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ALZHEIMER'S
| ARTHRITIS | CANCER
| DIABETES
HEART DISEASE | OSTEOPOROSIS
NEWS
Alzheimer's Disease at Age-Matters
Thanks to Beth Creason at about.com
The Seven Stages of Alzheimer's Symptoms
Do you
know what to expect during the course of Alzheimer's disease? There are
seven stages that describe each phase of this debilitating disease. Not
everyone who has AD will have all of these symptoms, nor will they
necessarily have the symptoms in the order I have listed, but, by using
this guide, you can get an idea of the progressive decline of the
patient's cognitive functions.
Alzheimer's
disease usually lasts from three to 20 years. During this time,
cognitive function steadily decreases. In many cases, patients do not
die of Alzheimer's itself, but other complications, such as pneumonia,
heart failure or infections.
Let's
examine the seven stages:
-
Stage
One: There are no symptoms at all. The patient has no memory
impairment nor does he have any visible signs of other cognitive
decline.
-
Stage
Two: The patient will notice some mild memory loss. He or she
will usually start by misplacing objects or forgetting names that
are well known to them. He or she may wonder about the memory loss,
but will usually blame it on aging.
-
Stage
Three: The victim will notice an increase in memory impairment.
They may make a trip to the store and forget how to get back home.
Their work performance may suffer because the patient may forget
important details while working on a project. They may start trying
to think of what a particular object is called, and the frequency of
forgetting names of people they should know well will probably
increase. Reading may become a problem, as the patient cannot
remember what he or she has just read. At this point, the patient
may lose or misplace something valuable, not remembering where they
put it. Concentration will become very difficult. Most victims will
go into denial during this stage, and will tend to have problems
with anxiety.
-
Stage
Four: In this stage, some long term memory loss will be seen.
When asked about news headlines or current events, they may have
difficulty in recalling what is happening. Travel becomes difficult
because of the anxiety it causes. The person may not be able to
handle their finances any longer because of confusion. The victim
will usually start to withdraw from anything that presents a
challenge. Denial is still prominent.
-
Stage
Five: The patient now has to have assistance with some
activities of daily living. They usually need help in selecting the
clothes they wear, as during this stage they tend to dress
inappropriately. They can still feed themselves and use the restroom
without assistance. They may have trouble remembering some family
members names, especially grandchildren or siblings, but can usually
tell you their own names or the names of their spouse or children.
They have trouble recalling such things as their address, or phone
number.
-
Stage
Six: The victim may now start forgetting the name of their
spouse or children. They usually cannot recall any recent events in
their lives. They may be able to recall things that have happened in
the past, but cannot go into detail about the events. They are
disoriented to time and place. When asked to count from ten, they
will usually not be able to do this. They may even have difficulty
in counting from one to ten. They may become incontinent, and will
require help with most activities of daily living, such as bathing,
toileting, dressing and sometimes eating. Delusions and paranoia may
be a problem. They may start having some difficult behavior
problems. Anxiety, agitation or violent behavior may occur.
-
Stage
Seven: Most communication skills are lost. Speech is
non-existent. The patient is incontinent. They will need help with
feeding and toileting. They will become unable to walk or control
other motor functions. During this stage, the person usually becomes
bedfast.
It's been
my experience that many patients will stay in stage five or six for a
long period of time. Some patients that I met several years ago that
were in these stages are still in the same stage. Not every
patient is the same, so the stages and length of time in each stage will
vary.
You can
help the patient by showing him or her a lot of love and patience.
Learning the different stages and knowing what to expect, will help you,
the caregiver.
BACK TO TOP
Behaviour of Alzheimer's Patients
Alzheimer's patients display a
variety of behaviours during the course of their disease. Find out what
they are and some methods of coping with each behavioural pattern.
Depression
Depression is a common problem with Alzheimer's patients, especially
when first diagnosed. Find out the symptoms of depression, some possible
causes and some of the strategies for coping.
Eating
and Feeding
Eating and/or feeding problems can become a difficult behaviour.
Sometimes the patient wants to overeat, and we also have the patients
who won't eat enough. Find out how to handle this.
Hallucinations
Find out some of the probable causes of hallucinations in Alzheimer's
victims, and read how you should handle this behaviour.
Hoarding
Read all about the hoarding behaviour. Find out why Alzheimer's patients
do this, and read some suggestions to help cope with hoarding.
Inappropriate
Sexual Behaviour
Alzheimer's patients sometimes display sexual behaviours that are
undesirable, but these behaviours are usually not sexual in nature at
all. Read about the reasons why they do this.
Incontinence
Incontinence is a problem usually in the middle and later stages of
Alzheimer's disease. Find out ways to help your loved one with this
behaviour.
Problems
with Bathing
For some carers, bath time can be a nightmare. Find out why your loved
ones act the way they do when it becomes time to bathe. Also find out
how to handle this difficult behaviour!
Repetitive
Actions
Repetitive actions are one of the most frustrating behavioural patterns
that carers must deal with. Learn some of the causes of this behaviour
and some coping strategies.
Sleeplessness
Find out some of the possible reasons why your Alzheimer's patient may
not be getting a good night's sleep, and read some suggestions to help
them
BACK TO TOP
DEPRESSION - The Causes and
what to try
Unfortunately, depression is a common
behaviour in Alzheimer's patients - especially in the early stages of
the disease. As always, there are several reasons why Alzheimer's
patients develop depression, but there are some coping strategies to
help lift the patient out of his or her depression. Let's explore both,
plus the symptoms of depression.
- Restlessness
- Feelings of hopelessness
- Suicidal thoughts
- Difficulty concentrating
- Withdrawing from peers
- Lack of interest or pleasure in activities
- Interruption of sleeping patterns
- Change in appetite
- Lack of energy
- Extreme fatigue
The Causes of Depression
- Depression may be caused from finding out the diagnosis of
Alzheimer's disease. This would be devastating to anyone.
- Knowing that one is losing physical and mental abilities could
cause depression as well as anxiety.
- If the patient has to move out of his or her home and give up
their possessions because of declining mental abilities, this
could set off depression.
- A change in surroundings.
- Not feeling useful or productive.
- Changes in brain chemistry.
- Some medications may cause depression.
What can YOU do?
- In the early stages of the disease, support groups, education
about the disease, and even therapy can help the victim deal with
his or her diagnosis.
- The carer also needs to keep reassuring the patient in the early
stages that they can still have some control over their lives by
participating in decisions made for their future.
- Medication may help the person suffering from depression brought
on by Alzheimer's.
- Make sure the victim knows you are always there to listen if he
or she wants to talk about their feelings.
- Avoid giving them false hope. It's better to face reality in the
situation.
- Encourage exercise and social interactions. If the patient feels
uncomfortable being with crowds, though, don't force them to
participate. You may choose to have friends and relatives visit on
a one-to-one basis.
- Discourage the use of alcohol, which may make the patient feel
"better" for a while. After the euphoria wears off, it
can trigger feelings of depression.
These are just a few things you can do to help the Alzheimer's
patient get over the depression they are suffering. In our opinion,
though, the main thing is to show them a lot of love and compassion,
and always let them know you are there for them.
BACK TO TOP
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TO BEHAVIOUR
EATING AND FEEDING PROBLEMS
Eating is a big problem for carers of Alzheimer's patients.
Sometimes the patient wants to eat constantly, which is not healthy.
You don't want them to gain too much weight, thereby creating other
health related problems. On the other end of the spectrum, you have
the patient who refuses to eat anything! So - why do these behaviours
occur, and what can you do about it?
First of all, let's look at why the patient wants to eat all of the
time.
There could be several different reasons why the Alzheimer's
patient displays the behaviour of over-eating. Some of them include:
- The Alzheimer's victim's brain does not function as it once did.
The person usually loses the ability to think logically and
rationally. They may not have the capacity to realise that they
are not really hungry.
- Emotional factors could cause the patient to over-eat. Food may
perhaps make them feel more secure, less anxious or in control.
- Side effects of some medications may cause the victim to feel
hungry most of the time.
- The patient could just be bored and find nothing to do except
eating.
- Depression could be a factor in the desire to eat all the time.
People with the problem of depression will usually display a
change in eating habits.
- Memory loss could also be a possible cause of this behaviour.
The patient may not remember that he or she just ate.
Here are some tips and possible solutions to help with the
over-eating behaviour:
- Instead of giving the patient three meals a day, offer him or
her five or six small meals a day.
- Keep a variety of low calorie snacks available, such as apples,
celery or carrots.
- Try to get the patient to go for a walk or engage in an activity
in order to take his or her mind off food.
- In extreme cases, you may have to lock foods up in your
cupboards, especially if the patient is overweight or on a special
diet.
Now, we'll take a look at some of the reasons why an Alzheimer's
patient won't eat, and some possible solutions for that
behaviour.
We've examined the problem of constant eating. Now let's look at
the problem of not eating enough. There are many factors why a person
with Alzheimer's disease won't eat. You will find a list of them
below.
Dental problems that may make eating painful, such as ill fitting
dentures, sores in the mouth or an infected tooth.
Anxiety or confusion can cause an Alzheimer's patient not to eat.
If they are anxious or nervous, you may have a hard time getting
them to sit still long enough to eat.
Vision problems may cause the patient to not want to eat. They
possibly may not be able to see the food clearly, therefore they
cannot recognise what it is.
Some medications such as anti-depressants may play a part in this
behaviour. Decreased appetite is a common side effect of the
anti-depressants.
Memory loss is a key factor in this behaviour. The victim may have
forgotten how to use the eating utensils, or he or she may have
forgotten that they have to eat in order to stay healthy.
Your loved ones could be suffering from agnosia. This occurs when
the brain is not able to process what the eye is seeing.
Now let's look at some possible solutions to this problem:
If you suspect a dental problem, make a dental appointment as soon
as possible.
Try keeping the atmosphere as calm as possible at mealtimes for
the Alzheimer's patient. Try to curb any loud noises or other
distractions before sitting the patient down to eat.
If you think the patient's medication could be the reason they are
not eating, try to discuss this with your doctor as soon as you can.
If the patient has vision problems, try urging them to wear their
glasses - especially at mealtime.
When memory loss is to blame, see if the patient will mimic you as
you go through the actions of eating (picking up your fork and
putting it to your mouth). If the patient does mimic you, he
or she may continue to eat once they taste the food. You may have to
repeat this process at each mealtime.
Try serving the patient finger foods. Sometimes this is easier for
them and they will be more apt to eat.
You might try serving just one food at a time, so as not to cause
any confusion for the victim. They may not feel so overwhelmed with
just one item at a time on their plate.
Give the patient as much time as needed to finish their meal.
Don't try to rush them, as this may only agitate them more.
Alternate the food with beverages to keep the throat from becoming
dry.
You may have to demonstrate chewing motions to the victim so that
they may mimic you.
Now that we have looked at the problems the carer could encounter
during mealtime, let's go on to examine the problems one may come up
against if the patient is in the stages in which they must be fed.
In later stages of Alzheimer's disease, some patients have
trouble chewing or swallowing. They may forget to chew at all and
swallow their food whole. They could have lost muscle control or
co-ordination. This could cause them to choke. Another common symptom
of the later stages of Alzheimer's is drooling, which is most likely
caused from weak muscles, medications or food being held in the mouth
and not swallowed.
Below are some suggestions to help with eating and feeding problems
in the later stages of Alzheimer's.
Make sure dentures fit properly.
Feed the patient foods that require little or no chewing. Some of
these would be soup, cottage cheese, mashed potatoes, applesauce,
scrambled eggs, pudding, yoghurt and milk shakes.
Sometimes the Alzheimer's patient will lose sensation in their
mouth. Gently move their chin to remind them to chew. Lightly stroke
their throat to remind them to swallow.
Try to serve the same texture foods during meals. You wouldn't
want to serve foods like milk and cereal because the milk is liquid
and the cereal is solid. The patient may get confused and not know
whether to chew or to swallow.
Make sure the patient is sitting up straight in his or her chair.
When they get ready to swallow their food, remind them to tuck their
chin (leaning head forward and tucking the chin down to the chest),
as this aids in the swallowing process.
For patients who are bedridden, try to make sure they are sitting
up as vertical as possible to prevent choking. Make sure you use
some type of covering to prevent spills on clothing or bedclothes.
Use an oversized spoon filled about half full of food. If you apply
slight pressure to the lower lip, the patient will usually be
prompted to open his or her mouth. For patients that tend to hold
food in their mouth, slight pressure with the spoon in the middle of
the tongue will usually promote a swallowing response. You should
also verbally prompt them to swallow.
You should learn the Heimlich manoeuvre in case of choking. If the
person can talk, cough or breathe, do not use this manoeuvre - if
they cannot do this, then you must help!
You may have to include nutritive supplements in your loved one's
diet if they still aren't eating, as they should. Most of the time,
even if the patient won't eat, you can usually get them to
drink liquids.
Make sure you do not use straws in liquids if the patient has a
swallowing problem. This can cause them to aspirate (liquid going
into the lungs) because the liquid goes into their mouth much faster
than if they were drinking out of a glass. Aspiration can easily
lead to pneumonia.
Your physician may be able to schedule a test that will tell if
your loved one has a swallowing problem (also called dysphasia).
Sometimes the patient may even have to have a thickener put in their
liquids if they are at high risk.
We hope some of these suggestions have helped you learn more about
eating and feeding problems
BACK TO TOP
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TO BEHAVIOUR
HALLUCINATIONS
Hallucinations are one of the many, many behaviours that
Alzheimer's victims display. Hallucinations are perceptions of things
such as, smells, sounds, physical sensations, tastes or visual objects
that are not really there. One lady would often smell bacon frying and
another who would see a bear lying beside her bed. Hallucination such
as seeing the bear can be terrifying to people with Alzheimer's
disease. This can cause them to become agitated or afraid to go to
sleep.
If your loved one starts experiencing hallucinations, it might be a
good idea to make a doctor's appointment. Often there are physical
factors that will contribute to the hallucinations, such as, bladder
or kidney infections, dehydration, side effects of medications or
intense pain.
Stay calm. Trying to convince the person that there is not really
anything there will only add to their agitation and confusion.
Gently reassure the patient that you are there to help. Hold their
hand and let them know that you'll protect them.
Try distracting the patient by suggesting a walk or perhaps a
snack or meal.
Sometimes washing the patient's face with cold wash cloth will
help get rid of the hallucinations.
Be honest with the patient. If they ask you if you see or hear a
particular thing, explain to the person that you know to them
the hallucination is very real, but that you do not see or hear what
they do.
Be aware that some of their hallucinations are often from past
experiences that they have been afraid of.
If none of these strategies work, consult with the physician about
prescribing medication for the patient.
The main thing to remember, as always, is to give your patient a
lot of love and support. Try to convince them that you will always be
there for them, so they don't have to be scared.
BACK TO TOP
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TO BEHAVIOUR
HOARDING
Sometimes in Alzheimer's patients you will see this hoarding
behaviour. Why they do this is not really known, but below you will
find some possible reasons for the behaviour.
The patient may be acting out their fears. They may be afraid (in
their minds) that if they don't take these things, then they won't
have them later on when they need them. Even if the item seems like
something that would never be of any use to us, they may feel they
will need it one day.
Memory loss can play a big part in why the patient hoards things.
They may pick it up, but then not remember where they put it or even
remember taking it to begin with!
Alzheimer's patients may take things and hoard them because it
makes them feel secure. The old saying, "The more the
better" applies here.
The most obvious reason the patient hoards things is because of
decreasing brain function. The patient doesn't realise that taking
things that are not theirs is wrong, so if they see something they
want, they take it and hoard it away.
Lock any money or valuables, such as jewellery, up in a safe place
away from the patient. Most Alzheimer's patients don't realise the
value of the items they collect, and may throw them away when they
are done with them.
Make sure you check your wastebaskets before getting rid of the
contents.
Some common hiding places are under cushions, in drawers, under
beds or in wardrobes.
Once you find a hiding place, be sure to check it periodically.
Hoarders will often use the same spot.
Get extras of anything you can, such as car keys, eyeglasses and
hearing aid batteries.
Lock up some of the rooms of the house so that the hoarder will
have fewer places to hide things and you will have a secure area.
Make up some "fake" purses or containers filled with
items that it is all right for the Alzheimer's person to keep and
hoard.
Display items that can be safely picked up by the patient, such as
a rack filled with hats or old junk jewellery.
Don't "take" things from the patient that they have
hoarded - offer to trade them for something else.
Remember - keep reminding yourself that the person with Alzheimer's
is not a thief and is not stealing from you. To them, anything lying
around is fair game. Taking the necessary precautions and keeping calm
about the behaviour is the answer to the problem.
BACK TO TOP
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TO BEHAVIOUR
INAPPROPRIATE
SEXUAL BEHAVIOUR
Sexual feelings and expression are a normal part of life. Although
some people with Alzheimer's or dementia lose interest in sex early in
the course of the disease, others may express more interest or make
advances toward people they believe are part of their past.
Many times Alzheimer's patients may engage in inappropriate sexual
behaviour. Such behaviours are usually not motivated by sexual desire,
but by an internal or external cue. For example, a woman may take off
her blouse because she is too hot, or a man may remove his pants
because he needs to use the toilet. Some of the more common
inappropriate sexual behaviours include:
- Undressing in public
- Inappropriate touching of oneself
- Inappropriate touching of others
- Making inappropriate remarks to others
- Masturbation
Regardless of why Alzheimer's or dementia patients act out these
sexual behaviours, do not get angry or laugh. It is embarrassing, but
it is also one of the difficult behaviours that is likely to happen at
some time or another. The best way to handle undressing issues it is
to quietly tell the patient that the behaviour is not appropriate and
lead them to the bathroom or out of public view.
Many times, undressing or touching oneself is not meant to be
sexually expressive. This could be an attempt at communicating a
certain need. Some of these needs could be uncomfortable clothing,
skin irritation, being too hot or undiagnosed medical problems, such
as urinary tract infections, intestinal obstructions, gynecological
problems caused by yeast infection or itching caused by the lack of
oestrogen.
If inappropriate touching of others is an issue, this could mean
the patient needs more affection. Try to increase the amount of
attention you give him or her. Hold their hand, give them a hug, or
reach out and pat their arm occasionally. They may also just need
reassurance of the carers presence, or it could even be that the
patient has trouble seeing clearly, and doesn't realise they are
touching places they shouldn't be.
Sometimes a person with Alzheimer's disease or dementia will
mistake someone for a spouse. This could lead to making inappropriate
remarks to others. Try to point out that the person is not their
spouse, and that their remarks are undesirable. This may be something
you will have to do time after time. Memory loss is a major part of
Alzheimer's, and the person may not remember from one time to the next
what you have told them.
Masturbation is usually not a response to sexual desire. Men and
women who masturbate may be looking for the good feelings it brings or
could be using it as a way of relieving frustrations. They don't
realise why they are doing it - they only realise that it makes
them feel better.
The main thing to remember is that the Alzheimer's or dementia
patient is not trying to intentionally embarrass you or make anyone
feel uncomfortable. Most of these inappropriate sexual behaviours have
nothing to do with real sexual feelings. The victim just needs your
patience and sensitivity, and most of all, they need to feel secure
and loved.
BACK TO TOP
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TO BEHAVIOUR
INCONTINENCE
Incontinence is not frequently talked about for some reason.
Perhaps people find it "embarrassing" or
"degrading", and that shouldn't be the case. It's a very
real problem that is no worse than any other behaviour exhibited by
the Alzheimer's victim. When urinary and faecal incontinence happens
to a person with Alzheimer's disease, there can be several reasons why
it is occurring. The main thing to keep in mind is, that for the most
part, the patient does not want to be incontinent any more than you want
them to be incontinent. Below you will find out some of the reasons
why a person could be incontinent, and then learn some tips on how to
prevent it.
Emotional stress. Is the patient anxious or upset about something?
Some medications, such as diuretics, tranquillisers or sedatives.
Beverages with a diuretic effect, such as coffee, tea or cola.
Inability to reach the toilet due to disorientation or physical
limitations.
With the nature of Alzheimer's, the patient could possibly just
forget some of their body signals, such as the urge to urinate or
they could forget where the bathroom is or what it is used for.
A kidney or bladder infection.
Bowel and bladder training. Make sure the patient goes to the
bathroom at regular intervals. The most favourable times are after
meals, before bedtime, upon rising from bed and every two hours
while awake.
Put a sign or picture on the bathroom door so that the patient
will know where that room is and what it is for. Leaving a light on
at night also helps.
Limit liquid intake in the evening. This only applies in certain
instances. If your patient gets plenty of liquids during the day
then it is all right to do this. However if you have problems
getting your patient to drink, then please do not with-hold liquids,
patients become dehydrated easily.
Have the patient wear clothing that is easy to remove such as,
sweat pants or slacks with elastic in the waist.
Watch for signs that your loved one may want to go to the
bathroom, such as a grimace or touching of the groin area.
Eliminate caffeine in the patient's diet. Caffeine has a diuretic
effect.
Be sure to praise or reward your loved one when they do use
the toilet. If they do happen to have an accident, make sure to clean
them up right away. Urine and faecal matter can cause infections,
pressure sores and odour. Wash and dry the patient thoroughly and
apply powder or ointment and a fresh pad if necessary. You have a much
happier patient when they are dry and comfortable!
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TO BEHAVIOUR
PROBLEMS
WITH BATHING
For some carers, bath time is a nightmare. Many times, Alzheimer's
patients are frightened or resistant when it comes to taking a bath.
There are many reasons why the patient may not want to take a bath.
We'll examine some of those reasons below and also look at some
suggestions to make bath time a more pleasant experience.
Depression could cause the patient to lose interest in personal
hygiene.
Physical illness could also cause the patient to lose interest in
personal hygiene.
If the hypothalamus region of the brain (the body's 'internal
thermostat' regulator), is damaged from Alzheimer's disease, this
could cause a changed sense of perception of hot and cold water
temperature.
Brain damage could also cause a different sensation of water.
Poor lighting and poor eyesight could play a role in not wanting
to bathe.
Not being able to find the bathroom.
Lack of privacy.
Room temperature too cold.
Water too deep.
Water too hot or cold.
Fear of falling.
Fear of water or of being hurt by it.
A disruption in the daily routine of the patient.
Unfamiliar carers, especially if home health workers come into the
home to help with bathing, etc.
The reason for taking a bath is forgotten.
Humiliation of being reminded to take a bath.
Agitated before starting the bath.
Feeling of being rushed by the carer.
Feeling embarrassed about being naked in front of another person.
Fatigue.
Fear of hair washing.
Patient kept waiting too long while caregiver prepares bath.
Fear of soap, wash flannel, running water, etc.
In "the good old days", most people did not bathe and
change their clothes as often as we do today. Taking a bath once a
week may have been the way the person did things in his or her home,
so bathing more often may be a source of upset to them.
Now we'll look at some suggestions on how to make bath time easier
for the patient and the carer.
PROBLEMS WITH BATHING: Helpful Advice
- Try to figure out the best time of day for the patient's bath.
Try to stay with the person's old bathing routine before they
developed Alzheimer's disease.
- Figure out when the patient is most relaxed, and what type of
bathing they would prefer – bath, shower, stand up wash, etc.
- Make sure the bathroom is warm and inviting.
- Give the patient privacy. Pull down the blinds or close the
curtains and doors.
- Provide plenty of lighting in the bathroom, especially in the
evening.
- Try showing the patient bathing instructions written by a doctor
on a prescription pad, such as: "Bathe 2-3 times
weekly."
- Prepare the bath ahead of time. Make sure to check the water
level.
- Lay out the soap, flannel, towel and clean clothes in sequence
of use so that the patient won't have to wait.
- Use a calm, quiet tone when announcing that the patient's bath
is ready.
- Explain to the patient one step at a time what to do. Combine
visual cues if needed.
- If the patient refuses, don't argue with him or her to the point
of getting them agitated. Wait until the person is in a good mood
to try and get them in the bath.
- Let the patient feel the water before getting into the tub. This
may help calm the person.
- If bathing is a difficult task, don't try to get them in the
bath every day. A stand up wash daily and a full bath every week
may be all right.
- Offer a reward for taking a bath, such as a favourite snack or
activity.
- Try making the bath separate from the hair washing. It may make
the patient less anxious about bath time.
- Play soft music in the background to try and soothe and calm the
patient.
- Try giving the patient a flannel to hold for distraction while
bathing.
- Wrap a towel around the patient's shoulders to make them less
self-conscious about being undressed. It's very important to
respect the person's privacy and dignity.
- Avoid forcing or arguing with the patient about taking a bath.
This only causes further agitation.
- Avoid using a commode chair when giving a shower. This
encourages the patient to be incontinent when bathing.
- Allow the patient to do as much of the bathing as possible.
Bathing is a very personal and private activity. It makes many
people feel very embarrassed when someone sees them without clothes
on. When a carer has to help a patient take a bath, it makes the
person realise that they have lost their independence. It is
important to realise that these feelings may contribute to some of
the resistance to bathing.
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REPETITIVE ACTIONS
Many times, people with Alzheimer's disease or other types of
dementia develop a behaviour that involves repeating the same
questions or actions over and over again. This can be very annoying,
but it helps to try and remember that this person very possibly does
not remember asking that question just moments before. Here are some
possible causes of the repetitive actions, and also some coping
strategies that may help you, as the carer, be able to handle the
behaviour much better.
Physical changes in the brain from diseases such as Alzheimer's.
Memory loss from dementing diseases.
Side effects of medications. This is especially true for
repetitive motions.
Misinterpreting sounds or sights, thereby causing anxiety.
Separation from loved ones, causing constant questions such as,
"Where's my husband/wife?"
Not understanding what is happening around the patient, resulting
in questions like "What are you doing?"
Inability to express needs. For example, hunger may be expressed
in the form of repeating the question, "What's for lunch?"
Trying to express emotions, such as fear, anger or insecurity.
Distract the person with a favourite activity or a favourite
snack.
Respond to the emotion instead of the specific question. The
person may simply need reassurance.
Remind with simple, brief statements. Don't remind the person that
he or she has asked the question before, as this could be upsetting
to them.
Try a gentle touch when verbal response doesn't help. Sometimes a
hug or a gentle shoulder massage is more reassuring than words.
Use a calm voice when responding to repeated questions.
Use simple written reminders with patients who can still read. For
example, a large sign hung in their room that says, "We will
eat supper at 6:00 PM."
For the patients who no longer read, use pictures instead. For
example, a picture of a toilet may replace the word "bath
room" on the bathroom door.
Don't discuss plans with the person until just prior to an event,
because it may cause agitation and repeated questions.
Ignore the behaviour or question. If there is no response, the
behaviour may stop. This must be used carefully, though, because
sometimes the patient may become angry or frustrated if the carer
does not answer them.
Use memory aids. Sometimes signs, large numeral clocks and
calendars will help orient some people.
Remove things that may cause repetitive questions. For example, a
coat stand with coats on it may cause the patient to ask, "Is
it time to go now?"
For repetitive movements such as rubbing hands together or tapping
hands on the table, occupy the person with some sort of activity, a
doll or a stuffed animal may be useful.
Have the patient's medications checked by a physician, because
sometimes certain medicine will produce repetitive action behaviour.
Remind yourself that the person with dementia does not have the
ability to remember because of changes in the brain. It is sometimes
helpful to keep a log or diary to help determine the causes of
repetitive actions. Does the action occur at a certain time of day?
Could the person be hungry, cold or hot? Keep track of when and what
events have occurred, and you may be able to stop the behaviour before
it starts.
Some repetitive behaviour, such as sticking the tongue in and out,
can be caused by too much of a sedating medication. If this type of
behaviour is occurring, you should be sure and tell your doctor.
Repetitive motions and questions can be one of the most frustrating
behaviours for carers. It will help to try and get away for a while.
Make a little time for yourself, and not only you, but also the
patient will benefit.
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SLEEPLESSNESS
Sleeplessness can have many different causes. A popular theory of
sleeplessness is that many older people don't seem to need as much
sleep as younger people do. This is not necessarily so when it comes
to people with Alzheimer's disease. Their sleep problems may be the
result of mental changes in which the portion of the brain that
controls sleep is damaged, or they could possibly be having dreams
that disturb them. A lack of exercise and taking naps during the day
could also be a cause of sleeplessness. First we'll explore the
reasons why the person may not be able to sleep, and then we will look
at some of the ways the carer may be able to help.
Sleeplessness could be a side effect of medication the person is
taking.
Medical conditions such as diabetes, alcoholism, heart disorders,
urinary tract infections and ulcers can all cause sleeplessness.
Arthritis pain, leg cramps and breathing difficulties can also
cause a person to not be able to sleep.
Depression may cause a person to wake up very early, for instance
at 2 AM. If they are using antidepressants, taking the dose at
bedtime may help.
Waking up in the middle of the night to use the bathroom can cause
sleep disturbances. This can be a frightening experience for people
who are confused.
Caffeine consumption during the day can cause sleeplessness.
If a person is hungry, this could be a cause of not being able to
sleep.
Disrupted sleep patterns due to progressive dementia. The ability
to sleep is said to deteriorate as the mental functions decline.
The patient could be too hot or too cold.
Sleeping too much during the day.
Not enough exercise.
Agitation from an upsetting situation, such as a bath or an
argument with the carer.
Find out some suggestions to help sleeplessness:
Make a doctor's appointment for your loved one to help identify
and treat any medical problems.
Treat pain with an analgesic, if approved by the physician.
Giving antidepressants at bedtime will help keep the patient from
being so sleepy during the day.
Have medications evaluated for side effects.
Determine whether the patient is too hot or too cold upon
awakening.
Provide plenty of lighting during the evening hours. Darkness or
shadows may contribute to agitation.
Be sure to keep a nightlight on during the night, so that the
patient can find the bathroom, if needed.
A commode or urinal next to the bed may be an option if the person
has trouble finding the bathroom.
Make sure the patient uses the bathroom before going to bed.
Make sure the bed is comfortable and familiar to the patient.
Try to maintain a set bedtime and waking routine.
Try bedrails on the bed. This may remind the person that they are
in bed. You will have to monitor this closely, though, because this
could lead to falls if the person tries to climb out of bed over the
rails.
Try to prevent daytime napping by getting the patient involved in
an activity.
Make sure the patient is getting adequate exercise.
Cut down on caffeine products such as coffee, tea, soft drinks and
chocolate. Eliminate ALL caffeine after 5 PM.
Make sure the patient is not hungry at night. Try offering them a
snack before going to bed. You might also try warm milk.
Avoid any upsetting activities, such as bathing, in the late
afternoon.
If the person refuses to sleep in their bed, let them sleep on the
couch on in a chair, if that is what they prefer to do.
Try softly playing, soothing music when they go to bed.
Keep in mind - drugs that induce sleep should only be used under a
doctor's supervision. Some patients that take sleeping pills become
more confused and anxious. Try all other methods before you consider
drugs.
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NEWS ON
ALZHEIMER'S DISEASE
Tuesday May 22 6:45 AM ET
Source Yahoo News
Japan Scientists Find Possible Alzheimer's
Cure
By Kazunori Takada
TOKYO (Reuters) - Japanese scientists have
discovered a substance that offers the best hope yet of a cure for
Alzheimer's disease (news
- web
sites), a researcher who headed the study said on Tuesday.
Alzheimer's, which causes dementia in patients
and is always fatal, is one of the most disturbing disorders among the
elderly, with one million patients in Japan and another four million in
the United States.
Ikuo Nishimoto, a professor of pharmacology and
neurosciences at Keio University in Tokyo, said his team has discovered
a protein, which the team has named humanin, that can stop the death of
brain cells that occurs in Alzheimer's patients.
But he also added that years of testing would
be needed to determine whether humanin, produced naturally by genes in
the rear part of the brain, can actually be used as a cure.
``The difference between what we have
discovered and what is currently used for treatment is that this
completely stops the death of brain cells,'' Nishimoto told Reuters in
an interview.
``This is the first step in completely curing
Alzheimer's disease.''
The discovery will be announced in a U.S.
science academy bulletin, ``Proceedings of the National Academy of
Sciences (news
- web
sites) of the United States of America,'' to be released later on
Tuesday.
Nishimoto said his team, which has only
conducted experiments in test tubes so far, will start testing the
substance in animals, and added that Keio University was currently
applying for a patent for humanin.
Alzheimer's disease has been in the spotlight
recently, after U.S. federal prosecutors charged a Japanese scientist
with stealing genetic material related to the disease and handing it
over to a Japanese government-funded research institute.
TESTS NEEDED
Nishimoto said that further testing will be
needed to determine whether humanin can actually cure Alzheimer's.
``Whether this can be used as a cure or not
will depend on the results of testing,'' he said, adding this process
could take as long as 15 years.
But Nishimoto said humanin has so far met all
the conditions required as the cure for the disease.
``Humanin has so far met the various required
conditions. For example, when you stop deaths of brain cells, it usually
causes cancer. But humanin does not have such side effects,'' he said.
Japan has positioned itself as one of the
leading nations in Alzheimer's research and many of its pharmaceutical
companies have launched major marketing campaigns for medications aimed
at slowing the early effects of the disease.
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