Find peace of mind as a caregiver – Daily Breeze



[ad_1]

By David W. Hart, Ph.D.

Collaborater

November is National Caregiver Awareness Month, and it looks like it's time to look at important issues for millions of families and friends who are dedicated, often to their own detriment, to caregiving. and the well-being of those they love.

The National Caregiver Alliance and AARP report that approximately 34.2 million Americans and nearly 3.5 million Californians have provided unpaid care to an adult aged 50 or over during last 12 months. In the United States, more than 16 million caregivers care for someone with Alzheimer's disease or related dementia. In total, the economic value of services provided by caregivers is estimated at nearly $ 500 billion. Yes, it's billion with a b. For some contexts, this number is higher than that of many state economies around the world.

David Hart, Ph.D.
  • Caregivers spend an average of 13 days per month on tasks such as shopping, medication recalls, transportation, laundry, meal preparation and housework.
  • More than 96% provide help for activities of daily living (ADL) such as personal hygiene, dressing, grooming, as well as getting up and getting up.
  • On average, caregivers spend 24.4 hours a week on care.
  • Caregivers caring for someone with Alzheimer's disease or other dementia report spending an average of 9 hours per day (Fisher, et al., 2011).

After reading the data, one can imagine that caregivers are stressed. Beyond stressed, in fact. It has been a special privilege to form support groups for dementia caregivers over the past 10 years, and the stories shared are both heartbreaking and inspiring.

What I hear most often, though, is that the standard guideline – natural caregiver, take care of yourself first and foremost – is not entirely helpful. The caregivers often report feeling like a dog paddling in dangerous waters, a person attached to the back, his head barely above the water, without a buoy in sight. No lifeboat, no coast guard, no oxygen. It may seem unrealistic, if not impossible, to prioritize oneself in extreme situations.

This does not mean that the advice is bad – it is not – but the decree is often given too early. The initial goal, in my work with caregivers, is to determine if the caregiver is legitimately in need of the caregiver's full assistance. In other words, can the care recipient swim a bit alone? The caregivers who attend my group are superheroes, aspire to absolute perfection and tend to overcompensate their loved ones by offering too much help. This type of trap is often linked to the caregiver's personality style and probably favors the care recipient's passivity and need.

[ad_2]
Source link