Saturday, April 28, 2007
The previous column said caregiving is not a healthy occupation.
Most caregivers report some depression, some health decline, some lack of taking care of their own health needs.
The problem, says Karin Little, is the way caregiving "kind of sneaks up on people. You tell them, `Hey, you're a caregiver' and they look shocked and then respond, `Oh yes, that's what I'm doing.'"
The lack of awareness – for most people – happens because most people needing care decline slowly. There's a need to take over more and more responsibility and suddenly you become the caregiver, she says.
Related columns
Part one: Caring for a loved one puts your health at risk
Part two: Caregiving can sneak up on you
Little is a family consultant with the Orange (Calif.) Caregiver Resource Center, which provides an array of services for caregivers.
Q: What's one of the basic personal needs caregivers tend to overlook?
A: Many times caregivers don't realize they need to have someone legally designated to care for them in event of an emergency.
We have our legal workshops because we find many do not have their own durable power of attorney for health care filled out. If something happens to the caregiver, no one is designated to step in and make decisions. So we provide them with information from an elderlaw specialist on wills, trusts, conservatorships, Medicare, Medicaid and so on.
Q: That's nuts-and-bolts stuff. What about the emotional drag of caregiving?
A: We have a class that really gives caregivers lots of tools for dealing with the emotional side. Like someone with Alzheimer's may ask the same question over and over, do other irritating things, wander away. The caregiver cannot change that person's behavior. We tell them the only one whose behavior can change is you. There are ways you can change your behavior and attitude to make situations less stressful.
Q: Do you work with caregivers outside of the classroom?
A: Of course. We have a counseling program with therapists trained in caregiving issues. They help deal with issues of anger, frustration, guilt, depression, anxiety. We offer six sessions on a sliding scale depending on income.
Then there are support groups that are ongoing. Some are focused on stroke survivors, Huntington's disease and so on.
Q: I think it would be a blessing to have someone outside the family to talk over these emotional issues.
A: Oh, yes. Caregivers often need someone dispassionate to talk to. They need someone to walk them through the problems of today and tomorrow.
You know, there is no timeline to caregiving. You don't know how long it will last. It could be five, 10, 15 years. The better care people receive, the longer they live.
Q: That's particularly tough on women who give up a job to be a caregiver.
A: Exactly. They put their lives on hold, lose out on benefits for their future, like Social Security and retirement plans. Then when they try to go back to work, they may need to retrain. Ouch, that's tough.
Q: What is one special need caregivers have that we haven't talked about?
A: Doctors and dentists who make house calls.
Comments
Patrice (anonymous) says...
I cared for my mom at home from 1993-1998. My dad died, my mom was physically and neorologically disabled due to several strokes. She was already deaf in one ear and extremely hard of hearing in the other, long before the strokes. Long story short, I could not bring myself to place a deaf, speech-disabled, physically and nuerologically-impaired woman in a nursing home. I worked in the human services field, and believed that my mom would be at an insurmountable disadvantage in an institutional setting. I left my full-time job and my apartment, and mved in to my mom's apartment, along with my son and his father. If I had any illusions about this being easy - they were soon gone! Was it easy -no! were there lots of problems - yes! However, I wouldn't trade the spiritual and emotional journey my family took for anything. My mother's doctor told me that, if I decided to care for my mother, it would be one of the most meaningful things I would ever accomplish. she was right. My mom lived died at home, in a living set up for her at the center of the home, so she would always feel included and special. She was at peace when the end came. One of the EMT's who came to our home at the end told me he had never seen a more peaceful, accepting death.
April 28, 2007 at 4:28 p.m. ( permalink | suggest removal )
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