by the principle that citizens have a right to control the use of their personal data and that they should have access to documents of public interest. The HCLU rejects the policy of subjecting drug dependent people and occasional drug users to criminal sanctions. We believe that increasing police rigor is not the right way of addressing the drug issue. Instead, support is needed for propagating information, and for prevention, treatment and rehabilitation. The organization monitors cases where the rights of individuals held in closed institutions are restricted (those detained by police, the arrested, the imprisoned, and the inmates of psychiatric institutions) as well as the powers of authorities to restrict the liberty of citizens, and the manner in which these powers are used in daily practice. The HCLU consistently monitors the formulation of new pieces of legislation that fall within its competence; right from the initial conception of a draft law down to its enactment. Before preparing a statement, the organization seeks counsel of eminent experts of the topic concerned: jurists, lawyers and physicians. We time the production of each of our statements to the day when parliamentary discussion of the concerned topic opens; and our statements are sent directly and especially to politicians, journalists and experts concerned. In the annex attached to our statements, we acquaint the Members of Parliament involved in the topic with our commentaries on, and recommended alternative wording of several articles of that bill. The HCLU publishes a Policy Paper Series. Each issue sums up the liberal position on a legal policy issue involving a fundamental right. It surveys the Hungarian scene, and outlines the main policy aim of the HCLU in that field. The Policy Papers are issued in Hungarian and in English as well. The organization systematically observes the activities of the European Union, the Council of Europe, the WHO, the UN and the World Medical Association. We collect recommendations and norms that such organizations issue concerning patient/provider relationship and medical interventions. We make these documents accessible in Hungarian. (For example, we have arranged the Hungarian translation and publishing of the Convention on Human Rights and Biomedicine of the Council of Europe and the Amsterdam Declaration of the WHO.) It is our aim to achieve adjustment of the Hungarian legal system to the most recent international legal norms, which means that laws and other legal instruments need adjustment. It is our policy to recommend to the competent authorities that Hungary should join the relevant international conventions. Members and advisors of the HCLU The highest body of the HCLU is the General Assembly. The general meeting selects the members of the Executive Committee. The members of the Executive Committee administer the daily work of the HCLU, they elect the Executive Director of the Union, and they may recommend the adoption of new members for the General Assembly. The members of the Executive Committee and the permanent staff of the HCLU carry the daily affairs of the organization. They discharge the publicly announced services, and they formulate the HCLU's position on key issues of legal policy. A Board of Advisors assists the work of the Executive Committee. The Board consists of renowned jurists, lawyers and physicians with whom we have evolved daily working relations. It is the duty of the Board of Supervisors - whose members are elected by the General Assembly - to supervise the activities and financial operation of the Executive Committee. Resources and accountability Since the HCLU is an independent non-profit organization, financial resources are largely provided by private foundations (eg. Open Society Institute, Trust for Civil Society in Central & Eastern Europe), donors (eg: Tiara Ltd., Concorde Securities Ltd.) and more and more often by private individuals. Its annual income increases every year, reaching 300 million HUF in 2011. The HCLU has 15 full-time and 15 part-time employees and dozens of volunteers working on 9 different programs. Innovations and achievements The HCLU has a variety of highly successful tools and a complex strategy to promote the case of human rights and to help those who are defenseless. Beyond classical legal defense methods (legal advocacy, legal counseling, strategic litigation), the organization maintains five websites and its Video Advocacy Program has created a unique genre of documentaries, which are regularly screened abroad by a wide public. The staff of the Program has conducted trainings in all parts of the world, while their movies frequently win awards at international film festivals. The HCLU is regularly present in the most popular Hungarian and foreign media platforms, and prestigious international organizations (eg. UN, Venice Commission, Parliamentary Committee of Council of Europe) request its opinion on certain issues. In 2009, the HCLU won a freedom of information case at the European Court of Human Rights. The right of access to state-held information as part of Article 10 of the European Convention on Human Rights has been formally recognized, as reflected in the ruling by the European Court of Human Rights. For the first time in the Court's practice, it declared that withholding information needed to participate in public debate on matters of public importance may violate the freedom of expression, and by doing so, gave a new, extended interpretation of the concept of freedom of expression. The HCLU has led a number of successful citizen mobilization campaigns in recent years. The organization has more than 30,000 fans, followers and supporters on social media platforms. Today, the HCLU has become the most significant public interest NGO in Hungary in the fields of freedom of speech, freedom of information and drug policy. The HCLU's Roma Program uses innovative methods such as Skype based legal aid service and video advocacy. Awards SozialMarie Award - 2012 - Unruhe Private Foundation (Austria) The Year's Pro Bono Lawyer - 2011 - Hungarian Chamber of Lawyers, PILnet (Hungary) IV. Roma Documentary Film Festival - 2011 - Depok Foundation (Hungary) Erste Award for Social Integration - 2011 - Erste Foundation (Austria) Kreativ Magazin Online Video Contest - 2011 - Kreativ Magazin (Hungary) Andras Fay Award - 2008 - OTP Bank Plc. (Hungary) SozialMarie Awards - 2007 - Unruhe Private Foundation (Austria) Justitia Regnorum Fundamentum Award - 2007 - Dr. Attila Peterfalvi, parliamentary comissioner of data protection and freedom of information NGO of the year - 2004 - NIOK Foundation (Hungary)