Health & Medical Question – Public Policy Meeting Summary Paper

Introduction

The purpose of this assignment was to attend a Public Policy Meeting, which was approved by the instructor. The meeting was held on October 24, 2022 at 9:00 AM located at Napa Valley, California. This paper will describe the components of the meeting. Included in this paper will be the purpose of the meeting, key participants and the description of the committee, key agenda items and background information. Additionally, this writer will continue with one specific topic that was discussed at the meeting and an explanation of the committee process. There will be an analysis of the key stakeholders’ position related to this specific topic along with key interactions that occurred at the meeting. The paper will also include outcomes of the meeting including specific topic or areas of focus.

Purpose of the Meeting

The meeting’s primary focus is on Alzheimer’s research, care, and services. It also focuses on long-term support services, with a special focus on hospice care, end-of-life care, and advanced care planning. There are many individuals already live with Alzheimer’s disease and are enduring significant difficulties. Speakers therefore attempt to resolve those problems. These days, they prioritize providing care for the local populations. Clinical care for individuals who are already coping with dementia will be discussed in the ensuing sessions. Additionally, they revisit the topic of the disease range. It is acknowledged that there are many difficulties as people approach more severe stages of their illnesses and attempt to maximize their quality of life. One of the discussion’s main points today is that. Additional assistance for caregiving is also discussed.

Key Participants and Description of the Committee

The meeting was headed by Cindy Carlson, a geriatrician at the University of Wisconsin School of Medicine and Public Health and theVA in Madison. The council comprised of Bruce Finke of the Indian Health Service, Helen Lamont, a designated federal officer for the advisory council, Matt Janicki from the University of Illinois, Lisa McGuire from the Centers for Disease Control and Prevention, Joe Montminy, a patient advocate for those living with Alzheimer’s, Helen Medsger, Shari Ling, a geriatrician and gerontologista caregiver representative to the advisory council, Ken Kim from the Center for Pan Asian Community Services, Joanne Pike, the president of the Alzheimer’s Association, Maria Ortega from Florida Atlantic University, Rhonda Williams from the Vermont Department of Health, and Venoreen Browne-Boatswain representing caregivers on the council (U.S. Department of Health and Human Services, 2022). Other members incorporated Randy Bateman, a neurologist at Washington University in St. Louis, Richard Hodes, a director of the National Institute on Aging, Amy Kelley, the deputy director of National Institute on Aging, Scotte Hartronft, a geriatrician and internist, and Joan Weiss, the deputy director at HRSA’s division of medicine and dentistry. Speakers of the meeting incorporated Dr. Neil Henderson, the emeritus professor and the first executive director of the Memory Keepers Medical Discovery Team. There were also Dr. Danetta Sloan, and Dr. Munoz and Sherrill Wayland.

Key Agenda Items

The meeting’s primary agenda item is support long term support services, clinical care and research. Details on community-based approaches to decrease disparities and provide end-of-life and hospice care with — through partnerships with the Black church — is another important component (U.S. Department of Health and Human Services, 2022).. The Latino population must also take cultural factors and end-of-life care into account. The final item on the agenda discusses how to encourage a just and inclusive hospice care for older people who are lesbian, gay, bisexual, transgender, and queer.

Background Information

Dr. Henderson asserts that there is no one method to approach native people about issues related to death and dying. In his opinion, native people today function and live according to a combination of tribal and colonial beliefs, if not always universally. The term “colonial” refers to individuals who are descended from European immigrants who arrived where there were already hundreds of thousands of native inhabitants (U.S. Department of Health and Human Services, 2022). Cosmology is the word used in anthropology to describe these topics when it comes to death and one’s final resting place.  The desire for an intact corpse at burial is one of the things that unites many tribes—not all, but a lot. People who are thought to be fully assimilated into their tribal society simply won’t hear of it. On the contrary, a lot more individuals have a combination of these views from both the perspective of the majority culture and the perspective of their own culture.  According to some, if it will benefit others, we should permit it.

People are encouraged to consider what it means to have multiple identities that overlap and how that may affect inclusion and equality at the end of life by adding the additional layers of being lesbian, gay, bisexual, transgender, or queer. LGBT seniors with dementia may experience an especially difficult set of conditions when trying to access assistance and encouragement (U.S. Department of Health and Human Services, 2022). They have a higher likelihood of aging alone, living alone, and having no dependent offspring. Additionally, they are more likely to experience prejudice and a lack of cultural literacy among providers, which are barriers to receiving excellent care and support.

One Specific Topic that was Discussed at the Meeting and an Explanation of the Committee Process

The meeting covered a variety of topics, including community-based participatory research and community-based research. Community-based research and community-based interactive research can occasionally be confused, according to SDr. Danetta Sloan. Community-based participatory research is a collaborative method with procedures designed in to ensure that the rigor is maintained (U.S. Department of Health and Human Services, 2022). Particularly in qualitative study, this has been debatable. Community-based strategies take into account the strengths that each person offers to the table. In order to combine understanding with actions for social transformation, it is also focused on action and starts with a subject that is significant to the community. In addition to contributing to a community’s overall health improvement, this also serves to lessen health disparities. The community is typically not engaged in the development of community-based research.  However, addressing the cultural barriers and developing trustworthy connections are more important overall.  Additionally, community-based study enables participants to make a more immediate difference. Making an immediate difference in the community, particularly through community-based partnerships, is possible.

Dr. Maria Ortega presided over the gathering as chair of the clinical subcommittee. The meetings were conducted by Carrie Molke, a long-term support specialist. Dr. Randy Bateman oversaw the study, and Dr. Joanne oversaw the subcommittee’s newest addition this past year. Members participate in the creation and delivery of services through committee processes, voice member opinions during decision-making, and assist in meeting member requirements through interaction. Members of the meeting had the chance to share various points of view and work on problems in groups. Members had the option of asking inquiries. At the opening and conclusion of the meeting, a 15-minute window was set aside for questions. Additionally, people submitted a letter or a request to speak to a committee about a topic that was on the schedule.

An Analysis of the Key Stakeholders’ Position related to this Specific Topic

Stakeholders are anyone with a personal interest in the results of the research being conducted, including participants in the study, residents, participants’ families, researchers, healthcare professionals, and decision-makers. The personal accounts of stakeholders and their words of concern for patient care help investigators make sure that their work is patient-focused and pertinent to those who might be affected by the research interventions.

Key Interactions that Occurred at the Meeting

There were effective interactions during the meeting. The meeting began with the chairperson addressing the key point and introducing the main speakers. Each speaker was provided an opportunity to address important issues related to the topic of discussion. Other members were also provided a chance to ask questions as speakers respond to their answers.

Outcomes of the Meeting Including Specific Topic Focus

Everyone who participated in this discussion and shared their knowledge and experience. They now have a lot to consider regarding both their personal and work lives and careers. Additionally, they would discuss how to use this data to generate a list of suggestions for the National Alzheimer’s Plan.

Conclusion

In conclusion, this writer attended a Public Policy Meeting, which was approved by the instructor. The meeting was held on October 24, 2022 at 9:00 AM located at Napa Valley, California. This paper described the purpose of the meeting, key participants and the description of the committee, key agenda items and background information. Additionally, this writer focused on one specific topic that was discussed at the meeting and an explanation of the committee process. An analysis of the key stakeholders’ position related to this specific topic along with key interactions that occurred at the meeting was completed. The outcomes of the meeting were also discussed along with areas of focus.

Reference

U.S. Department of Health and Human Services. (2022, November 3). October 2022 Meeting of the Advisory Council on Alzheimer’s Research, Care, and Services | Part 2 [Video]. YouTube. https://www.youtube.com/watch?v=Uw9Z-UBnjR8