Feb 7 • 10:04 UTC 🇫🇮 Finland Yle Uutiset

"I don’t need a day off from Erkki," says Tuula Heikkilä, who cares for her spouse – the welfare area disagrees

Tuula Heikkilä, a caregiver for her husband Erkki who suffers from Alzheimer’s, expresses frustration over new welfare policy changes that limit caregiver support.

Tuula Heikkilä, a 77-year-old caregiver for her 91-year-old husband Erkki, who has been battling Alzheimer's disease for eight years, shares a positive outlook on their life together. However, they are facing disappointment due to a new welfare policy change in South Karelia, which affects nearly 1,000 caregivers in the region. This change limits the use of the caregiver relief service voucher to only organizing care during the caregiver's time off, eliminating its flexibility for other supportive services like rehabilitation and cleaning.

The new approach has sparked concerns among caregivers like Tuula, who believe that this policy overlooks the individual needs of families in similar situations. Tuula argues that the current system has functioned well for them, allowing for customized support tailored to their unique circumstances. The impending changes underscore a growing tension between the welfare region and the caregivers, as they navigate the availability and practicality of essential services that contribute to their quality of life.

With the welfare area emphasizing standardized support, caregivers feel increasingly isolated in addressing their specific needs, which could have broader implications for mental health and familial relationships. The decision to restrict the use of the service voucher is seen as detrimental by many, raising questions about the prioritization of caregiver well-being in regional health policies and the future relationship between caregivers and welfare authorities.

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