Dementia Can Change A Person's Personality

Being diagnosed with dementia will affect people in different ways. The service user could become withdrawn and depressed, this will affect their well-being and how they look after and treat them self’s. They can start to self-harm or neglect them self’s through personal hygiene or through there eating, eating too much or too little. They may even become so depressed and down in mood

the importance of relationships and interactions with others to the person with dementia, and their potential for promoting well‑being.

The medical model of dementia dominated the traditional approach to dementia care until the 1990’s. The emergence of a social model of dementia after that time was partly to this dominance. It was also part of a wider social and civil rights movement at that time which people with disability were viewed and

“Alzheimer`s disease is called a family disease” (ALZlive), because it impacts every family member who is slowly watching a loved one decline. Alzheimer’s disease has an impact on caretakers because caregivers can lead to a variety of emotions, from guilt to anger. When dealing with a client who has Alzheimer; caretakers have a huge responsibility, which can cause stress or depression. If the caretaking is a family member it might lead to finical problems, which can lead to the hard and controversial decision of putting someone in a nursing home, that is better equipped. Guilt is the main emotion that a caretaker can express “I have never spoken to my mother`s doctor, it occurs to me that other children of

and risk. People with dementia can have mood swings and there personality can even change altogether. As carers we need to set boundaries to keep a person safe without infringing on a there rights, which can be difficult, especially in the advanced stages of dementia but there are some effective techniques to aid.

All forms of dementia can affect the way a person communicates, so in time they may have to find different ways of expressing themselves and their feelings. As a carer your non-verbal communication will become important, your body language, facial expressions, gestures, eye contact and tone of voice will have to be taken into account when you are communicating with a sufferer. In the early stages of some forms of dementia people may have difficulty finding the right word they are looking for, and in the later stages of some forms of dementia the words could be lost completely. As the dementia progresses, it gets a lot

Individuals with dementia have impairment in mental capacity and people can discriminate against when it comes to exercise their rights. People with dementia face a poor quality of life which lead the person to be isolated and loss his self esteem.

Some carers may not feel they can approach the person because the assume they are violent. If a person gets violent it is due to frustration and not being able to express themselves and you should always try to work out what it is that triggers the outburst or what is frustrating the individual. It helps if you know how to approach the person so they don’t get agitated. You should always try to form positive relationships with the individuals and by getting to know them better, you will be able to provide them with better care.

and risk. People with dementia can have mood swings and there personality can even change altogether. As carers we need to set boundaries to keep a person safe without infringing on a there rights, which can be difficult, especially in the advanced stages of dementia but there are some effective techniques to aid.

• Every individual, including individuals with dementia, has their unique life history, lifestyle, culture and preferences, including their likes, dislikes, hobbies and interests, which makes an individualised approach in care necessary.

1.4 The impact the behaviours of carers and others may have on an individual with dementia include becoming more confused and frustrated as they do not understand what you are telling, are using body language that suggests something different to what you are saying. They may feel you are telling them off or

They observe that family caregivers were concerned about possible damage to the self-image of older adults and were uneasy about exposing them to upsetting situations. This is evidence enough that fundamental change in clinical practice is called for and that there are barriers that tend to affect services access by dementia sufferers and family caregivers.

Dementia is the loss of brain function it’s most likely to affect memory , thinking , language , and behavior. With certain caregivers they should feel comfortable because they can have a lot of frustrations during this time . According to “What Does Dementia Feel Like” it states “it's the feeling you get when things don't make sense or you don't know what you should be doing. If someone seems angry with you it can feel terrible remember that it's not your fault. They may not be able to control their emotions anymore.” Caregivers should always stay calm and repeat what was being said to make the patients feel more comfortable like you are on their side.

At some point in our lives we have probably all known someone that had or has dementia. Dementia is a generalized term that refers to the progressive, irreversible decline in mental function. Dementia is a disease that not only affects the patient but also affects the patient’s loved ones. Caring for a loved one with dementia can be very difficult and heart breaking but there are lots of resources to help.

With dementia, independence is lost. The unreliability of short-term memory and confusion makes it difficult to be around the person. and leads to more isolation from friends. Support and comfort come from praising the tasks that can be accomplished and offering frequent reminders of place and time.