IAHPC is a global non-profit, charity organization dedicated to the promotion and development of palliative care. Its mission is to collaborate and work to improve the quality of life of patients with advanced life-threatening conditions and their families, by advancing hospice and palliative care programs, education, research, and favorable policies around the world. Its vision is to help to increase and optimize the availability of and access to hospice and palliative care for patients and their families throughout the world.
29 April 2022 - 28 April 2022
Speakers from the Lancet Commission on Pain and Palliative Care and the Stanford-Lancet Commission on the North American Opiod Crisis will present their findings, followed by discussion from representatitves from the International Narcotics Control Board, the WHO, UNODC and civil society experts.
28 April 2022
Chairs of the Lancet Commission on Pain and Palliative Care and the Stanford-Lancet Commission on the North American Opioid Crisis will present the main findings of their reports, followed by a discussion on the way forward with civil society experts and representatives of the International Narcotics Control Board, the World Health Organization, and UNODC.
News9 September 2021
The global pandemic of untreated pain as a side effect of almost a century of drug control, exacerbated by the COVID-19 pandemic, has created a secondary public health crisis—suicides, heart attacks, and chronic conditions associated with serious health-related suffering.
News18 July 2019
This decision by the WHO puts a decade of progress towards allowing millions of people access to controlled substances for pain relief at risk.
News1 June 2018
The CSTF has been re-launched to support civil society participation in the upcoming Ministerial Segment of the 62nd Session of the CND.
Blog31 January 2018
World Cancer Day asks us to reflect on how we can play our part, as a collective or as individuals, in reducing the global burden of cancer. The “global burden of cancer” is actually an aggregate of the very real burden that falls on individual people: on cancer patients, their family members and their caregivers. In the vast majority of cases, people face severe untreated pain, financial worries, often bankruptcy, and psycho-spiritual distress. My part in reducing that burden is to advocate for the mainstreaming of palliative care — which alleviates the “total pain” brought on by cancer and other life limiting illnesses — throughout public health systems. I do this because it is a matter of social justice, and because I witnessed my mother’s severe unrelieved cancer pain and could do nothing to help her at that time. She died at only 51 from liver cancer, which had metastasised to her bones. It was an agonising death because her doctors had sent her home (to us, in the capital city of a high-income country) to die with no palliative care, inadequate pain management, and a family that had no clue how to look after, or communicate with a dying person, or process our grief. Decades later, I know her pain could have been easily relieved if her doctors and nurses had been properly taught how to manage it. Today, in 2018, in that same country, such a situation would be the exception rather than the rule, unless the patient was poor, homeless, in prison, undocumented, or in a substandard nursing home. But it is the rule in the vast majority of low- and middle-income countries, where patients and families facing cancer and the dying process have little or no pain relief or palliative care. Unlike our family, though, which was very privileged, many will become destitute, lose their lands, and have to take their children out of school because they must use scarce cash to pay for medications and treatments, rather than school fees, and food. Catastrophic out-of-pocket expenses for cancer care drive millions of households into poverty every year. Universal health coverage, one target of the Sustainable Development Goals, could stop this tragedy in its tracks. Bridging the global abyss in access to internationally controlled essential medicines for the relief of severe pain, including cancer pain, for instance would cost around USD145 million per year, according to the Lancet Commission, a fraction of the USD100 billion the world spends every year on drug control. Properly licensed pharmacists and prescribers, including nurses, can dispense controlled medications such as morphine through a well set up supply chain, safely and with minimal fear of diversion or non-medical use. I have seen this work in rural Uganda, where the Palliative Care Association works with the Narcotics Commissioner to provide training for police officers. I have been out with nurse prescribers, physicians, and volunteers to the poorest slums in Kampala, Addis Ababa, Nairobi, Bogota, and Montevideo, and have seen how oral morphine can be brought safely and compassionately to cancer patients where they live, to make their last months, weeks, and days endurable, and even times of grace. Between 30-50% of all cancers are preventable; most are treatable with early detection and access to radiotherapy and medication; all can be palliated. All patients and families can be provided with ethical communication and services to relieve the physical, spiritual, and psycho-social pain that inevitably accompanies serious illness. This calls for health system strengthening, universal healthcare, and the political will to make population health (not just treatment and prevention of disease) a centrepiece of global and national health approaches. Chapter Two of the Outcome Document of the UN General Special Session on the World Drug Problem (2016) contains many suggestions and recommendations to help member states improve access to internationally controlled medicines for the treatment of severe pain, palliative care, and substance use disorder. Successfully implementing those recommendations entails the participation and expertise of civil society organisations, including palliative care associations, national competent authorities, and patient groups. IAHPC is helping partners and governments operationalise those recommendations to relieve preventable, severe health related suffering of patients, including cancer patients, around the world. Further reading and useful links International Agency for Research on Cancer Union for International Cancer Control WHA 70/32 Cancer Resolution WHO Cancer Fact Sheet Worldwide Hospice and Palliative Care Alliance
Publications23 January 2017
In the British Medical Journal, Katherine Pettus argues that because of policies to prevent illicit drug use, patients in most of the world lack palliative care and suffer severe untreated pain.
16 September 2017 - 19 September 2017
Entitled "Palliative care is public health: principles to practice", this will be an opportunity for hospices, and the organisations with whom they collaborate, to share, learn and network internationally.
News18 May 2015
In order to feed into the report being prepared by the Office of the High Commissioner for Human Rights for the UNGASS, NGOs from all over the world have submitted their contributions on how drug control affects human rights.