Solving Day to Day Problems


 
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Solving day-to-day problems

Communication

As Alzheimer's disease progresses, the patient may not understand clearly what is happening around them or what is wanted from them. This is a difficult problem for both the patient and caregiver. Some techniques that might help communication include:

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Daily grooming

On occasion your patient may refuse to bathe. The reason for this may be that the bathing has become too complicated to complete, or the patient becomes afraid of water. Vision problems also make it difficult to distinguish the shape of the tub or shower. The person may have forgotten how to operate the water control knobs or may no longer remember what to do with the soap and washcloth. As Alzheimer's disease progresses, coordination becomes affected and this adds to safety concerns.

Whatever the reasons, avoid discussing with your patient whether or not a bath is needed. Simply say that it is "bath time." This can work more effectively if you are adhering to established routines such as time and place for a bath.

Remember to remove the lock from the bathroom door and remove razors and electrical appliances (hair dryer, curling iron) from the cabinets. Here are a few tips that might help bath time go more smoothly:

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Dressing

Patients should be encouraged to continue to dress themselves as long as they are able. The past grooming habits of the patient should be considered. Routines often work the best in all daily activities.

Here are a few suggestions that might extend your patient's independence:

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Driving

When should the Alzheimer's patient stop driving? This question is more complex than it seems. The reason: Driving is a habitual skill, and many Alzheimer's patients can appear capable of driving competently well into the disease.

Nevertheless, some troubling questions remain. For example, could the patient react instantly in an emergency? Are reflexes and muscular coordination still good? Are eyesight and hearing unimpaired? Can decisions still be made quickly and accurately? If there is any doubt about the answer to any of these questions, then the risks of driving are probably too high.

Driving tends to be an emotional subject because it represents personal independence, so try to discuss the situation calmly with the patient. Possible reactions include relief, anger and stubbornness. Offer sympathy and understanding. The Alzheimer's patient will need to express these legitimate feelings of distress and loss. But, for safety's sake, you'll have to remain firm.

It may be hard for you to "lay down the law" to a spouse or parent. However, since a confused driver is a danger to everyone, you really have no choice. If the patient insists on having the car keys, you can disable the car by unscrewing the distributor cap. (Some caregivers solve the problem by parking the car away from the house for a while.)

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Mealtime

Meals can be the high point of an Alzheimer's patient's day. You can increase the enjoyment by establishing a regular routine, minimizing distractions, and serving dishes that take the patient's limitations into account. Here are some strategies that may help:

Other possible problems: Some Alzheimer's patients forget they've just eaten and ask for another meal. That's when your posted schedule will come in handy Don't argue-find a distraction instead. For example, tell your patient to complete an activity with you first. The activity will divert attention away from eating.

What about the patient who raids the refrigerator? You may have to lock it, especially if it contains foods forbidden for medical reasons. Or you may need to find another place to store certain foods-a small refrigerator in the basement, for example. Try to keep healthy snacks on hand to forestall indiscriminate munching.

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  Sleeping problems

Your Alzheimer's patient will probably experience changes in his or her sleeping patterns as the disease progresses. Restlessness and sleeplessness at night are common and can be stressful for the caregiver, as this can lead to the wandering behavior described later in this chapter. Some tips to minimize sleeping problems are:

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Social Interaction

Many patients, especially in the early stages of the disease, go through bouts of depression as they begin to realize that Alzheimer's disease is changing their personalities and their lives. Social interaction during these early stages can sometimes ward off depression and be stimulating. Do not force your patient to interact with others, but encourage him or her to be as socially active as possible. Encourage participation in a non-demanding task or job, or in simple activities that provided enjoyment in the past.

A recent development that provides structured social interaction is the support group designed specifically for Alzheimer's patients. These groups give patients a chance to talk to others who are going through the same types of changes and are experiencing the same emotions. They can be themselves without worrying about making a mistake and feeling foolish or out of place. The groups are not available in every community, but you should check with the local hospital, churches and adult day care centers, or perhaps consider starting one in your community.

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"Sundowning"

For unknown reasons, many Alzheimer's patients became restless and agitated in the early evening, around sundown. This is called "sundowning." Some suggestions to minimize these symptoms include:

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Toileting

Alzheimer's patients sometimes have difficulty getting to the bathroom in time. A physical exam will allow the doctor to determine if there is an underlying medical problem.

If there is no underlying medical problem, then the accidents are due to confusion caused by Alzheimer's disease. The patient may have trouble remembering what to do when the urge to urinate occurs. Some patients have trouble remembering where the bathroom is-or remembering in time to get there. The following can help:

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Wandering

Wandering is one behavior exhibited by an Alzheimer's patient that may be difficult to understand. The consequences of this behavior could be disastrous if the patient leaves a safe and secure area. However, wandering or pacing within a secure area will not harm anyone, and can even have a calming effect on some patients. If this activity is not harmful to the patient nor particularly bothersome for you, all that is necessary is a clear pathway in the home.  

If wandering becomes a concern and the patient's safety is in jeopardy, some means of prevention must be sought. The caregiver should observe the patient to determine whether the wandering seems aimless or has a purpose. Since Alzheimer's patients usually have difficulty communicating, it is not an easy task to discover the reason for the wandering. Try keeping a written diary for a few days to help uncover a reason for the wandering. Observing the patient will usually give some clues:

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Catastrophic behavior

As the disease progresses, changes occur in the brain and body. At times, Alzheimer's patients will become overwhelmed by confusion and will become extremely upset. Oftentimes, behavior problems occur in the evening. Perhaps dealing with a confusing and seemingly threatening environment all day has tired the patient, causing negative emotions to surface. The best way to stop catastrophic behavior before it happens is to try to determine the source of the problem. If your patient has a catastrophic reaction:

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