Gardening Tools

Wednesday, 10 June 2009

Dementia, Telling it to the kids

LifeWire) - When a grandparent or other loved one is diagnosed with Alzheimer's disease, it can be the children of the family who are most affected. Adults are capable of understanding the disease, its symptoms and what to expect. Parents and other relatives need to pass along this knowledge - in an age-appropriate way - to children who will be impacted by the disease.

Breaking the News

At any age, children can sense discord and stress in their environment, so it's important to address any concerns before kids make erroneous assumptions.

The conversation will differ depending on the child's age. For younger children, you don't necessarily need to use the term Alzheimer's disease. Instead, talk about how the child's loved one is sick, will have trouble remembering things and might sometimes be confused. Be sure to mention that their loved one will probably get sicker and that it's important for the family to help out. Depending on their level of understanding, try to prepare them for the changes they'll see in their loved one.

Teenagers, who are more capable of understanding the diagnosis, should hear more details, such as how long their loved one is expected to live and what treatment options are available. Talk to them before inviting a loved one to move in for full-time care. While parents might not always abide by teens' opinions, it's important that everyone's voice be heard.

Reassure children that Alzheimer's disease is not infectious. If the loved one was diagnosed before age 65, talk to older teens about the possibility that the disease is inherited. If early-onset Alzheimer's disease has affected several immediate relatives, the family might consider genetic testing for the disease.

Continue to talk to children and teens about the situation when the disease progresses to the point where their loved one no longer recognizes them. Acknowledge their feelings and assure them that their loved one still loves them and still appreciates their visits. Allow them to grieve this loss, and don't force them to continue visiting if they are truly uncomfortable.

Emotions and Reactions

Children can experience a variety of emotions relating to their loved one's condition, but they might not volunteer their feelings. In some cases, parents might need to anticipate these emotions and be proactive about initiating a conversation.

These emotions can include:

Fear that parents, other relatives or they themselves might be diagnosed with the disease
Anxiety, sadness or fear regarding changes in their loved one's behavior or personality
Frustration over having to say things many times or needing to repeatedly identify themselves
Remorse over acting frustrated or guilt about not having the disease themselves
Self-consciousness about being in public with their loved one or, if the loved one lives with the family, feeling ashamed of their living situation
Remember, kids and teenagers don't always express their emotions in the same ways that adults do. Instead of talking about their fears, worries and guilt, they might exhibit behavioral problems, be distracted from schoolwork, avoid interaction with the family and even complain about physical ailments. If this occurs, try having another conversation; if necessary, ask a trusted teacher, another adult or a school counselor to sit in on it.

Parenting Strategies

Offer continuous support to children while they cope with their loved one's disease. It's important to allow them to express themselves, to avoid judging their feelings and to answer all of their questions as honestly as possible. For more help, visit the Alzheimer's Association website for kids and teens.

It can also be helpful to engage the children in family-related activities, such as making a family tree or looking at old photographs. These activities can help children feel connected to their loved one.

Parents or guardians can also engage children in making a memory book for their loved one. Memory books, which have been shown to ease behavioral symptoms in people with Alzheimer's disease, usually consist of family photos and other memorabilia. The book can help a loved one with Alzheimer's disease reconnect with memories. Children can also write a letter or draw a picture for their loved one to be included in the book.

Sources:

Bourgeois, Michelle. "History of Memory Books." Department of Communication Disorders: Research Lab and Caregiver Resources. 2007. Florida State University. 23 May 2008 .

Callone, Patricia, Connie Kudlacek, Barbara C. Vasiloff, Janaan Manternach, and Roger A. Brumback. . A Caregiver's Guide to Alzheimer's Disease: 300 Tips for Making Life Easier. First. New York: Demos Medical Publishing, 2006.

"Helping Children Understand Alzheimer's Disease." Alzheimer's Care. Apr. 2007. Alzheimer's Society of Canada. 3 Jun 2008. .

"Talking to Teens and Kids." ALZ.org. 27 Oct. 2006. Alzheimer's Association. 3 Jun 2008. .

LifeWire, a part of The New York Times Company, provides original and syndicated online lifestyle content. Betsy Lee-Frye is an independent journalist living in Kansas City, Mo. Her work has appeared in The Dallas Morning News, Better Homes and Gardens Special Interest Publications and Kansas City Magazine.
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The Dementia Café, share experience, make new friends

The Dementia Café is a place to get advice, share experiences and make new friends.

It's aim is to build a community of carers and people with Dementia who can support one another through the most difficult situations when dealing the effects of dementia. If you have been diagnosed with dementia; are caring for someone with dementia; or are involved with any aspect of the illness, please register on the website and join the community.




Please click on the Message Board logo to be taken to The Dementia Café Message Boards page. Once registered, you'll be able to post messages, get replies, and join in the discussions.


Why not register and get involved ?



Message Boards





Please click on the Online Support logo to open the Online Support page.


Come and join in the discussions !

Early Indiactors, Dementia, Alzheimer's

Early symptoms
Every person is unique and dementia affects people differently - no two people will have symptoms that develop in exactly the same way. An individual's personality, general health and social situation are all important factors in determining the impact of dementia on him or her.

The most common early symptoms of dementia are:

Memory loss
Declining memory, especially short-term memory, is the most common early symptom of dementia. People with ordinary forgetfulness can still remember other facts associated with the thing they have forgotten. For example they may briefly forget their next-door neighbour's name but they still know the person they are talking to is their next-door neighbour. A person with dementia will not only forget their neighbour's name but also the context.

Difficulty performing familiar tasks
People with dementia often find it hard to complete everyday tasks that are so familiar we usually do not think about how to do them. A person with dementia may not know in what order to put clothes on or the steps for preparing a meal.


Problems with language
Occasionally everyone has trouble finding the right word but a person with dementia often forgets simple words or substitutes unusual words, making speech or writing hard to understand.

Disorientation to time and place
We sometimes forget the day of the week or where we are going but people with dementia can become lost in familiar places such as the road they live in, forget where they are or how they got there, and not know how to get back home. A person with dementia may also confuse night and day.

Poor or decreased judgement
People with dementia may dress inappropriately, wearing several layers of clothes on a warm day or very few on a cold day.


Problems with keeping track of things
A person with dementia may find it difficult to follow a conversation or keep up with paying their bills.

Misplacing things
Anyone can temporarily misplace his or her wallet or keys. A person with dementia may put things in unusual places such as an iron in the fridge or a wristwatch in the sugar bowl.

Changes in mood or behaviour
Everyone can become sad or moody from time to time. A person with dementia may become unusually emotional and experience rapid mood swings for no apparent reason. Alternatively a person with dementia may show less emotion than was usual previously.


Changes in personality
A person with dementia may seem different from his or her usual self in ways that are difficult to pinpoint. A person may become suspicious, irritable, depressed, apathetic or anxious and agitated especially in situations where memory problems are causing difficulties.

Loss of initiative
At times everyone can become tired of housework, business activities, or social obligations. However a person with dementia may become very passive, sitting in front of the television for hours, sleeping more than usual, or appear to lose interest in hobbies.

If you are experiencing any of these symptoms or are concerned about a friend or relative, visit your doctor and discuss your concerns.

Where next?
Diagnosis
Frequently Asked Questions
World Alzheimer's Day™ 2002 - Recognising dementia
About Alzheimer's disease

Tuesday, 9 June 2009

Alzheimer's, Dementia, Poetry, Please submit your

Poetry

Have a go at writing poetry yourselves if you've never done it, before opportunity knocks at diagnosis' door.
Please send us your poems at friends@alzheimersforum.org.
Barry has compiled a book of poems called Poetic Thoughts taken from Alzheimer's Forum and Alzheimer's Society websites about Alzheimer's and dementia. Have a look and read them at your leisure.
Latest poems
Left Alone, by Barry
My day started with harmony I was feeling on a highSince my body and mind had awakened seeing eye to eye,But my exultation within was not that long to remainAs I'd forgotted this day I was to be left alone again.
'Twas 7 in the morning as my darling gave me a kiss and a hugWith the dilemma in her eyes much clearer than the sky above,I'm not that far away she soothingly and withassurance expressed,Just keep a calm mind and don't let yourself get stressed.
As she walked out the door I locked it tight from behind,Switching on the alarms for some extra security of mind,If intruders should encroach to confuse my day even more,Then a piercing warning would echo through the solitudeof my air.
Thus my lonesome day slowly pursued its own path,I wandered from room to room with my inner fears noone to convey,But what if I should stumble? And now where is my lunch, I cried!Thought I'm sure you must have told me you had preparedit in advance.
Then disorientation seized me as the walls all started to close in,Is that my shadow on the wall? Or is it an evil spirit within?I was trying to conquer the hallucinations now castbefore my eyes,When all of a sudden scurrying commotions overhead did arise,Was it merely trickery inside my ears? Or maybe it's just a mouse!
So I tried watching the TV but it was to be of little avail,Since the voices and images to my mind had all become veiled,I sat at the computer to write down my inner fears of the day,Yet my eyes and fingers would not correspond in the same way,Yes, my early morning harmony lay around me shattered in affray.
Then as the evening moon finally took turn from the sinking sunMy wife at last returned, her day's hard labour had been done,She embraced me ever lovingly asking, 'Have you been ok?'I nodded with a smile and a Yes, it's been a very good day!But now it's even better that you're back in my arms,As we lay our heads together on pillows of soft silky downI quietly gave thanks to God that my lonely day was at an end.
Of Two Perspectives, by Barry
We live in our own world of delusions and fearsThat distraught our mind throughout days and nightsBut do we reflect about the one we most loveBe it our partner, husband or wife?They take upon their shoulders our continuous careWithout thoughts of themselves or their quality of life,Yet do we remember to give that loving embrace?Or do we cast criticisms, emotions and tears to their face,We should never forget the one we truly love so dear,Giving them space to cope with their own inner fears,Time to be alone with their own thoughts to dwell,Some solitude in peace from the turmoils of our hell,Yes the problem is complexity from both points of view,As we want eternal loving affection, but then so do you.This is surely an equation that even Einstein couldn't solve,It's just one more conundrum in an illness that has no resolve,Now one thing I realise as the days slowly languish byAs I can see from the anguish within your own loving eyes,This illness is not only affecting the life of just me,But tearing out the heart and soul of the one most dearest to me.
The Fight Never Ends, by Norrms:
Is it too soon to be talking of this?Secretly remembering our first kiss,Of how you will manage when I'm gone,When my fight is finished, over and done,I ask you this with tears in my eyes,Trying to stifle a million cries,Don't be so silly, you'll outlast me!Is always your answer, but please will you see,I neeed to make sure that life will be kind,And then you can rest and have peae of mind,I need to say this before the AD,Removes all my memories and steals them from me,I didn't mean to make you cry,Just want to be sure that you will get by,You take hold of my hand and say, Listen to me,You're going nowhere, why can't you see,We are in this together, no matter how long,Nobody's singing their last song,You have provided for us, all of your life,And I'm proud to say that I am your wife,We have wonderful kids, and grandchildren too,All of them grateful for the kindness from you.Then I say, Shh, please just let me say,That when my time comes, no matter what day,You shall remember, that very first kiss,And how all our life has been absolute bliss,And do me one favour, is my question to you,When you look up, at a sky that's so blue,Always remember, I will always love you,And please say goodby to all of my friends,Especially on TP, The Fight Never Ends.
You can read previous poetry contributions by clicking on the links below. The most recent contributions are at the end of the list.
Information on Poetry
The times that were not!
I once eloped with a petticoat
'Blog, blah, blah, blah'
Look at life
My shadow
Memories
Two poems
Don't treat me like a mattress
Simple as ABC
Has Life Passed By?
My Sister
Of Endless Days
Tree of Life
Reality or Dream
Perspective
There is no turning back
Now I have gone
Laughing at dementia and why not
A passing year
A poem by Frank - let the words flow
Distant Memories
My Mum and Dad's day with Alzheimer's
Never a Typical Day
Memories Lament
Going Too Fast?
Field of Dreams
Watching the World Go by
Ups and Downs
Bewildered
Gardening with Alzheimer's
It's OK to be scared
The Time Has Come
The Fight Never Ends
Of Two Perspectives
Say to yourself
You are never alone
Friends
Moments
My, my, another day
For one more day
Coping or not... with Alzheimer's
Of my eyes
Who can help?
He Gave In But He Never Gave Out
Of my Dementia
Spirit of Life
Of Courage
Do You Remember?
Reflections of Timeless Love within Dementia
Misty Horizons
Out of the Shadows
Nan
Al Zimer
Of the night
Hello Alzheimer's
The Alzheimer's Train
That's Asda Price
Distorted Day
Love's Lone Rose
Explaining to Mum
Gone Wandering
Alzheimer's Mountain
If My Eyes Could Talk
In Remembrance
I've Got Through Another Day
Betwixt Two Worlds
Just Once More
Left Alone

Alzheimer's and Dementia Forum

Welcome to Alzheimer's Forum

Your weekly magazine on the web

A website designed and written by people with dementia from around the world.

Being diagnosed with dementia does not mean the end of life. We still have brains, we can still laugh and cry. We still have feelings!

This website highlights how having any type of dementia or memory related problem can affect us all through the different stages of the illness.

'Dementia is not just an illness - it's a whole new way of life for us and for our families.'

Although this website is designed for people with memory problems, even families and carers will find it of use in broadening awareness of the illness.

We're in a class of our own worldwide. This website is written BY and FOR people with dementia

WANTED!
People with dementia involved in trying to make a change
The Bradford Dementia Group at Bradford University are looking for 25 people across the UK who are interested in bringing about change or who speak out or campaign on issues which matter to them.
They are looking for a variety of people: it may be that you are involved in community events, or that you write letters to newspapers, sign petitions or speak out in public. Maybe you keep a blog, have volunteered your skills to get better services or are involved in campaigns on a local or national level.
Whatever your level of involvement, they are interested in finding out why you get involved and how your activities affect you, your family and your life in general. The project will take place from August 2009.
To volunteer you need to

  • have a dementia diagnosis
  • be interested in changing things, speaking out or campaigning
  • be prepared to talk to a researcher
  • be prepared to keep a diary for up to one month; you can keep a written, photo or audio diary, whichever suits you best.

They are also looking for 5 people with dementia who are interested in piloting the materials they are going to use to make sure they have got them right. The pilot will last two weeks and will take place in June 2009.

If you are interested in finding out more please email socialchange@bradford.ac.uk or ring EJ on 01274 236 494 or Ruth on 01274 236 468.

What's new on Alzheimer's Forum

  • A FIRST! 2009 CALENDAR - you can still download the remaining months of the year.
    For the first time on Alzheimer's Forum, download and print a calendar for 2009. You will find it in the Multimedia section under Photos. We also have a Screensaver calendar and you can download and use each month as your screensaver.

  • Alzheimer's Forum is viewed from around the world Have a look at our summary of website views and a breakdown of the pages viewed to see the global impact of this website. Thank you for your support and for making Alzheimer's Forum so successful in broadening the awareness of Alzheimer's and dementia.

  • We have lots of new contributions under Thoughts and Experiences. Barry has written of his own thoughts about the Two Perspectives of Dementia, to show how the illness has affected him.

  • Go to the Multimedia section and listen Barry talk about the Four years within Alzheimer's. Download and print the new book Poetic Thoughts - a book of poems about Alzheimer's and dementia.

  • There are lots of new word puzzles for you to try. Have a look at our latest puzzle, it's all about the things you will find at the seaside.

  • Do you have a Predicament of the Month? Please send us your thoughts for the current predicament: WALKING, STUMBLING, BUMPING INTO EACH OTHER OR EVEN TRYING TO CROSS THE ROAD - HOW DOES IT AFFECT YOU? Email us and let us know. Share your views with others.

  • Look at the new poems in the Poetry section. There are two new very thought provoking poems from Norrms and Barry. Maybe you could send us a poem. Sometimes it's easier to get the message across through a poem. Why not have a go?

  • Remember you are never alone so email us as we want to hear from you. Click on the links on the left-hand-side menu to browse the contributions from other visitors to our website. Email us at friends@alzheimersforum.org.

Dementia and Sexuality

Sexuality and dementia
DownloadSexuality and dementia (pdf)
Information for people with dementia, their carers and their families. It looks at sexuality and intimacy when someone with dementia is living at home.
As dementia progresses needs change: existing relationships may have to adapt, new relationships may form, desires may fluctuate. What does not change is the right of every adult to be sexually alive should they wish to be so, regardless of age, ability or sexual preference. Sexuality is a basic need which people with dementia and their carers should be able to express without fear of disapproval.
Key pointsExisting relationshipsBalancing needs and desiresUnderstanding behaviour which seems sexualNew relationshipsSafe sexFurther helpFurther reading
Key points:
People with dementia have lived with their sexuality for much longer than they have lived with dementia.
Not everyone with dementia is old – in Scotland there are approximately 1600 people with early onset dementia (under 65).
Not everyone with dementia is heterosexual.
Not everyone chooses to exercise their right to be a sexual being.
Couples who work on their relationships can keep them stronger for longer.
Maintaining a healthy sex-life can improve overall quality of life for carers and people with dementia
Carers need to consider their own needs alongside those of people with dementia.
Sex and sensuality encompass a kaleidoscope of feelings and activities; from the deepest longings for mutual affection to the simple enjoyment of the company of a loved one. Sexuality also covers a gamut of behaviours – touching, kissing, caressing and cuddling, genital intercourse with mutual orgasm and feelings of closeness and being wanted and valued as a human being -Sex, Intimacy and Aged Care
Existing relationships
All relationships change with time. However, the increased physical and emotional dependency between partners which dementia brings can have a massive impact on even the strongest relationships.
People with dementia experience its progression in different ways and at different rates. As the ability to cope with ordinary life is gradually impaired, alterations in personality, presentation and behaviour (including sexual behaviour) may become more obvious. Loss of memory, declining physical health, inability to concentrate and growing confusion lead to greater dependency on carers. Inevitably this will impact on relationships and affect the way in which partners relate to each other both physically and emotionally.
Being provided with intimate personal care by a loved one can be a positive emotional experience for some people with dementia. For others it represents a loss of dignity and can have negative impact on how they feel about a sexual partner and about themselves.
Similarly for carers, the emotional effect of a partner’s increased dependency and need for physical care might change their sexual feelings towards them. Some carers may simply be too tired for sex or too emotionally overwhelmed to expend precious energy on the sexual aspects of their relationship. There are no easy solutions to coping with the ongoing changes in relationships. However, understanding that these changes are experienced by many people and having some insight into their causes can help.
Seeing beyond dementia
Sometimes what appear to be personality changes in a person with dementia are caused by sheer boredom, frustration at a misunderstood situation, unfamiliar surroundings or tasks which have become too difficult. Depression can be an underlying cause of personality changes in people with dementia but it can be successfully treated. Carers too can become overwhelmed, frustrated, depressed, anxious and stressed - emotions which their partner may sense and in turn be affected by.
It is important for many couples to have a safe place (this might be a friend, a support group, a helpline, a confidential internet chat-line, a counsellor) in which to air emotional issues affecting their relationship. Supportive family and friends are often vital both to the person with dementia and his or her carer. Support groups for people with early stage dementia and for carers are an excellent way for some people to exchange feelings, experiences and frustrations.
Other coping mechanisms that people have found useful include planning positive time apart to relax and build-up self-esteem. Some people are able to retain their sense of self by channelling energy into creative projects like writing poetry, listening to music, gardening, painting or keeping a journal.
If time apart is difficult to arrange or is not wanted then couples can focus on the positive aspects of their relationship by engaging in activities they still enjoy doing together. For example, putting together albums of photos and souvenirs which prompt positive reflections of past and present events, taking short trips to places and people they like visiting, dancing to favourite music, working together to complete simple household projects like baking or gardening. (See Alzheimer Scotland’s Activities booklet for more ideas.)
Redefining sexual intimacy
Redefining sexual intimacy is an enormous challenge, especially as the needs of both partners must be considered. A person with dementia may experience a loss of sexual manners and appear to be less thoughtful than they once were. A partner can address this by taking a more active role in finding a way to make sex pleasurable for both.
Although a person with dementia may forget how they used to please their partner and themselves during sex, what they will not lose is the need for intimacy and touch. However, for both partners feelings of guilt, despair, resentment, anger, worry and fear for the future can interfere with their ability to sustain a close intimate relationship. Therefore communication between partners is vital – sharing feelings and thoughts is a far more positive response to stress than nursing anxieties and grievances.
Increased interest in sex
Sometimes a person with dementia forgets that they have just had sex, or tries to initiate more sex than their partner can cope with. If a partner feels unequal to a person with dementia’s sexual needs then perhaps they can help them to masturbate in private. Where repeated demands for sex become overwhelming then gentle diversionary tactics may help such as getting involved in an activity together, or avoiding outright refusal by saying -
maybe later after I’ve...
Reduced interest in sex
Whilst some people with dementia may lose interest in sex they are likely to retain their need for physical contact. Gentle stroking and touching may be enough to replace a full sexual relationship and there are several other ways to incorporate touch into a care routine. For example, regular kissing and cuddling or patting and rubbing to allay distress and to communicate reassurance and love. The positive benefit of gentle hand massage using aromatherapy oils has been reported(1) and is another simple way to enjoy the feeling of shared touch.
For partners who no longer share a bed it may help the person with dementia to have something to cuddle, such as a soft toy, covered hot water bottle or even a pillow. This may seem a patronising response but should not be dismissed if it is found to be of comfort, especially to someone who has been used to the presence of another warm body beside them in bed for most of their adult life.
Different approaches
Physical ill-health or the side-effects of medication may affect either partner’s ability to have vigorous intercourse. Mutual masturbation and fondling can provide a less physical substitute but still be a rewarding way in which to express love and desire for each other. You should speak to your doctor if you think the side-effects of medication may be having an adverse effect or if you are worried about problems which may have an underlying physical cause – such as inability to have or to maintain an erection, premature ejaculation, vaginal dryness or loss of libido. (See Alzheimer Scotland’s booklet – Getting help from your doctor.) Couples should feel comfortable with whatever works for them within the context of a loving relationship and they should try not to be embarrassed if they need to seek help.
Balancing needs and desires
In some relationships the partner who is the carer may feel guilty because they still wish to have sex but the person with dementia has become passive and unresponsive. In these circumstances some carers start to feel that continuing to have sex with their partner is an abuse of the relationship, whilst others see maintaining their sex life as quite normal. Men in particular may feel that they are taking advantage of a partner who is compliant and unable to signal enjoyment, or indeed consent. It is important to learn to read non-verbal signals and to respect any sign of fear or reluctance from a partner with dementia. If this does becomes a matter of concern, it may help to speak to other carers, a relationship counsellor, or to a psychiatrist (see Further help).
Those involved with the support and care of the person with dementia will need to determine a number of things including:
is your partner still able to recognise you?
is your partner able to say no or able to show an ability to express their wishes and views?
As with all of us, a person with dementia’s sex life is deeply personal. If a person with dementia becomes the subject for discussion with professionals, their confidentiality and right to be treated with dignity and respect should be maintained, as should that of their carer.
Sexual aggression and an excessive interest in sex
Sometimes people with dementia can show an excessive interest in sex. They may appear to be sexually aggressive, demanding repeated sex from partners or they may attempt to have sex with people other than their partner. They may masturbate frequently or try to touch other people inappropriately. However, all of these kinds of behaviour are fairly rare(4) .
Dementia causes gradual damage to the brain which can change the way a person behaves. As with any behaviour it is helpful to consider the reasons the apparently sexual behaviour has occurred. Is the person with dementia signalling their need for closeness and reassurance? Are they angry because they no longer feel able to satisfy their partner? Could it be a by-product of medication they have been prescribed? This last is especially important as some drugs, including some anti-depressants, have side-effects which can cause excessive sexual interest and sexual arousal.
In extreme situations, where sexual aggression occurs, it may be difficult to manage. This is especially so when male partners are still physically strong. A carer may have to seek help to keep their partner, themselves and those around them safe in situations where the attentions of the person with dementia are violent or too persistent. It is important for a carer to recognise that their partner’s behaviour may be a component of their illness.
Domestic violence is a difficult subject to discuss because of the shame associated with it and an added sexual element may make it more embarrassing. For some couples the behaviour may be part of a long-learned pattern in a relationship which has been exacerbated by dementia. Although this is a difficult problem to discuss, other carers may provide useful help by sharing their experiences and advice. Day care workers, community psychiatric nurses (CPNs) and psychiatrists should also be a good source of practical support and guidance.
Understanding behaviour which seems sexual
There may be times when a person with dementia behaves in sexually inappropriate ways. For example, undressing at the wrong time, exposing themselves, masturbating in public, making what seem like sexual approaches, using obscene or sexually explicit language. Although this can embarrass a carer it is vital to remember that dementia affects a person’s understanding of social situations and therefore their ability to behave as might be expected.
Realising that apparently sexualised behaviour is the effect of dementia and seldom involves sexual arousal can help to depersonalise it and gives a carer the emotional distance to devise strategies for managing. Rather than "sort" the behaviour, it is helpful to consider the reasons why a person, any person – not just a person with dementia, would behave that way. For example, are they:
removing clothes because they are too hot, itchy, tight or uncomfortable?
exposing themselves because they need to go the bathroom?
bored and frustrated?
mistaking someone else for their partner?
expressing a need for touch?
misinterpreting the behaviour of other people?
How to help
When sexualised behaviour happens in public it is hard not to be shocked and to over-react. However, it is important to try to remain calm and not to communicate anger or distress to the person with dementia. What is not a good solution is to stop going out in public. Becoming isolated is bad for both carers and people with dementia.
Try to focus on the reasons why the person with dementia is behaving in a particular way (see above) and, if it is causing embarrassment, to distract them with something else.
If necessary, lead the person with dementia away from the situation, calmly and gently. Unless the situation is serious try to avoid physically restraining the person with dementia, as this may cause them to become more frustrated.
Speak to family and friends about understanding and dealing with potentially embarrassing situations.
Seek practical advice from other carers, and from social workers and healthcare professionals.
Learn from previous experiences. Try to identify the circumstances in which this behaviour is likeliest to happen. Are there cues? For example – is it when the person with dementia is tired or bored, is restless, starts blushing, or when they start picking at their clothing, or when they are in the company of particular people?
If you do manage to identify situations and/or triggers you will you be more prepared and better-equipped to cope if they happen again. Also, when you need a break from caring, you will be able to pass on practical guidance about how to look after your partner to a substitute carer.
New relationships
Respecting autonomy
Older people with dementia are faced with society’s reluctance to accept that sex is not the sole preserve of the young. Whilst younger people with dementia are less likely to have their sexual needs questioned they too may find that relatives worry on their behalf.
People with dementia are usually capable of forming new intimate relationships. Relatives, especially grown-up children, may have difficulty in acknowledging that parents are sexually alive or feel resentment that a new partner appears to be taking the place of a parent who has died. But all adults, regardless of age, have the right to make choices about their relationships and to have a private life. If those closest to a person with dementia are satisfied that their friend or relative is not physically or mentally vulnerable as the result of a relationship, and that no-one else is being harmed, then they should not attempt to interfere.
As long as a person with dementia is able to make decisions about their life then these decisions should be respected. Whilst a person with dementia is still capable of understanding what they are doing they may choose to set up a welfare power of attorney. A welfare power of attorney allows a person to make their wishes for the future clear and it only comes into force when the person to whom it applies becomes incapable. For more information see Alzheimer Scotland’s booklet Dementia - Money and Legal Matters: A Guide.
If protection becomes necessary
If families are still concerned that a relative with dementia is open to physical or emotional abuse in a relationship, then there are steps they can take. Initially they should share their fears with any professionals involved with their relative, such as GPs and social workers. If it becomes necessary to consult others about a person with dementia it is essential to respect their dignity and right to privacy. Those involved with the support and care of the person with dementia will need to determine a number of things including:
is that person comfortable with the relationship?
is that person still able to avoid exploitation?
is that person’s behaviour consistent with their prior beliefs and values?
is that person capable of saying no?
Sexual abuse of a person with dementia can constitute a criminal offence. It may also be a reason for the local authority to intervene to protect that person. Where an adult is unable to take decisions to protect their own interests, there are procedures to allow a family member to act on their behalf. For example, the person with dementia may have granted a welfare power of attorney. It is also possible for a family member or other concerned persons to seek an intervention or guardianship order.
For more help with this you can speak to your local authority social work department, a solicitor, the Public Guardian or the Mental Welfare Commission (see Further help). For more information see Alzheimer Scotland’s booklet Dementia - Money and Legal Matters: A Guide. Whatever the level of capacity of a person with dementia, their rights must come first.
Safe sex
The risk of sexual infection does not diminish with age. Contraception should still be a consideration for men of all ages and for younger women in heterosexual relationships. Sexually transmitted diseases (STDs), including HIV (human immunodeficiency virus) which causes AIDS (acquired immunodeficiency syndrome) are a potential danger to all those who are sexually active. Although most people in long-term relationships will have addressed the need for safe sex, in new relationships it is important that both partners discuss how they are going to protect themselves. GPs are a good source of advice on both family planning and safe sex.
Further help
For carers and people with dementia
Alzheimer Scotland Dementia Helpline The 24 hour Dementia Helpline, 0808 808 3000 is for:
people with dementia
carers
relatives
and anyone concerned about dementia.
DASN – Dementia Advocacy and Support NetworkA worldwide organisation run by and for those with dementia working together to improve their quality of life. As well as information about dementia, their website has links to chat rooms where people can meet on-line and to their e-mail community.Website: www.dasninternational.org/
Relationship counselling
GPSome surgeries now have NHS counselling services available.
Person Centred Therapy ScotlandTel: 0870 7650871E-mail: info@pctscotland.co.ukWebsite:www.pctscotland.co.ukHave a leaflet called 'Finding a counsellor in Scotland' and a directory of counsellors.
Couple Counselling Scotland40 North Castle Street, Edinburgh. EH2 3BNTel: 0131 225 5006E-mail: enquiries@couplecounselling.orgWebsite:www.couplecounselling.org/ Offers couples and individuals an opportunity to explore their intimate personal relationships in a safe and comfortable setting.
SPOD (Association to Aid the Sexual and Personal Relationships of People With a Disability)286 Camden Road, London. N7 OBJHelpline: 020 7607 8851. Tuesday 11.00am - 2.00 pm, Thursday 11.00am - 2.00pmE-mail: info@spod-uk.orgOffers advice on sex, sexuality and personal relationships tailored to the needs of disabled people.
The British Association for CounsellingBACP House, 35-37 Albert Street, Rugby. CV21 2SG.Tel: 0870 443 5252 (calls charged at national rate)E-mail: information@bacp.co.ukWebsite:www.bacp.co.uk Has a searchable database of therapists and holds a list of trained counsellors and psychotherapy organisations.
Lesbian, gay, bisexual and transgender support
Gay and Lesbian Carers Network, Alzheimer's SocietyGordon House, 10 Greencoat Place, London. SW1P 1PHE-mail: gaycarers@alzheimers.org.ukTel: Roger - 01843 220932, Arthur - 01273 628047, Bruce - 01865 847471 , Sally - 020 8675 0660Lesbian women and gay men caring for a partner, relative or friend with dementia face many challenges. The Network has trained and skilled volunteers able to offer a listening ear.
Scottish lesbian and gay switchboardsProvide telephone counselling and support on: sexuality, relationships and ‘coming out’; safer sex and sexual health and information on social life, support groups, housing, legal issues and employment. The service is completely confidential - regional numbers listed below.
Ayrshire - 01292 619 000Borders Gay Switchboard -Thursdays 7:30pm - 10 pm, Tel: 01896 756 611LGBT Youth Scotland: Dumfries & Galloway Service - Tel: 01387 739888; text line 0778 527 4147; e-mail: dandg@lgbtyouth.org.uk . Runs a group every Friday evening (6-9.30) for LGBT people over 26 plus a lunch-time drop in every Tuesday (12-2). Contact Christine.Layden@lgbtyouth.org.ukDundee LGB Switchboard - Mondays 7pm - 10 pm, Tel: 01382 202 620Fife Friend Fridays - Fridays 7:30pm - 10pm, Tel: 01592 266 688Grampian LGB Switchboard - Wednesdays and Fridays 7pm - 10pm, Tel: 01224 633 500Lothian Gay & Lesbian Switchboard - Nightly 7:30pm - 10pm, Tel: 0131 556 4049Lothian Lesbian Line - Mondays and Thursdays.7:30pm - 10pm, Tel: 0131 557 0751Moray LGB Switchboard - Men: Fridays. 7pm - 10pm, Tel: 01343 541 188 , Women: Thursdays 7pm – 10pmStrathclyde G&L Switchboard - Nightly 7pm - 10pm, Tel: 0141 332 8372Strathclyde Lesbian Line - Wednesdays 7:30pm - 10pm, Tel: 0141 354 0400
Help with intervention or guardianship orders
Mental Welfare Commission for ScotlandArgyle House, 3 Lady Lawson Street, Edinburgh. EH3 9SHTel: 0131 222 6111E-mail: enquiries@mwcscot.org.ukWebsite: www.mwcscot.org.ukSafeguards the rights and welfare of people with mental illness and learning disability both in hospital and living in the community.
Public GuardianOffice of the Public Guardian, Hadrian House, Callander Business Park, Callander Road, Falkirk. FK1 1XRTel: 01324 678300, Fax: 01324 678301E -mail: opg@scotcourts.gov.ukWebsite: www.publicguardian-scotland.gov.ukThe Public Guardian registers continuing and welfare powers of attorney, authorisations to access funds, guardianship orders and intervention orders pronounced in terms of the Act.
Further reading
Sex, Intimacy and Aged Care by Barbara ShermanJessica Kingsley Publishers Ltd, London 1999. £13.95.This book challenges us to examine our own attitudes. Stories of the experiences of caregivers, families of people affected by dementia illustrate the difficulties encountered by sexual partners, as well as the complexity of the situations confronting professional careworkers.
Sexuality and Dementia Video and Training Handbook by Carole ArchibaldUniversity of Stirling, 1994.Training handbook and supporting video focusing on the expression of sexuality by people with dementia and the subsequent difficulties experienced by care staff.It costs £40 to buy the full training pack, or £9.00 for the carers’ video but both can be borrowed from the Dementia Services Development Centre (details below). They also have, available for loan only, an American video about heterosexual couples where one partner has dementia, called A Thousand Tomorrows. Contact:Dementia Services Development Centre, University of Stirling, Stirling. FK9 4LATel: 01786 467740
Activities - a guide for people concerned about their memory, people with dementia and their carers, Alzheimer Scotland. £1.50 (post and packing free within the UK) – single copies free to carers and people with dementia in Scotland via the 24 hour Dementia Helpline 0808 808 3000. For carers who look after someone who has moderate to severe dementia and need help with planning daily activities. Keeping someone with dementia busy and engaged will become more difficult as the dementia progresses. However by focusing on what he or she can do, even when the illness is quite advanced, you can both enjoy a range of stimulating activities and outings together.
Getting help from your doctor – a guide for people worried about their memory, people with dementia and their carers, Alzheimer Scotland. £1.50 (post and packing free within the UK) - single copies free to carers and people with dementia in Scotland via the 24 hour Dementia Helpline 0808 808 3000. It will help you to find out how doctors and other health workers can help you. The information in this booklet will also help relatives or carers of people with dementia, and there is a section especially for them.
Don’t make the journey alone, Alzheimer Scotland. £1.50 (post and packing free within the UK) - single copies free to carers and people with dementia in Scotland via the 24 hour Dementia Helpline 0808 808 3000. Clearly presented information about dementia written by people with dementia for people with dementia.
Dementia – Money and Legal Matters: A Guide, Alzheimer Scotland. £3.50 (post and packing free within the UK) - single copies free to carers and people with dementia in Scotland via the 24 hour Dementia Helpline 0808 808 800. A 52 page booklet. This information is for people with early stage dementia and for people helping or caring for someone with dementia.
Acknowledgements
Thanks to Dr Carole Archibald of the Dementia Services Development Centre at the University of Stirling and staff at Alzheimer Scotland.
Feedback
Alzheimer Scotland actively seeks the views of people with dementia and their carers. If you have any comments or suggestions about this information sheet please send them to:Information DepartmentAlzheimer Scotland22 Drumsheugh GardensEdinburgh EH3 7RNE-mail: alzheimer@alzscot.org

Getting Help, Dementia Patients and their Caregivers,

From country to country there is wide variation in the provision of care for people with dementia and their caregivers. In many countries there will be little or no care outside the family. However, wherever you live, there are some basic things that caregivers need.
These are:
medical help with diagnosis and care
help with the task of caring
rests (breaks, respite) from caring
regular health checks for you the caregiver
information about home care, day centre, or nursing home care
In some countries, you can get help and support for the day-to-day tasks of caring. There is a wide range of support and information available, so do not be afraid to ask. Remember you are not alone.
The topics you will find here cover:
sources of help and information
community care
day care
respite care
nursing and residential homes
choosing a home
questions to ask a home
making the move
Sources of help and information
"It is worth looking for help, even though it may seem hard to find."
There are many people and organisations in both the voluntary and professional sectors to make caring easier for you. The main contacts who can help you find support include:
the doctor in charge of the person with dementia
local social services
your national Alzheimer's association
National Alzheimer associations often have local branches, who can inform you about the services available in your area. The societies may comprise of fellow caregivers. These people will understand your needs, fears and concerns, and can be an invaluable source of information and support. A list of national Alzheimer's associations is available.
Opportunities also exist for caregivers to learn about dementia, and how to care for someone with dementia. Local groups often have speakers and run practical sessions on caring. It is also possible that more formal courses are organised at both regional and national levels. Consider attending these courses, as they will help you cope with the needs of someone with dementia.

Community care
"Getting help at home may allow you both to keep your independence."
Community care is a general term for services provided to help people with an illness or disability continue living in their own homes. In some countries there are a number of different services designed to support people in their own homes, however these will vary from country to country.
To obtain hospital services in the community, you need to contact the person's doctor or specialist. They will then detail the help available to you, and how to get it. For other services, you may need to contact your local social services department.
If you are the main caregiver, and you share your house with the person with dementia, or spend a large proportion of your time looking after them, there maybe help you can get too. It is worth contacting the person's doctor or local dementia support group for more information.
Day care
"Day care allows you to continue looking after the person while also giving you time to yourself."
If you are unable to look after someone with dementia all the time, for example during the day when you have to work, you may consider using day care centres. These provide care facilities when you need time to yourself regularly.

Respite care
"Respite care can give you some time to yourself."
Respite care means having someone look after the person with dementia, while you have a break from the responsibility of caring. It is important that you are able to get rest as a caregiver. You will not be able to look after someone with dementia if you are not fit yourself - this means having time-off.
Respite care takes a number of forms. Usually, the person goes into hospital or a nursing home for a week or two. In other cases, a caregiver will come to your home and look after the person, while you take a break.
Where nursing homes offer respite services, consider using these to see if the person might consider staying there when the time comes to move them to a home.

Nursing and residential homes
"Ease the pain of putting the person you care about into someone else's care by choosing an appropriate home."
Making the choice to move someone you care deeply about into a nursing or residential home is one of the most difficult choices you will have to make. Yet the move can be made easier if you take time to select the right home.
The main difference between nursing and residential homes is that residential homes look after people who are more active and alert. Nursing homes generally have a greater number of registered nurses on their staff in order to provide 24-hour nursing care.

Choosing a home
"Make sure the home you choose has both the right level of care and type of atmosphere to suit the person."
When choosing a home, you first need to check that the home can care for someone with dementia. Get as much information about homes from the person's doctor, social services and local dementia support group.
Once you have a list of home's names and numbers, call and make appointments to visit as many as possible. Ask questions and, from your visits, select a shortlist of homes that you think will provide the right level of care, with the right atmosphere to suit the person.
Then visit all the homes on the short-list, taking the person with you. If the home offers respite care services, see if the person can stay there, to find out if they will be happy there.
The whole process can take a long time and be very painful. However it is important that you spend time to make the right choice. In the long-term, this will make life more comfortable for the person and help you feel better about the move.

Questions to ask a home
"Asking questions will help you choose the right home for the person with dementia."
This is a list of questions that you might consider asking when looking for a home. Ask yourself:
where is the home situated? Will it be easy for friends and family to visit?
is the home friendly, welcoming and homely?
is it well furnished?
is it clean and sweet smelling? There should be no smell of urine.
do the staff treat people with tact and respect when helping them with bathing or visiting the toilet?
are there activities going on? How are chairs arranged? Is the television just left on all day?
Ask the nursing home:
are there places to get out to? Are outings arranged?
is there a safe garden to walk in?
are there enough rooms for residents to sit in?
what is the home's practice about smoking?
is there access for wheelchairs or walking frames? Are the toilets and baths suitably adapted?
are single rooms available?
can you take the person's own furniture and other possessions?
can residents use their own rooms to be private, and do the staff respect their need for privacy?
will they have their own toilet? Are there enough toilets and bathrooms for all the residents?
what is the food like? Is the food prepared at the home appealing and nutritious? Are choices offered at mealtimes? Are special diets catered for?
will the person be able to eat in their own room if he/she wishes?
will he/she be able to eat at a different time, or have a snack, just like at home?
what are the arrangements for medical care?
are dental treatment and chiropody available?

Making the move
"Make the move easier by continuing to care for the person after they have moved into the home."
Good planning and preparation is the best way of reducing stress around the move. Guilt is often a key factor in making the move, so it is important that you recognise this feeling for what it is. Do not forget that you are doing this for their benefit, as well as yours and your family's. Nothing you do will change the outcome of dementia, so all you can do now is make sure that the person is comfortable, safe and reasonably content.
Your role as a caregiver does not need to stop here. You can continue to provide the person with your care by visiting them regularly and helping at mealtimes and with baths. This will make the whole transfer less traumatic for you both.
Where next?
Living and caring for a person with dementia
Find your local Alzheimer association
Help for carers

Every day Challenges for a Caregiver

Here we look at the everyday challenges that a caregiver has to cope with and suggest ways in which these can be met. The subjects are:
bathing and personal hygiene
dressing
toileting and incontinence
cooking
eating
driving
alcohol and cigarettes
sleeping problems
repetitive questioning and behaviour
clinging
losing personal items
hallucinations and delusions
sexual relationships
inappropriate sexual behaviour
wandering
violence and aggression
depression and anxiety

Bathing and personal hygiene
"Make bathing an enjoyable, relaxing and stress free activity - not a forced chore."
Someone with dementia may forget to bathe, not recognise the need, or have forgotten what to do. In this situation you must respect the person's dignity when helping.
Associate washing with an activity, such as going to a restaurant or visiting friends, this may prompt the person to wash. Rather than forcing the person to wash, try to make it enjoyable and relaxing. Use praise and encouragement when the person is freshly bathed, rather than criticism of their cleanliness. A shower, or stand-up wash may be easier than a bath. However, if the person has not been used to a shower it may seem alarming and is best avoided.
Simplify bathing and allow the person to do as much as possible unaided. They may know they need to wash, but may have forgotten what to do. Gently remind them of the required steps as they wash themselves. If the person appears embarrassed when bathing, keeping portions of their body covered may be helpful. If the person refuses to be washed, try again later when their mood may have changed. If you constantly have problems with washing, seek support and get someone else to do it.
Finally think about safety. Bathrooms can be wet and slippery, so use grab rails, non-slip mats or an extra chair. These all help prevent accidents.

Dressing
"Make dressing an enjoyable shared activity."
A person with dementia often forgets how to dress and may not recognise the need to change clothes. Use dressing as a simple way of keeping the person active and helping them retain their sense of independence and self-esteem.
Allow plenty of time for dressing, make sure the atmosphere is calm and warm. If the person is struggling, lay out clothes in the order they should put them on, or verbally suggest which item of clothing the person should put on. As the disease progresses, you may have to pass the items of clothing to the person and explain how or help to put the clothes on.
Some items of clothing are easier to put on than others. Use wide-necked tops, baggy trousers and non-skid slip-on shoes, as these all help make dressing easier. Try to ensure that the person with dementia is comfortable with the clothes selected, involving them in the selection process.

Toileting and incontinence
"Confusion is often the cause of incontinence, so limit large drinks, label the toilet door with signs and dress the person in loose clothing."
The person with dementia may lose the ability to recognise when to go to the toilet, where the toilet is, or what to do when in the toilet. Confusion is often the cause of incontinence, but sometimes there are other possibilities so get professional advice.
There are some steps you can take to reduce the risks of accidents occurring. Limit large drinks last thing at night and create a schedule for going to toilet, for example regularly throughout the day and before getting into bed. Frequent toilet trips reduce the risk of accidents happening. During the night consider waking the person regularly and suggesting they go to the toilet. Remember that a person with dementia can be easily confused and might need taking to the toilet, especially if it is not near the bedroom. A chamber pot or commode by the bedside may be helpful in an emergency.
Around the house, use signs with bright colours and large letters to label the toilet door and leave it open to make it easy to find. Finally, make sure that clothing can be easily removed, as this makes going to the toilet easier.
Skin can be damaged if left exposed to urine, so make sure that the person with dementia showers or washes daily. If you cannot shower the person immediately after an accident, consider using baby wipes to clean the affected skin, and carrying spare clothing with you.
Incontinence means more work for you as a caregiver, which can be both upsetting and distasteful . These feelings are understandable and it is important that you contact someone to talk about the problem and your feelings. Your doctor or nurse and members of support groups will have come across these problems before and will be able to offer you help and support.

Cooking
"The ability to cook may be lost."
Assess how well the person can do their own cooking. While it is important that they maintain their independence for as long as possible, their health must not suffer. Poor physical condition, due to dementia, can result in the person injuring themselves with burns or cuts when cooking. Installing safety devices and removing sharp utensils from the kitchen can reduce chances of injury.
For the person, their ability to cook may diminish in the later stages of dementia. It may be hard for them to give up this role, if they are used to looking after themselves, their family or partner, so try and make cooking an enjoyable shared activity.
The inability to look after themselves poses problems if the person lives alone, with an increased risk of injury. Provide meals, or a meal service, and try to see that enough nutritious food is eaten.

Eating
"Eating is important! So get help if you are having difficulty coping."
People with dementia often forget if they have eaten, or how to use utensils. You may have to remind the person how to eat. Consider suggesting the use of a spoon instead of a knife and fork. Ask your doctor to put you in contact with a local occupational therapist, who could give you further information about devices that help with eating.
Finger food is easier to manage and not as messy. You can also cut the food up into small pieces to prevent choking. Remind the person to eat slowly and be aware that they may not be able to sense hot or cold, and could burn their mouth on hot food or liquids.
As the disease progresses, physical problems may arise such as not being able to chew properly or swallow. You may need to serve different portions of food one at a time to make eating easier . In the later stages of dementia the person may need to be fed or you may have to mash or liquidise all food. If the person has difficulty swallowing, you may need to consult your doctor to learn a technique to stimulate swallowing.

Driving
"Driving is a symbol of independence, so approach the subject of no longer driving with care."
People with dementia may no longer be aware that their judgement is impaired and reactions slower. Research suggests that a proportion of people in the early stages of dementia retain the ability to drive, but this ability can be lost easily. This problem can be difficult to handle, so you should approach the subject with care.
Discuss the subject with the person gently, and suggest using public transportation instead of driving. If the person has stopped driving, try to maintain their independence by suggesting they organise a taxi or mini-cab account.
If driving remains a problem, consider selling the car if you do not need it yourself. This way the person with dementia may not be continually reminded of the car. If you still need a car, consider making the keys hard to find, or suggest driving for the person.
If you cannot dissuade the person from driving, it may be necessary to consult with your doctor or the drivers licensing authority. Depending on your country, rules will apply whereby people with certain medical conditions can no longer drive, or need to re-take a driving test. Make sure you and the person adhere to your local regulations.

Alcohol and cigarettes
"Supervise drinking and smoking to make sure accidents don't happen."
There is no problem for a person with dementia drinking alcohol in moderation if their medication allows. However the person may forget they have just had a drink and so have another one. This cycle can lead to repetition with the person becoming drunk or unmanageable.
In these cases, try to reduce the amount of alcohol being drunk, by either reducing the number of bottles of alcohol available in the drinks cabinet, or emptying or diluting some of them. It might also be worth distracting the person with another activity, so that they do not think about drinking.
Cigarettes introduce a greater danger because of the risk of fire and damage to health. Always supervise the person when smoking, or try to discourage smoking altogether. Make sure that the clothes they wear and the furniture in the house are fire-resistant. Consider fitting a smoke alarm, which can alert you to any danger.

Sleeping problems
"Increasing daily activities and discouraging sleeping during the day, will help the person sleep at night."
The person with dementia may be restless at night and disturb the family. People with dementia can get disorientated in time and no longer recognise the difference between night and day. This can be the most exhausting problem as a caregiver.
Establishing a routine to keep the person with dementia busy is the first priority. The routine should keep them as busy and active as possible and discourage sleeping during the day, for example, long walks add more physical activity to the day and should help the person sleep at night.
Don't feed the person a large meal in the evening, and after the day's activities, keep the evening fairly quiet and relaxed. As bedtime approaches, make the person as comfortable as possible, with a warm and inviting bedroom.
If practical measures fail to improve matters, you may need to use sleeping pills in order to cope. Generally, these should be avoided in people with dementia. Your doctor can advise you on the best course of action.

Repetitive questioning and behaviour
"Repetitive questioning is caused by memory problems giving a general feeling of insecurity."
Dementia can make a person forget what they have said or done from one moment to the next, leading to repetitive questioning and actions. This may cause irritation for you the caregiver.
Rather than answering the question again and again, it may be helpful to say that everything is fine and try to make the person more secure. It might help to write the answer down. If the same question comes up again, you can direct the person to a written answer. Try to distract the person by changing the subject or giving hugs, if appropriate for the person.

Clinging
"Clinging behaviour can be difficult; try to deal with clinging behaviour by using memory joggers, activities or sitters to distract the person while you step away."
The person with dementia may become extra dependent on you and follow you everywhere. This can be frustrating, difficult to handle, and rob you of your privacy. The person may act this way as a result of feeling insecure and fear that when you leave them, you will not return.
Whenever you leave a person with dementia, it is important that you tell them you will come back. If necessary write this information down for the person. Another method is to provide them with something to occupy their attention while you step away.
If you need more space and time to yourself, you may want to call on a sitter. The sitter can be someone from a support group, or a member of your family or a friend. Either way, this will give you time to relax without having to worry about the person. Such breaks help you cope with caring for someone with dementia.

Losing personal items
"Don't argue about lost items, they can usually be found after a quick search."
An inevitable part of dementia is forgetting where objects were placed. This behaviour is caused by insecurity, combined with a sense of loss of control and of memory. In some cases the person will accuse you and others of taking the missing objects. It is vital to respond to the accusations without confrontation or anger . The first step is to agree with the person that the item is lost and help find it. It is pointless getting into an argument over the loss and will only upset you and the person.
What often happens is that when items go 'missing', the person will hide them in a place to prevent them from disappearing again. They then forget about this hiding place. If you look carefully, you will probably find the hiding place, so check these first in the search for the missing item.
You should make sure that you keep copies or spares of important items, such as keys, spectacles and documents. Try limiting the amount of valuables and money left about the house. This reduces the chance of a real theft occurring. Finally, always check waste baskets before emptying them, this prevents accidental loss of items.

Hallucinations and delusions
"Hallucinations and delusions are real to the person so deal with them, don't dismiss them."
It is not uncommon for the person with dementia to experience hallucinations or delusions.
If the person is experiencing an hallucination, they might see or hear things that are not there; for instance, figures at the foot of the bed, or voices in the room. Do not dismiss the validity of what the person has just seen, but distract them by drawing their attention to something real in the room. Hallucinations can be associated with poor vision, so it is worth a trip to the opticians for a check-up. Keep rooms well lit to ensure that the person is not misinterpreting what is going on around them. Also, check with your doctor about medications that are being used, they may contribute to the problem.
A delusion is a false belief. For example, the person may believe that they are under threat of harm from the caregiver. To the person this delusion is real and causes fear, and may result in distressing self-protective behaviour. Do not argue about the validity of what they believe, but try reassuring and comforting them if they are frightened. Your calm voice and holding hands gently can help calm the person down and bring them back to reality.

Sexual relationships
"Don't be afraid to discuss this and related issues with professionals trained to listen and help."
For some couples, sexual intimacy continues to be a satisfying part of their relationship, but dementia may alter the person's attitude. Gentle cuddling and holding may be mutually satisfying, and will let you know if he or she is able or inclined to engage in further intimacy. It is wise to be patient. The person may not respond in the same way as before, or may seem to lose interest.
The opposite may occur too. The person may make excessive demands for sex, or behave in a manner that makes you feel uncomfortable. If this is a problem, you may consider sleeping in a separate bedroom. Whether this becomes a permanent feature is a difficult decision to make, but one you must make if necessary.
You may feel guilty about yours or your partner's needs. Seek help from other caregivers or professionals you trust and don't be afraid to discuss these and related issues with a professional trained to understand and help you manage. In some countries there are people with special skills in this area, such as psychologists, social workers or counsellors who can provide advice and guidance.

Inappropriate sexual behaviour
"Remember, stay calm, avoid confrontation, and distract the person with another activity."
A person with dementia may display inappropriate sexual behaviour, but it is rare. Behaviour may include undressing in public, fondling genitals, or touching someone in an inappropriate way.
In responding, try not to over-react and never forget that it is the disease taking effect. Distracting the person with another activity is a useful way of defusing a situation. If the person removes their clothing, then calmly, quickly and gently discourage the behaviour and encourage another activity.

Wandering
"If the person is lost, seek help immediately and don't delay calling the police."
This is a worrying problem which needs managing. The person with dementia may wander around the home or leave the house and wander around the neighbourhood. If possible, prevent them from leaving the home without your knowledge, by making sure your home is secure.
Safety is a primary concern when the person with dementia is out in public alone. Make sure they have identification on them and keep an up-to-date photograph of them, in case they get lost.
If the person is lost, then alert your neighbours, friends and local police immediately. It is worth warning the police in advance of the person's condition and the possibility that they may get lost. Check the usual shops that they visit to eliminate those from the search.
When the person is found, avoid confrontation and showing anger - speak calmly, with acceptance and love. It is not their fault, but a problem associated with dementia.

Violence and aggression
"Violence and aggression are caused by the illness."
From time to time, the person may become angry, aggressive or violent. It is not a personal attack on you, but a part of their illness. There are many reasons why a person with dementia may feel angry. They may not like being helped with things they used to do on their own, or may simply be frustrated due to an inability to do things.
These short-term changes happen for a variety of reasons such as the person's sense of loss of social control and judgement, loss of the ability to express negative feelings safely, and loss of the ability to understand the actions and abilities of others. It is therefore worth finding and avoiding the causes of unwanted certain reactions.
If the person feels angry, aggressive or violent, keep calm and try not to show fear or alarm. Give them more space and try to draw their attention to a calming activity.
This is one of the most difficult things to cope with for a caregiver, and if violence occurs often, you will need to seek help. Talk to someone for support, and speak with your doctor about help with managing the person.

Depression and anxiety
"Depression is serious but treatable, so seek help and advice on how to deal with it."
The person with dementia may experience depression and be withdrawn and unhappy, speaking and thinking slowly. Dementia is a disabling disease, and it is understandable for a person with dementia to be depressed at times, so don't expect the person to recover from depression immediately.
Depression and anxiety can affect daily routines and interest in food, resulting in declining health. It is essential to provide more love and support for the person during these periods. Contact their doctor, who will be able to help or offer a referral to a counsellor, psychologist or psychiatrist. Treat this problem seriously and seek help.

I Have Dementia

I have dementia
If you have been told that you have Alzheimer's disease, vascular dementia or another dementia then this section is for you.
If you are experiencing memory problems or are having difficulties in performing everyday tasks visit your doctor. There may be reasons, other than dementia, for your problems and the doctor will be able to check.
If you have been diagnosed with dementia, finding this out can come as a shock, even if you have felt that something was not quite right. You may have lots of questions about what this means, what happens next with your family, social and working lives, and who can help you.
It is important to know that you are not alone. You may be able to get help, support and information from:
Your family and friends
Your doctor
Health and social workers
Counsellors
Alzheimer associations and other voluntary groups
Where next?
Life after diagnosis
Account of a personal experience
Why is early diagnosis important?
Younger people with dementia (aged under 65)
Treatments
Finding help
Other resources
These Alzheimer associations have content aimed at people with dementia on their websites:
Alzheimer's Association (USA)
Alzheimer's Australia
Alzheimer's Society (England, Wales, Northern Ireland)
Alzheimer Scotland
Alzheimer Society (Canada)
Alzheimer's Association Japan (in Japanese)
Romanian Alzheimer Society (in Romanian)
Other sites that may be helpful:
'Facing Dementia' - Health Scotland publication
Dementia Advocacy and Support Network International (DASNI) - an organisation for those diagnosed with dementia, working together to improve quality of life
"Survivre avec une maladie d'Alzheimer" - website in French created by a person with dementia in Switzerland

The Personal and Emotional Stress of Caregiving and Looking after Yourself

The personal and emotional stress of caregiving and looking after yourself
The personal and emotional stress of caregiving and looking after yourselfAlzheimer's disease not only affects the person with dementia, it affects the entire family. The greatest burden is placed on the caregiver. The personal and emotional stress of caring for a person with dementia are enormous and you need to plan ways of coping with the disease for the future. Understanding your emotions will help you successfully cope with the person's problems as well as your own. You are an important person in the life of the person with dementia. Without you the person would be lost. This is why it is essential to take care of yourself.Here we look more closely at your emotions and needs as a carer. The topics we will talk about include:griefguiltangerembarrassmentlonelinessfamily supportsharing problemstaking time-outknow your limitsnot blaming yourselfseeking and taking advice.Grief"Try to accept that feelings of grief are a natural response to the situation."Because of Alzheimer's disease, you may feel that you have lost a companion, friend or parent, and grieve for the way they used to be. Many caregivers find themselves shifting between hope and despair, thinking the person may get better, then knowing they will not. Also, because dementia is progressive, just when you think you have adjusted, the person may change again. It may be devastating when the person no longer recognises you.Try to focus on what makes life as pleasant as possible for you both, and look for the parts of the person's personality that still remain.It is important that you find someone to talk to. Sharing your feelings with family, friends and other caregivers is one way of coping with the grief. Many caregivers have found that joining support groups is a good way to get encouragement and assistance to keep going.Guilt"It is common to feel guilty."It is common to feel guilty for being embarrassed at the person's behaviour, for anger at the person, or for feeling that you can not carry on and are thinking about nursing home placement.The decision to move someone you care about or love into a nursing home is a difficult and painful decision to make. Yet caring for someone with dementia can become a 24-hour occupation and there comes a time when short breaks of respite care will not provide sufficient relief. Eventually, you risk damaging your own health if you do not consider moving the person to a home, where they can get the 24-hour help they need.You may find it helpful to talk to other caregivers and friends about the feelings of guilt. Just because the person you are care for goes to a nursing home, it does not mean giving up your caregiver responsibilities. Indeed the care home may be grateful for your help at mealtimes or with bathing. Continuing to help in this way will help relieve your feelings of guilt.Anger"Getting angry is normal."It is important to remember that you are not perfect. It is normal for you to lose your temper and get angry at times - as do all other caregivers. Your anger may be mixed. It may be directed at the person, yourself, the doctor, or the situation, depending on the circumstances. It is important to distinguish between your anger at the person's behaviour, resulting from the disease, and your anger with the person, as this will help you to cope better.Try to understand the person's behaviour that is upsetting you and see if you can stop or reduce it, as it will not help either of you to lose your temper. If you think you are going to lose your temper, go into another room or into the garden and give vent to your feelings away from the person with dementia.It may be helpful to seek advice from friends, family, or a support group. Sometimes people feel so angry that they are in danger of hurting the person they care for - if you feel like this, you must seek professional help. Many local support groups have caregivers' contacts, with whom you can talk to and get advice from. Use these people to get help when you need it.Embarrassment"Ease any embarrassment by taking the courage to explain the situation to people around you."You may feel embarrassed when the person displays inappropriate behaviour in public or disrupts the neighbours. It may take some courage, but by explaining the disease and the concept of dementia to friends and neighbours, you will help them understand the person's behaviour.Look for support from other caregivers who have experience of similar problems. Sharing your feelings with other caregivers will enable you to cope better and the embarrassment may fade.Loneliness"Try to maintain friendships and keep social contacts, as loneliness makes caregiving harder."Many caregivers withdraw from society and, along with the person with dementia, are confined to and around their homes. Being a caregiver can be lonely - you may have lost the companionship of the person, as well as social contacts, due to the demands of being a caregiver.Loneliness makes coping with the problems of caregiving harder, so try to keep in contact with friends, and see if they can offer extra help. Explain the problems of dementia and that they, as friends, can help by providing you, or the person with dementia, some companionship.Maintain your own social engagements and take breaks from looking after the person. This will give you time and space to recharge your batteries and help you feel better about yourself.Consider joining a support group. Here you will find people with similar problems, who can help you get over the rough patches and provide a social life, where you do not have to be separated from the person you are caring for.Family support"The family can be the greatest source of help."For some caregivers their immediate family is the greatest source of help. For others it is the biggest source of distress. If this is the case, you may feel that you have been left to cope as a caregiver on your own, which can lead to bitterness and resentment. If you are feeling distressed because family members are not supporting you, try to find out why they are not helping. It may be helpful to call a family meeting to discuss the care of the person.If you cannot get help from your immediate family then try to get help from elsewhere. Accept help from other family members and do not take on the burden of caring alone. Try to arrange breaks from caring to give you the respite care you need. You may find that by looking after yourself, you feel less stressed about the lack of family support.Sharing problems"Share your problems."You need to share your feelings about your caregiving experiences with others. If you keep them to yourself, it may be more difficult for you to look after the person with dementia, as you may begin to resent them or get angry with them. Try to think ahead and have someone to turn to in an emergency.You will most likely find that your friends have not stopped liking or caring about you, and would probably be quite happy to listen or help if you let them know how. Try to accept support when others offer it, even if you do feel you are troubling them.If you can realise that the problems and feelings you are experiencing are a natural response to your situation, it will be easier for you to cope. If you do not want to bother your friends then seek professional help from the person's doctor or the local support group.Taking time-out"Make time for yourself."It is essential to make time for yourself. As a caregiver you risk isolation by looking after someone with dementia. This can cause loneliness and sometimes anger or resentment towards the person with dementia. Taking time-out allows you to spend time with others. Enjoy your favourite hobbies and, most importantly, enjoy yourself.Support groups, social services and some nursing homes provide day care help, where you can leave the person with dementia in safety and comfort while you can enjoy time to yourself or with the rest of your family. Use the support available to you, so that you can have a rest.Know your limits"Be aware of how much you can take, and seek help if caring becomes too much for you."How much can you take before it becomes too much? Looking after someone with dementia is a demanding role, which may be complicated by:your own physical or health problemslack of sleepfinancial uncertainty.Most people will come to realise how much they can take before caring becomes too demanding. If your situation is too much to bear, take action, seek additional support, and call for help to prevent or avoid a crisis.Not blaming yourself"Dementia is no one's fault, the disease is the cause."Do not blame yourself or the person with dementia for the problems you encounter. This is particularly hard if the person cannot remember who you are or if they are violent. Remember the disease is the cause not the person.If you feel your relationships with friends and family are fading, don't blame them or yourself. Try to find what is causing the breakdown and discuss it with your friends and family. These relationships can be a valuable source of support for you and the person with dementia.Seeking and taking advice"Learning to seek and take advice can help you be a better caregiver."Learning to accept help may be new to you. More often than not, family, friends and neighbours may want to do something to help you and the person with dementia.Self-help groups (a group for caregivers) can be another source of help for you. They provide an opportunity to get together with other helpers and caregivers, who may already have experienced the problems you are facing. Through their combined experience, these groups can be an invaluable source of help, comfort and encouragement.Your doctor, community nurse or social worker may also be able to help you. They will be able to provide you with help and advice about looking after the person and the support available. If they cannot answer your problems themselves, they will usually be able to put you in contact with someone who can.Alzheimer's disease not only affects the person with dementia, it affects the entire family. The greatest burden is placed on the caregiver. The personal and emotional stress of caring for a person with dementia are enormous and you need to plan ways of coping with the disease for the future. Understanding your emotions will help you successfully cope with the person's problems as well as your own. You are an important person in the life of the person with dementia. Without you the person would be lost. This is why it is essential to take care of yourself.Here we look more closely at your emotions and needs as a carer. The topics we will talk about include:grief guilt anger embarrassment loneliness family support sharing problems taking time-out know your limits not blaming yourself seeking and taking advice.Grief"Try to accept that feelings of grief are a natural response to the situation."Because of Alzheimer's disease, you may feel that you have lost a companion, friend or parent, and grieve for the way they used to be. Many caregivers find themselves shifting between hope and despair, thinking the person may get better, then knowing they will not. Also, because dementia is progressive, just when you think you have adjusted, the person may change again. It may be devastating when the person no longer recognises you.Try to focus on what makes life as pleasant as possible for you both, and look for the parts of the person's personality that still remain.It is important that you find someone to talk to. Sharing your feelings with family, friends and other caregivers is one way of coping with the grief. Many caregivers have found that joining support groups is a good way to get encouragement and assistance to keep going.[Photo]Guilt"It is common to feel guilty."It is common to feel guilty for being embarrassed at the person's behaviour, for anger at the person, or for feeling that you can not carry on and are thinking about nursing home placement.The decision to move someone you care about or love into a nursing home is a difficult and painful decision to make. Yet caring for someone with dementia can become a 24-hour occupation and there comes a time when short breaks of respite care will not provide sufficient relief. Eventually, you risk damaging your own health if you do not consider moving the person to a home, where they can get the 24-hour help they need.You may find it helpful to talk to other caregivers and friends about the feelings of guilt. Just because the person you are care for goes to a nursing home, it does not mean giving up your caregiver responsibilities. Indeed the care home may be grateful for your help at mealtimes or with bathing. Continuing to help in this way will help relieve your feelings of guilt.[Photo]Anger"Getting angry is normal."It is important to remember that you are not perfect. It is normal for you to lose your temper and get angry at times - as do all other caregivers. Your anger may be mixed. It may be directed at the person, yourself, the doctor, or the situation, depending on the circumstances. It is important to distinguish between your anger at the person's behaviour, resulting from the disease, and your anger with the person, as this will help you to cope better.Try to understand the person's behaviour that is upsetting you and see if you can stop or reduce it, as it will not help either of you to lose your temper. If you think you are going to lose your temper, go into another room or into the garden and give vent to your feelings away from the person with dementia.It may be helpful to seek advice from friends, family, or a support group. Sometimes people feel so angry that they are in danger of hurting the person they care for - if you feel like this, you must seek professional help. Many local support groups have caregivers' contacts, with whom you can talk to and get advice from. Use these people to get help when you need it.[Photo]Embarrassment"Ease any embarrassment by taking the courage to explain the situation to people around you."You may feel embarrassed when the person displays inappropriate behaviour in public or disrupts the neighbours. It may take some courage, but by explaining the disease and the concept of dementia to friends and neighbours, you will help them understand the person's behaviour.Look for support from other caregivers who have experience of similar problems. Sharing your feelings with other caregivers will enable you to cope better and the embarrassment may fade.[Photo]Loneliness"Try to maintain friendships and keep social contacts, as loneliness makes caregiving harder."Many caregivers withdraw from society and, along with the person with dementia, are confined to and around their homes. Being a caregiver can be lonely - you may have lost the companionship of the person, as well as social contacts, due to the demands of being a caregiver.Loneliness makes coping with the problems of caregiving harder, so try to keep in contact with friends, and see if they can offer extra help. Explain the problems of dementia and that they, as friends, can help by providing you, or the person with dementia, some companionship.Maintain your own social engagements and take breaks from looking after the person. This will give you time and space to recharge your batteries and help you feel better about yourself.Consider joining a support group. Here you will find people with similar problems, who can help you get over the rough patches and provide a social life, where you do not have to be separated from the person you are caring for.[Photo]Family support"The family can be the greatest source of help."For some caregivers their immediate family is the greatest source of help. For others it is the biggest source of distress. If this is the case, you may feel that you have been left to cope as a caregiver on your own, which can lead to bitterness and resentment. If you are feeling distressed because family members are not supporting you, try to find out why they are not helping. It may be helpful to call a family meeting to discuss the care of the person.If you cannot get help from your immediate family then try to get help from elsewhere. Accept help from other family members and do not take on the burden of caring alone. Try to arrange breaks from caring to give you the respite care you need. You may find that by looking after yourself, you feel less stressed about the lack of family support.[Photo]Sharing problems"Share your problems."You need to share your feelings about your caregiving experiences with others. If you keep them to yourself, it may be more difficult for you to look after the person with dementia, as you may begin to resent them or get angry with them. Try to think ahead and have someone to turn to in an emergency.You will most likely find that your friends have not stopped liking or caring about you, and would probably be quite happy to listen or help if you let them know how. Try to accept support when others offer it, even if you do feel you are troubling them.If you can realise that the problems and feelings you are experiencing are a natural response to your situation, it will be easier for you to cope. If you do not want to bother your friends then seek professional help from the person's doctor or the local support group.[Photo]Taking time-out"Make time for yourself."It is essential to make time for yourself. As a caregiver you risk isolation by looking after someone with dementia. This can cause loneliness and sometimes anger or resentment towards the person with dementia. Taking time-out allows you to spend time with others. Enjoy your favourite hobbies and, most importantly, enjoy yourself.Support groups, social services and some nursing homes provide day care help, where you can leave the person with dementia in safety and comfort while you can enjoy time to yourself or with the rest of your family. Use the support available to you, so that you can have a rest.[Photo]Know your limits"Be aware of how much you can take, and seek help if caring becomes too much for you."How much can you take before it becomes too much? Looking after someone with dementia is a demanding role, which may be complicated by:your own physical or health problems lack of sleep financial uncertainty.Most people will come to realise how much they can take before caring becomes too demanding. If your situation is too much to bear, take action, seek additional support, and call for help to prevent or avoid a crisis.[Photo]Not blaming yourself"Dementia is no one's fault, the disease is the cause."Do not blame yourself or the person with dementia for the problems you encounter. This is particularly hard if the person cannot remember who you are or if they are violent. Remember the disease is the cause not the person.If you feel your relationships with friends and family are fading, don't blame them or yourself. Try to find what is causing the breakdown and discuss it with your friends and family. These relationships can be a valuable source of support for you and the person with dementia.[Photo]Seeking and taking advice"Learning to seek and take advice can help you be a better caregiver."Learning to accept help may be new to you. More often than not, family, friends and neighbours may want to do something to help you and the person with dementia.Self-help groups (a group for caregivers) can be another source of help for you. They provide an opportunity to get together with other helpers and caregivers, who may already have experienced the problems you are facing. Through their combined experience, these groups can be an invaluable source of help, comfort and encouragement.Your doctor, community nurse or social worker may also be able to help you. They will be able to provide you with help and advice about looking after the person and the support available. If they cannot answer your problems themselves, they will usually be able to put you in contact with someone who can.