Relevant bibliographies by topics / Pacific Islander American Personal narratives

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  1. Journal articles
  2. Dissertations / Theses
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Academic literature on the topic 'Pacific Islander American Personal narratives'

Author: Grafiati
Published: 4 June 2021
Last updated: 9 February 2022

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Journal articles on the topic "Pacific Islander American Personal narratives"

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Alber, Julia M., Chari Cohen, Amy Bleakley, Sanam F. Ghazvini, Brenda Trang Tolentino, Rebeca Almeida, and Beth L. Chance. "Comparing the Effects of Different Story Types and Speakers in Hepatitis B Storytelling Videos." Health Promotion Practice 21, no. 5 (January 19, 2020): 811–21. http://dx.doi.org/10.1177/1524839919894248.

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Chronic hepatitis B, a condition associated with severe complications, disproportionately affects Asian Americans and Pacific Islanders in the United States. Increasing testing among this population is critical for improving health outcomes. This study compares different types of video narratives that use storytelling techniques to an informational video (control), to examine whether narratives are associated with higher hepatitis B beliefs scores and video rating outcomes. A sample of Asian American and Pacific Islander adults ( N = 600) completed an online survey where they viewed one of four video conditions, three of which included storytelling techniques and one with informational content. Results indicated that parental stories received significantly higher perceived effectiveness ratings ( M = 3.88, SD = 0.61) than the older adult personal stories ( M = 3.62, SD = 0.74), F(3, 596) = 3.795, p = .010. Parental stories also had significantly higher perceived severity scores ( M = 3.83, SD = 0.69) compared to the young adult stories ( M = 3.73, SD = 0.74) and the informational videos ( M = 3.83, SD = 0.69), F(3, 596) = 7.72, p < .001. The informational videos ( M = 4.10, SD = 0.65) received significantly higher message credibility ratings than the older adult personal stories ( M = 3.84, SD = 0.70), F(3, 596) = 4.71, p = .003. Follow-up tests using Bonferroni correction revealed that parental stories ( M = 3.98, SD = 0.64) and young adult personal stories ( M = 3.934, SD = 0.76) scored significantly higher on speaker ratings than the older adult personal stories ( M = 3.698, SD = 0.77). Results suggest that storytelling has the potential for connecting with a specific audience in an emotional way that is perceived well overall. Future research should examine the long-term impact of hepatitis B personal story videos and whether the addition of facts or statistics to videos would improve outcomes.
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Pang, Valerie. "The Beliefs of Successful Asian American Pacific Islander Teachers: How Culture Is Embedded In Their Teaching." AAPI Nexus Journal: Policy, Practice, and Community 7, no. 1 (2009): 55–82. http://dx.doi.org/10.36650/nexus7.1_55-82_pang.

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Equal educational opportunity is highly dependent on the beliefs and abilities of teachers. However, there is a dearth of research on Asian American Pacific Islander (AAPI) education and the beliefs of successful AAPI educators. Their contributions have been marginalized in the field of education. This research studied the beliefs of nineteen AAPI educators of a successful low-income (82%), 98 percent minority (75% AAPI and 23% Latino) K–8 school. Student achievement levels are beyond what would be expected with an Academic Performance Index (API) of 860. Any score above 800 is considered exceptional in California. Cultural values are embedded in the belief system of the teachers, and these beliefs result in high teacher personal efficacy and collective efficacy. These then influence teacher behaviors as evidenced by utilized instructional strategies, contributed informal leadership roles, and the long-term stability of the school.
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Taitingfong, Riley, Cinnamon S. Bloss, Cynthia Triplett, Julie Cakici, Nanibaa’ Garrison, Shelley Cole, Julie A. Stoner, and Lucila Ohno-Machado. "A systematic literature review of Native American and Pacific Islanders’ perspectives on health data privacy in the United States." Journal of the American Medical Informatics Association 27, no. 12 (October 15, 2020): 1987–98. http://dx.doi.org/10.1093/jamia/ocaa235.

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Abstract Background Privacy-related concerns can prevent equitable participation in health research by US Indigenous communities. However, studies focused on these communities' views regarding health data privacy, including systematic reviews, are lacking. Methods We conducted a systematic literature review analyzing empirical, US-based studies involving American Indian/Alaska Native (AI/AN) and Native Hawaiian or other Pacific Islander (NHPI) perspectives on health data privacy, which we define as the practice of maintaining the security and confidentiality of an individual’s personal health records and/or biological samples (including data derived from biological specimens, such as personal genetic information), as well as the secure and approved use of those data. Results Twenty-one studies involving 3234 AI/AN and NHPI participants were eligible for review. The results of this review suggest that concerns about the privacy of health data are both prevalent and complex in AI/AN and NHPI communities. Many respondents raised concerns about the potential for misuse of their health data, including discrimination or stigma, confidentiality breaches, and undesirable or unknown uses of biological specimens. Conclusions Participants cited a variety of individual and community-level concerns about the privacy of their health data, and indicated that these deter their willingness to participate in health research. Future investigations should explore in more depth which health data privacy concerns are most salient to specific AI/AN and NHPI communities, and identify the practices that will make the collection and use of health data more trustworthy and transparent for participants.
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Potočnik, Nataša. "The South Pacific in the works of Robert Dean Frisbie." Acta Neophilologica 34, no. 1-2 (December 1, 2001): 59–71. http://dx.doi.org/10.4312/an.34.1-2.59-71.

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Robert Dean Frisbie (1896-1948) was one of the American writers who came to live in the South Pacific and wrote about his life among the natives. He published six books between 1929 and his death in 1948. Frisbie was horn in Cleveland, Ohio, on 16 April1896. He attended the Raja Yoga Academy at Point Loma in California. Later he enlisted in the U. S. army and was medically discharged from the army in 1918 with a monthly pension. After his work as a newspaper columnist and reporter for an army newspaper in Texas, and later for the Fresno Morning Republican, he left for Tahiti in 1920. In Tahiti he had ambitious writing plans but after four years of living in Tahiti, he left his plantation and sailed to the Cook Islands. He spent the rest of his life in the Cook Islands and married a local girl Ngatokorua. His new happiness gave him the inspiration to write. 29 sketches appeared in the United States in 1929, collected by The Century Company under the title of The Book of Puka-Puka. His second book My Tahiti, a book of memories, was published in 1937. After the death of Ropati 's beloved wife his goals were to bring up his children. But by this time Frisbie was seriously ill. The family left Puka-Puka and settled down on the uninhabited atoll of Suwarrow. Later on they lived on Rarotonga and Samoa where Frisbie was medically treated. Robert Dean Frisbie died of tetanus in Rarotonga on November 18, 1948. Frisbie wrote in a vivid, graceful style. His characters and particularly the atoll of Puka-Puka are memorably depicted. Gifted with a feeling for language and a sense of humor, he was able to capture on paper the charm, beauty, and serenity of life of the small islands in the South Pacific without exaggerating the stereotypical idyllic context and as such Frisbie's contribution to South Pacific literature went far deeper than that of many writers who have passed through the Pacific and wrote about their experiences. Frisbie's first book The Book of Puka-Puka was published in New York in 1929. It is the most endearing and the most original of his works. It was written during his lifetime on the atoll Puka-Puka in the Cook Islands. It is a collection of 29 short stories, episodic and expressively narrative in style. This is an account of life on Puka-Puka that criticizes European and American commercialism and aggressiveness, and presents the themes of the praise of isolation, the castigation of missionaries, and the commendation of Polynesian economic collectivism and sexual freedom. At the same time, the book presents a portrait of Frisbie himself, a journal of his day-to-day experiences and observations and avivid description of the natives on the island. Frisbie's unique knowledge of the natives and their daily lives enabled him to create in The Book of Puka-Puka an impressive gallery of vi vid, amusing, yet very real and plausible Polynesians. The second book of Robert Dean Frisbie to appear in print was My Tahiti (1937), a book of -memoirs, published in Boston. My Tahiti is a book of 30 short stories about the author and his living among Tahitians. Again, Robert Dean Frisbie is the main hero in the book and as such the book is autobiographical in a sense as well. This book is a personal record which has charm and distinction as it has sincerity, which is in the men, women and children of Tahiti, and which brings an effortless and unpretentious humor to depict a South Seas idyll and a quiet poise to withstand the insidious romance of the tropical islands, too.
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Chow, Julian, Grace Yoo, and Catherine Vu. "Welfare Reform and the Delivery of Welfare-to-Work Programs to AAPIs: What Works?" AAPI Nexus Journal: Policy, Practice, and Community 5, no. 2 (2007): 77–97. http://dx.doi.org/10.36650/nexus5.2_77-97_chun-chungchowetal.

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The passage of the Personal Responsibility and Work Opportunity Act (PRWORA) of 1996 has major implications for low-income Asian American and Pacific Islander (AAPI) populations. The purpose of this paper is to provide an overview of the research currently examining the impact of welfare reform on AAPI recipients and the welfare-to-work services available to this population. This article highlights AAPI participation and their timing-out rates in California’s CalWORKs program and their barriers to transitioning to work. Four welfare-to-work program models and recommendations are presented to illustrate strategies that can be used to address the unique needs of AAPI in order to alleviate their high risk for timing-out: one-stop-shops, transitional jobs programs, providing comprehensive and family focused services, and additional research and evaluation of programs specific to assisting the AAPI population on CalWORKs.
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Palos, Guadalupe R., Megan Hebdon, Sara McComb, Richard W. Wagner, and Maria Alma Rodriguez. "Survivors' narratives of the value of cancer survivorship care plans and clinical services." Journal of Clinical Oncology 34, no. 3_suppl (January 20, 2016): 57. http://dx.doi.org/10.1200/jco.2016.34.3_suppl.57.

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57 Background: Providers in primary care practice can benefit from having a better understanding of cancer survivors’ perceptions of the value of survivorship treatment summaries and care plans. Our objective was to qualitatively explore survivors’ perceptions of care received in dedicated outpatient clinics for survivors of breast, genitourinary (GU), and head/neck cancers. Methods: This study was conducted from August 8, 2014 to October 2, 2014 in 3 clinics, selected on variation in infrastructure, patient populations, and disease site. A convenience sample of survivors scheduled for an appointment in these clinics was eligible. Semi-structured interviews were conducted by research staff trained in qualitative methodology. Demographic and clinical data were collected. Groups explored a) experience with care/services, b) value of care plan, service coordination and clinic operations and c) gaps/strengths in transition to clinics. Descriptive statistics were used to summarize and analyze demographic and clinical data. Discussions were transcribed verbatim with confirmation of themes among a team of researchers. Results: A total of 36 survivors, X= 62.3 (SD = 10.9) years, were interviewed. Of these 27.8% breast survivors, 38.9% head/neck, and 33.3% GU, with X= 8.33 (SD = 5.83) years since their cancer diagnosis. Of these, 80.5% were Caucasian, 8.3% Hispanic/Latino, and 5.6% Asian/Pacific Islander, and 5.6% African-American. 61.1% were male and 78.6% married or living with someone. Survivors cited concerns about inconsistency in methods used to distribute care plans to survivors, inadequate communication about the purpose of the care plan, and vague recall of receiving care plans. Survivors reported the value of receiving survivorship care were “having an awareness of what’s up the road, establishing a constant relationship with their provider and addressing gaps in care”. Conclusions: The value of offering survivorship care is supported by the narratives of these survivors. Additional training and education on effective communication about survivorship care plans may be useful to oncology specialists and primary care providers.
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Smith, Matthew Lee, Caroline D. Bergeron, SangNam Ahn, Samuel D. Towne, Chivon A. Mingo, Kayin T. Robinson, Jamarcus Mathis, Lu Meng, and Marcia G. Ory. "Engaging the Underrepresented Sex: Male Participation in Chronic Disease Self-Management Education (CDSME) Programs." American Journal of Men's Health 12, no. 4 (January 22, 2018): 935–43. http://dx.doi.org/10.1177/1557988317750943.

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Females are more likely than males to participate in evidence-based health promotion and disease prevention programs targeted for middle-aged and older adults. Despite the availability and benefits of Stanford’s Chronic Disease Self-Management Education (CDSME) programs, male participation remains low. This study identifies personal characteristics of males who attended CDSME program workshops and identifies factors associated with successful intervention completion. Data were analyzed from 45,375 male CDSME program participants nationwide. Logistic regression was performed to examine factors associated with workshop attendance. Males who were aged 65–79 (OR = 1.27, p < .001), Hispanic (OR = 1.22, p < .001), African American (OR = 1.13, p < .001), Asian/Pacific Islander (OR = 1.26, p < .001), Native Hawaiian (OR = 3.14, p < .001), and residing in nonmetro areas (OR = 1.26, p < .001) were more likely to complete the intervention. Participants with 3+ chronic conditions were less likely to complete the intervention (OR = 0.87, p < .001). Compared to health-care organization participants, participants who attended workshops at senior centers (OR = 1.38, p < .001), community/multipurpose facilities (OR = 1.21, p < .001), and faith-based organizations (OR = 1.37, p < .001) were more likely to complete the intervention. Men who participated in workshops with more men were more likely to complete the intervention (OR = 2.14, p < .001). Once enrolled, a large proportion of males obtained an adequate intervention dose. Findings highlight potential strategies to retain men in CDSME programs, which include diversifying workshop locations, incorporating Session Zero before CDSME workshops, and using alternative delivery modalities (e.g., online).
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Callander, Denton, John A. Schneider, Asa Radix, Basile Chaix, Roberta Scheinmann, Gia Love, Jordyn Smith, et al. "Longitudinal cohort of HIV-negative transgender women of colour in New York City: protocol for the TURNNT (‘Trying to Understand Relationships, Networks and Neighbourhoods among Transgender women of colour’) study." BMJ Open 10, no. 4 (April 2020): e032876. http://dx.doi.org/10.1136/bmjopen-2019-032876.

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IntroductionIn the USA, transgender women are among the most vulnerable to HIV. In particular, transgender women of colour face high rates of infection and low uptake of important HIV prevention tools, including pre-exposure prophylaxis (PrEP). This paper describes the design, sampling methods, data collection and analyses of the TURNNT (‘Trying to Understand Relationships, Networks and Neighbourhoods among Transgender women of colour’) study. In collaboration with communities of transgender women of colour, TURNNT aims to explore the complex social and environmental (ie, neighbourhood) structures that affect HIV prevention and other aspects of health in order to identify avenues for intervention.Methods and analysesTURNNT is a prospective cohort study, which will recruit 300 transgender women of colour (150 Black/African American, 100 Latina and 50 Asian/Pacific Islander participants) in New York City. There will be three waves of data collection separated by 6 months. At each wave, participants will provide information on their relationships, social and sexual networks, and neighbourhoods. Global position system technology will be used to generate individual daily path areas in order to estimate neighbourhood-level exposures. Multivariate analyses will be conducted to assess cross-sectional and longitudinal, independent and synergistic associations of personal relationships (notably individual social capital), social and sexual networks, and neighbourhood factors (notably neighbourhood-level social cohesion) with PrEP uptake and discontinuation.Ethics and disseminationThe TURNNT protocol was approved by the Columbia University Institutional Review Board (reference no. AAAS8164). This study will provide novel insights into the relationship, network and neighbourhood factors that influence HIV prevention behaviours among transgender women of colour and facilitate exploration of this population’s health and well-being more broadly. Through community-based dissemination events and consultation with policy makers, this foundational work will be used to guide the development and implementation of future interventions with and for transgender women of colour.
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Holloway, Ian, Elizabeth Wu, Jennifer Gildner, Vincent Fenimore, and Paula Frew. "Vaccination Response to an Ongoing Meningitis Outbreak: Uptake and Attitudes among Men Who Have Sex with Men in Los Angeles, CA." Open Forum Infectious Diseases 4, suppl_1 (2017): S418. http://dx.doi.org/10.1093/ofid/ofx163.1046.

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Abstract Background Men who have sex with men (MSM) are at high risk for invasive meningococcal disease (IMD). Following a 2016 IMD outbreak in Southern California, public health officials issued an advisory that urged at-risk adult gay and bisexual men, and all people with HIV, to obtain immunizations. Despite public health efforts to increase MCV4 coverage, uptake and acceptance among MSM remains unknown. Thus, our study sought to: (1) estimate reported MCV4 immunization among MSM in Los Angeles, CA; and (2) document the facilitators and barriers to the newest vaccination recommendation following the recent outbreak. Methods From November 2016 through February 2017, we used venue-based sampling to recruit MSM in Los Angeles (N = 513). Eligible participants completed a 30-minute iPad survey that included items on MCV4 status, sexual behavior, vaccination knowledge and behaviors among other factors. Chi-square and independent sample t-tests were used to determine bivariate associations. Statistically significant variables from bivariate analyses were included in a multivariate logistic regression model predicting MCV4 uptake. Results Participants were young (M=33, SD=10) and racially/ethnically diverse: White (35.7%), Black/African American (14.6%), Hispanic (36.5%), Asian/Pacific Islander (4.1%), Other (9.2%). Reported MCV4 immunization among MSM (25.4%) and MSM living with HIV (37.7%) was low. Statistically significant correlates of MCV4 uptake in our multivariate model included: younger age (aOR=2.51), prior STI diagnosis (aOR=2.21), believing MCV4 vaccination was important (aOR=3.45), having confidence in the MCV4 vaccine (aOR=5.43), and knowing someone who had received the vaccination (aOR=5.79). Conclusion MSM’s perceived health risk, vaccine confidence, and knowledge of someone who received the MCV4 vaccine were important indicators of meningitis immunization in this outbreak context. Provider and public health education efforts may be enhanced by messages that emphasize personal health risks, the safety and efficacy of MCV4, and the importance of meningococcal vaccines for men’s health. Popular opinion leader programs facilitated by someone who had been vaccinated are warranted to enhance MCV4 uptake. Disclosures All authors: No reported disclosures.
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Damien, Hansra, Ramdial Jeremy, Martinez Gianni, Farooq Faheem, Alfredo Torres, Saravia Diana, Ashwin Mehta, and Eugene Ahn. "Disparities Between Patient and Hematology/Oncology Physician Expectations for Integrative Oncology in an Ethnically Diverse Population." Blood 124, no. 21 (December 6, 2014): 2641. http://dx.doi.org/10.1182/blood.v124.21.2641.2641.

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Abstract Purpose: Evidence shows increased patient utilization of various integrative care modalities. In part, patients desire greater self-empowerment to potentially manage their symptoms, improve quality of life and overall outcomes. Measurements of patient and physicians opinions regarding the importance of integrative care are lacking. We aim to compare expectations of what “comprehensive care” means between hematology/oncology physicians and patients. Methods: Approval from the University of Miami IRB was obtained prior to initiation of data collection. Adult patients (pts) and hematology/oncology physicians (MDs) at an academic tertiary care medical center in Miami, Florida were enrolled to complete a survey. Demographics collected include: age, gender, race, & ethnicity. Clinical information collected include cancer subtype and treating hematologist/oncologist. The survey consisted of 7 questions assessing personal opinions on “comprehensive care”. The questions specifically asked “In addition to standard care, it is important to incorporate/provide” nutrition services, exercise therapy, spiritual/religious counseling, supplement/herbal advice, support groups, music therapy, or other complimentary medicine services (acupuncture, massage, relaxation therapy). Answers were recorded on a 5 point Likert scale (1=highly disagree, 2= disagree, 3=neutral, 4=agree, 5= highly agree) then converted into 2 categories (1,2,3= neutral/disagree vs. 4,5=agree). Fisher’s exact test with 2 sided p-value used to compare significance between MDs & pts responses. Results: 670 pts and 55 MDs enrolled from June 2013 to May 2014. Pts demographics included a mean age 55 with range 18-88 with 44% male and 56% female. 57% of patients were Hispanic vs. 43% not Hispanic. 81% were white, 11% black/African American, 2% Asian/Pacific Islander, and 6% other. 17% of patients had hematologic disorders (85% malignant 15% benign) vs. 83% of patients had solid oncologic malignancies. MD demographic data will be reported in poster. Survey results: 83% of pts agree that nutritional advice is important vs. 67% of MDs, p=0.01. Significant disparities were also seen for exercise therapy (86% vs. 73% respectively, p=0.02), spiritual/religious counseling (69% vs. 50% respectively, p=0.01), supplement/herbal therapies (86% vs. 56% respectively, p=0.0001), music therapy (66% vs. 30% respectively, p=0.0001), and “other complementary services” such as acupuncture, massage and relaxation therapy (70% vs. 45% respectively, p=0.004). The lone service that did not demonstrate significant disparity of opinion was support groups (72% vs. 68% respectively, p=0.5). Conclusion: A significant majority of adult hem/onc patients seen at a major academic institution in South Florida feel that it is important to incorporate nutrition advice, exercise therapy, spiritual/religious counseling, supplement/herbal advice, support groups, music therapy, and other complimentary services such as acupuncture, massage and relaxation therapy as part of their “comprehensive care”. With the exception of support groups, MDs tend to value integrative oncology services significantly less than patients do. It is expected that increased availability and utilization of integrative oncology modalities at tertiary hospital sites could improve patient satisfaction and quality of life, and enhance patients’ therapeutic alliance with their medical team and plan as patient and physician definitions of “comprehensive care” more closely merge. This is the first study published to our knowledge that examined disparities between patient and physician expectations for comprehensive care in an ethnically diverse, predominantly Hispanic population. Disclosures No relevant conflicts of interest to declare.
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Dissertations / Theses on the topic "Pacific Islander American Personal narratives"

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Talusan, Liza A. "The formation of scholars| Critical narratives of Asian American and Pacific Islander doctoral students in higher education." Thesis, University of Massachusetts Boston, 2016. http://pqdtopen.proquest.com/#viewpdf?dispub=10118448.

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This dissertation addresses the formation of scholar identity as informed by an identity- conscious approach to doctoral student socialization, doctoral student development, and racial identity as expressed through the critical narratives of Asian American and Pacific Islander doctoral students in the field of higher education. The study explored the intersections of race, doctoral student socialization, and doctoral student development — three areas that have been approached as separate entities in existing literature. By using life history methodology and narrative inquiry, this study contributed to a more thorough understanding of racialized experiences in doctoral studies. Critical narrative was used as a methodological approach concerned with power and language in society where individuals can concretely question their own realities and identify the socio-ideological influence of systems on their practices and beliefs (Souto-Manning, 2012). Rather than use terminology of counter-narrative, which positions a narrative as counter to an existing dominant narrative, the use of critical narrative is highlighted as a way to position the stories of Asian Americans and Pacific Islanders as their own central story. This inquiry advances our understanding of ways to create and sustain more inclusive and engaging learning environments that support racial diversity in higher education and to better understand the barriers that have socially and historically marginalized Asian Americans and Pacific Islanders both in general and in doctoral education. Recommendations for practice include developing identity-conscious approaches to scholar formation, including but not limited to inclusive pedagogy and curriculum; mentoring and advising; culturally affirming networks; program and organizational orientation; and doctoral student support. A model of identity-conscious scholar formation is presented in which socialization, development, and racial identity must be operationalized as bidirectional and interactional processes.

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Books on the topic "Pacific Islander American Personal narratives"

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Kirby, Lawrence F. Stories from the Pacific: The Island War, 1942-1945. Manchester, Mass: Masconomo Press, 1994.

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Radike, Floyd W. Across the dark islands: The war in the Pacific. New York: Presidio, 2003.

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Helmet for my pillow: From Parris Island to the Pacific, a young Marine's stirring account of combat in World War II. New York: Bantam, 2010.

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Bill, Marvel, ed. Islands of the damned: A marine at war in the Pacific. New York: New American Library, 2010.

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Burgin, R. V. Islands of the damned: A marine at war in the Pacific. New York: New American Library, 2010.

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Burgin, R. V. Islands of the damned: A Marine at war in the Pacific. New York: NAL Caliber, 2010.

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Astor, Gerald. Crisis in the Pacific: The battles for the Philippine Islands by the men who fought them. New York: Donald I. Fine Books, 1996.

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The unspoken bond: Stories about the Naval Hospital corpsmen and the Marines they served with and the battles they fought in the Pacific during the Second World War, beginning with Guadalcanal-Tulagi, 1942. London [Ont.], Canada: Third Eye, 1998.

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Baskett, Dave. Recollections of service in the 6th Reconnaissance Group in World War II: Colorado Springs, Australia, the Pacific Islands, Okinawa, and Japan. [Casper?: s.n., 1998.

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Elizabeth, Osborne. Torres Strait Islander women and the Pacific War. Canberra: Aboriginal Studies Press, 1997.

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Book chapters on the topic "Pacific Islander American Personal narratives"

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"Pathography/Illness Narratives." In The Routledge Companion to Asian American and Pacific Islander Literature, 467–76. Routledge, 2014. http://dx.doi.org/10.4324/9781315779089-48.

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