Can I make a Lasting Power of Attorney after being diagnosed with Dementia?

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Can I make a Lasting Power of Attorney after being diagnosed with Dementia?

As you may know, a Lasting Power of Attorney is put in place so that someone that you trust implicitly (known as Attorneys) can manage your finances & property and/or your health & welfare decisions on your behalf.

A Lasting Power of Attorney must be put in place whilst the Donor (the person giving the Power) has capacity, and a Certificate Provider is required to certify this in order for the Lasting Power of Attorney to be registered by the Office of the Public Guardian.

Once diagnosed with Dementia is it too late to make a Lasting Power of Attorney?

Whether a Lasting Power of Attorney can be created and registered after a Dementia diagnosis will depend on how soon the diagnosis takes place and whether that individual has capacity, lucid or ‘good’ days and is still of sound mind.

If the individual still has capacity or has lucid days where they are clear on their finances, current affairs and appear to be unaffected by the Dementia then it may well be that a Lasting Power of Attorney can be prepared at this time and instructions taken from the individual. 

A Certificate Provider will meet with the individual and go through, carefully and sensitively, the current circumstances and ask questions as to that individual’s circumstances and personal affairs, as well as current affairs in the news and media, to ascertain their general capacity and mental wellbeing. If the Certificate Provider is content that the intended Donor has capacity, and they are aware of the importance of the Lasting Power of Attorney and the extent of the Power that they are giving to their Attorneys, then the Lasting Power of Attorney can be applied for and registered.

When registering a Lasting Power of Attorney, it may be necessary to notify people that an application is being made in order to protect the Donor. Notification can be given to up to five people although this cannot be given to those that are being appointed as the Attorneys. This provides extra security for the Donor and allows the person, or people, being notified of the intended registration the opportunity to object to the Power being registered for any of the following reasons:-

  • if they believe that the Donor does not have mental capacity;
  • if the person being notified has a genuine belief that the Donor was under undue pressure to give the Power or is a victim of fraud;
  • if the person being notified has a genuine belief that the Attorney would act in a way that is beyond their powers under the Power or would not be in the best interests of the Donor;
  • if the Donor of the intended Attorney, or Attorneys, have already passed away;
  • if the Donor and intended Attorney were married or in a civil partnership and this has now ended;
  • if the intended Attorney does not have the mental capacity to be appointed as an Attorney;
  • if the Attorney is bankrupt;

Having both Lasting Powers of Attorney in place means that, the Donor is able to appoint the people they know and trust (whilst still of sound mind to make such a decision) to make decisions for them when they are unable to do so for themselves, and takes an unnecessary stress away from both them and their loved ones at, what is already, a difficult time.

We are always happy to have a chat with you about putting a Lasting Power of Attorney in place, the Powers that are available and whether this is still a viable option for either yourself or a loved one.

If you would like to have a free chat about Lasting Power of Attorneys, please contact us on or 01727 865 121

A is for Alzheimer’s

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A is for Alzheimer’s
5 Early Signs of Alzheimer’s...
All beginning with A

Here we take a look at five of the early signs of Alzheimer’s and exactly what they mean…

Agnosia is where an individual is unable to recognise familiar objects, tastes, sounds or other sensations.

Amnesia is memory loss.

Anomia is the inability to remember the correct names of things.

Aphasia is where an individual is unable to express themselves through speech.

Apraxia is where an individual does not use an object for it’s correct use as they are unable to identify the object.

It is important to remember that having one, or a couple, of these symptoms does not necessarily mean that you or a loved one has Alzheimer’s and you should always seek professional advice but it is always important to keep an eye on changes and an early diagnosis can be so beneficial for those diagnosed and their loved ones.

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How does Dementia affect sleep?

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How do the most common types of Dementia affect sleep?

You may notice that those living with Dementia, especially in the later stages, seem to spend a lot of time sleeping, but why is this?

We understand that it may seem out of the ordinary, even concerning, for the caregivers and the loved ones of those living with Dementia if a change in sleeping habits is seen, especially a marked increase in the amount an individual is sleeping but there could be an explanation…

As the Dementia progresses the damage to the brain increases and this can cause the person living with Dementia to sleep more, especially as the individual becomes more frail.

The damage to the brain, of a person living with Dementia, will make their usual daily activities much more of a task and more complex, making it more draining on the individual and causing them to sleep more, both during the day and at night.

Medication prescribed to those living with Dementia, to control and alleviate their symptoms, may also contribute to how someone living with Dementia sleeps and how drowsy they are feeling during the day. This again, may cause someone living with Dementia to sleep more.

It is not uncommon for those living with Dementia to increase the amount that they sleep during the day which leads them to being restless and unable to sleep during the night time and so although it may, at first instance, appear as though the individual is sleeping more, it may well be just that their routine, and the times that they sleep, have changed.

One common symptom of Dementia is disorientation to time and place. This can have a major impact on an individual’s sleep as when they are disorientated to time they may be unaware of whether it is day time or night time, when they initially wake and so get up and ready for the day in the early hours of the morning or during the night. This will, of course, impact the time that they are able to stay awake in the day.

Specific types of Dementia may cause specific symptoms that will affect the quality of an individual’s sleep, or even their ability to sleep at all. Symptoms may include hallucinations, breathing difficulties and restless legs, all of which can disturb an individual’s sleep or make getting to sleep extremely difficult.

As individual’s age, our quality of sleep declines and we have less deep sleep, which helps us to feel refreshed and rested and also keeps the brain healthy. Thus, we may find ourselves sleeping more to achieve that feeling of being refreshed and rested and this is no different for those living with Dementia.

It is, however, important to remember that where there is a sudden change in an individual’s sleeping pattern or behaviour, or something just doesn’t seem right, then you should always seek the opinion of a GP or healthcare professional to ensure that there is no underlying issue, such as an infection, that requires attention.

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What to do after being diagnosed with Alzheimer’s

What to do after being diagnosed with Alzheimer’s

Whether receiving a diagnosis for yourself or a loved one, it is a very difficult time, so much information to take in and lots of changes on the horizon. It can be overwhelming.

Depending on where you are on your journey when the diagnosis takes place, may depend on the amount of information you already have and what is available.

Here we set out a simple list of steps that should be taken upon diagnosis to help you set off on the right path…

Knowledge is Power

You may have had experience with Alzheimer’s or Dementia before, or this may well be your first encounter, either way there may be symptoms that you are not aware of or have not experienced before.

The more you can learn the better. The phrase “forewarned is forearmed” comes to mind. The more we know, the better we can prepare.

There is a lot of support around online, groups, professionals, carers, families and individuals that have also been diagnosed all navigating a similar journey. Linking up with these groups and support can be beneficial mentally and emotionally.

Allow yourself to feel

As we have said, receiving a diagnosis for yourself or a loved one, is a very difficult time, so much information to take in and lots of changes on the horizon. Allowing yourself to go through the emotions you are feeling is okay.

You are not superhuman or a robot and taking time to acknowledge and process those emotions is invaluable.

There is no ‘correct path’ of emotions to take and so feelings of sadness, anger, frustration, disappointment and disbelief are all natural feelings.

Getting into a Routine

Getting organised and into a routine can really help, not only in terms of getting into good habits but to help set out early where everyone is, what should be done when and to know what is expected when. This is vital as the Alzheimer’s or Dementia progresses as routine and structure will be a necessity.

Alzheimer’s affects memory and so having a structured routine can help keep track of medication, appointments, activities and day-to-day tasks.

Routine can help to reduce stress, anxiety and frustration and increase independence and feelings of security.

Ensure your LEGAL and FINANCIAL affairs are in order

Managing your financial and legal affairs is impossible once capacity is lost. 

A diagnosis of Alzheimer’s or Dementia does not automatically mean that capacity is lost and so arranging the correct legal authorities are in place, whilst you have capacity to do so is vital.

You may consider reviewing your Will but also putting Lasting Powers of Attorney in place so that the person that you choose, and trust, has the authority to deal with your matters (financial, property, health and welfare) when you are no longer able to do so.  

We are always happy to have a free chat with you about this – CLICK HERE

Look at what CAN be done

Once a diagnosis is received is very easy to see this as a disabling disease that will only get worse and therefore discount capabilities, activities and all those things that were much loved prior to the diagnosis.


It is so important to consider what can still be achieved, the preferences, opinions and desires of the person living with Alzheimer’s.

A diagnosis doesn’t always mean that a person is incapable and they won’t necessarily lose their desire to carry out those activities that they used to love. Being able to carry this on for as long as is safe can be great for independence, self-esteem not to mention physical, emotional and mental wellbeing.

Consider a Care Plan

It is inevitable that as the Alzheimer’s or Dementia progresses the need for care will increase, as will appointments with an array of professionals.

There may be a range of people helping with care, loved ones, family, friends and professionals, and a care plan can assist with setting out who is responsible for what, what is expected and when this is expected.

Having a plan for now, as well as having discussions about what may be needed as the condition progresses, and how this could be catered for can save a lot of stress in the future.

Diagnosis is NOT the End

It is natural to feel that there is no light at the end of the tunnel or struggle to see what there is to be grateful for when receiving a diagnosis of Alzheimer’s or Dementia as the road ahead can seem somewhat bleak and overwhelming however, this doesn’t have to be the case.

Taking into account point 5 above and looking at what can be done means that it is not the end…fun can still be had, knowledge can still be gained and relationships can still develop. 

Yes, things will be different but that does not mean it has to be worse.

You are NOT alone

Remember, whether you are the one that has been diagnosed, a loved one or caregiver…you are NOT alone.

There are lots of support groups out there, those that you can attend locally and National support groups that you can access online.

We have a list of upcoming events that maybe local to you on our website HERE.

There are no stupid questions and so we should not be afraid to ask for help or assistance.

Everyone’s journey is different, neither right nor wrong. We all have different experiences and can learn something new.


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Decluttering to Create an Organised Home for Independent Living

Decluttering to Create an Organised Home for Independent Living

The home of someone living with dementia may have become cluttered because of a change in habit i.e. they prefer to keep their possessions where they can see them rather than store them away and risk not being able to find them or because they have lost the ability to look after their living space.

I wanted to share my experience of working with families in the early stages of dementia to create a safe living environment for longer independent living


Difficulties of Living in A Cluttered Environment

Living in a cluttered environment can make day to day living more difficult and confusing for someone with dementia.

It may cause: 

  1. Increased anxiety and stress from not being able to find what they need
  2. Increased confusion as useless things become mixed up with important items
  3. Increased risk of tripping as it becomes more difficult to differentiate one object from another
  4. Increased hygiene risk as it’s more difficult to clean a cluttered space
  5. Increased fire risk making emergency access more difficult


The Importance Of An Uncluttered and Simplified Home

Creating an uncluttered and simplified home can help to increase the chances of someone living with dementia to maintain independence for longer, in a safe environment. They can continue to perform daily tasks and avoid situations which may cause confusion.

In early dementia it is common for an individual to mislay items around the home and become upset about not finding the things that they need.

I have worked closely with my clients’ adult children or carers to create a new simplified living environment. This can be a stressful and emotional time for everyone. I have found that it works better if the changes can be made in the early stages when they are more likely to understand the need for it. At this stage they can be involved with the decision-making process of where to keep key items and making decisions on which items are important to keep and those that they no longer need.


Blissfully Organised’s Top Tips to Create an Uncluttered and Safe Living Space


Create a decluttering and organisation action plan for each room. The objective is to create a safe and comfortable living space. Understand the items that are important to them and their daily routine – medicines, keys, toiletries, clothing and kitchen essentials (their favourite mug etc). Once you know which items are essential you can start to eliminate unnecessary items. Simplifying the number of items will make it easier to find what they need, i.e. in the kitchen you can reduce the number of cups, plates, cutlery, glasses to the minimum required. In the bathroom you can simplify the items to have one of each, i.e. shampoo, toothpaste and toothbrush, soap, hairbrush etc.


Designate fixed locations for everything in the home, i.e. medicines, glasses, keys etc. 

Agree where key items should be stored in each room.


Keep frequently used items in view i.e. utensils in the kitchen or toiletries in the bathroom.


Never simply move things without communicating its new home. This can cause a great deal of stress.


You can label drawers or use photos so they can more easily find what they need in cupboards without having to have everything in view.


My clients are often reluctant to let things go because they feel that it may be useful one day or is wasteful to throw it away. 

I find it’s very important to reassure a client that the things that they no longer need will be recycled to a valuable new home.

If you need further advice or support on decluttering and organising the living space of a relative in the early stages of dementia please do not hesitate to contact me. 

I would love to support you.

Tracy Ross

Professional Organiser

Blissfully Organised

Tel: 07818 423 376

What are your thoughts?

Do you have an experience you would like to share?

Or, is there a topic you would like us to write about?

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