How to Preventing Back Injuries When Lifting Someone

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Protecting and ensuring the safety of elders is of prime importance for home caregivers. However, many don't stop to think about protecting themselves from injury. By protecting the caregivers, we also provide a safe and secure environment for such care. Preventing injuries, especially back and shoulder injuries (the most common), can be achieved through proper education and attention to body positioning when lifting, turning and transferring patients from one location to another.

Many caregivers taking care of parents or grandparents are simply not suited for such physical stress. With the physical demands of physically lifting, turning and transferring loved ones, injury is common. In fact, it is estimated that musculoskeletal injuries that occur as a result of lifting or moving patients affects nearly 52 percent of caregivers.

Most caregivers in home environments are in their 40s, and 50s. Keeping them, as well as their loved ones, safe and healthy is vital. Learning how to practice good body mechanics in all aspects of home care is essential in preventing injuries.

Common Injuries

One of the most common injuries suffered by caregivers in a home setting is back injuries. Other dangers include exposure to needle sticks when caring for someone with diabetes or someone who needs supervised injections, as well as blood-borne pathogens that may be contained in saliva, urine, and blood. In addition, exposure to contagious illnesses or diseases may also occur. Still, by far, the most prevalent injuries among caregivers are those that involve the back, neck and shoulder joints.

Diane Sewell, an Assistant Director of Nursing at a long-term care center with 30 years of geriatric care experience states, "Most of the causes of injuries to home caregivers are back injuries caused by improper body mechanics when it comes to lifting. If an elder is receiving physical therapy at a facility that is aware of a situation where a family member is going to be taking care of an elderly parent at home, they will often suggest that the caregiver join in a therapy session to learn how to correctly transfer the person in different care scenarios."

 
 

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DT

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Apr 16, 2011

My biggest problem is simply lack of Rest. You note that I do not say lack of Sleep - the need to be constantly alert does not make my sleep "restful". I do not think I have had a really decent night's sleep for the last 5 years, since mom started having difficulty getting around, at night she may have to get up and go to the bathroom, sometime she can't sleep herself and likes to get up and wander around, get a snack, drink of water, whatever. I always add that Invariably a suggestion is made that perhaps a relative can help to relieve me sometime, and I always have to answer No, there is no one. I can lie down at any tme day or night and fall asleep, and do, but that does not mean I can rest.

 
 

mrjess5

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Apr 16, 2011

Icare for my 86 year old mother and she has both Dementure & Alzihmers she was diagnoied 2 years ago and I too don't get the right amount of sleep. I put locks on the doors and I'm going to put a bell on both doors so that if she tries to go out the door , I set up a baby monitor so that I can also hear her. She goes to an adult day care while I go to work at the loc al high school for three hours. My neice and I are her only caregivers at this time and we are in a carehome program here in R.I. and the team comes in once a week for 8 wks. to see how things are going then it will be once a month and they get me her supplies if I need anything and they show a lot of support with what I' m going through. My mom used to be able to do income taxes for people and she used to be a private secutary now she's having a great deal of remebering who her granddaughter and I are at times.When she speaks its very hard to understand her ,her words come out all jumbled and it frustrates her,but I try to understand her. I'm making a speach board for her so that it will be a lettle easier for her to communicate with me. Dayle from R.I.

 
 

bobstitt1942

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Apr 16, 2011

Totally agree with the lack of sleep. It does not take too many nights to go completely bonkers.

My wife has a form of dementia and she cannot speak. Sometimes she understands me, sometimes she does not. I get her up once during the middle of the night to give her a pill. Some nights she sleeps through, other nights and even days she is pacing in the house or in the yard. When she first started pacing I called it "taking out the garbage", because she always ended up in the area where we kept the garbage and I was assuming she thought I forgot it.

She quit for about 6 months and now she is back to doing it again. Here are some of the things I have done.
We moved out of the bedroom, she sleeps on the couch and I sleep in my recliner, which is surprisingly comfortable.
I have the TV programmed for 3 days ahead to her favorite shows. Our TV is old and I assume you can do this much easier with newer TVs. I start the programming at 2:00 am because usually this is about the time she gets restless.

When she wakes up I help her into the bathroom and then ask her if she wants to go back to sleep or watch TV for awhile. If she wants to watch TV I turn it on and it goes to one of her favorite shows and I set the sleep button to an hour or two.

Sometimes it helps.

If I feel restless, I just take a melatonin table and read a book until I fall back to sleep. If she paces, I have gotten to the point where I can just ignore her.

Another thing that helps is my daughter has moved back home with us and is here at times so I can completely fall asleep at times and not worry about her.

When I get adequate sleep I feel like I can cope with anything. If I cannot, that's when I start thinking about my shack in the deep woods where the only one I have to worry about is myself.

 
 

quakerite

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Apr 17, 2011

As a registered nurse, I thought I had it covered when I moved my 93-yr-old aunt in with me. I quickly discovered I didn't know anything either about her condition or about the changes I would have to make. I had to quit my job because my aunt can't be left alone and the adult day care where she goes doesn't open till 8. The stress got to where I began having severe dizzy spells and sky-high blood pressure. Plus, I didn't know how to manage someone with dementia. I began attending workshops, reaching out to counselors at her day care, talking to the nurses there - that was huge!They made me see that to provide care for my aunt, I would have to be in great shape. I went to a massage therapist who does crano-sacral adjustment - that was immediate relief! I got back into meditation and yoga. The day care hired me pt - it's way less than I made before, but it works a lot better for me and my aunt. And recently I added a zumba class twice weekly; my aunt goes with me once a week and the participants fuss over her, make her comfortable, and just love her (which of course she loves!). On the second day I pay a CNA to sit with her. There is still stress, still adjustments (it's been over a year now), but we're managing. Every 2 months I put her in a short-term respite care for a week - that is good for both of us! I see stressed out family members everyday at the adult day care and when I tell them about resources, about destressing, they say they're too busy, too stressed. Trust me, taking care of yourself is the best and smartest thing you can do for your loved one.

 
 

lynatals

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Apr 18, 2011

Caring for an ailing loved one is not only physically demanding but often times emotionally draining as well. In situations were the loved one suffers from Dementia or Alzheimer's sleep deprivation is not uncommon.

Individuals who feel that this may be beneficial to them should contact their States Area on Aging. The phone numbers can usually be obtained through the States Department of Social Services.

Once a request is made to the Intake Department, a they will then contact the person and conduct an initial inquiry to see if they may qualify. If they do, a Case manger will then usually come out to the home to do a more in-depth assessment in order to determine the number of hours/days and type of care that they would recommend and be able to cover through their State's program

 
 

mrjess5

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Apr 18, 2011

Hi I'm Dayle from R.I. and i'm in a program where the nurse and case worker are coming out to check and see if I need help with my mom and the program is run dy the Stated of R.I. elderly affairs and they pay me for careing for my 86 year old mother who has both Alzhimers and Dementure it is a good company that I 'm with because they have compasion for the care giver and the patient. Everyone who cares for the elderly should look into this program. And yes mI am sleep deprived but I WILL NOT PUT MY MOM IN THE NURSING HOME!!!!!

 
 

DT

Give a Hug

Apr 20, 2011

mriess - Your determination to keep your mom out of a nursing home does you credit. I have a kind of agreement several years ago with my mother that if she has to go to a nursing home it will be her choice first, but I am now looking at the practical side of it. Our house is one of those small "picturesque" cottages built in 1938 and is simply not set up for dealing with an invalid without major reconstruction. When you consider hallways and doors that are too narrow for wheelchairs and only one bathroom that does not have room enough to turn a walker around, something alternative may have to be considered. I mean, unlike a lot of contributors my mom does not have dementia or alzheimers or anything like that but if I have to start carrying her around in the house, I simply cannot because I have physical problems if my own and she will have to be bedridden. As the end time approches we all are fearful of dieing alone in a strange and impersonal nursing home, but there seems to be fewer and fewer options ( I am already looking at the probability that I will) and she will become more and more reluctant to suggest it herself, and in her fear she does not really care or consider what the consequences are on me. Something is going to have to give sooner or later.

 
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