Family centred care is essential when caring for a sick child. The impact of illness touches everyone therefore the family is the unit of care rather than the child being separated out without consideration of the whole family.
It is important to remember that parents should be recognized as being experts as far as their child’s needs are concerned acknowledging that they know their child the best. It is also important to remember that they also carry the burden of both the illness and the decision making.
As adults we are able to articulate our needs, for children it is harder to express what they need. Often children will display behaviour which is not usual for them. They become withdrawn, cry or scream. Their play may alter and they may act out and changes can often be seen in their drawings both in topic and colour choices.
Children are very good at being able to interpret the behaviour of those around them, gaining insight into their condition. Sick children make use of various coping mechanisms, as do we as adults when dealing with issues of pain, fear and anxiety. The coping mechanisms are dependant on the developmental age and understanding of the child.
Children often try to protect their parents and other adults in their lives. They often perceive that the topic they wish to discuss is too uncomfortable or stressful for the adults they love. Therefore they may deny the reality of their situation to protect those around them.
The emotional link that parents have with their children in most cases allows them to feel safe. Therefore, it is important for parents and health professionals to encourage open communication while respecting their right to privacy in regard to their thoughts and emotions. The use of play and artwork allows the child to express themselves concerning issues that may be troubling them. It is important not to make assumptions about what a child knows or understands.
Children who live with illness require the adults in their lives to be honest and real. They need us to listen, giving them time to share their thoughts and feelings. As a health professional I am mindful of providing care and support to families to enhance their quality of life as they live with the impact of illness.
(Ward, 2005)
Cynthia Ward CEO
Cynthia's Blog
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Resiliency in Action
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Xmas Greetings 2012
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Resiliency in Evidence
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The importance of hearing from children, young people and their families
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The Wisdom of Learning from Others - 26 June 2012
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Parents the unseen heroes when caring for children with complex health needs:
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Building Resiliency in Children - 29 April 2012
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Holiday a mixed time for families - 31 January 2012
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Listening to families - 20 December 2011
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Huge generosity makes True Colours Long Lunch a great success - 7 November 2011
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Challenge to gain sufficient funding to continue service - 30 September 2011
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Staying resilient in the face of chronic illness - 31 August 2011
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Facing the challenge of Winter - 31 July 2011
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Parents expertise develops through necessity, not choice - 27 June 2011
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Children’s rights in healthcare - 30 April 2011
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“There is nothing safe about this life” - 21 March 2011
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Our hearts reach out to Christchurch - 28 February 2011
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How will we face the New Year - 31 January 2011
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Support helps team keep standing - 20 December 2010
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Long Lunch fundraiser was an awesome event - 12 November 2010
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We all want our voice heard - 30 September 2010
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“Making sense gives meaning to the experience” - 30 August 2010
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“Seen, heard and understood” - 12 July 2010
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Extra vigilance is exhausting for parents - 3 June 2010
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Illness and loss have huge impact on team - 26 April 2010
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“The greatest treasure” - 22 March 2010
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Children require honesty - 9 March 2010
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The many friends of True Colours - 20 February 2010
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Committed to best practice - 2 February 2010
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Therapeutic space complete thanks to Paul Newman Own Foundation - 25 January 2010



