Many of us have been anxiously watching the news from Ukraine and wondering what we can do to help. SWHPN is part of the World Hospice and Palliative Social Workers (WHPCSW.net) community. We are coming together now to support our HAPC colleagues in Ukraine, who are facing a humanitarian emergency through a critical lack of necessary medical supplies for patients in hospices, palliative care settings, and hospitals. These vulnerable patients and their families, as well as healthcare staff, are unable to leave the country while Russia is attacking.
 
SWHPN is collecting donations of funds and ensuring they get distributed to bona fide organizations and NGOs on the ground in Ukraine, Poland and Romania. The WHPCSW is actively helping connect people throughout our network. The head of the Ukrainian Association of Palliative and Hospice Care is asking for donations of needed medical supplies. Our contact in Ireland is planning to buy the supplies and get them to another contact at the Poland/Ukrainian border, and from there, we are working to secure transport to hospices throughout the country. You can help by donating here.

In March of 2021, the Improving Access to Mental Health Act of 2021 was introduced in the House. This bipartisan bill, co-sponsored by Senator Debbie Stabenow (D-MI), Senator John Barrasso (R-WY), and Representative Barbara Lee, MSW (D-CA), will address gaps in services that Clinical Social Workers are able to provide under current law. 

There are 42 cosponsors in the House and 5 in the Senate. Per the NASW advocacy alert, we need at least 175 cosponsors in the House and over 50 in the Senate to demonstrate broad support for this bill and elevate it to potential consideration. It is anticipated that this might be a topic of focus in the coming months due to a recent request from the Senate Finance Committeeabout concerns that every American should be able to access high-quality behavioral health care when needed. 

Finding time to keep updated on pending palliative care legislation can be a challenge for busy palliative care practitioners. However, political advocacy work is as important as direct care work, and in some instances, may have the potential to improve lives and decrease suffering on a much larger scale. There is an urgent need to improve equitable access for all people who could benefit from palliative care, especially those who have been unfairly impacted by systemic racism and other forms of oppression in health care. This type of change will require some changes in public policy and laws. The palliative care community can work together to influence these changes through increasing engagement in political palliative care practice. 

Political palliative care is not partisan. Policy advocates view frontline healthcare professionals as important potential contributors for political action and advocacy due to their unique knowledge, proximity, and insight into the lives of the patients they care for. For patients with complex long-term healthcare needs, such as those served in palliative care, this type of practitioner advocacy can help communicate the perspective of a population of patients who may not be as well-equipped to communicate their experiences barriers to care and unmet needs.

The Congressional Social Determinants of Health (SDOH) Caucus is a bipartisan effort of lawmakers started in July of 2021 to improve approaches for addressing health disparities experienced by persons disproportionately impacted by SDOH and improve well-being. In this effort, the Caucus is seeking comments and feedback from the public on challenges and opportunities related to SDOH by September 21, 2021.