Alzheimer’s disease is the most common type of dementia.
There are over half a million people living in the UK, with Alzheimer’s disease (AD).
Alzheimer’s can affect different parts of the brain, but mostly impacts the hippocampus, the area responsible for our day-to-day memory.
Alzheimer’s will steadily degrade neurological capability by blocking connections between nerve cells with protein buildup in the form of amyloid plaques and tangles. As the connections between cells are lost they die, the brain tissue and function also dies with them.
Being a progressive disease, it gets worse over time and as for now it’s incurable.
Those living with this condition can still live a long, happy and fulfilled life.
In this guide we discuss the different available options. The option you choose with vary, depending on the stage and your personal journey with Alzheimer’s.
Alzheimer’s Research UK have found, only 39% are living in a care home. The remainder live in the community, using services such as live-in care.
There are advantages of a care home, they are quicker to access and to organise as local authorities are experienced towards using them. Making the process of getting everything in place easier.
Those who have acute, late-stage symptoms may benefit from specialist facilities. Medically-led care services like a nursing home will have a medical professional assisting your loved one at all times. It is best to look at the care plan to determine if this is right for your loved one.
Care homes’ with specialist Alzheimer’s care facilities, tend to be more expensive and are harder to find, although there are a good option depending on the level of care needed.
The cost of residential care facilities can vary too. The average cost can be around £845 per week, this can increases too as there is a difference in regional costs. For example, you may pay over £1500 in South East England and in London.
We can provide specialist Live-in care for Alzheimer’s or dementia, having a experienced and trained carer live in your home to take care of you. They will provide help and support with everything as the condition progresses. The level of support and care received depends what is needed at early stages, to more intensive support in the later stages.
In the earlier stages you may want to start considering care options.
On the onset of any condition, it would be beneficial you get as much information as possible. Speaking to your loved one’s GP and there are many established charities, such as the Alzheimer’s Society, Dementia UK and Independent Age you can contact and learn more.
You might start noticing your loved one’s forgetfulness and lack of orientation on a daily basis. This is when you might want to plan and understand the help available to you and changes that would be needed to make.
Your loved one may be prescribe a number of treatments, that will help them to live a longer, happier and more fulfilled life. Life expectancy can be up to 20 years following diagnosis.
Current drug treatments for early-stage Alzheimer’s are focused on a temporary easing of symptoms such as memory problems and lack of concentration.
These drugs are:
• Donepezil — brand names Aricept, Donepezil common drugs used to treat confusion associated with Alzheimer’s, usually taken before bed. This can help with improved focus, awareness and cognitive ability. .
• Rivastigmine — brand name, Exelon Rivastigmine taken twice a day. Prescribed for early-stage symptoms of Alzheimer’s, also for Parkinson’s and Dementia for cognitive ability and awareness.
Further evidence also shows the below can help slow the onset:, living well with any form of dementia is not just about potential drug treatments. It’s also about taking a holistic perspective towards wellbeing. There is an increasing body of
• Regular exercise — It doesn’t have to be intensive training. Keeping active can mean simply taking a walk around the local park or neighbourhood. Or is it could be going for a light weekly swim, or doing simple yoga or tai chi exercises.
• Staying sociable — Is increasingly linked with reducing the impact of memory loss and may slow neurological degeneration. Keeping current social networks or meeting new people by joining community clubs could help.
• Mental activity — Using your brain is proven to reduce cognitive decline, slowing the impact of Alzheimer’s Disease. From reading the morning paper, completing puzzles such as crosswords or sudoku, or doing arts and crafts.
For more information, read our guide on living well with dementia.
When it comes to care, this time of the diseases progress is all about being adaptable, calm and patient with increasingly difficult circumstances. This can severely impair someone’s ability to remain independent, meaning they can become increasingly reliant on someone helping them out.
For family carers, the middle stages can spell the start of frequent personal care requirements. These are generally characterised by support with washing, dressing and occasionally toileting – although this can vary significantly from person to person.
If you’re looking after a loved one, you may start to notice individual quirks related to their cognitive decline. In response, you’ll likely have developed strategies to cope.
However, with the support and advice from a medical professional or GP, the middle stages are the best time to put a professional carer in the home.
This will allow your loved one to begin to accept them into their routine for the most acute stages that are unfortunately yet to come. That aside, they can simply be a great support, offering lots of practical help.
As the symptoms become increasingly acute, so does the level of care that’s required. The later stages can be identified by a steep deterioration in someone’s condition. This can be an incredibly distressing time, and not one in which one family member should be left to cope caring alone.
Realistically, even if you’ve held off on getting outside help, as the disease intensifies you should really assess getting support. A live-in carer can help your loved one feel as comfortable, safe and supported as possible throughout this difficult and extraordinary time. This support can also give you the time to enjoy their company for the rest of the time they have.
Here is a run through of the kind of tasks your carer may undertake during the later stages of Alzheimer’s:
A vital component of late-stage Alzheimer’s care is ensuring the person being cared for is sufficiently fed. Clearly, as a person becomes increasingly inactive, the amount of they food required is reduced. However, it’s still vital they are well sustained and get to enjoy their favourite meals as much as is possible.
During the later stages of Alzheimer’s, the following could be required to support healthy eating and drinking.
In the later stages of neurological degeneration, trouble toileting is likely to become an increasing problem. This is for a variety of reasons.
It may be that mobility issues prevent someone from reaching the loo in time. It might be because sensual impairment stops someone from being able to feel they need to go. For some, it’s not being able to communicate to a carer that they need the toilet. And for others, issues with orientation can mean they’re unaware of where the toilet is.
The less mobile a person with late-stage Alzheimer’s becomes, the increased likelihood that they’ll be bed or chair-bound. This can have significant implications for someone’s skin and bone health. Problems such as pressure sores, frozen joints and the deterioration of the skin are all fairly common for those living with Alzheimer’s.
If these aren’t kept on top of, they can lead to a serious deterioration in someone’s health. Luckily, a carer is able to spot the signs and help relieve some of these symptoms. Here’s some of the things they can do:
Staying in a sedentary position increases the likelihood of contracting pneumonia and the flu. Reducing risk is about taking a more holistic approach to avoiding infection.
As people in the later stages are more prone to infection, bumps and cuts, they may occasionally feel in pain. However, this can be an issue if they’re unable to communicate that this is the case. It takes a carer with experience to understand when a person is feeling pain. They can do this by:
‘Palliative’ can be a bit of a confusing word. In short, it just means support for someone with a terminal illness. It’s a necessary step for someone with Alzheimer’s when symptoms have begun to deteriorate to the point in which they can no longer cope alone.
Palliative care may be needed for a few weeks, months or years. There are no limits. It’s all about ensuring anyone with a terminal condition is able to live out the rest of the time they have left with dignity, without discomfort or distress.
Usually, we find it’s best for families to choose a live-in carer with palliative experience when they know a loved one is facing a life-limiting condition.
For Alzheimer’s, this would be in the middle stages. As continuity is crucial, it can really bring that additional peace of mind to know you’ve someone the whole family will get used to and trust.
This differs from palliative care because it’s focused on those very final stages of someone’s life. It’s usually additional to any long-term support you may have put in place from a live-in carer.
Realistically, this is something families will only consider in the final weeks and months of someone’s life. With that in mind, it’s about helping someone pass away in a peaceful and dignified way, in as much comfort as possible and those they love around them.
It’s at this point that any advance decisions and advance statements relating to someone’s later moments will be taken into account.