Support of a child after brain tumour diagnosis
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Support of a child after brain tumour diagnosis

Rachel Perrow Neuro-oncology and solid tumour clinical nurse specialist, Bristol Royal Hospital for Children, University Hospital Bristol NHS Foundation Trust

Rachel Perrow describes one family’s experience after their child’s emergency admission to a high dependency unit

‘Sam’ was a six-year-old boy with medulloblastoma causing obstructive hydrocephalus and ataxia. Surgery, rehabilitation and possible long-term disability or neurological deficit were prepared for thoroughly by Sam and his family with the help of a multidisciplinary team. Full resection was successful but was followed by posterior fossa syndrome. His parents, who were under great stress throughout, were encouraged to communicate their concerns in a designated environment and to assist in their child’s rehabilitation. A care plan ensured that they were involved with, but not overwhelmed by, his needs and the long-term prognosis.

Nursing Children and Young People. 25, 4, 14-18. doi: 10.7748/ncyp2013.05.25.4.14.e177

Correspondence

rachel.perrow@uhbristol.nhs.uk

Peer review

This article has been subject to open peer review

Conflict of interest

None declared

Accepted: 12 December 2012

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