IAHPC Advocacy Program
The content of this section is under the coordination of Dr. Katherine Pettus, PhD, the IAHPC Advocacy Officer. If you wish to suggest any additional resources to add to this page, please contact Dr. Pettus via our website.
What is Palliative Care Advocacy?
Through this program, the IAHPC, in collaboration with other UN approved non-governmental organisations, seeks to ensure that access to palliative care and to essential medicines for pain relief and palliative care are included in international policy documents and strategies, as components of the right to health. Ideally, national palliative care organisations can leverage these international documents, usually approved by members of their own governments, to improve palliative care delivery for their patients and secure public funding. IAHPC works on the drafting and implementation of resolutions, agreements and strategies with international agencies of the United Nations, including the World Health Organisation and with governments by invitation. We also train palliative care providers who are members of palliative care associations to do advocacy for specific needs in their countries and regions.
Frequently asked questions
- What is a palliative care policy advocacy? Structured communication between national, regional, and global palliative care associations (non-governmental organisations) and government representatives, at the local, national, regional, and international levels.
- Why does IAHPC do palliative care advocacy? To improve care for the patients and families cared for by our members. Our advocacy includes encouraging governments to improve access to internationally controlled essential medicines such as morphine by collaborating, upon request, to review and revise unduly restrictive laws and regulations, educate prescribers, and raise public awareness raising of the benefits of rational access to controlled medicines.
- Who can do palliative care advocacy? Members of a palliative care or other professional associations or institutions. IAHPC advocacy is done by individuals and teams in an institutional context that is framed by the United Nations system. National advocacy is done in the context of your own government.
- How can I do palliative care advocacy? It depends on the issue and on what level you want to work: local, regional, national, international, or a combination. Advocacy is done by individuals, but through institutions.
- Join your national, regional, and international palliative care organizations.
- Stay current by reading the IAHPC newsletter!
- Get to know your lawmakers and regulators). Invite them to visit your program and see your work firsthand.
- Participate in social media (create and join accounts on Twitter, Facebook, Linked in, and Youtube.) IAHPC has all those accounts. You can “follow” us and stay current. (we can help!)
- Ensure your association designates an advocacy focal point to engage in direct communication: letters, emails, etc. with lawmakers, and with regional and international palliative care organisations (we can help!)
- Get to know journalists and representatives of traditional media: learn to write press releases, editorials, and co-author journal articles (we can help)
- Participate in a delegation with your national, regional, or international association in meetings where public health issues are debated and policy goals are set out in resolutions and consensus documents (we can help)
2020 IAHPC Advocacy Initiatives
Western Pacific Region Advocacy Network Initiative
Principles of Palliative Care Advocacy, Dr. Katherine Pettus
IAHPC Statement, Presented by Harmala Gupta, ED of CanSupport
IAHPC Question to interactive Panel
Reconvened 63rd Session of Committee on Narcotic Drugs
Statement of IAHPC on Agenda Item 5, Cannabis. Dr. Dingle Spence
Statement of IAHPC on Agenda Item 9, Controlled Medicines Supply Chains. Heloisa Broggiato.
Integration of Palliative Care into National COVID Response Plans per WHA73/1
Information and registration
International Federation on Aging Town Hall Series. Palliative Care for Older Persons: A Rights Based Approach
Dr. Katherine Pettus, Advocacy Officer Presentation November 13, 2020
73rd World Health Assembly extended
IAHPC Statement to WHA73 Extended
WHO Regional Meetings
70th Session of the Regional Meeting for Europe
Video of Dr. Lukas Radbruch, IAHPC Board Chair delivering the IAHPC statement
Commission on Narcotic Drugs, Release of the World Drug Report June 26, 2020
Statement of Dr. Abidan Chansa, Zambia for IAHPC and Vienna NGO Committee on Drugs Re Access to Controlled Medicines
IAHPC Report from WHA
63rd Meeting of Commission on Narcotic Drugs
Presentation of Ms. Heloisa Broggiato to CND63 High Level Side Event on Increasing Access to Internationally Controlled Essential Palliative Care Medicines
IAHPC statement to CND 63 on Item 6
Nota de Información de parte de IAHPC
Promoción de la sensibilización, la educación y la capacitación como parte de un enfoque amplio para garantizar la disponibilidad de sustancias fiscalizadas y el acceso a ellas con fines médicos y científicos y mejorar su uso racional.
IAHPC Briefing Note
Promoting awareness-raising, education and training as part of a comprehensive approach to ensuring access to and the availability of controlled substances for medical and scientific purposes and improving their rational use.
Ongoing IAHPC Advocacy Initiatives
IAHPC Concept Note for WHO Group of Friends of Palliative and Long Term Care
IAHPC/WHPCA/ICPCN Concept Note for Nursing Palliative Care SIde Event at WHA73
WHO Public Hearing on Guidelines Scoping Document -- WHO guideline on ensuring balanced national policies for access and safe use of controlled medicines
IAHPC and Dr. Lukas Radbruch Statements for WHO Public Hearing on Guidelines Scoping Document.
146th Meeting of the World Health Organization Executive Board Meeting
Statement of IAHPC to WHO EB146 on Primary Health Care
Statement of IAHPC to WHO EB146 on Universal Health Coverage
IAHPC Presentation to G2H2 at Pre-WHO EB146 Civil Society Briefing
IAHPC Briefing Note
- please register online here by 23:59 Geneva local time Sunday 12 January 2020.
- please write to the WHO Secretariat and request that the meeting be webcast for registrants who cannot attend in person.
- please write to your permanent mission in Geneva (contact list here), request that they accept the Secretariat's invitation to attend the meeting, and enclose some information about the situation regarding palliative care and access to palliative care medicines in your country. If you need more information on this, or data, contact me and/or consult our data map and website resources.
Please send me the letter you write to your Permanent Mission or BCC me, so we can track contacts with missions upload as examples of national advocacy. Two letters that have already been sent from Uganda are here: APCA Letter to Uganda Geneva Mission
, HAU Letter to Uganda Mission in Geneva