Department of Global Public Health, Karolinska Institutet, Solna, Sweden.
Global Health and Development, Faculty of Social Sciences, and New Social Research, Tampere University, Tampere, Finland.
BMC Public Health. 2021 Jan 25;21(1):208. doi: 10.1186/s12889-020-10015-w.
A child's long-term illness or disability is always a serious matter that impacts the whole family. Costs related to an illness can substantially affect a family's financial situation. To date, there is little research on how parents experience available support for financial assistance. Surveys in Finland have found that families of children with long-term illnesses and disabilities could experience financial struggle and perceive the state provided financial support system as too complex. This article aimed to explore how caregivers of children with long-term illnesses perceived their financial situation, need for financial support and experienced its provision by the state in the Helsinki greater region.
Convenience sampling was used. Participants were contacted through peer-support groups on Facebook. Eleven mothers of children with varying long-term illnesses and disabilities residing in the Helsinki greater region were interviewed using in-depth interviews. Recordings of the interviews were transcribed and analysed using framework analysis. An analytical framework was built to label the dataset, which was then charted. Lastly, themes were formed through descriptive analysis.
The main findings showed how the burden of caring for a child with a long-term illness or disability causes fatigue, which affects a family's financial situation holistically. This affected both employment and financial management, but also receiving information about and applying for the state provided allowances. Mental resources were further depleted by seeking information and applying for allowances. This contributed to a vicious cycle between parental fatigue and financial struggle. Participants found the allocation of funds inequitable across the country. Finally, participants thought the allowance was insufficient in compensating for time spent caring for their child's illness and did not consider their mental strain.
Even in a welfare state such as Finland, caregivers of children with long-term illnesses are at risk of poverty and struggle with the organization of state provided financial support. Policies should be designed to ensure equity across the country and consider how the parental fatigue should be addressed. The study has implications for achieving sustainable development goals on wellbeing and reducing poverty.
儿童长期患病或残疾始终是一个严重的问题,会影响整个家庭。与疾病相关的费用可能会极大地影响家庭的财务状况。迄今为止,关于父母如何获得经济援助支持的研究甚少。芬兰的调查发现,患有长期疾病和残疾的儿童的家庭可能会面临经济困难,并认为国家提供的经济支持系统过于复杂。本文旨在探讨长期患病和残疾儿童的照顾者如何看待他们的财务状况、对经济支持的需求以及他们对国家提供的经济支持的体验。
采用便利抽样法。通过 Facebook 上的同伴支持小组联系参与者。对居住在赫尔辛基大都市区的 11 名患有各种长期疾病和残疾的儿童的母亲进行了深入访谈。对访谈的录音进行了转录,并使用框架分析法进行了分析。构建了一个分析框架来标记数据集,然后对其进行图表化。最后,通过描述性分析形成了主题。
主要发现表明,照顾患有长期疾病或残疾儿童的负担会导致疲劳,从而全面影响家庭的财务状况。这不仅影响了就业和财务管理,还影响了获取和申请国家提供的津贴的信息。寻求信息和申请津贴进一步耗尽了精神资源。这导致了父母疲劳和经济困难之间的恶性循环。参与者认为全国资金分配不均。最后,参与者认为津贴不足以补偿照顾孩子疾病所花费的时间,也没有考虑到他们的精神压力。
即使在像芬兰这样的福利国家,长期患病儿童的照顾者也有陷入贫困的风险,并难以组织国家提供的经济支持。应制定政策以确保全国范围内的公平,并考虑如何解决父母疲劳问题。这项研究对实现福祉和减少贫困方面的可持续发展目标具有重要意义。