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The Necessity of Counseling

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Many caregivers go through periods of stress, depression, and frustration. These are normal human responses. Feeling them does not in any way mean that a caregiver is inadequate. Most caregivers pour their heart and soul into their task, and the emotional toll can sometimes be quite devastating.

When asked about signs of caregiver "burnout" or stress, Shawn Hertz, of the Los Angeles Caregiver Resource Center says, "They become more resentful… there are quite a few red flags, and they cut across medical symptoms, physical symptoms, psychological symptoms and social symptoms. That's the important thing to remember about stress: it doesn't just affect one aspect of our lives. It affects all the major aspects of our lives that make us a whole person."

Caregivers who receive regular emotional support are much more apt to be able to handle difficult decisions, situations, and to help clarify needs of care receivers. Whether such emotional support is personal, through one-on-one contact with a supervisor, counselor, religious member of the community, or group support, the availability of counseling may prove invaluable to maintaining high-quality care.

Caring for loved ones often brings caregivers a great sense of accomplishment, but at times, overwhelming demands may affect a caregiver's physical condition, in addition to many other aspects of their life. It is not uncommon for caregivers to occasionally feel anger, frustration, and then grow anxious or guilty for those feelings.

One of the most devastating effects of the demands of caregiving, however, is depression. The Family Caregiver Alliance has estimated that nearly 20 percent of family caregivers suffer from some form of depression, and that over 40 percent of caregivers of Alzheimer's patients suffer from mild to moderate stages of depression during and after extended periods of care.

Of course, not all caregivers will suffer from depression, anxiety, or feelings of inadequacy, but for those who do, learning how to understand and address those feelings is one of the greatest benefits of counseling.

Being able to confide in someone about emotions or frustrations often helps to head off depression and feelings of confinement in many caregivers. The responsibilities of caring for a family member, especially one suffering from various stages of Alzheimer's, can feel like a jail sentence to many. This has nothing to do with how much someone loves their family member, but with the constant and needy demands of those suffering from it.

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195Austin said
Sep 2, 2008

I did not even realize how angery I was until my therpisist pointed it out and it did take a long time to learn how to cope with my problems but when she told me no one was going to recuse me which I was waiting for- I had to rescue myself which I did even though I was angery with her for telling me that- now that I have I really feel good about myself and everyone tells me how good I look and for the first time ever I am happy and content- the problems are still there but now I feel I can deal with them and still have a life besides being a caregiver,

anne123 said
Jun 5, 2010

This article recommends finding someone we caregivers can talk to openly about our challenges with caring for our elders. I have found that it is more helpful for me to express myself on this forum than with friends. That's why I feel that agingcare.com is such a necessary and productive resource.

MrsGrasshopper said
Jun 5, 2010

I appreciate the advice and understanding I receive from this program. My mother is 97 years old with dementia. She is becoming more and more beligerent and helpless at the same time. I know I need to get out more if not for my sake for my husband's sake. He helps me so much and puts up with her behavior. I can afford to get away but I am always afraid a cargiver will abuse her while I am away any length of time. How do you overcome this feeling. I feel that I am now seriously endangering my mental and physical health.

JamesJHC said
Jun 5, 2010

I feel like I am about to go crazy!!!! My mother was diagnosed with Dementia two years ago. I try going to school and work, plus make sure she is taken care of. She is a very needy person and had every medical problem she sees on tv. Sometimes I'm not sure if the problems are real or just a way to get attention. I don't have family close by, so this leaves me to try and handle everything. She lives with me, and gets very angry if I don't spend every minute with her. I keep taking her to the doctor and they say that nothing is wrong with her. What do I do now?

spiralli said
Jun 5, 2010

Oh I totally get the hypochandriac mother thing! Mine is exactly the same, its really hard, I feel for you SO much.

I need to see a therapist but my insurance does not cover it. Do any of you have any suggestions? I need someone who is aquainted with Dementia care giving. Help Please and Thank you!

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