All Stories

  1. Inconvenient Truths and Uncomfortable Stories: Nursing Children and Managing Pain
  2. “Sharing the Horrible Moment”; the Experiences and Perceptions of Children of Being Held for Clinical Procedures: An Exploratory Qualitative Study
  3. Cultural reproduction of knowledge and identity: Impact of a competency-based curriculum on knowledge engagement and identity construction in second year undergraduate nursing students in England – A constructivist grounded theory study
  4. Measures of identity in adolescents/young adults with long-term physical health conditions: a systematic review
  5. A feasibility randomised controlled trial of an exergaming device aimed at improving mobility in children with cerebral palsy
  6. ‘In the Midst of a Thunderstorm’: Young People's Experiences of Physical Restraint in Inpatient Mental Health Services in the UK
  7. Randomised controlled trial of online behavioural sleep intervention for children with epilepsy
  8. Exploring the Views of Children With Cerebral Palsy, Their Parents and Physiotherapists on Participating in a Feasibility Randomised Controlled Trial Testing an Exergaming Device: A Qualitative Study
  9. “I’d probably trip over it because it’s bumpy”: A qualitative exploration of the lived experiences of ambulatory children with cerebral palsy walking in challenging environments
  10. Establishing Consensus on the Breakthrough Pain Assessment Questionnaire-Self Report (BTPAQ-SR) for Typically Developing Children and Young People (8–25 yrs) with Life-Limiting and Life-Threatening Conditions: An International e-Delphi Study of Expert ...
  11. Perspectives of stakeholders on running ‘Pill School’ in community settings: a survey based study
  12. Talking the Walk (Along): Lessons Learned From Engaging With Children With Cerebral Palsy and Their Parents for Investigating Lived Experiences of Falls
  13. Involved, interrupted or ignored? Triadic communication in children's non-urgent X-ray procedures
  14. Digital healthcare interventions to support parents with acutely ill children at home: A systematic review
  15. Coming in hot: using emotional journey maps to examine parental perceptions associated with presentation of their child with fever to the emergency department in England
  16. My A–T pack: a qualitative study of the utility, acceptability, design, and content of a family-designed and owned information pack relevant to the lives of children and young people living with ataxia telangiectasia
  17. Assessing the performance of paediatric early warning scores to predict critical deterioration events in hospitalised children (the DETECT study): a retrospective matched case-control study
  18. Children’s perspectives on the acceptability of medicine, how to assess acceptability and the development of the Theoretical Framework of Children’s Medicine Acceptability: a qualitative study
  19. Editorial: Pain and relationships
  20. Are challenging walking environments linked to falls or risk of falling in children with cerebral palsy? A systematic review
  21. Virtually the same, but remotely different: health professionals, parents and children’s experiences of remote out-patient consultations
  22. Romancing With Pain: A Survey Study of Young Adults With Chronic Pain
  23. Neighbourhood socioeconomic conditions and emergency admissions for ambulatory care sensitive conditions in children: a longitudinal ecological analysis in England, 2012–2017
  24. Coming in hot: a qualitative investigation into perceptions of parents and doctors of reasons for the presentation of children with fever to the emergency department in England
  25. Understanding the importance of therapeutic alliance during physiotherapy treatment for musculoskeletal pain in children: a scoping review
  26. Children with cerebral palsy avoid stepping in potholes with mediolateral changes in foot placement that cause laterally instability
  27. Narrative Accounts of Youth and their Mothers with Chronic Headache
  28. Definition and Assessment of Paediatric Breakthrough Pain: A Qualitative Interview Study
  29. The Concept of Child-Centred Care in Healthcare: A Scoping Review
  30. Being Participatory Through Animation
  31. A rapid systematic review of breakthrough pain definitions and descriptions
  32. Parental sleep‐related practices and sleep in children aged 1–3 years: a systematic review
  33. A cross-sectional survey of healthcare professionals supporting children and young people with epilepsy and their parents/carers: which topics are raised in clinical consultations and can healthcare professionals provide the support needed?
  34. The Concept of Child-Centered Care in Healthcare: A Scoping Review
  35. “A hard-won capability”: the experiences of parents managing their babies' medicines after discharge from a neonatal unit
  36. How real-time images of the eardrum help parents and children make better decisions about care
  37. Designing a novel protocol to investigate mechanisms of falls in children with cerebral palsy, informed by lived experiences
  38. “I’d go slow and hope I don’t fall” Exploring lived experiences of children with cerebral palsy walking in challenging environments
  39. The economic burden experienced by carers of children who had a critical deterioration at a tertiary children’s hospital in the United Kingdom (the DETECT study): an online survey
  40. Developing rights-based standards for children having tests, treatments, examinations and interventions: using a collaborative, multi-phased, multi-method and multi-stakeholder approach to build consensus
  41. Using technology to reduce critical deterioration (the DETECT study): a cost analysis of care costs at a tertiary children's hospital in the United Kingdom
  42. A shared love: reciprocity and hopefulness in romantic relationships of young adults with chronic pain
  43. Health literacy among children living with a long-term condition: ‘What I know and who I tell’
  44. Communication during children's X-ray procedures and children's experiences of the procedure: A scoping review
  45. Feeling stretched: Parents’ narratives about challenges to resilience when their child has a tracheostomy
  46. ‘ZOOMing’ in on Consulting with Children and Parents Remotely to Co-Create Health Information Resources
  47. Changing Agendas on Sleep, Treatment and Learning in Epilepsy (CASTLE) Sleep-E: a protocol for a randomised controlled trial comparing an online behavioural sleep intervention with standard care in children with Rolandic epilepsy
  48. A cross sectional study investigating dynamic balance when stepping to targets in children with cerebral palsy compared to typically developing children
  49. The impact of parent treatment preference and other factors on recruitment: lessons learned from a paediatric epilepsy randomised controlled trial
  50. Dietary Therapy to Improve Nutrition and Gut Health in Paediatric Crohn’s Disease; A Feasibility Study
  51. OP029 [Emerging Sciences / Technology » Innovations]: THE CLINICAL EFFECTIVENESS OF DYNAMIC ELECTRONIC TRACKING AND ESCALATION TO REDUCE CRITICAL CARE TRANSFERS (THE DETECT STUDY)
  52. Unsettling the fluidity of practice and dealing with threat: the experiences of paediatric pharmacists in response to the admission of adult COVID-19 patients requiring intensive care in a paediatric tertiary hospital
  53. Parents supporting parents to reduce the risk of bronchiolitis (a respiratory virus)
  54. Clinical utility and acceptability of a whole-hospital, pro-active electronic paediatric early warning system (the DETECT study): A prospective e-survey of parents and health professionals
  55. Parents’/caregivers’ fears and concerns about their child’s epilepsy: A scoping review
  56. Navigating uncertain illness trajectories for young children with serious infectious illness: a modified grounded theory study
  57. Parents’ experiences and perceptions of the acceptability of a whole-hospital, pro-active electronic pediatric early warning system (the DETECT study): A qualitative interview study
  58. Health professionals’ initial experiences and perceptions of the acceptability of a whole-hospital, pro-active electronic paediatric early warning system (the DETECT study): a qualitative interview study
  59. ‘I feel like my house was taken away from me’ : Parents' experiences of having home adaptations for their medically complex, technology‐dependent child
  60. Changing Agendas on Sleep, Treatment and Learning in Epilepsy (CASTLE) Sleep-E: A protocol for a randomised controlled trial comparing an online behavioural sleep intervention with standard care in children with Rolandic epilepsy
  61. Multicentre, randomised controlled feasibility study to compare a 10-week physiotherapy programme using an interactive exercise training device to improve walking and balance, to usual care of children with cerebral palsy aged 4–18 years: the ACCEPT st...
  62. ‘It’s my back…’; developing the coming to spinal clinic resource to improve the health literacy of young people with adolescent idiopathic scoliosis and their parents
  63. ‘It doesn't feel like our house anymore’: The impact of medical technology upon life at home for families with a medically complex, technology-dependent child
  64. Defining usual physiotherapy care in ambulant children with cerebral palsy in the United Kingdom: A mixed methods consensus study
  65. “Communicating Lily’s Pain”: A reflective narrative commentary about co‐creating a resource to provoke thinking and change about assessing and managing the pain of children with profound cognitive impairment
  66. Healthcare Professionals’ Experiences of the Barriers and Facilitators to Pediatric Pain Management in the Community at End-of-Life: A Qualitative Interview Study
  67. Using an animation to enhance parents and professionals’ communication and assessment of pain in children with profound cognitive impairment
  68. Seeing lockdown through the eyes of children from around the world: Reflecting on a children's artwork project
  69. How parents share and limit their child’s access to information about COVID-19: A mixed methods online survey study
  70. “Pain talk”: A triadic collaboration in which nurses promote opportunities for engaging children and their parents about managing children’s pain
  71. Using methods across generations: researcher reflections from a research project involving young people and their parents
  72. Ataxia and mobility in children following surgical resection of posterior fossa tumour: A longitudinal cohort study
  73. Navigating uncertain illness trajectories for young children with serious infectious illness: a mixed-methods modified grounded theory study
  74. Children and young people’s contributions to public involvement and engagement activities in health-related research: A scoping review
  75. Children’s pictures of COVID-19 and measures to mitigate its spread: An international qualitative study
  76. Is paediatric endotracheal suctioning by nurses' evidence based? An International Survey
  77. Paediatric Outpatient Parenteral Antimicrobial Therapy (OPAT): An e-survey of the experiences of parents and clinicians
  78. “People play it down and tell me it can’t kill people, but I know people are dying each day”. Children’s health literacy relating to a global pandemic (COVID-19); an international cross sectional study
  79. Two‐Stage Revision Hip Arthroplasty with or without the Use of an Interim Spacer for Managing Late Prosthetic Infection: A Systematic Review of the Literature
  80. The impact of digital educational interventions to support parents caring for acutely ill children at home and factors that affect their use: systematic review protocol (Preprint)
  81. Impact of Digital Educational Interventions to Support Parents Caring for Acutely Ill Children at Home and Factors That Affect Their Use: Protocol for a Systematic Review (Preprint)
  82. How nurses use reassurance to support the management of acute and chronic pain in children and young people: An exploratory, interpretative qualitative study
  83. Romantic Relationships in Young People with Long-Term Health Conditions: A Scoping Review
  84. Developing a Framework to Support the Delivery of Effective Pain Management for Children: An Exploratory Qualitative Study
  85. Crohn's and colitis: New research offers insights into caring for young people
  86. Depression, anxiety, and loneliness among adolescents and young adults with IBD in the UK: the role of disease severity, age of onset, and embarrassment of the condition
  87. Sustaining, Forming, and Letting Go of Friendships for Young People with Inflammatory Bowel Disease (IBD): A Qualitative Interview-Based Study
  88. Communication styles between family carers and children with leukaemia in occupied Palestinian territory
  89. A systematic review of the organizational, environmental, professional and child and family factors influencing the timing of admission to hospital for children with serious infectious illness
  90. Physical restraint of children and adolescents in mental health inpatient services: A systematic review and narrative synthesis
  91. Holding Their Own and Being Resilient: Narratives of Parents over the First 12 Months of Their Child Having Tracheostomy
  92. “I Don’t Like to Make a Big Thing out of It”: A Qualitative Interview-Based Study Exploring Factors Affecting Whether Young People Tell or Do Not Tell Their Friends about Their IBD
  93. Not a nurse but more than a mother: the everyday geographies of mothering children with complex heath care needs
  94. Experiencing place identity and place belongingness at a children’s hospice: Parents’ perspectives
  95. Stories as findings in collaborative research: making meaning through fictional writing with disadvantaged young people
  96. Communicating Pain: The Challenge of Pain Assessment in Children with Profound Cognitive Impairment
  97. Working back to the future: strengthening radical social work with children and young people, and their perspectives on resilience, capabilities and overcoming adversity
  98. Using participatory drama workshops to explore children’s beliefs, understandings and experiences of coming to hospital for clinical procedures
  99. Home-based treatment for a serious bacterial infection
  100. Exercise and Physical Therapy Interventions for Children with Ataxia: A Systematic Review
  101. “It’s a lifeline”: Generating a sense of social connectedness through befriending parents of disabled children or children with additional need
  102. Coming ‘Home’: Place bonding for parents accessing or considering hospice based respite
  103. Core Health Outcomes in Childhood Epilepsy (CHOICE): Development of a core outcome set using systematic review methods and a Delphi survey consensus
  104. The absent-present researcher: data analysis of pre-recorded parent-driven campaign videos
  105. Parent’s experiences of their child’s withdrawal syndrome: a driver for reciprocal nurse-parent partnership in withdrawal assessment
  106. Child Centred Care: Challenging Assumptions and Repositioning Children and Young People
  107. Can children be treated safely with parenteral antimicrobial therapy for serious bacterial infection
  108. Toward developing consensus on family-centred care: An international descriptive study and discussion
  109. New steps of change
  110. ‘Place bonding’ in children’s hospice care: a qualitative study
  111. International commentary on Phiri et al. ‘Registered nurses’ experiences pertaining to family involvement in the care of hospitalised children at a tertiary government hospital in Malawi’
  112. A review of literature about disfigurement, the body and clothing and accessories
  113. A qualitative study of health professionals’ views on the holding of children for clinical procedures: Constructing a balanced approach
  114. The practice of writing
  115. Evaluating a telehealth intervention for urinalysis monitoring in children with neurogenic bladder
  116. The concept of child-centered care in healthcare
  117. Inequality and poverty
  118. Holding children for procedures: An international survey of health professionals
  119. Being Participatory: Researching with Children and Young People
  120. Getting poetic with data: Using poetry to disseminate the first-person voices of parents of children with a disability
  121. A systematic evidence synthesis of interventions to engage children and young people in consultations about their long-term conditions
  122. Participatory Research: Does It Genuinely Extend the Sphere of Children’s and Young People’s Participation?
  123. Participatory Research in the Past, Present and Future
  124. Core Health Outcomes In Childhood Epilepsy (CHOICE): protocol for the selection of a core outcome set
  125. A sense of belonging: The importance of fostering student nurses’ affective bonds
  126. Parenting a Child With Complex Health Care Needs: A Stressful and Imposed “Clinical Career”
  127. Young children's experiences of growing up with a chronic illness
  128. Consulting with children, parents and a teacher to shape a qualitative study
  129. Using videos made by parent as part of a campaign to raise awareness
  130. Peer review: A good but flawed system?
  131. Parent-to-parent peer support for parents of children with a disability: A mixed method study
  132. Looking towards the horizon: changing landscapes and a shift to a more equitable future for children, young people and their families
  133. Getting published: Only one step in disseminating your findings
  134. Nursing judgement and decision-making using the Sedation Withdrawal Score (SWS) in children
  135. Creating authentic video scenarios for use in prehospital research
  136. Accuracy and Efficiency of Recording Pediatric Early Warning Scores Using an Electronic Physiological Surveillance System Compared With Traditional Paper-Based Documentation
  137. Developing a web-based resource for parents of young children undergoing day surgery
  138. Misleading information, exaggeration and the need to act
  139. Auto-driven Photo Elicitation Interviews in Research with Children: Ethical and Practical Considerations
  140. Optimizing Numeric Pain Rating Scale administration for children: The effects of verbal anchor phrases
  141. Developing a Sense of Knowing and Acquiring the Skills to Manage Pain in Children with Profound Cognitive Impairments: Mothers’ Perspectives
  142. Language, disfigurement, stigma and clothing
  143. In pursuit of an optimal model of undergraduate nurse clinical education: An integrative review
  144. Perseverance and parents of children with complex health care needs
  145. Parallel-Serial Memoing
  146. Pain experience, expression and coping in boys and young men with Duchenne Muscular Dystrophy – A pilot study using mixed methods
  147. Personal qualities necessary to care for people with dementia
  148. Is undernutrition prognostic of infection complications in children undergoing surgery? A systematic review
  149. “Knowing the Places of Care”: How Nurses Facilitate Transition of Children with Complex Health Care Needs from Hospital to Home
  150. The Impact of Immersive Outdoor Activities in Local Woodlands on Young Carers Emotional Literacy and Well-Being
  151. Navigating Uncertainty: Health Professionals’ Knowledge, Skill, and Confidence in Assessing and Managing Pain in Children with Profound Cognitive Impairment
  152. Social relationships, loneliness and adolescence
  153. Holding Children for Clinical Procedures: Perseverance in Spite of or Persevering to be Child-Centered
  154. The context, influences and challenges for undergraduate nurse clinical education: Continuing the dialogue
  155. Transition
  156. Generic training will not prepare nurses of right calibre to care for children and families
  157. Support for Children’s Protagonism
  158. ‘If you see something, say something’
  159. Bladder augmentation in children and young adults: a review of published literature
  160. Motivational Interviewing Post-Stroke
  161. Young women with a disorder of sex development: learning to share information with health professionals, friends and intimate partners about bodily differences and infertility
  162. Parents’ and children’s beliefs and concerns about taking medicines
  163. Identifying Continence OptioNs after Stroke (ICONS): an evidence synthesis, case study and exploratory cluster randomised controlled trial of the introduction of a systematic voiding programme for patients with urinary incontinence after stroke in seco...
  164. A Qualitative Study of Communication between Young Women with Disorders of Sex Development and Health Professionals
  165. ‘We don't have recipes; we just have loads of ingredients’: explanations of evidence and clinical decision making by speech and language therapists
  166. Technology adoption in health care
  167. Identifying continence options after stroke (ICONS): a cluster randomised controlled feasibility trial
  168. Misunderstood as mothers: women's stories of being hospitalized for illness in the postpartum period
  169. Advancing health and well-being through children’s rights
  170. Service user involvement in practitioner education: Movement politics and transformative change
  171. Holding and restraining children for clinical procedures within an acute care setting: an ethical consideration of the evidence
  172. Parenting a sick child
  173. Be my guest! Challenges and practical solutions of undertaking interviews with children in the home setting
  174. How arts-based approaches can put the fun into child-focused research
  175. Development and validation of the Liverpool infant bronchiolitis severity score: a research protocol
  176. Child poverty
  177. ‘Just kids playing sport (in a chair)’: experiences of children, families and stakeholders attending a wheelchair sports club
  178. ‘Being a presence’
  179. The assessment and management of children's pain
  180. The restrictions to the use of codeine and dilemmas about safe alternatives
  181. Paediatric intensive care nurses' and doctors' perceptions on nurse-led protocol-directed ventilation weaning and extubation
  182. Parents’ experiences and views of caring for a child with a tracheostomy: A literature review
  183. Looking for an ordinary life
  184. Modernising health visiting practice whilst keeping compassion in care
  185. Stigma, health and incarceration
  186. ‘I am closer to this place’—Space, place and notions of home in lived experiences of hospice day care
  187. ‘Do I, don’t I ask for help?’
  188. Researching children's health experiences: The place for participatory, child-centered, arts-based approaches
  189. Editorial
  190. Editorial
  191. Editorial
  192. A UK and Irish survey of enteral nutrition practices in paediatric intensive care units
  193. Parents need to protect: influences, risks and tensions for parents of prepubertal children born with ambiguous genitalia
  194. Children’s well-being: Priorities and considerations
  195. Reflections on the ethics of Internet newsgroup research
  196. Developing and Implementing an Appreciative ‘Quality of Care’ Approach to Child Neglect Practice
  197. The Identification of Acute Stroke: An Analysis of Emergency Calls
  198. Autobiography as genre for qualitative data: A reservoir of experience for nursing research
  199. Home-Based Care for Special Healthcare Needs
  200. Social support for mothers in illness: A multifaceted phenomenon
  201. FUNdamentally important: humour and fun as caring and practice
  202. Deconstructing child and adolescent mental health: questioning the‘taken-for-granted’…
  203. Searching for harmony: parents’ narratives about their child’s genital ambiguity and reconstructive genital surgeries in childhood
  204. Assessment of acute pain in children: development of evidence-based guidelines
  205. Key Working for Families with Young Disabled Children
  206. Editorial: A day at the beach or …
  207. Time-use diaries are acceptable to parents with a disabled preschool child and are helpful in understanding families' daily lives
  208. A structured observation of the interaction between nurses and patients during the administration of medication in an acute mental health unit
  209. Mothering disrupted by illness: a narrative synthesis of qualitative research
  210. Addressing end of life care issues in a tertiary treatment centre: lessons learned from surveying parents’ experiences
  211. Appropriated landscapes: the intrusion of technology and equipment into the homes and lives of families with a child with complex needs
  212. A simple act?
  213. Taking a deep breath . . . or two ... or three?
  214. Living with type 1 diabetes: perceptions of children and their parents
  215. Tick box for child? The ethical positioning of children as vulnerable, researchers as barbarians and reviewers as overly cautious
  216. Re-visioning the doctoral research degree in nursing in the United Kingdom
  217. Examining the British PhD viva: Opening new doors or scarring for life?
  218. Fear, failure, outrage and grief: the dissonance between public outrage and individual action?
  219. Editorial: Nursing amidst stories (and knowing what to do with them)
  220. Parents’ narratives about their experiences of their child's reconstructive genital surgeries for ambiguous genitalia
  221. Global health: time for a safer, fairer world
  222. What pain assessment guidelines tell us and what they may miss
  223. Commentary on Shields L, Pratt J & Hunter J (2006) Family centred care: a review of qualitative studies. Journal of Clinical Nursing 5, 1317-23
  224. Analgesia Review
  225. Pain Assessment
  226. Medical Procedures
  227. Postoperative pain
  228. Background
  229. Quick reference summary of recommendations and good practice points
  230. ‘Good’ and ‘bad’ stories: decisive moments, ‘shock and awe’ and being moral
  231. The influence of culture on diabetes self-management: perspectives of Gujarati Muslim men who reside in northwest England
  232. Guidance, Guidance Everywhere, but One you Need to Read: 0-18 years: guidance for all doctors
  233. Bunny hops and creative thinking about getting youngsters active
  234. Percutaneous Endoscopic Gastrostomy Feeding in Nursing Homes
  235. Parenting: a glut of information
  236. An exploration of best practice in multi-agency working and the experiences of families of children with complex health needs. What works well and what needs to be done to improve practice for the future?
  237. Children in handcuffs and detained behind bars. Where in the world?
  238. Kicking Eeyore into touch: ‘Living-strong’, ‘nursing-strong’ and being appreciative and solution-focused
  239. Chronic pain in children and adolescents
  240. Far away and close to home... stones, stories and health care
  241. Weight monitoring of breastfed babies in the United Kingdom - interpreting, explaining and intervening
  242. APPRECIATING WHAT WORKS: DISCOVERING AND DREAMING ALONGSIDE PEOPLE DEVELOPING RESILIENT SERVICES FOR YOUNG PEOPLE REQUIRING MENTAL HEALTH SERVICES
  243. ‘One expertise among many’— working appreciatively to make miracles instead of finding problems
  244. Thingamijigs, wotsits and the naming of things
  245. A letter to myself - stay angry, keep caring...
  246. From Peter, Jane and Tiptoes to literacy as freedom
  247. Weight monitoring of breastfed babies in the UK - centile charts, scales and weighing frequency
  248. “They’ve got to be as good as mum and dad”: Children with complex health care needs and their siblings’ perceptions of a Diana community nursing service
  249. A spoonful of sugar helps the medicine go down...
  250. Evaluating Student Paediatric Advanced Nurse Practitioners’ Experiences of a Paediatric Pharmacology Module: In the Context of Reflective Learning
  251. If I have to Say it One more Time, I Swear I’m Gonna Kill Someone
  252. Touching the Void – Taking Decisions and Finding Solutions
  253. Pain narratives and narrative practitioners: a way of working ’in-relation’ with children experiencing pain
  254. ‘Bloods Taken, CXR Later, No Change’
  255. Ducks Might Quack... Children and Domestic Violence in Rural Areas
  256. Bernie,... do you know what?
  257. Methodological issues and complementary therapies: researching intangibles?
  258. If you've `Gone Busted' - A Nurse will Fix you
  259. Think Child, Not Refugee
  260. It’s Dead …it Doesn’t Work Anymore, but will it Get Better?
  261. A pain workshop: an approach to eliciting the views of young people with chronic pain
  262. Clients' experiences of frozen shoulder and its treatment with Bowen technique
  263. The transition of adolescents with diabetes from the children's health care service into the adult health care service: a review of the literature
  264. Big Elephants Fighting Whilst Children’s Policy Misses Out?
  265. Adaptation and negotiation as an approach to care in paediatric diabetes specialist nursing practice: a critical review
  266. Dealing with uncertainty: parental assessment of pain in their children with profound special needs
  267. On ’Irafs and Other Amazing Things …
  268. Health Inequalities: A Blight on Children’s Lives and Futures
  269. An evaluation of a children's drug therapy service
  270. Chronic Pain in Childhood and the Medical Encounter: Professional Ventriloquism and Hidden Voices
  271. A pilot study to evaluate the effectiveness of Bowen Technique in the management of clients with frozen shoulder
  272. Ways of working: CCNs and chronic illness
  273. Reflections of a cynical optimist
  274. So-knit 1, purl 1… clone1?
  275. Childhood Chronic Illness: a continuing challenge
  276. Children - silent consumers of health care
  277. Public health for children: the Green Paper
  278. Children's health care: a new era or more rhetoric?
  279. Children's nursing-a cause for celebration
  280. Children's nurses as critical thinkers
  281. An asthmatic in‘Wonderland’: a patient's perspective of Accident and Emergency
  282. Complementary therapies and management of chronic pain
  283. Nursing Care and Management of Children's Perioperative Pain