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Results: 1 to 20 of 138

1.

Biographical disruption, abruption and repair in the context of motor neurone disease.

Locock L, Ziebland S, Dumelow C.

Sociol Health Illn. 2009 Nov;31(7):1043-58. doi: 10.1111/j.1467-9566.2009.01176.x. Epub 2009 Jul 29.

PMID:
19659736
[PubMed - indexed for MEDLINE]
2.

How people with motor neurone disease talk about living with their illness: a narrative study.

Brown J, Addington-Hall J.

J Adv Nurs. 2008 Apr;62(2):200-8. doi: 10.1111/j.1365-2648.2007.04588.x.

PMID:
18394032
[PubMed - indexed for MEDLINE]
3.

Non-finite loss and emotional labour: family caregivers' experiences of living with motor neurone disease.

Ray RA, Street AF.

J Clin Nurs. 2007 Mar;16(3A):35-43.

PMID:
17518867
[PubMed - indexed for MEDLINE]
4.

Living with motor neurone disease: lives, experiences of services and suggestions for change.

Hughes RA, Sinha A, Higginson I, Down K, Leigh PN.

Health Soc Care Community. 2005 Jan;13(1):64-74.

PMID:
15717908
[PubMed - indexed for MEDLINE]
5.

Revisiting biographical disruption: exploring individual embodied illness experience in people with terminal cancer.

Reeve J, Lloyd-Williams M, Payne S, Dowrick C.

Health (London). 2010 Mar;14(2):178-95. doi: 10.1177/1363459309353298.

PMID:
20164165
[PubMed - indexed for MEDLINE]
6.

Caregiver bodywork: family members' experiences of caring for a person with motor neurone disease.

Ray RA, Street AF.

J Adv Nurs. 2006 Oct;56(1):35-43.

PMID:
16972916
[PubMed - indexed for MEDLINE]
7.

Exploring the transitional process from receiving a diagnosis to living with motor neurone disease.

Mistry K, Simpson J.

Psychol Health. 2013;28(8):939-53. doi: 10.1080/08870446.2013.770513. Epub 2013 Mar 6.

PMID:
23464923
[PubMed - indexed for MEDLINE]
8.

Experiences of dying, death and bereavement in motor neurone disease: a qualitative study.

Whitehead B, O'Brien MR, Jack BA, Mitchell D.

Palliat Med. 2012 Jun;26(4):368-78. doi: 10.1177/0269216311410900. Epub 2011 Jun 28.

PMID:
21712334
[PubMed - indexed for MEDLINE]
9.

I've never not had it so I don't really know what it's like not to: nondifference and biographical disruption among children and young people with cystic fibrosis.

Williams B, Corlett J, Dowell JS, Coyle J, Mukhopadhyay S.

Qual Health Res. 2009 Oct;19(10):1443-55. doi: 10.1177/1049732309348363.

PMID:
19805806
[PubMed - indexed for MEDLINE]
10.

'All in the same boat'? Patient and carer attitudes to peer support and social comparison in Motor Neurone Disease (MND).

Locock L, Brown JB.

Soc Sci Med. 2010 Oct;71(8):1498-505. doi: 10.1016/j.socscimed.2010.06.043. Epub 2010 Aug 10.

PMID:
20719422
[PubMed - indexed for MEDLINE]
11.

Experiencing and controlling time in everyday life with chronic widespread pain: a qualitative study.

Richardson JC, Ong BN, Sim J.

BMC Musculoskelet Disord. 2008 Jan 11;9:3. doi: 10.1186/1471-2474-9-3.

PMID:
18190693
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Quality of life issues in motor neurone disease: the development and validation of a coping strategies questionnaire, the MND Coping Scale.

Lee JN, Rigby SA, Burchardt F, Thornton EW, Dougan C, Young CA.

J Neurol Sci. 2001 Oct 15;191(1-2):79-85.

PMID:
11676996
[PubMed - indexed for MEDLINE]
13.

Coping with motor neurone disease--an analysis using self-regulation theory.

Earll L, Johnston M, Mitchell E.

Palliat Med. 1993;7(4 Suppl):21-30.

PMID:
8269176
[PubMed - indexed for MEDLINE]
14.

Encountering the downward phase: biographical work in people with multiple sclerosis living at home.

Boeije HR, Duijnstee MS, Grypdonck MH, Pool A.

Soc Sci Med. 2002 Sep;55(6):881-93.

PMID:
12220091
[PubMed - indexed for MEDLINE]
15.
16.

A comparison of mood and quality of life among people with progressive neurological illnesses and their caregivers.

McCabe MP, Firth L, O'Connor E.

J Clin Psychol Med Settings. 2009 Dec;16(4):355-62. doi: 10.1007/s10880-009-9168-5. Epub 2009 Jul 29.

PMID:
19639395
[PubMed - indexed for MEDLINE]
17.

Disrupted lives and threats to identity: the experiences of people with colorectal cancer within the first year following diagnosis.

Hubbard G, Kidd L, Kearney N.

Health (London). 2010 Mar;14(2):131-46. doi: 10.1177/1363459309353294.

PMID:
20164162
[PubMed - indexed for MEDLINE]
18.

Experiences of living with motor neurone disease: a review of qualitative research.

Sakellariou D, Boniface G, Brown P.

Disabil Rehabil. 2013 Oct;35(21):1765-73. doi: 10.3109/09638288.2012.753118. Epub 2013 Jan 22. Review.

PMID:
23336121
[PubMed - indexed for MEDLINE]
19.

Living with amyotrophic lateral sclerosis/motor neurone disease (ALS/MND): decision-making about 'ongoing change and adaptation'.

King SJ, Duke MM, O'Connor BA.

J Clin Nurs. 2009 Mar;18(5):745-54. doi: 10.1111/j.1365-2702.2008.02671.x.

PMID:
19239541
[PubMed - indexed for MEDLINE]
20.

Sudden illness and biographical flow in narratives of stroke recovery.

Faircloth CA, Boylstein C, Rittman M, Young ME, Gubrium J.

Sociol Health Illn. 2004 Mar;26(2):242-61.

PMID:
15027986
[PubMed - indexed for MEDLINE]

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