Open-ended personal interviews were conducted with 20 women with early stage breast cancer attending a regional cancer centre in Southwestern Ontario. We explored three related issues: (1) the extent to which these women perceived that they had treatment options; (2) their understanding of treatment benefits and risks; and (3) the role they wanted for themselves and their oncologists in treatment decision-making. We found, first, that many women who were presented with the choice to undergo some form of adjuvant treatment versus no treatment felt that 'doing nothing was no choice'. Second, when interpreting probabilistic information on treatment benefits and risks, some women retained the idea of probability but thought that they personally would beat the odds. Others transformed the information to make it more personally meaningful, and still others assessed their risk status by comparing themselves with friends or relatives having the same disease. Third, many women preferred some form of shared treatment decisionmaking process with their oncologists. Women perceived treatment decisions as either 'right' or 'wrong' which raised the issue of blame for a 'bad' decision should the cancer return. Implications of these findings for clinical practice and for models of treatment decision-making are discussed.

Many substance users report that they experience multiple barriers that produce significant challenges to linking with treatment services. Being on a waiting list is frequently mentioned as a barrier, leading some people to give up on treatment and to continue using, while prompting others to view sobriety during the waiting period as proof they do not need treatment. This ethnographic study examines the views that 52 substance users have of the waiting time before treatment and the strategies they created to overcome it. Understanding how substance users react to waiting time itself and in relation to other barriers can lead to services that are effective in encouraging treatment linkage.

The results of this study confirm a body of literature that supports the effectiveness of case management in improving linkage with treatment. The role of motivational interviewing in improving linkage was not supported. Results are discussed in the context of other case management and motivational interviewing linkage studies.

Waiting time is a contemporary reality of many drug abuse treatment programs, resulting in substantial problems for substance users and society. Individual and system factors that influence waiting time are diverse and may vary at different points in the treatment continuum. This study assessed waiting time preceding clinical assessment at a centralized intake unit and during the period after the assessment but before treatment entry. The present study included 577 substance abusers who were enrolled in a large clinical trial of two brief treatment interventions in a midsize metropolitan area in Ohio. Bivariate analyses identified individual and system factors that influenced preassessment and postassessment waiting time, as well as total wait to treatment services. Multivariate analyses demonstrated that longer wait time for an assessment is influenced by being court referred, less belief in having a substance abuse problem, and less desire for change. A shorter wait to actually enter treatment is predicted by having a case manager, being more ready for treatment, and having less severe employment and alcohol problems. The different influences present during the two waiting periods suggest that assessment and treatment programs need to implement system changes and entry enhancement interventions that are specific to the needs of substance abusers at each waiting period.

A elaboração de um significado para a compreensão e a convivência com a esquizofrenia constitui uma das maneiras de os familiares lidarem com a doença e a evidencia como um fenômeno culturalmente constituído. A partir de uma abordagem antropológica, este estudo entrevistou 14 familiares de 8 pacientes com diagnóstico de esquizofrenia, buscando formular uma compreensão da esquizofrenia através dos conceitos e imagens do universo cultural e social familiar. Os dados produzidos foram analisados segundo metodologia qualitativa. Três categorias de concepção de doença são discutidas, Problema de Nervoso, Problema na Cabeça e Problema Espiritual. Argumenta-se que as concepções analisadas podem ser compreendidas como construções culturais e discute-se a importância desta abordagem para a compreensão da evolução da doença e para a elaboração de programas de intervenção culturalmente apropriados.