Alzheimer’s Caregivers Six Times More Likely to Develop Dementia

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While it may seem cruelly ironic, studies have indicated that people who act as caregivers for loved ones (particularly loved ones) with Alzheimer's have a heightened risk for developing dementia themselves.

On average, it is estimated that this increased risk translates to a caregiver being six times more likely to develop dementia than a non-caregiver.

Numerous investigations have shown that caregivers for people with Alzheimer's have consistently ranked lower than same-aged non-caregivers on assessments of memory, attention, and cognitive functioning. This measurable decrease in cognitive capabilities is thought to put caregivers at greater risk for developing dementia.

Researchers have theorized that a combination of several different factors including; caregiver isolation, and increased stress contributed to this increased vulnerability to dementia.

Isolation

Social isolation is an often overlooked side-effect of having a loved-one who has been diagnosed with Alzheimer's disease.

For a variety of reasons, many of which have to do with being uncomfortable in the presence of a dementia-stricken person, family and friends that used to come over and visit may become more distant in light of an Alzheimer's diagnosis.

When this is compounded by the fact that their loved one can no longer emotionally engage with them in the way that they used to, the caregiver is often left with a hollow shell of their former social life.

Stress

Caregiving for a person who has Alzheimer's is an extremely taxing endeavor that can lead to the development of excessive secretions of cortisol, the hormone that is discharged when a person is stressed.

Too much cortisol can weaken a person's immune system, damage their ability to learn, elevate blood pressure, and increase inflammation in the brain. Research has shown that inflammation of the brain hastens the development of dementia.

In addition, the extreme amounts of stress associated with being a caregiver can also cause changes in lifestyle habits that can increase their risk of dementia. Caregivers may not have the time or the energy to exercise regularly or eat a well-balanced diet. The combination of a sub-par diet plan and deficient exercise program has also been proven to increase a person's risk for developing dementia.

What this means for caregivers

Sometimes, the best way to care for your loved one is to care for yourself.

The combination of the isolation and stress associated with being a caregiver can lead to more serious conditions like depression, a mental condition that increases your risk of developing dementia.

It is essential that you take a break from being a caregiver once in a while. Fight the urge to identify solely with your role as a spouse or loved one—just because you share an intimate bond with the elder you're caring for doesn't mean that you don't deserve a break.

Engaging in activities like yoga, exercise, hobbies, anything social, etc. will serve to rejuvenate your mind and stave off the depression and stress that can contribute to your risk of developing dementia.

Research has also pointed to the remarkable benefits that can be derived from caregiver support groups. Whether it is an in-person or online group, being able to share your trials and triumphs with a collection of caregivers who know where you are coming from is priceless.

For more information on caregiver support:

Getting Caregiver Support When You Have No Time

11 Ways to Stop Caregiver-Related Depression

 
Read more about: dementia caregiver
 

Comments

 
  •  Comments 1 to 10 of 15 
 
 

pinksea741

Give a Hug

Jun 1, 2011

Wow. that will certainly make people think more than twice before caring for their parents/relatives. I sure hope they take care of themselves first...even if it is for a hour walk away from the house.

 
 

Everyone is always saying to "take care of yourself," but how do you exercise, take a walk, even go to a support group when your parents need you there 24/7? It is more stressful to either leave them home alone or arrange for a neighbor or friend (a stranger to mom) come in for an hour or two.

 
 

bobbie321

Give a Hug

Jun 1, 2011

ehhhh, now this.

I was a caregiver for almost 6 years and would never have done it had I known what I was getting into. I loved my mom more than anything but I love me too.

Now I am in my post caregiving life and am in the middle of nice people and taking courses for my new career. I believe that you have to keep learning to save yourself from joining this statistic.

Chris in Fl I hear you. When I was a 24.7.365 caregiver I didn't even have time to do things like put cream on my hands.... When mom got cream, I got some from osmosis....

Friends always offered to come and sit with mom and when I would ask they would always be busy.... never failed and so no one EVER came. not once.

If I get it just drop me off somewhere; I would never do this to another person.

lovbob

 
 

maggiesue

Give a Hug

Jun 1, 2011

I don't want this "catching" disease. This is enough information to convince me to get out of the caregiving business. It's been 8 years of hell with no end in sight. Why should I sacrafice my life for someone who's la-la?

 
 

bernie1

Give a Hug

Jun 1, 2011

I have been a caregiver for my wife for 12 years. Social life is nought. Lots of sad moments when I remember the early years of our life (married 59 years). My wife was very active and energetic. Now she is a shell. Stressed day is normal for me. But, I wouldn't trade it in for anything else in the world. Lots of love over the years. I worry about what will happen to her if I go first. All in all, I am glad to be her caregiver. Being able to help the Love Of My Life function is worth the stress and depression that goes with it all. Bernie G.

 
 

crstrob

Give a Hug

Jun 1, 2011

I have been contemplating bringing my husband home from the nursing home soon as I am getting ready to retire. He is in end-stage Alzheimer's (at the age of 66), has probably had Alz. for 10 years, and has been in the nursing home the past year due to progression of the Alz. I have been tossing around whether I can handle him (physically). He can't walk/talk/feed himself and a hoyer lift has to be used to get him from a bed to a chair and back. He is the love of my life and I so want us to be together. However, the article, your comments, and advice from others give me reason to really think this out before making a final decision..

 
 

yearight

Give a Hug

Jun 1, 2011

I understand that you love your husband and want to be together, but, you can spend time with him in the NH. He is total care and that is exhausting. You can't leave him alone. If you are financially set you could take him home and hire caregivers to do all the heavy lifting and someone to care for him so that you can sleep and run errands, etc. But if you do not have the finances I would strongly suggest that you leave him in the NH and just spend as much time as possible there with him. You are not abandoning him. Don't feel guilty. I wish you the best.

 
 

jeannegibbs

Give a Hug

Jun 1, 2011

Statistics can be a little misleading. Is it really that caregivers have dementia more often than noncaregivers, or could it be that caregivers get DIAGNOSED with dementia more often. Many people have had dementia several years by the time it is officially diagnosed. It may have taken 5 years to conclude that Pop has dementia. Mom has been taking care of him. Her children now know what to look for, what to suspect, and how to proceed. What are the chances that Mom will go 5 years with dementia before being diagnosed? I would say very, very small. The difference in the rate of diagnosis can make a big difference in the statistical picture. I don't think that fully explains the differences -- stress and isolation have got to be way up there also. And the advice for us caregivers to take care of ourselves is spot on.

I'm just not too panicked about catching dementia from my husband.

 
 

PCVS

Give a Hug

Jun 2, 2011

JeanneGibbs makes a very good point. On the other hand, if the assertion is valid it might mean that there is a viral component to at least some forms of dementia after all.

On the third hand, isolation, poor nutrition, exhaustion and so forth can lead to lower functioning and this in itself can make people susceptible to all manner of illnesses. That said, no matter how bad it's been, I keep allocating the better part of the grocery budget to healthy foods, so at least I've been ahead there.

On the fourth hand, I think there are two books every caregiver should be provided with: First is "The Power." Second is "36 Hour Day."

 
 

There is also the heredity and genetic factor. The risks of developing dementia are higher if someone in your family has it, I believe. My mom had it and her brother had it and my great aunt had it. This most likely leaves me more vulnerable to it. It scares me but what can I do? I took care of my mom for over 5 years and have other risk factors including depressing and stress.

 
  •  Comments 1 to 10 of 15 

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