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Family unit members caregivers was met with collected loss

Our dataset out of qualitative interviews while focusing groups indicated that way of life which have dementia is to be knew essentially because the getting entangled inside an ambiguous and remote lives. Family unit members caregivers sensed swept up when you look at the a great prospectless coming, while they even more eliminate the feeling regarding equality and reciprocity, and you can struggle to handle subsequent knowledgeable backup and ambiguity rather than one guarantees except the newest confidence out-of passing. Due to the volatile however, modern development of the illness, staying in experience of new diseased person need a continuing efforts to attune. They usually had to see a unique equilibrium, refamiliarize themselves that have a modified condition.

Inside data, i basic looked for to spell it out what it method for live with dementia on position out of loved ones who were employed in the new proper care of their family

Furthermore, we aimed to explore how friends caregivers addressed contingency and you will dealt which have dementia while the related ongoing losses event. Our very own studies depicts the event of your loved ones normally getting classified because an intricate grieving procedure in which he’s https://datingranking.net/pl/benaughty-recenzja/ to cope with thus-called ‘compounded serial losses’ that are numerous and you will cyclic in general. Blandin and you will Pepin arranged a principle of ‘alzhiemer’s disease grief’ so you can translate the sort away from losses and you may suffering inside the alzhiemer’s disease. Our very own studies supports its concept, and the theory off unclear losings [27–29]. It illuminates new ambiguity of your own compiled losses skills on the experience the lingering changes is volatile, changing, and you will lacking all the quality [16, twenty seven, twenty eight, 30–32]. Our very own findings show one to writing about that it ambiguity is just one quite demanding aspects of coping with alzhiemer’s disease.

Seeing it persistent progression of the condition and working with the accompanying not sure changeability suggests in itself just like the an extremely demanding procedure having romantic family relations, as well as for their family influenced by dementia

Amazingly, because annoying contact with ongoing loss is actually preferred from inside the respondents’ tales, the ways it individual friends caregivers was away from uniform. Particular participants think it is nearly unbearable, not just for the people which have alzhiemer’s disease but also for on their own. Other respondents, yet not, demonstrated significant resilience. To help you an elevated otherwise decreased extent they were able to render up resistance and you may face the tough task of controlling the fresh new experience off dementia as an element of their life. Inspite of the demanding effort it expected, they for some reason the time by themselves toward state and you may remained in a position to determine meaning and value in daily life. Our very own results underline the necessity of usually trying to the latest an approach to attune, link and you can reconnect. As the Taylor said: a portion of the concern should not be if the other has been able to accept your, but rather if the body’s nonetheless offered (social) recognition..

When the particular be seemingly better in a position to deal with and adjust to the contingencies out-of dementia than others, an appealing real question is how this improvement might be said. Into the current literature, that it real question is have a tendency to noticed off either an encumbrance perspective [3–8, 10], otherwise a quality-of-lifetime direction [nine, 34–38], commonly starting from an emotional-behavioural paradigm. They work on step 1) predictors out of burden eg stress, depressive and you will/or despair symptoms; 2) chance facts such as for example behavioral problems from the care receiver, standards of your own condition and you may/otherwise poor economic situation; 3) coping measures of caregiver; otherwise cuatro) quality-of-life domain names such as for example health and powers of one’s caregiver, supportive public ecosystem, and other tips particularly own methods. Our very own findings suggest that the explanation regarding exactly how friends caregivers package with regards to requiring work and you will spots will be based upon a combination of each one of these issue. Although not, the overall performance go beyond which psycho-behavioural symptomatic strategy by firmly taking a more alternative lifeworld means one takes into account both heartbreaking load-experience, and also the imagined lifestyle, instead of focussing on one side or perhaps the other. I advise that instance a great lifeworld knowledge results in the into the-breadth understanding of the brand new each and every day truth out of relatives caregivers, therefore the grand perception it’s to their lifestyle.

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