Britt-Marie Ternestedt

Ragnhild Hedman, Ingrid Hellström, Britt-Marie Ternestedt, Görel Hansebo, Astrid Norberg (2018). Sense of Self in Alzheimer’s Research Participants

Britt-Marie Ternestedt (2017). Att bli sedd och förstådd i dödens närhet: Dialogens betydelse

Jane Österlind, Britt-Marie Ternestedt, Görel Hansebo, Ingrid Hellström (2017). Feeling lonely in an unfamiliar place: older people’s experiences of life close to death in a nursing home

Åsa Rejnö, Gunilla Silfverberg, Britt-Marie Ternestedt (2017). Reasoning about truth-telling in end-of-life care of patients with acute stroke.

Mona Söderlund, Agneta Cronqvist, Astrid Norberg, Britt-Marie Ternestedt, Görel Hansebo (2016). Conversations between persons with dementia disease living in nursing homes and nurses: qualitative evaluation of an intervention with the validation method

Ragnhild Hedman, Görel Hansebo, Britt-Marie Ternestedt, Ingrid Hellström, Astrid Norberg (2016). Expressed Sense of Self by People With Alzheimer’s Disease in a Support Group Interpreted in Terms of Agency and Communion

Kristina Ek, Birgitta Andershed, Eva Sahlberg-Blom, Britt-Marie Ternestedt (2015). "The unpredictable death"-The last year of life for patients with advanced COPD: Relatives' stories.

Berit Seiger- Cronfalk, Britt-Marie Ternestedt, Lise-Lotte Franklin Larsson, Eva Henriksen, Astrid Norberg, Jane Österlind (2015). Utilization of palliative care principles in nursing home care: Educational interventions

Cecilia Håkansson, Berit Seiger Cronfalk, Eva Henriksen, Astrid Norberg, Britt-Marie Ternestedt, Jonas Sandberg (2014). First-line managers’ views on leadership and palliative care in Swedish nursing homes

Cecilia Håkanson, Berit Seiger Cronfalk, Eva Henrikssen, Astrid Norberg, Britt-Marie Ternestedt, Jonas Sandberg (2014). First-Line Nursing Home Managers in Sweden and their Views on Leadership and Palliative Care

Eva Ekwall, Britt-Marie Ternestedt, Bengt Sorbe, Helena Sunvisson (2014). Lived experiences of women with recurring ovarian cancer.

Viktoria Wallin, Ida Carlander (Goliath), Per-Olof Sandman, Britt-Marie Ternestedt, Cecilia Håkanson (2014). Maintaining ordinariness around food: partners' experienceies of everyday life with a dying person.

Britt-Marie Ternestedt, Astrid Norberg (2014). Omvårdnad ur livscykelperspektiv – identitetens betydelse

Ragnhild Hedman, Ingrid Hellström, Britt-Marie Ternestedt, Görel Hansebo, Astrid Norberg (2014). Social positioning by people with Alzheimer's disease in a support group

Elisabeth Bergdahl, Eva Benzein, Britt-Marie Ternestedt, Eva Elmberger, Birgitta Andershed (2013). Co-creating possibilities for patients in palliative care to reach vital goals: A multiple case study of home-care nursing encounters

Ida Carlander (Goliath), Britt-Marie Ternestedt, Jonas Sandberg, Ingrid Hellström (2013). Constructing family identity close to death

Jane Österlind, Britt-Marie Ternestedt (2013). De 6 S:n -en modell för personcentrerad palliativ vård

Britt-Marie Ternestedt, Birgitta Andershed (2013). Den palliativa vårdens utveckling

Britt-Marie Ternestedt (2013). Döden i samhället

Anette Henriksson (Alvariza), Kristofer Årestedt, Eva Benzein, Britt-Marie Ternestedt, Birgitta Andershed (2013). Effects of a support group programme for patients with life-threatening illness during ongoing palliative care

Ragnhild Hedman, Görel Hansebo, Britt-Marie Ternestedt, Ingrid Hellström, Astrid Norberg (2013). How people with Alzheimer's disease express their sense of self: Analysis using Rom Harré's theory of selfhood

Britt-Marie Ternestedt, Astrid Norberg (2013). Identitet

Astrid Norberg, Britt-Marie Ternestedt (2013). Jämlikhet inför döden

Astrid Norberg, Britt-Marie Ternestedt (2013). Jämlikhet inför döden: Finns den?

Mona Söderlund, Agneta Cronqvist, Astrid Norberg, Britt-Marie Ternestedt, Görel Hansebo (2013). Nurses’ movements within and between various paths when improving their communication skills – an evaluation of validation method training

Birgitta Andershed, Britt-Marie Ternestedt, Cecilia Håkanson (2013). Palliativ vård: begrepp & perspektiv i teori och praktik

Joakim Öhlén, Britt-Marie Ternestedt (2013). Palliativt forskningscentrum vid Ersta Sköndal högskola och Ersta sjukhus i Stockholm

array Britt-Marie Ternestedt, Jane Österlind, Ingela Henoch, Birgitta Andershed (2012). De 6 S:n - En modell för personcentrerad palliativ vård

Britt-Marie Ternestedt (2012). Den sista tiden i livet: Äldres döende och död

Cecilia Håkanson, Eva Sahlberg-Blom, Britt-Marie Ternestedt, Henry Nyhlin (2012). Learning about oneself through others: experiences of a groupbased patient education programme about irritable bowel syndrome

Jane Österlind, Görel Hansebo, Janicke Andersson, Britt-Marie Ternestedt, Ingrid Hellström (2011). A discourse of silence: professional carers resoning of death and dying in nursing homes

Ida Carlander (Goliath), Britt-Marie Ternestedt, Eva Sahlberg-Blom, Ingrid Hellström, Jonas Sandberg (2011). Being me and being us in a family living close to death at home

K Blomberg, C Widmark, Britt-Marie Ternestedt, S Törnberg, Carol Tishelman (2011). Between youth and adulthood: Focus-group discussion with 30 year-old women abot cervical cancer and its prevention in urban Sweden

Elisabeth Bergdahl, Eva Benzein, Britt-Marie Ternestedt, Birgitta Andershed (2011). Developing nurses’ way to reflect over caring relationships through clinical supervision with a structured reflection; an action research approach

Ida Carlander (Goliath), Britt-Marie Ternestedt, Eva Sahlberg-Blom, Ingrid Hellström, Jonas Sandberg (2011). Four aspects of self-image close to death at home

K Blomberg, Carol Tishelman, Britt-Marie Ternestedt, S Törnberg, A Levál, C Widmark (2011). How can young women be encouraged to attend cervical cancer screening?: Suggestions from face-to-face and internet focus group discussions with 30 year-old women in Stockholm, Sweden

Cecilia Håkanson, Eva Sahlberg-Blom, Henry Nyhlin, Britt-Marie Ternestedt (2011). Learning to live with irritable bowel syndrome.: The influence of a group-based patient education programme on peoples’ ability to manage illness in everyday life.

Anette Henriksson (Alvariza), Eva Benzein, Britt-Marie Ternestedt, Birgitta Andershed (2011). Meeting the needs of family members of persons with life threatening illness: a support group programme during ongoing palliative care.

Eva Ekwall, Britt-Marie Ternestedt, Bengt Sorbe, Ulla Hällgren Graneheim (2011). Patients' perceptions of communication with the health care team during chemotherapy for the first recurrence of ovarian cancer

K Ek, Britt-Marie Ternestedt, Birgitta Andershed, Eva Sahlberg-Blom (2011). Shifting life rhythms: Couples' stories about living together when one spouse has advanced chronic obstructive pulmonary disease

Kristina Ek, Birgitta Andershed, Eva Sahlberg-Blom, Britt-Marie Ternestedt (2011). Struggling to retain the living space: Patients´ stories about their lives as living alone with severe chronic obstructive pulmonary disease

Ida Carlander (Goliath), Eva Sahlberg-Blom, Ingrid Hellström, Britt-Marie Ternestedt (2011). The modified self: family caregivers' experiences of caring for a dying family member at home

Cecilia Håkanson, Eva Sahlberg-Blom, Britt-Marie Ternestedt (2010). Being in the patient position: experiences of health care among people with irritable bowel syndrome

Inger James, Birgitta Andershed, Bengt Gustavsson, Britt-Marie Ternestedt (2010). Emotional knowing in nursing practice: In the encounter between life and death

Britt-Marie Ternestedt (2010). En värdig död och en identitetsfrämjande vård

Inger James, Birgitta Andershed, Bengt Gustavsson, Britt-Marie Ternestedt (2010). Knowledge Constructions in Nursing Practice: Understanding and Integrating Different Forms of Knowledge

Lise-Lotte Dwyer, Görel Hansebo, Birgitta Andershed, Britt-Marie Ternestedt (2010). Nursing home residents’ views on dying and death: nursing home employee’s perspective

Berit Seiger Cronfalk, Britt-Marie Ternestedt, Peter Strang (2010). Soft tissue massage: early intervention for relatives whose family members died in palliative cancer care

Britt-Marie Ternestedt (2009). A dignified death and identy-promoting care

Lise-Lotte Dwyer, Birgitta Andershed, Lennart Nordenfelt, Britt-Marie Ternestedt (2009). Dignity as experienced by nursing home staff

Eva Benzein, Astrid Norberg, Eva Sahlberg Blom, Britt-Marie Ternestedt, Birgitta Andershed (2009). Ett vårdvetenskapligt perspektiv på forskning i livets slutskede: erfarenheter från Sverige

Karin Blomberg, Anette Forss, Britt-Marie Ternestedt, Carol Tishelman (2009). From 'silent' to 'heard': professional mediation, manipulation and women's experiences of their body after an abnormal Pap smear.

Berit Seiger Cronfalk, Peter Strang, Britt-Marie Ternestedt (2009). Inner power, physical strength and existential well-being in daily life: relatives' experiences of receiving soft tissue massage in palliative home care.

Jane Österlind, Görel Hansebo, Rikard Lindqvist, Britt-Marie Ternestedt (2009). Moving on a roundabout at the end of life-What counts? Waiting times for transfer to sheltered accommodation for older people in Sweden.

Astrid Norberg, Britt-Marie Ternestedt (2009). Omvårdnad som huvudämne i sjuksköterskeutbildningen

Britt-Marie Ternestedt, Astrid Norberg (2009). Omvårdnad ur ett livscykelperspektiv

Cecilia Håkanson, Eva Sahlberg-Blom, Henry Nyhlin, Britt-Marie Ternestedt (2009). Struggling with an unfamiliar and unreliable body: the experience of irritable bowel syndrome

Inger James, Birgitta Andershed, Britt-Marie Ternestedt (2009). The encounter between informal and professional care at the end of life

Berit Seiger Cronfalk, Britt-Marie Ternestedt, Peter Strang, Maria Friedrichsen (2009). The existential experiences of receiving soft tissue massage in palliative home care: an intervention

ILK Karlsson, M Ehnfors, Britt-Marie Ternestedt (2008). Five nurses' experiences of hospice care in a long-term perspective

Karin Blomberg, Britt-Marie Ternestedt, Sven Törnberg, Carol Tishelman (2008). How do women who choose not to participate in population-based cervical cancer screening reason about their decision?

Kristina Ek, Britt-Marie Ternestedt (2008). Living with chronic obstructive pulmonary disease at the end of life: a phenomenological study

Jane Österlind, Görel Hansebo, Göran Lantz, Britt-Marie Ternestedt (2008). Pathways in end-of-life care for older people: care managers' reasoning.

Lise-Lotte Dwyer, Lennart Nordenfelt, Britt-Marie Ternestedt (2008). Three nursing home residents speak about meaning at the end of life

C Tishelman, M Bergenmar, B-M Bernhardson, K Blomberg, S Börjeson, H Foderus, H Leveälahti, Eva Sahlberg-Blom, Britt-Marie Ternestedt (2008). Using undergraduate nursing students as mediators in a knowledge transfer programme for care for patients with advanced cancer.

Inger James, Birgitta Andershed, Britt-Marie Ternestedt (2007). A family's beliefs about cancer, dying, and death in the end of life.

Britt-Marie Ternestedt (2007). Att få vara den man är i dödens närhet

Britt-Marie Ternestedt (2007). Forskning som speglar vården i livets slutskede: sammanställning av aktuell forskning [Fulltext]

Gunilla Silfverberg, Britt-Marie Ternestedt (2007). Hemmet och vårdetiken

Karin Jackson, Britt-Marie Ternestedt, Anders Magnuson, Jens Schollin (2007). Parental stress and toddler behaviour at age 18 months after pre-term birth.

Ewa Ekwall, Britt-Marie Ternestedt, Bengt Sorbe (2007). Recurrence of ovarian cancer-living in limbo

Joakim Öhlen, Birgitta Andershed, Christina Berg, Ingvar Frid, Carl-Axel Palm, Britt-Marie Ternestedt, Kerstin Segesten (2007). Relatives in end-of-life care--part 2: a theory for enabling safety

Kent Wall, Hjörtur Oddsson, Britt-Marie Ternestedt, Anders Jonzon, Eva Nylander, Jens Schollin (2007). Thirty-year electrocardiographic follow-up after repair of tetralogy of Fallot or atrial septal defect.

Inga Lill Källström Karlsson, Margareta Ehnfors, Britt-Marie Ternestedt (2006). Patient characteristics of women and men cared for during the first 10 years at an inpatient hospice ward in Sweden.

Britt-Marie Ternestedt (2006). Patients and their primary care providers identified 4 goals of life sustaining treatment.

Karin Jackson, Britt-Marie Ternestedt, Anders Magnuson, Jens Schollin (2006). Quality of care of the preterm infant--the parent and nurse perspective.

Lise-Lotte Franklin, Britt-Marie Ternestedt, Lennart Nordenfelt (2006). Views on dignity of elderly nursing home residents

Britt-Marie Ternestedt, Lise-Lotte Franklin (2006). Ways of relating to death: views of older people resident in nursing homes.

Britt-Marie Ternestedt (2005). Barn med medfödda hjärtfel: vad säger den psykosociala forskningen?

Britt-Marie Ternestedt (2005). Expressed desire for hastened death by patients with advanced cancer had several meanings and uses.

Britt-Marie Ternestedt (2005). Hjälp att leva livet ut

K Kallenberg, Britt-Marie Ternestedt (2005). Självbestämmande i dödens närhet

Carol Tishelman, Britt-Marie Bernhardson, Karin Blomberg, Sussanne Börjeson, Liselotte Franklin, Eva Johansson, Helena Leveälahti, Eva Sahlberg-Blom, Britt-Marie Ternestedt (2004). Complexity in caring for patients with advanced cancer

K Segesten, Birgitta Andershed, C Berg, I Frid, C-A Palm, Britt-Marie Ternestedt, Joakim Öhlén (2004). Kommentarer

Karin Jackson, Britt-Marie Ternestedt, Jens Schollin (2003). From alienation to familiarity: experiences of mothers and fathers of preterm infants.

Ewa Ekwall, Britt-Marie Ternestedt, Bengt Sorbe (2003). Important aspects of health care for women with gynecologic cancer

Britt-Marie Ternestedt, Birgitta Andershed, Monika Eriksson, Ingrid Johansson (2002). A Good Death. Development of a Nursing model of care.

Ann-Britt Ivarsson, Ingrid Söderback, Britt-Marie Ternestedt (2002). The meaning and form of occupational therapy as experienced by women with psychoses: A phenomenological study

Birgitta Andershed, Britt-Marie Ternestedt (2001). Development of a theoretical framework of understanding about relatives´ involvement in palliative care.

Birgitta Andershed, Britt-Marie Ternestedt (2000). Being a close relative of a dying person. Development of the concepts: Involvement in the light and in the dark.

Birgitta Andershed, Britt-Marie Ternestedt (1999). Involvement of relatives in the care of the dying in different care cultures. Development of a theoretical understanding.

Birgitta Andershed, Britt-Marie Ternestedt (1998). Involvement of relatives in the care of the dying in different care cultures. Involvement in the dark or in the light?

Birgitta Andershed, Britt-Marie Ternestedt (1998). The illness trajectory - for patients with cancer in two different cultures of care.

Birgitta Andershed, Britt-Marie Ternestedt (1997). Patterns of care for patients with cancer before and after the establishment of a hospice ward

Ragnhild Hedman, Ingrid Hellström, Britt-Marie Ternestedt, Görel Hansebo, Astrid Norberg (). Being a research participant with Alzheimer’s disease: Expressions of sense of self

Mona Söderlund, Agneta Cronqvist, Astrid Norberg, Britt-Marie Ternestedt (). Conversations between residents with dementia disease and nurses: evaluation of an intervention with the Validation method

Lise-Lotte Dwyer, Birgitta Andershed, Britt-Marie Ternestedt, Lennart Nordenfelt (). Nursing home staff's reasoning about death and dying