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Conference Proceedings - School of Nursing & Midwifery - Trinity ...

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<strong>School</strong> <strong>of</strong> <strong>Nursing</strong> & <strong>Midwifery</strong>, <strong>Trinity</strong> College Dublin: 8 th Annual Interdisciplinary Research <strong>Conference</strong><br />

Transforming Healthcare Through Research, Education & Technology: 7 th – 9 th November 2007<br />

<strong>Conference</strong> <strong>Proceedings</strong><br />

with a poor appetite and reduced energy levels. Uncertainty was<br />

repeatedly expressed about what could now be viewed as normal<br />

with respect to many aspects <strong>of</strong> their recovery. Awareness <strong>of</strong><br />

mortality and uncertainty about the future were prominent. For<br />

some this increased feelings <strong>of</strong> isolation as they realised they could<br />

never completely share the horror <strong>of</strong> the experience they had<br />

endured.<br />

For the purpose <strong>of</strong> this presentation two <strong>of</strong> the post-discharge<br />

categories will be considered, communication and information and<br />

elimination as well as the themes incorporated within them.<br />

Sections <strong>of</strong> the participants’ transcripts have been used to clarify<br />

and enhance the discussion.<br />

Communication and Information<br />

Each individual’s physical condition, disease state, emotional state<br />

and social circumstances was inextricably linked with their need for<br />

information. Most <strong>of</strong> the participants had been given a leaflet<br />

providing basic information on day-to-day activities, feelings and<br />

emotions, diet and bowel activity, sexual activity and follow up. It<br />

also provided the contact information for such organisations as<br />

Cancer BACUP, Cancerlink and Colon Cancer Concern. For some,<br />

returning home was a particularly anxious time because they felt<br />

that they had received insufficient information prior to discharge to<br />

be able to understand the ‘new normality’ particularly in respect to<br />

bowel function. Others felt that whilst the information valuable to a<br />

degree it was too general, lacking in clarity, detail and specificity to<br />

their individual needs.<br />

‘Once you get home, there is no one to answer questions or fears.<br />

How long will it take for my tummy not to go tender, weeks,<br />

months? At night I want to pass urine, every one and a half hours,<br />

no sleep or very little. When will this settle? I open my bowels<br />

slightly every day, about four times a day, only a little. But what if<br />

I feel constipated, what do I do? Do I take anything? Nurses from<br />

your surgery have no real knowledge <strong>of</strong> your condition and they’re<br />

only able to change dressings’ (8).<br />

‘And I don’t know how much I can do, because they say no heavy<br />

lifting for six weeks, but what is heavy lifting? If you lift a kettle <strong>of</strong><br />

water, you tend to feel it pulling’ (17).<br />

The importance <strong>of</strong> information pertaining to resuming self-care<br />

after colorectal cancer surgery has been previously reported<br />

(Galloway and Graydon, 1996; Saegrov and Harding, 2004;<br />

Simpson and Whyte, 2006). The findings <strong>of</strong> this study concur in<br />

that they highlight the need for more detailed, personalised<br />

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