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Home / Health Conditions / Alzheimer's / Laurie Hernandez: Caring For Someone With Alzheimer’s Is Not Easy

Laurie Hernandez: Caring For Someone With Alzheimer’s Is Not Easy

“My family really came together when it was [time] to take care of my grandmother,” says Hernandez in a My Story video for the Alzheimer’s Association. She comes from a very tight-knit family and was very close with her grandmother. “Seeing how much Alzheimer’s affected my dad and seeing how he reacted towards his mom having it…it was really hard for us as well.”

Being a caregiver for someone with dementia or Alzheimer’s Disease is extremely difficult. The Alzheimer’s Association recently released a survey that shows the impact that this disease has on families, especially when they’re caregivers and this is what they found:

*Far too many caregivers are doing it alone. The survey found two out of three caregivers (64%) felt isolated or alone in their situation, and more than four in five caregivers (84%) would have liked more support with caregiving tasks, particularly from their family.

* The No. 1 reason people said they did not help with providing care for someone with Alzheimer’s or another form of dementia was they felt as though another family member had already taken on the responsibility (74%), followed by their not living in the same area (62%).

*Alzheimer’s is one of the costliest diseases affecting seniors. People greatly fear to become a burden to their families as they age, but they are not planning accordingly. For example, 70% of people fear being unable to care for themselves or to support themselves financially, but only 24% have planned financially for their families in preparation for any future caregiving needs. Moreover, 74% of people said they would prefer a paid caregiver, but only 15% have financially planned for one.

*Alzheimer’s stress can bring families closer or tear them apart. Relationships between siblings were found to be the most strained, stemming from not having enough support in providing care (61%) as well as the overall burden of caregiving (53%). Among all caregivers who experienced strain in their relationships, many felt like their efforts were undervalued by their family (43%) or the person with the disease (41%).

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