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An interview guide was designed to address three major domains: 1 ; wishes for care at the end-of-life, 2 ; preferences for information about the illness, and 3 ; the meaning of death. Corresponding questions on the semi-structured interview guide included: 1 ; What wishes do you have for your own end-oflife care? Where would you like to be when you die? Whom would you like to have at your bedside at the time of your death? 2 ; To what degree would you like to have a detailed explanation concerning the selection of treatment? To what extent would you like to be part of the decision-making for your treatment? 3 ; What does death mean to you? In this paper, we have focused only on the results from the first and third domains. Participant consent Procedures for recruiting and obtaining consent differed between the hospitalized and outpatient participants. To reduce stress for the hospitalized participants, a written copy of the interview questions was given to the subjects at the time they consented to being involved. In the process five patients declined to participate further. Interviews were then conducted one to three weeks later. Hospitalized participants received interviews in a private conference room near their own rooms. Each interview lasted about an hour. Since it was not feasible to circulate the questionnaires prior to in the outpatient environment, outpatient participants were interviewed at the point their consent was gained. Thus outparticipants were not able to consider the questions in advance nor did they have the time to reassess their desire to participate. However we did consult nurses in advance about suitable patients for this inquiry and after receiving consent from the outpatients that were recommended, we again considered whether or not the interview questions would be acceptable to each individual. Finally, all consenting outpatients were interviewed. We also used a private conference room to interview outpatient subjects. Each interview lasted between 40 and 90 minutes. Interviews were recorded on audiotapes and transcribed verbatim. Data analysis We analyzed this qualitative data using the.
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Shiro Yokohama, Yosui Tamaki, Satoshi Okamoto, Mituyoshi Okada, Kazunobu Aso, Takenao Hasegawa, Masaru Aoshima, Masakazu Haneda, Second Department of Medicine, Asahikawa Medical College, Asahikawa, Japan Yoshihiko Tokusashi, Naoyuki Miyokawa, Department of Surgical Pathology, Asahikawa Medical College, Asahikawa, Japan Masashi Yoneda, Department of Gastroenterology, Dokkyo University School of Medicine, Mibu, Japan Kimihide Nakamura, Health Care Administration Center, Obihiro University of Agriculture and Veterinary Medicine, Obihiro, Japan Supported by a Grant-in-Aid for Scientific Research C ; from the Japan Society for the Promotion of Science, No. 15590613, and a grant for Research on Intractable Disease from the Japanese Ministry of Public Welfare Correspondence to: Dr. Shiro Yokohama, Second Department of Medicine, Asahikawa Medical College, Midorigaoka higashi 2-1-1-1, Asahikawa 078-8510, Japan. yokohama reha.or.jp Telephone: + 81-166-682454 Fax: + 81-166-682459 Received: 2005-05-31 Accepted: 2005-06-24 2006 The WJG Press. All rights reserved.
One ipriflavone metabolite, daidzein, undoubtedly contributes to its bone-sparing capacity see alternative medicine alert , december 2000.
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Fifteen core themes were identified, namely: a ; the cause and onset of psoriasis is the result of multiple triggers and is not merely a consequence of stress; b ; for irene, the cause of psoriasis was related to the genetic component on her father's side of the family and the onset was a consequence of her suffering from a bacterial infection; c ; the importance of the doctor patient relationship in terms of being provided with adequate information on psoriasis and the need for empathy on the part of doctors; d ; trial and error prescriptions, the inefficacy of these treatments and also the need to alert patients to the adverse side-effects of prescribed medications; e ; stigmatised by feeling categorised by the medical profession and experiencing stigma in the workplace; f ; emotional dimensions of self and the consequent suffering of a reactive depression; g ; education of medical doctors to the trauma patients endure and education of the general public that psoriasis can deplete the immune system; h ; medical aids and the need for chronic support; i ; life skills and assertiveness training as a method of self-empowerment; j ; empowerment through sharing in group psychotherapy; k ; the need for medical psychotherapists and the networking of dermatologists with psychologists; l ; the importance of self-care and personal hygiene; m ; the development of the personal and spiritual dimensions of self as a method of emotional coping; n ; learning to trust the physical body; and finally, o ; positive meaning-making in self-development and reaching out to in need.
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