Doing Participatory Action Research in a Racist World Western Journal of Nursing Research Volume 28 Number 5 August 2006 525-540 © 2006 Sage Publications 10.1177/0193945906287706 http://wjn.sagepub.com hosted at http://online.sagepub.com Colleen Varcoe University of British Columbia, Vancouver This exploration of the racial power dynamics in a participatory action research project with women who had experienced intimate partner violence discusses the challenges inherent in doing participatory action with antiracist intent and offers suggestions for overcoming these challenges. To engage in this type of research, explicit commitment to the goals of an antiracist intent needs to be shared as widely as possible. Fostering such shared commitment demands that the social locations of all involved be interrogated continuously. Such interrogation, however, needs to be prefaced with understanding that individuals are not representative of particular power positions or social identities or locations and with critical attention to how language and social structures shape racism and other forms of dominance. Being inclusive must be understood as complex and the influence of diverse agendas and perspectives acknowledged and taken into account. In the face of such complexity, “success” in research may need redefinition. Keywords: racism; participatory research; violence; women; nursing research; Canada C urrently engaged in a large participatory action research (PAR) project, my fourth as a principal investigator, I continuously reflect on what I have learned. In particular, I continue to be challenged by doing nursing research with diverse women in a society imbued with, and often structured by, racism. In this article, I recount some of the processes involved in one PAR project to share my evolving ideas regarding doing such research. I conclude with a discussion of recommendations for other nurse researchers who aim to engage in participatory research within an antiracist paradigm. Author’s Note: The author gratefully acknowledges the participation of all the women in this project, including those who left in anger. Also appreciated are the reviews of earlier drafts of this article by two of the participants (not named for reasons of confidentiality), two anonymous reviewers, and Dr. Annette Browne, University of British Columbia. Finally, the research referred to in this study was generously supported by the BC Health Research Foundation. 525 526 Western Journal of Nursing Research Background Participatory research has become an increasingly popular approach in nursing research (Henderson, 1995; Holter & Schwartz, 1993; Lindsey & McGuinness, 1998). In part, this popularity is because of the congruence between the concern of nursing with people who are marginalized and the goals of PAR. These goals are to place the less powerful at the center of knowledge creation, shift peoples’ lived experience of marginalization to the center (Hall, 1992), and place the tools of research “in the hands of deprived and disenfranchised people so that they can transform their lives for themselves” (Park, 1993, p. 1). Both the moral commitments of nursing in working with people who are marginalized and the commitments of PAR oblige researchers to continually work to readdress hierarchies, power, and privilege (McIntyre & Lykes, 1998, 2004). Race is a central axis of power and privilege in the Western world, and proponents of PAR have repeatedly emphasized the importance of attending to race, particularly as it intersects with gender, ethnicity, sexual orientation, and physical and mental abilities (Hall, 1992; Metzler et al., 2003; Rivera, 1999; Spigner, 1999; Stanfield & Dennis, 1993; Sullivan et al., 2003). Indeed, some argue that PAR has potential as a tool of resistance against the interlocking oppression of race, gender, culture, and class. As Spigner (1999) has noted in the health field, however, the research establishment is overwhelmed by well-meaning nonminority researchers who, although they recognize racism and its consequences on health, cannot reconcile the contradiction of nonminority researchers doing research with people marginalized by their minority status in the name of empowerment. Recognition of this contradiction has led to emphasis on the importance of researchers from minority groups (DionStout, Kipling, & Stout, 2001; Douglas, 1998; Spigner, 1999; Washington, Napoles-Springer, Forte, Alexander, & Perez-Stable, 2002) as well as calls to engage explicitly with issues of race. Although race has no validity as a biological construct, race and racism shape social experience, having profound effects on peoples’ lives. Nurse researchers are paying increasing critical attention to the use and construction of race in nursing research (e.g., Anderson, 2000; Phillips & Drevdahl, 2003). Drevdahl, Taylor, and Phillips (2001, in press) analyzed the use of race and ethnicity in nursing research literature, finding significant inconsistency in their use and their meanings. Despite the importance of attending to race and racism within both nursing research and participatory research, however, nurse researchers have paid little attention to the power dynamics of race and racism in participatory research. Thus, this article reports on the research processes in a PAR study as those processes relate to such dynamics. Varcoe / Participatory Action Research 527 Project Violence Free During a 5-year period (1999 to 2003), I, along with a group of women who had experienced intimate partner abuse, obtained funding and conducted a study of formal system responses to violence against women. For our study, we used ethnographic methods within a PAR framework. The project took place in two suburban communities in western Canada. The impetus for the project arose from recognition by both service providers and the women they served that the responses by health care, social welfare, and legal systems required analysis and improvement. Early meetings between myself, service providers, and the women they served led to the women deciding to direct the project and partner with me. The purpose of the project was to develop a process through which women who experience violence could collaborate with service providers to diminish barriers to living violence-free and improve the way services are offered. The project also was intended to facilitate the empowerment of women who experienced violence by recognizing the importance of their experiences and providing opportunities for them to talk, listen, learn, and advocate on their own behalf toward changing practices and policies. During the 3 years of data collection, the research team, composed of myself, a number of the women (some served as paid researchers), and several community researchers and hired research assistants interviewed a total of 46 women who experienced partner abuse and 38 service providers. Documentary data from the women and service providers were collected. Following completion of the study, we contracted an independent researcher to conduct postparticipation interviews with 6 active participants regarding their experience of involvement in the study. The women participated in the design of the study, the writing of two successful funding proposals, analysis of the data, and a range of specific actions and dissemination strategies, including publications. Participation varied depending on each woman’s interests. The women were interested in writing lay publications but had little interest in academic publications; thus, only 2 women made comments on earlier drafts of this article. Challenges of “Doing” PAR in Complex Contexts In general, the research team encountered a gulf between the rhetoric of PAR and the reality of conducting participatory research with participants who have survived often-unspeakable abuse. The literature on PAR provided little guidance regarding how to do research with women whose lives are continually disrupted by abuse, who have serious mental illnesses, who have drug or alcohol problems, or who just want to stop talking about violence and get on 528 Western Journal of Nursing Research with their lives. There was little direction regarding how to work across quite different political commitments and philosophical orientations. Most taxing, however, was the absence of discussion regarding how to work with racism. The members of the research team identified themselves in relation to ethnicity and race in varied ways. Although my father is aboriginal, I have not lived within aboriginal culture, but I have experienced racism occasioned by my appearance or by revealing my ancestry. Two members of the research team identified as members of particular racialized groups and as “women of color.” All other members of the research team identified as White, Caucasian, or European Canadian. All of us shared a commitment to ending violence against women, and some were declared feminists. Some of us had a commitment to inclusion and some, a commitment to active antiracism. As the principal researcher, I used my power to involve immigrant women, aboriginal women, and other racialized women in the project, although I thought doing so was at odds with my intention to power share. One of the other women was explicitly committed to such inclusivity. These moves, particularly in the context of global events following the attacks on the World Trade Center in New York, provided a catalyst for power dynamics that erupted frequently and forcefully. What follows is an analysis of those experiences that may provide ideas for working with race and power in participatory research and a basis for further discussion. The Politics of Participation The women’s experiences and relative disadvantages shaped their participation. All of the women had direct experience of intimate partner violence to the extent that it became a central feature of their lives. Their participation was both a testimony to the centrality of their experiences of violence and, according to the women, was a meaningful way of dealing with those experiences. Dealing with the aftermath of violence, however, shaped and limited participation in some ways. For women who had income, child care, transportation (particularly personal vehicles), and facility in English, it was relatively easy to participate. Not surprisingly then, the women who were most active in directing the research were predominantly White, middle-aged, English-speaking women with some employment income. Women with little or no income, no private transportation, limited English, or membership in racialized groups found it more challenging to participate. If a few of us had not been committed to including racialized and immigrant women, the project might have proceeded with less conflict and possibly without racial conflict. Given the varied commitments and identities within the group, and given world events, we Varcoe / Participatory Action Research 529 struggled continuously. The conflicts and challenges began with decisions regarding hiring staff, continued through decisions regarding how to use the budget, and have not yet ended, extending to the question of how to write an article such as this in a respectful manner. The conflicts and controversies around the politics of participation point to the complexity of the ideal of inclusion, the influence of diverse agendas and perspectives, the limitations of naming social locations in certain ways, and the power of ideological frames. The Complexity of Inclusion Critiques of racism in science (Harding, 1993); critiques of exclusion from research because of race, class, or gender (e.g., Cannon, Higginbotham, & Leung, 1988); and critiques of feminism’s failure to grapple with more than gender in countering such exclusion (hooks, 1992) have led to greater awareness of the need for inclusivity in research. In response to these critiques, associated calls for anti-Eurocentric and anticolonialist approaches, and more generalized calls for attention to the relationship among research ethics, empowerment, and voice, participatory approaches have grown in popularity. Thus, I began this research with explicit concern for inclusivity. In particular, I began this research with an express concern about racialization that arose from several interrelated sources. First, my earlier research (Varcoe, 1996, 2001) heightened my awareness of the dynamics among racism, classism, and the health and health care of women who experience violence. Second, I was aware of the lack of research on racialized women in general and in particular on racialized women who experience violence. When beginning this research, there were few studies of the particular challenges faced by racialized women, immigrant women, and aboriginal women, and I was committed to addressing this deficit. Finally, my analysis of my own experiences of violence was that my relative “success” as a survivor of various forms of violence was facilitated by the advantages I had in speaking English as my first language, having access to good education, having enjoyed a progressively better standard of living from rural poverty to my current middleclass status, and “passing” as White unless I revealed my aboriginal ancestry. Thus, we included in the research proposal explicit plans to include as diverse a group of women as possible. Although the women who were involved in these initial stages supported inclusivity, in retrospect, none of us adequately anticipated the challenges we would face. During the 3 years, we expanded beyond the initial group, eventually involving a wide range of women. The literature on cross-cultural and feminist thinking and research prepared me to be acutely aware of my power and privilege as a researcher. Such literature, however, tends to dichotomize the researcher and the researched as 530 Western Journal of Nursing Research though each is a homogenous group characterized by its difference from the other. For instance, Selby (1998) spoke of the importance of research relations when “there are ‘haves’ and ‘have-nots’” (p. 13). The prototype for discussing power relations appears to be situations in which a lone White researcher studies “others.” For example, Patricia Hill Collins (1993), from whom I took considerable guidance regarding the intersections of race, class, and gender, described a pattern of relationships she calls voyeurism: “From the perspective of the privileged, the lives of people of color, of the poor, and of women are interesting for their entertainment value” (p. 37). Although these warnings are important, they offered little guidance as we entered the messy power relations that arose in trying to do research with women whose education ranged from elementary school to graduate school, whose income ranged from single-income social assistance to $80,000 a year and whose ethnicity and immigration status reflected the diversity of Canada itself (with, in the end, a relative overrepresentation of immigrant and aboriginal women). The “haves” and “have-nots” dissolved into an infinite range of “have mores,” “have much mores,” “have much less,” and so on, and “the privileged” was rendered an unstable category. The attempt to be inclusive added complexity to the diverse and sometimes competing perspectives and agendas operating in this project. Different Perspectives: Different Agendas Although all members of the research team and all participants appeared united by the goals of the study and by concern for violence against women, we each brought different understandings and reasons for participating. My reasons for doing this research were not entirely altruistic. I was a “new” academic with a research program to develop, albeit delighted that the research permitted me to harness my passionate anger about violence, the position of women in society, racism, and the inadequacies of nursing and health care system responses to violence against women (Morrow & Varcoe, 2000; Varcoe, 1997). And, my perspective—explicitly feminist and antiracist—was only one perspective that, despite my efforts and power, failed to dominate. I had only a rudimentary notion of what it meant to do research in an antiracist manner. Each other person also had her own reasons for participating. In general, all of the women expressed a desire to “do something.” The women talked about wanting to “make a difference,” “change things,” and “try to help other women who have gone through this or could be going through it.” The women who were initially involved were united both by their concern for violence and their own difficulties trying to get support within formal systems. They did not express any particular commitment to my agenda of inclusion but seemed supportive or at least did not challenge my agenda. Varcoe / Participatory Action Research 531 As we were committed to making the project as participatory as possible (a shared agenda, I believe), the women and I collaborated on every phase, beginning with the development of the proposal and the hiring of staff. The hiring process was when I first became aware of the fallacy of the assumption that I (the highly educated, articulate researcher) was the one wielding power. The women were clear that they wanted to hire a woman who had helped many of them in their own healing process; my input in this decision was irrelevant. She knew the community well and had been instrumental in starting the project. The women accepted my argument, however, that given that this woman was White, if we wanted to involve women of color, immigrant women, and aboriginal women, we needed to hire a woman from one or more of these communities. Thus, we hired a woman with explicit political commitments to women of color and immigrant women who was strengthened by her own identity as a woman of color and an immigrant. During the next 3 years, the project evolved with a core group of women participating actively in every element of the study and taking on other initiatives that stemmed from, but were separate from, the research project. For example, the women developed a local anti-violence media campaign, consulted with the provincial justice department on a stalking brochure, and held fund-raising events for nonresearch activities. The group grew and shrank as new women joined and others dropped away, but the ethnicity of the group remained predominantly European Canadian. Paid staff actively pursued the involvement of aboriginal and immigrant women, with the result that the research involved an incredibly diverse group of women, but none joined the core group despite invitations to do so. Thus, there were three “layers” of participation: (a) the research team composed of myself, the paid staff, and those “participants” who were active in all phases of the research (the research grant paid interested women $15 an hour for research work and the women determined what work qualified as “volunteer” versus “paid”); (b) women who guided the research to a lesser degree and participated actively in selected actions, such as a youth forum; and (c) the aboriginal and immigrant women who were interviewed and participated in data analysis but who remained separate from the overall guidance of the project and related social activities. Each participated for her own reasons—some of which were made explicit (e.g., my desire to develop my research program, employment for others), some of which were shared (e.g., the desire to change the system responses to abuse), some of which were not shared (e.g., the desire to tell one’s story), some of which were hinted at (e.g., the support for self-development, available through media and other workshops funded by the project), and some of which were unknown. These various perspectives and agendas often collided. For example, earlier I claimed that it was “relatively easy” for more privileged women to participate. 532 Western Journal of Nursing Research All the women did not see it this way. Even though some women had employment, postsecondary education, income well above poverty levels, and English-language fluency, their participation occurred in the context of struggles to put their lives together in the aftermath of interpersonal violence, and many were still being harassed by ex-partners, frequently through their children (Varcoe & Irwin, 2004). The women often talked about the challenges of participating and some women emphasized that they wanted these challenges recognized and not diminished through comparison with other women who may face different challenges. Some objected to extra effort being made to include women who did not speak English (e.g., paying for interpreters and multilingual support workers) or new immigrants (e.g., holding meetings in a location familiar to the women). As well as the hourly wage for research work, the research grant provided child care and transportation for all participation, including “actions” (e.g., videotaping, workshops) and related social activities (e.g., lunches). Because a number of women wanted the extra income, there was some conflict and competition regarding who should get the paid work, even though there was more money and work than the women could do. These tensions revealed deep divisions among us and the inadequacy of the ways we dealt with our own social locations in relation to one another. Beyond Naming Social Locations Naming one’s social location has become a common feature of much qualitative research. In 1994, Visweswaran called locating oneself an “increasingly sterile” maneuver (p. 49). In response to essays by Lather (1994) and Fine (1994), Daphne Patai (1994) protested that “this tiresome reflexivity” has become a “mental game” (p. 66), arguing against “the pretence that the world’s ills are set right by mere acknowledgement of one’s own position” (p. 67). We lived the complexity behind these critiques. In this project, the fiction of the powerful researcher and the less powerful yet homogenous “researched” unraveled. The romantic emancipatory possibilities of PAR were exposed as dreams in the light of the realities of our racist and inequitable world. Rather than having overengaged in tiresome reflexivity, however, our failure seems to me to have been the failure to explicitly take into account the complex ways in which power and privilege were continuously operating and shaping our work. Race was particularly problematic. One of the women who self-identified as a woman of color continually put the issue of race “on the table,” as I did (but less often). Other team members expressed no interest in discussing race. Our interest in race seemed to be directly proportional to the hue of our skin color. Everyone engaged in analysis of my position as the powerful researcher, initially at my instigation, and gradually as part of the project culture. There Varcoe / Participatory Action Research 533 was little or no interest, however, in engaging in reflection regarding how the social positions of other participants might be operating. From the beginning of my engagement with the women, I had continually expressed concern that I not dominate and sought to “take a back seat.” In fact, I probably overdid it. For example, when discussing our methodology, one woman became frustrated with my desire for them to make decisions. “You’re the researcher, Colleen. Just tell us!” The women wanted to “get on with it,” were interested in action, and often expressed impatience with the seemingly slow research process. Several commented in postparticipation interviews that the research was “more involved than I thought” and that the “actions” were less immediate than they had expected. Thus, among the research team members, there was a sense of impatience, an orientation toward “action,” and little interest in “navel gazing,” particularly when issues such as race seemed irrelevant to their interests. So the insidious rhetoric of equality found purchase. The idea of all women who experience violence being on an “even playing field” surfaced repeatedly in analysis sessions when issues of race were raised. With one early exception, the women decided not to participate in analyzing their own interviews, leaving the women free to compare their own experiences to those of the women whose interviews were being analyzed. “I hope she doesn’t think that she had problems because she was an immigrant!” Thus began the analysis of our first interview with a woman of color and thus began one of many sessions laden with racial conflict. The speaker went on to say that her reaction to the interview story (which related to horrendous physical and emotional abuse compounded by grave difficulty getting formal support) was that the interviewee “didn’t have it that bad” in comparison to herself and that she hoped that the woman realized that the system was “that bad” regardless of “being an immigrant” (by “immigrant,” she was referring to the woman’s membership in a racialized group, not referring to her status as a newcomer to Canada). Responses dissolved into two camps: Some defended the initial speaker, whereas those committed to antiracism pointed to the particular barriers that the woman encountered and emphasized the invisible “race privileges” that others enjoy (including most in the room at the time). Everyone seemed angry. One woman said that others were being “attacked because they are White” and left, never to return to analysis. Those of us who remained buried the conflict as quickly as possible, perhaps partly because we had all experienced so much conflict and violence in our lives. We all conspired to treat the conflict as a problem of process—we agreed that people ought to be able to react with their biases and hold them up for scrutiny without being “attacked.” I tried to reframe the exchange as “intellectual” discussion. A seemingly important difference between the “office 534 Western Journal of Nursing Research staff” (myself and the paid researchers) and the rest of the women was that we had both significantly more formal education (two of us with graduate degrees) and experience in community leadership positions and meetings. We were familiar with debates and presenting and defending arguments. The women had previously called the lively and impassioned theoretical debates among the staff and myself “fights,” and at this point I tried to reframe this “fight” as a theoretical debate that the women were now joining. In doing so, I helped to gloss over the deeper differences that were to plague our project. In this context, explicit naming of social locations became a liability in the absence of commitment to critical reflexivity by all. Others increasingly saw each person as representative of her particular social location. So, for example, some dismissed concerns about race as the “personal problems” of those raising such concerns. Increasingly, my concern about my positional power was raised to curtail my influence, and some women saw me as “taking sides” with the women of color when issues of race arose. Most poignantly, one woman claimed that women of color were not joining the project because articulate women of color (such as one member of our research team) were intimidating, and my reaction to this was dismissed as “taking sides.” The day after the attacks on the World Trade Center, our analysis meeting erupted in anger as one of the women interpreted another’s concern for backlash against Muslims as a defense of the attacks and stormed out of the meeting. Although these dynamics played out in ways that were disturbing and challenging, they are not particular to this project but rather reflect much wider ideological and discursive frames. Ideological Frames Of course, this work was not done in a vacuum. Rather, this research was done in Canada, where liberal racism (Henry, Tator, Mattis, & Rees, 2000) is masked by the ideology of multiculturalism (Ng, 1995). In this ideological frame, “multiculturalism provides a way of managing a society with multi-ethnic and multi-racial groupings” (Ng, 1995, p. 6), and state policy dictates that all groups should be treated equally and obfuscates any need to redress entrenched inequalities. These notions of multiculturalism and equality are linked to the strategy of “cultural sensitivity,” an approach in which those with privilege ought to be “sensitive” to difference but are not obligated to challenge the marginalization and stigma that generally accompany difference from the dominant group. These ideological frames undergirded our research. Living in Canada within the rhetoric of multiculturalism, all of us were well schooled in Varcoe / Participatory Action Research 535 multiculturalism that defines “cultural” problems as mismatches between “minority” and dominant cultures, overlooks political and economic forces, makes the “different” culture the problem, and assumes a “level playing field” that overlooks the historical impact of colonization, immigration, and racism (Henry et al., 2000). We had limited experience in antiracist work; I had begun to take an actively antiracist stance in my work as a teacher and one of the staff had years of experience as an antiracist political activist, but none of us had tried a project of this complexity or scope. We failed to adequately account for the operations of our own social locations and to adequately account for the racist context and the broader racializing discourses. Although we were explicitly aware of the need for particular strategies to involve women of color, immigrant women, and aboriginal women in the project, we were unprepared for the scope of the challenge. Not surprisingly perhaps, then, most did not see a need to go beyond inviting participation. There was no question whether garage sales, formal meetings, and barbecues with White women would be inviting to a more diverse group. Indeed, some expressed resentment when women of color were offered paid work or when “more” was done to facilitate participation (i.e., driving to give someone a ride). But Did We Fail? In the end, the women produced a powerful video that included a wide range of women. They dominated a conference attended by hundreds of service providers from the justice and social service systems. A number of nursing students completed community health and research placements with the group. Diverse women presented at conferences, did “speaks” to various aboriginal groups, consulted with policy makers, contributed to publications (e.g., Varcoe & Irwin, 2004; Varcoe, Jaffer, & Earhardt, 2002; Varcoe, Jaffer, & Kelln, 2002), and even had fun. Everyone learned something; many learned a lot. I learned that I would do some things exactly the same and some things differently. Having a colleague with similar philosophical commitments worked effectively for me. My role as “employer,” however, conflicted with the role of colleague. Several women quit the project in anger—I suspect at least partly because they saw me as “taking sides.” I could not freely discuss these dynamics with paid staff because such discussion would involve talking about one employee with another, and group discussions reinforced the view that I was taking sides. I now prefer to have a co-investigator who is not an employee, with whom I can problem solve and debrief. 536 Western Journal of Nursing Research Having a funding agency that was committed to community-based research facilitated our work. The funding body was supportive of the kinds of strategies (child care, transportation, an accessible “storefront” research office, and interpreters) necessary to do participatory research with women and with people whose first languages are not the “official” languages of the country. This degree of support for the study (when other funding bodies are known to have greater restrictions on what are considered “eligible” research expenses) were critical to mounting and sustaining this study. Being clear about the goals of the project in the beginning was very useful. In the future, however, I will negotiate commitment to goals in more detail. I now know that it is important to surface as many “hidden” agendas as possible and then to negotiate commitment not only to my own goals but also to those of the participants. It became increasingly clear that the group could not meet all the participants’ goals, and unfulfilled expectations caused bitterness that could have been avoided. Being aware of power differences and positionality, or “location,” and bringing my own privilege to the attention of the other participants were, I believe, important and useful. I think that “location” or exploring one’s subjectivity must be done, however, in a much more complex way. Having one member of the research team (albeit the “most” powerful) engage in reflexive analysis of her own social location is not adequate to set the ills of a research project to rights. Rather, all participants should be required to explore their positionality in a manner that is relative, relational, contextual, and continuous. That is, it would have been useful to explore in an ongoing manner how each member’s power operated differently in relation to other participants and in different contexts. For example, because of her extensive network and history with the community of local service providers, one of the women was in a powerful position to facilitate or limit relationships between service providers and the research team. Indeed, her less-thancongenial withdrawal from the project coincided with an abrupt cessation of participation by many local service providers. Since then, however, I have found it useful to preface such discussions of social location with strategies to pre-empt “White defensiveness” (Aveling, 2002; Roman, 1993) or indeed defensiveness regarding other positions of dominance. Following others such as Gillespie, Ashbaugh, and DeFiore (2002), emphasizing that it is racism, social inequities, dominance and uncritical acceptance of privilege that is problematic (not White-ness or other positions per se). To optimize the engagement of everyone regardless of their particular identities, I also focus on how racism is institutionalized and embedded in language. Stressing that individuals are not representative of particular Varcoe / Participatory Action Research 537 power positions, social identities, or locations can open up the possibility of a wider range of critical analyses rather than simple dichotomization into powerful or oppressed. Such strategies might have lessened the entrenchment of individuals into positions shaped by their claimed social location. In addition, we might have fostered critical analysis when some women who were members of racialized groups expressed class and “caste” bias towards others. Dealing with the power and privilege conferred by various positions of power ought to have been an explicit focus for everyone. In the absence of attention to the dynamics of an inherently racist social context, commitment to an antiracist agenda by a few participants was not sufficient to achieving that agenda. In the future, I will include an antiracist agenda in my negotiation of project goals and be more explicit regarding the possible consequences of such an agenda. It was unreasonable, and perhaps naïve, to expect that a group of community participant–researchers without prior experience in either research or antiracism could take on a project of this nature without support in confronting racism. We had workshops on interviewing, research methods, group process, and ethics. At a minimum, a workshop on racism and working within diversity should have been our starting point. We found many ways to value diversity. We attempted to identify and value each woman’s individual skills and help her match those to her contribution in the project. We valued and sought the diversity of women’s experiences. We knew the importance of employing women from the participant’s communities, and we used an advisory committee with representatives from various sectors. We did not go far enough, however, to support the inclusion of racialized women or to foster an antiracist agenda. I now try to ensure that there is meaningful commitment to an antiracist stance at the outset of any project. I attempt to ensure diversity in both hired staff and the “reference group” (such as an advisory committee). Selby (1998) urged researchers to ensure that there is a reference group composed of members of the “culture” being studied. However, as this project illustrates, the “culture being studied” is bound to be diverse in itself; thus, such a reference group needs to be diverse. In our case, greater diversity in ethnicity, class, and education would have been warranted. I now make the value of “cultural brokerage” explicit—by making such skill a component of job descriptions and foregrounding the importance of such work on a daily basis. If I had done so, it would have been clear that facilitating the development of trust and communication with various immigrant and aboriginal communities, groups, and individuals was work that deserved time and attention, and 538 Western Journal of Nursing Research complaints by some that one of the staff was “not doing her job” when doing such work might have been forestalled. I also make explicit how different needs for participation might require different resources. So, for example, in some projects an honorarium for very poor women might be larger than for those who have an income well above the poverty line. Or twice as much time might be allocated for research assistants to recruit nonEnglish-speaking participants. Finally, I have learned to redefine success and failure in such research. There were many intangible successes in this project that included increased skills and confidence among the participants, new relationships and connections, new awareness of issues in various communities, and so on. We initially expected the same level of academic success (e.g., presentations, publications) as with nonparticipatory, noninclusive studies. I now endeavor to set expectations (for myself and funding bodies) in ways that accommodate the unique requirements of PAR. Disagreement and loudly expressed anger marked the exercise of power. Continued participation in the project despite conflict suggested some degree of resolution of conflict, coupled with commitment. Thus, I count conflict, tenacity, and survival of the project as markers of success. If nurse researchers (and those from other disciplines) want to engage in empowering research, they ought to expect to get overpowered once in a while. 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(2004). “If I killed you, I’d get the kids”: Women’s survival and protection work with child custody and access in the context of woman abuse. Qualitative Sociology, 27(1), 77-99. Varcoe, C., Jaffer, F., & Earhardt, P. (2002). Woman abuse in a global context: Women immigrating to Canada (Research report). Vancouver, Canada: University of Victoria. Varcoe, C., Jaffer, F., & Kelln, P. (2002). Protecting women? Women’s experiences of seeking protection from abuse by intimate partners. Victoria, Canada: University of Victoria. Visweswaran, K. (1994). Fictions of feminist ethnography. Minneapolis: University of Minnesota Press. Washington, A. E., Napoles-Springer, A., Forte, D. A., Alexander, M., & Perez-Stable, E. J. (2002). Establishing centers to address treatment effectiveness in diverse ethnic groups: The MEDTEP Experience. Ethnicity & Health, 7(4), 231. Colleen Varcoe, PhD, RN, is an associate professor at the University of British Columbia School of Nursing. Her research focuses on women’s health with an emphasis on violence and inequity, and the culture of health care with an emphasis on ethical practice. She is currently undertaking a longitudinal study of the health and economic effects of violence and a participatory project examining rural maternity care for aboriginal women.