What Caregivers Can Expect as the Disease Progresses
| What Caregivers Can Do to Decrease Stress
| What Can Be Done to Reduce Caregiver Burden
There are millions of Americans who have
Alzheimer’s disease. And with this, there are the millions who are unpaid caregivers for a person with Alzheimer’s or another form of
dementia. The health and emotional stability of people who care for Alzheimer’s patients directly affects the patients themselves, and thus should be an important part of the patients’ care plans.
What Caregivers Can Expect as the Disease Progresses
- A decline in logical thinking and judgment
- Inappropriate social behaviors
- Confusion and disorientation
- Rummaging and hiding objects
- Aggressiveness, anger, and frustration
- Night wakefulness
- Refusal to eat
What Caregivers Can Do to Decrease Stress
- Recognize common precursors to wandering, such as restlessness and disorientation.
- Reassure and reorient the person.
- Reduce noise levels and confusion.
- Involve the person in productive daily activities and exercise.
- Have a written plan for yourself if the person does wander.
- Keep a recent photograph of the person to give to police if the person does wander.
- Inform the police and your neighbors of the person’s tendency to wander.
- Have the person wear bright, distinctive clothing.
Protect your valuables, and hide dangerous or toxic products from the person. Take some time to:
- Lock cabinets and specific rooms.
- Store valuables and unsafe substances out of reach of the person.
- Learn where the person tends to hide objects.
You can also create diversions. Try these tips:
- Use a basket of towels or laundry. They may repeat folding the items in the basket for a period of time.
- Give them a box of mixed objects to sort out, such as screws, bolts, or beads.
- Create a special place, such as a chest of drawers, a box, or chest.
Talk to the doctor about adjusting medication if behavior does not improve.
- Identify the immediate cause, if possible.
- Do not take the person’s belligerence personally.
- Reassure the person.
- Do not confront the person about their behavior, it may be beyond his control.
- Avoid using restraint. This may further frustrate the person.
- If needed, step back and stand away from the person. Give the person a safe space to let their anger play out.
- Try a relaxing activity, such as having the person listen to soothing music.
- Look for patterns in potential anger triggers.
- Don’t argue with the person about whether or not what they are talking about is real.
- Increase lighting so there are less shadows.
- Remove mirrors.
- Stay calm. If safe to do so, provide reassuring words and a comforting touch.
- Limit intake of caffeine.
- Increase physical activity during the day.
- Limit naps.
- Establish a nighttime routine, including calming elements, such as a bath and a warm drink, such as milk.
- Keep a nightlight on.
- Provide the person with a number of small meals throughout the day rather than a few large meals.
- Make the person’s favorite food.
- Provide finger food.
- Provide soft foods that don’t require chewing.
- Remove distractions during mealtimes.
- Have a different caregiver help the person with eating.
What Can Be Done to Reduce Caregiver Burden
The daily routine of caring for a chronically ill person can put tremendous physical and emotional strain on caregivers, particularly for families who have assumed care responsibilities more recently. Here are some tips on coping with the stress that may come with caring for someone with Alzheimer's:
- Know that there is help available. You are not alone. Adult day care, in-home assistance, visiting nurses, and Meals-on-Wheels are some services that may be helpful.
- It is okay to ask for help from family and friends. Also consider joining support groups or an online community.
- Take care of yourself. Be mindful of what you eat, get plenty of exercise, and get enough rest.
- Squeeze in some personal time. Stroll around the mall, have lunch with friends, or just take a nice walk.
- Manage your stress level.
- Do not be hard on yourself or the situation.
Accept changes that may come with meeting the needs of someone with Alzheimer's. Sometimes care beyond what you can provide is needed. This includes in-home caregiver services and residential care.
- Get your legal and financial planning in order. Talk with an attorney about legal, financial, and care issues.
The importance of easing the mental and physical burdens of those who care for Alzheimer’s patients cannot be underestimated, as the health of Alzheimer’s patients is closely related to the health of their caregivers. But your health is important too. So be sure to take care of yourself as you care for others.
2013 Alzheimer’s disease facts and figures. Alzheimer’s Association website. Available at: http://www.alz.org/downloads/facts_figures_2013.pdf. Published 2013. Accessed June 17, 2013.
Alzheimer's caregiving tips: Rummaging and hiding things. National Institute on Aging website. Available at: http://www.nia.nih.gov/sites/default/files/Alzheimers_Caregiving_Tips_Rummaging_and_Hiding_Things.pdf. Accessed June 17, 2013.
Caregiver center. Alzheimer’s Association website. Available at: http://www.alz.org/living_with_alzheimers_caring_for_alzheimers.asp. Accessed June 17, 2013.
Gaugler JE, Kane RL, Kane RA, Clay T, Newcomer RC. The effects of duration of caregiving on institutionalization.
Gonyea JG, O'Connor MK, Boyle PA. Project CARE: a randomized controlled trial of a behavioral intervention group for Alzheimer's disease caregivers.
Last reviewed June 2013 by Michael Woods, MD
Please be aware that this information is provided to supplement the care provided by your physician. It is neither intended nor implied to be a substitute for professional medical advice. CALL YOUR HEALTHCARE PROVIDER IMMEDIATELY IF YOU THINK YOU MAY HAVE A MEDICAL EMERGENCY. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with any questions you may have regarding a medical condition.
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