The Daily Mail has recently carried an an article by Dr Keith Souter about why dementia gets worse when the sun goes down – and what anxious carers can do to make things better.
Speech and Language Therapists also have a part to play in the care of dementia patients because of the effect the condition can have on a person’s ability to communicate.
Their communication can start to become more difficult particularly in relation to finding the right words and remembering names of people and places.
But there are things that you can do to help facilitate better communication between yourself and the person with dementia, which this article outlines.
The article in the Daily Mail states “Looking after someone with dementia can stretch people to their limits, and there are many in this situation. In England alone, there are more than 670,000 unpaid carers helping someone with dementia……
…….The early stages of the disease bring changes that may be so subtle that some friends and acquaintances are unaware that there is anything wrong – and this stage can continue for many years.
But as the disease progresses and more damage is done to the brain, symptoms become more pronounced: difficulties with communication become more intense and issues such as getting dressed or managing day-to-day affairs become more problematic.
This marks the beginning of the middle stage, the longest stage, which can last for several years. It’s when the condition becomes more challenging and extra help may be needed.
However, there will be good days as well as bad. The following can help . . .
Establish routines
In the early stages of dementia, it’s the short-term memory that’s most affected, making it harder for patients to keep track of the day, or even what time of day it is.
I’ve found that sticking to a routine helps keep someone with dementia better orientated, and gets their body clock into a rhythm.
In the early stages, aim to establish fixed times of day for the following – it may help to write this on a board that’s kept next to a calendar (cross it off to show what day it is) and a clock, so that they know what to expect when.
- Bed and getting-up times.
- When to take medication.
- Meal times.
- Shopping days.
- Leisure time such as TV, radio or social times.
In the middle stages of dementia, routines may still be useful but patients can be more prone to mood changes, so be flexible. Encourage but don’t coerce.
When behaviour changes
The middle stage of dementia inevitably heralds changes in behaviour. This can be one of the toughest things to cope with, for at times it may seem as if the person you know and love has gone. The following are common:
Clinginess
This can be very draining as some people with dementia do not like to let their carer out of their sight. Clinginess is the return of a psychological reflex from our toddler years – a toddler will cry when their mother moves away or when a stranger approaches.
As the dementia progresses, the loss of nerve cells in the brain allows old reflexes that were replaced in adulthood by more complex brain pathways to resurface.
What to do: The best way to deal with it is by diluting contact – try introducing other regular carers as soon as the person being cared for starts to display any clingy behaviour. The clinging behaviour may now apply to many people, not just one.
Wandering
Around 60 per cent of those with dementia wander – pacing around the house or outside of the home – and the problem is they can get lost, as the damage to the hippocampus part of the brain means they lose their sense of orientation.
What to do: If they tell you they’re going out don’t argue but speak calmly and tell them they don’t need to as they are ‘staying here’ tonight.
Avoid busy places such as shopping centres. People with dementia may find these disorientating and when they get home this disorientation can continue and induce wandering so they may feel the urge to leave the house.
Wandering about the house at night can arise from a need to go to the loo. Ensure they don’t have too much fluid before bed and install night-lights to help prevent falls. Painting the walls and doors a matching colour makes it less likely that the person with dementia will find their way out.
You could also consider moving the lock higher up the door to a less familiar place.
You may want to consider installing movement sensors to alert you to potential problems.
Anxiety
Worrying for no reason or displaying physical symptoms such as palpitations are signs that the dementia patient may be suffering with anxiety.
What to do: Try to identify what’s causing it – have there been more people round than normal, or have they had too much caffeine? Many of the triggers may be unavoidable, but it can help to keep their surroundings as comfortable and relaxing as possible.
Put pictures and familiar possessions around them. Pleasant smells such as flowers, baking aromas and soap may trigger memories that help distract them from their anxious feelings.
Playing music can also be calming. Talking to them can distract them, too. But never talk down to them or use childish language as this could make them angry.
Anger and aggression
It can be confusing when someone who was once so patient and tolerant becomes prone to temper tantrums.
What to do: It’s important to consider any physical reasons that might be making them this way.
Pain is a common cause of anger in those with dementia, as are urinary or chest infections, a stroke, or even something as simple as not having had enough sleep.
If you suspect any of these is possible, then speak to a doctor.
Speak to the person with dementia reassuringly, in a calm manner. Use music or a calming activity such as massaging or stroking their hand or brushing their hair to distract them.
If, however, they seem aggressive do not put yourself in danger. If necessary, move back and wait for them to calm down.
Often people with dementia have good and bad days but also good and bad times during a given day – and often they may display more symptoms and anxiety as the light starts to fade, becoming confused, agitated, restless or showing repetitive behaviours.
This pattern is referred to as ‘sundowning’.
It’s not clear why this happens – it’s possible it’s to do with a disruption to brain chemicals affecting the body clock. Two-thirds of those with Alzheimer’s disease experience sundowning.
It can occur at any stage of the condition, but tends to peak at the middle stage and lessen as the disease progresses.
What to do: Keep the person busy at sundown and in the early evening. Avoid stimulants such as coffee or alcohol at this time of day as this may make them more excitable. A rocking chair can help as it is soothing and relaxing. It may also help to introduce more light into the room.
LOOK THEM IN THE EYE WHEN YOU TALK
With dementia, the parts of the brain that normally deal with understanding, thought processing and language deteriorate.
The patient may struggle with nuances and may lose their sense of humour; they may also get frustrated and cross when they can’t quickly bring to mind the words they need.
Furthermore, they may seem to get stuck in a loop and repeat the same question again and again.
The following strategies can help tackle these issues:
- Before you start talking always engage eye contact to help get the person with dementia to focus on you. There can be a tendency for them to look away and this makes it harder for them to concentrate on the conversation.
- Be careful about asking questions they may be unable to process. For example, if they’re upset don’t ask what’s wrong as they may not know, or are unable to put it into words. Instead, tell them: ‘You seem to be upset; let’s think how we can make you feel better.’
- Finishing sentences for them can increase frustration. It’s better to ask if they’d like you to find words for them if they’re having difficulty.
- Watch their body language as this can give you clues about how they are feeling. For example, repetitive movements can mean they are anxious or scared, while withdrawing may mean they feel overwhelmed.
- If they’re doing something obviously wrong, for example putting dishes in the washing machine or clothes in a food cupboard, don’t ask them why or castigate them – the reasoning side of their brain has been affected and pointing out their mistakes will only cause them embarrassment and frustration.
Better to say: ‘You seem to have put the crockery in the washing machine. Did you mean to put them in the dishwasher?’
■ Dr Souter is a retired GP and fellow of the Royal College of General Practitioners. Adapted by LUCY ELKINS from Your Guide To Understanding And Dealing With Dementia by Dr Keith Souter, published by Summersdale.
For more information go to the Daily Mail
Written by Rachel Harrison, speech and language therapist, on behalf of Integrated Treatment Services.