Are Alzheimer’s Caregivers the Forgotten?

Forty percent of Alzheimer’s caregivers end up suffering from depression.

Do you want to see this happen to a loved one or friend?

One issue that really frustrates me is the treatment of Alzheimer’s caregivers. Most Alzheimer’s caregivers hear people tell them how wonderful they are for taking care of their loved one. As a caregiver, I learned to appreciate these compliments. They help, they really do.

However, if you have a friend or a loved one that is an Alzheimer’s caregiver and that is all you do — it is not enough. Many Alzheimer’s caregivers are forgotten by family and friends. This is a sad truth that is rarely discussed.

I meet and talk to caregivers all the time. It is not unusual for them to tell me that as time goes on, and as Alzheimer’s worsens, one by one their family and friends fade away. This is understandable — Alzheimer’s is scary and disconcerting. It is hard to accept, hard to understand, and hard to watch as it progresses.

It is not unusual for the friends and family to continue to call and give the caregiver the old "rah rah sis boom bah," and then they get back their own life.

Meanwhile, the caregiver puts their life on hold — or worse they have no life — while caring for an Alzheimer’s sufferer. Calling and letting the caregiver "vent" is helpful, very helpful, but it is not enough.

Like it or not, if you are a family member or friend of an Alzheimer’s caregiver and you are not helping them–you have abandoned them. I am sure this sounds harsh.

Caregivers need help. A few hours, here and there, to get away from it all is an important step in improving their lives. Some time to enjoy the world outside their home.

Why am I so passionate and adamant about this?

Forty percent of Alzheimer’s caregivers end up suffering from depression — four out of ten. Do you want to see this happen to a loved one or friend?

Alzheimer’s is a sinister disease–it kills the brain of the person suffering from Alzheimer’s.

It will try to kill the brain of the Alzheimer’s caregiver.

I really don’t believe this problem is well understood.

Here are my immediate suggestions.

  • If you know an Alzheimer’s caregiver, find a way to organize the troops–family and friends–and get involved. Somebody has to take the initiative and if you are reading this article–take charge now.
  • If you know a family that is dealing with Alzheimer’s send them the link to this article and encourage them to organize up their own troops and do something.
  • Nothing works better than a small team of caregiver helpers. The key words here are: team and team work.

Here are some actions that will improve the life of the caregiver and help them avoid depression.

  • The Alzheimer’s caregiver needs to get away from it all. They need a respite every few days. This means someone must taking over while they go do something they enjoy. You might find this difficult to believe, but when I get to go to the store, take my time, and look around at the surroundings — it is a treat. I bet you take it for granted.
  • Invite your Alzheimer’s caregiver and their loved one over for lunch or dinner. Most Alzheimer’s caregivers tell me that one of the biggest problems they face is socialization. If you don’t believe me–ask. Socializing really benefits the Alzheimer’s sufferer (see: A Wonderful Moment). What is not as apparent is how much it benefits the Alzheimer’s caregiver.
  • This one is tough but could very well keep the caregiver from becoming depressed. Many sufferers of Alzheimer’s get up in the middle of the night. This means the caregiver needs to get up with them. Sleep deprivation often leads to depression, and it can cause erratic behavior. Imagine going night after night without sleeping well.
  • Do you know an Alzheimer’s caregiver? Ask them when was the last time they went to a movie? You might be surprised when you hear the answer (I mean went to the movies, not watched). Solve this problem through team work: one person can look after the sufferer, and the other one can take the caregiver to the movie. This is a "get away from it all experience" that is really beneficial to the mental health of the caregiver.

Here is something I learned over my years of talking to caregivers.

Many caregivers get abandoned by friends and family. The reasons for this vary widely–ranging from denial, dysfunction, to fear of Alzheimer’s. Many times friends and family while living their own busy lives fail to realize what is happening to the caregiver. An Alzheimer’s caregiver might vent to you or me about their difficult day; but, they rarely tell friends and family that they need help. Worse, they rarely get asked directly from friends and family what they need most personally.

I am not talking about running down to the grocery store to pick up a quart of milk.

Let me summarize.

  • Forty percent of Alzheimer’s caregivers end up suffering from depression. You can do something about this problem.
  • The best solution is to organize a small group of people, and to come up with a plan to assist the Alzheimer’s caregiver.
  • You might consider adopting an Alzheimer’s caregiver.

I know from my own experience that if you take action you’ll end up feeling good about yourself. Action will change and enrich your life.

Don’t allow Alzheimer’s to take control of the caregiver — form a team to take control of the problem. The caregiver gets a life, the sufferer gets more effective care, and the team gets the wonderful feeling that comes along with doing something and getting involved.

Note: I realize the above does not apply to all families and friends of Alzheimer’s caregivers. On the other hand, I know that this article is about one of life’s little secrets…

Posted with permission from The Alzheimer’s Reading Room. Original article appears here.

Bob DeMarco is an Alzheimer’s caregiver and editor of the Alzheimer’s Reading Room. The Alzheimer’s Reading Room is the number one website on the Internet for advice and insight into Alzheimer’s disease. Bob taught at the University of Georgia, was an executive at Bear Stearns, the CEO of IP Group, and is a mentor. He has written more than 700 articles with more than 18,000 links on the Internet. Bob resides in Delray Beach, FL.


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  • http://www.inhomehealthcaregiver.com/ Care Giver

    Thanks for this call to arms to help caregivers. It’s funny to think of a caregiver needing a caregiver. But it’s true. Support groups help, but getting actual tangible from the people in our life – who should be our support group – can make all the difference.

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  • http://Windows brenda guider

    I know what you mean, my mother is in the last stages of dementia, i have cronic back pain, i have bills and debt so i have to work. My mother is pretty good thanks to the LORD, she can get up ,walk, talk, she very seldom eats, she lives on Ensure, Boost, and Carnation Breakfast Drinks. I take care of her by my self. I thank GOD for Palmetto Senior Care, they take care of her while i’m at work.
    My doctor has put me on disability until december first, so my pay check will be gone.
    Does anyone out there help financially scraped caregivers financially or are we truely on the back burner.