Literature DB >> 17852224

Become your own advocate: advice from women living with scleroderma.

Cindy Mendelson1, Janet L Poole.   

Abstract

PURPOSE: Systemic sclerosis (SSC) affects 300,000 people in the USA and has a significant effect on an individual's functional ability. The purpose of this study was to outline the key components of living with the illness and to identify the information that those who are newly diagnosed would need to initiate a successful course of disease self-management. The results will provide the groundwork for development and testing of a self-paced education program for patients with SSC.
METHOD: Focus groups were conducted with 11 women diagnosed with SSC.
RESULTS: Analysis of the transcripts yielded three themes, Secure Effective Medical Management, Live Your Life, and Learn Everything You Can. The thread Become Your Own Advocate wove these three themes together and illustrated that taking control of SSC is ultimately a function of self-advocacy.
CONCLUSION: For patients with SSC, taking control of their illness was a necessary component of maintaining the highest quality of life possible. A positive attitude, a strong support system, a commitment to moving forward with life, and access to high-quality, timely information all provided the participants with the tools to develop and implement a strategy of self-advocacy in disease management.

Entities:  

Mesh:

Year:  2007        PMID: 17852224      PMCID: PMC2768647          DOI: 10.1080/09638280601029480

Source DB:  PubMed          Journal:  Disabil Rehabil        ISSN: 0963-8288            Impact factor:   3.033


  24 in total

Review 1.  The concept of theme as used in qualitative nursing research.

Authors:  L DeSantis; D N Ugarriza
Journal:  West J Nurs Res       Date:  2000-04       Impact factor: 1.967

2.  Patient education in arthritis: randomized controlled trial of a mail-delivered program.

Authors:  J F Fries; C Carey; D J McShane
Journal:  J Rheumatol       Date:  1997-07       Impact factor: 4.666

Review 3.  Collecting and analysing qualitative data: issues raised by the focus group.

Authors:  J Sim
Journal:  J Adv Nurs       Date:  1998-08       Impact factor: 3.187

4.  Psychological adjustment to systemic sclerosis.

Authors:  V L Malcarne; H L Greenbergs
Journal:  Arthritis Care Res       Date:  1996-02

5.  Body image dissatisfaction among women with scleroderma: extent and relationship to psychosocial function.

Authors:  Lisa M Benrud-Larson; Leslie J Heinberg; Christy Boling; Jeffrey Reed; Barbara White; Fredrick M Wigley; Jennifer A Haythornthwaite
Journal:  Health Psychol       Date:  2003-03       Impact factor: 4.267

6.  Scleroderma lung: pathogenesis, evaluation, and current therapy.

Authors:  H T Co; J A Block; W Sequeira
Journal:  Am J Ther       Date:  2000-09       Impact factor: 2.688

7.  Qualitative analysis: what it is and how to begin.

Authors:  M Sandelowski
Journal:  Res Nurs Health       Date:  1995-08       Impact factor: 2.228

8.  Correlates of the disability index of the health assessment questionnaire: a measure of functional impairment in systemic sclerosis.

Authors:  P J Clements; W K Wong; E L Hurwitz; D E Furst; M Mayes; B White; F Wigley; M Weisman; W Barr; L Moreland; T A Medsger; V Steen; R Martin; D Collier; A Weinstein; E Lally; J Varga; S Weiner; B Andrews; M Abeles; J Seibold
Journal:  Arthritis Rheum       Date:  1999-11

9.  Factors related to oral hygiene in persons with scleroderma.

Authors:  J L Poole; C Brewer; K Rossie; C C Good; C Conte; V Steen
Journal:  Int J Dent Hyg       Date:  2005-02       Impact factor: 2.477

10.  The use of the Health Assessment Questionnaire (HAQ) to determine physical disability in systemic sclerosis.

Authors:  J L Poole; V D Steen
Journal:  Arthritis Care Res       Date:  1991-03
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  11 in total

1.  Evaluation of a mail-delivered, print-format, self-management program for persons with systemic sclerosis.

Authors:  Janet L Poole; Betty Skipper; Cindy Mendelson
Journal:  Clin Rheumatol       Date:  2013-05-09       Impact factor: 2.980

2.  New directions for patient-centred care in scleroderma: the Scleroderma Patient-centred Intervention Network (SPIN).

Authors:  Brett D Thombs; Lisa R Jewett; Shervin Assassi; Murray Baron; Susan J Bartlett; Angela Costa Maia; Ghassan El-Baalbaki; Daniel E Furst; Karen Gottesman; Jennifer A Haythornthwaite; Marie Hudson; Ann Impens; Annett Korner; Catarina Leite; Maureen D Mayes; Vanessa L Malcarne; Sarosh J Motivala; Luc Mouthon; Warren R Nielson; Diane Plante; Serge Poiraudeau; Janet L Poole; Janet Pope; Maureen Sauve; Russell J Steele; Maria E Suarez-Almazor; Suzanne Taillefer; Cornelia H van den Ende; Erin Arthurs; Marielle Bassel; Vanessa Delisle; Katherine Milette; Allison Leavens; Ilya Razykov; Dinesh Khanna
Journal:  Clin Exp Rheumatol       Date:  2012-05-29       Impact factor: 4.473

Review 3.  The patient experience of Raynaud's phenomenon in systemic sclerosis.

Authors:  John D Pauling; Lesley Ann Saketkoo; Marco Matucci-Cerinic; Francesca Ingegnoli; Dinesh Khanna
Journal:  Rheumatology (Oxford)       Date:  2019-01-01       Impact factor: 7.580

4.  Factors related to self-efficacy in persons with scleroderma.

Authors:  Una Buck; Janet Poole; Cindy Mendelson
Journal:  Musculoskeletal Care       Date:  2010-12

5.  Living with scleroderma: patients' perspectives, a phenomenological study.

Authors:  Fatma Ilknur Cinar; Vesile Unver; Sedat Yilmaz; Muhammet Cinar; Fatma Yilmaz; Ismail Simsek; Hakan Erdem; Salih Pay; Ayhan Dinc
Journal:  Rheumatol Int       Date:  2011-11-17       Impact factor: 2.631

6.  Randomized Controlled Trial to Evaluate an Internet-Based Self-Management Program in Systemic Sclerosis.

Authors:  Dinesh Khanna; Jennifer Serrano; Veronica J Berrocal; Richard M Silver; Pedro Cuencas; Sharon L Newbill; Josephine Battyany; Cynthia Maxwell; Mary Alore; Laura Dyas; Robert Riggs; Kerri Connolly; Saville Kellner; Jody J Fisher; Erica Bush; Anjali Sachdeva; Luke Evnin; Dennis W Raisch; Janet L Poole
Journal:  Arthritis Care Res (Hoboken)       Date:  2019-02-05       Impact factor: 4.794

7.  Concepts of functioning and health important to people with systemic sclerosis: a qualitative study in four European countries.

Authors:  Tanja A Stamm; Malin Mattsson; Carina Mihai; Juliane Stöcker; Alexa Binder; Bettina Bauernfeind; Georg Stummvoll; Gunvor Gard; Roger Hesselstrand; Gunnel Sandqvist; Oana Draghicescu; Ana Maria Gherghe; Malina Voicu; Klaus P Machold; Oliver Distler; Josef S Smolen; Carina Boström
Journal:  Ann Rheum Dis       Date:  2011-06       Impact factor: 19.103

8.  Comparative analysis of educational needs of patients with rheumatic diseases selected based on the Polish version of the Educational Needs Assessment Tool (Pol-ENAT).

Authors:  Matylda Sierakowska; Stanisław Sierakowski; Justyna Sierakowska; Elżbieta Krajewska-Kułak
Journal:  Reumatologia       Date:  2016-10-05

9.  Functioning in the emotional sphere and ways of coping with chronic connective tissue disease.

Authors:  Justyna Sołowiej-Chmiel; Matylda Sierakowska
Journal:  Reumatologia       Date:  2018-10-31

10.  The educational needs of people with systemic sclerosis: a cross-sectional study using the Dutch version of the Educational Needs Assessment Tool (D-ENAT).

Authors:  Anne Schouffoer; Mwidimi E Ndosi; Thea P M Vliet Vlieland; Jorit J L Meesters
Journal:  Rheumatol Int       Date:  2015-08-31       Impact factor: 2.631

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