Why can it be difficult to decise whether or not a person is an informal carer and does it matter?

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Why can it be difficult to decide whether or not a person is an informal carer and does it matter? Base your answer on the case of someone you know, or have read about in K100.

How can we determine as to whether a person is an informal carer, and why should we be labelling people?

It is said that there are four complications that need to be considered when deciding to label a person as an informal carer

  • Interdependence
  • Duration and frequency
  • Labelling
  • Networks

 I am going to be looking at all four of these taking experiences from my personal life, and also looking at other sources to try and ascertain why it is difficult, and whether it matters to label people as informal carers. I will be looking into my Father Andrew’s experience with informal care as my case study.

 Andrew was diagnosed with Multiple Sclerosis a few years ago, and his health had severely deteriorated in a matter of months. Unfortunately Andrew could not do much for himself (although encouraged) this led to him having most things done for him. He had formal carers who would come in the morning and evening to help him in and out of bed, wash, dress, and change his colostomy bag. His informal carers (family and friends) also looked after Andrew, and at the time would not have labelled themselves as informal carers.

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Looking into the first complication interdependence as Andrew’s daughter I felt uncomfortable doing the things that formal carers would do such as wash him as this would not be socially acceptable, however I would shop, clean, cook, deal with financial matters, and help maintain his flat. Other family members would help with this as well as my sister, uncles, and grandmother, and to a point my young children who would help by reading to him or by playing games such as “I spy”. This did show that he was very dependant on us but also we were dependant on him ...

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