Alzheimer's Travel Anxiety Research Paper

Allow the person with dementia and their family plan and make arrangements for the future

Family/friends: when an individual is given a diagnosis of dementia it impacts on their friends and family too, they may feel angry or guilty but may also have an overwhelming fear of what they can do to support the sufferer and each other at present and in the future. Will they be able to cope with the level of commitment to the individuals needs on top of their own daily trials? Not to mention the added financial/emotional stress. Support services are available for care givers alongside the person suffering with dementia via Gp, social services or online forums.

After Alzheimer's is diagnosed in a parent, or other elderly family member, the caregiver has the task of deciding what the best form of care for the patient is. In order to do this they have to fully understand what the disease is, and

If you’re a caregiver you know that some days are better than others, but when you’re caring for a person who suffers from Alzheimer’s it can feel like things change from minute to minute. The professionals at Senior Care Transition Services provide free resources and senior living advice to people in the Dayton, OH, area who are looking for in home care providers, medical services, senior services, and assisted living communities. They know how trying caring for someone with Alzheimer’s can be and they have 3 valuable tips for all of the dedicated caregivers out there:

Alzheimer’s disease can have a big effect on family members around the person with the disease; it would be upsetting seeing a loved one got through such a major change in their behaviour and their mental capability. If you live with someone with Alzheimer’s and they are wondering in the middle of the night and have sleep difficulties and this can disturb the family in the house. Also if they are wondering around in the middle of the night around the community the police may pick them up, meaning they are again disturbed as the police will need to contact someone to make sure that the person is ok. There are also worries about financial problems that the Alzheimer’s sufferer may have, if they cannot manage

The goals the National Social Advocacy Association for Alzheimer’s Patients is to collaborate with long term healthcare facilities in establishing an innovative, comprehensive social advocacy, intervention, and advance treatment programs in healthcare facilities serving or providing Alzheimer’s patients. One that will help stimulate the “Central Nervous System and Peripheral Nervous Systems sensory” nerves which will increase the cognitive and mobility functions in Alzheimer’s Patients Marieb, (2006). In addtiont to reducing caregiver’s burnouts, eliminate Alzheimer’s patients injuries due to neglect, increase caregiver’s social awareness of Alzheimer’s disease and its risks facts,

People with Alzheimer’s try to continue doing normal everyday activities. Depending on how bad the progression of the disease is, this could be a very dangerous situation for them and could make their loved one’s very worried. One time, my grandpa decided that he was going to go to the store to buy groceries. So he took the car keys, hopped in the car and drove to the grocery store without my grandma realizing that he had gone. He bought some groceries then started going back

They may still be able to drive, work, and engage in social activities. However, they will notice that they are forgetting things such as doctor’s appointments. They may not be able to find the correct word to describe something simple such as a banana being yellow. They may also become reckless with their money, perhaps donating thousands to any charity that calls them. Moderate Alzheimer’s is typically the longest stage and one may notice more significant changes with the client such as not bathing, “sundowning” which is being more awake and pacing during the evening hours when they should be sleeping. The damage inside their brain makes it difficult to perform daily tasks such as cooking or cleaning. As time progresses, more memory is lost and the thought of them driving can lead to accidents or them becoming lost and unfamiliar with their surroundings even though they have lived in an area all their life. In the final stage, Alzheimer’s disease, will take away their ability to speak, control movement, and eventually the brain will stop the life sustaining body systems and they will die. In the final stage, they will need caregiving around the clock, which takes a tremendous toll on their family.

Psychosocial treatments can be affective for both the family as well as for the person who is diagnosed with Alzheimer’s. Part of this includes normalization of degradation of the illness, as well as providing the family with the proper tools to communicate with their loved one. For example, it can be important to learn to communicate questions that include the answer in them to ease the stress of the person who is trying to recall a word or person they may have seen. For instance, instead of asking “Who came to see

Dementia is an extremely common disease among the elderly, with 4 million Americans currently suffering from the Alzheimer’s type alone. Figures show that 3% of people between the ages of 65-74 suffer from the disease, rapidly increasing to 19% for the 75-84 age bracket, and as high as 47% for the over 85s. Therefore, it is easy to see why Dementia is such a large part of many people’s lives, whether they are suffering from the condition themselves, or have an elderly relative who requires full time care just to undertake simple day to day tasks. The disease can be extremely traumatic for the patient and their families, as the person, who may have been extremely lively and bright throughout their

Alzheimer 's disease is a condition that affects the cognitive status of many people around the world regardless of wealth, ethnicity, intelligence or any other factor. A specific case study that demonstrates the destructive nature of the disease can be seen in the case of Akram. Akram was an 80-year-old woman with a past medical history of hypertension, diverticulitis, transient ischemic attack (TIA), and diabetes. Her history did include a serious head injury at the age of 45 from an automobile accident, but she recovered well after some time in the hospital. As she aged, she could remember childhood friends and family from 20+ years ago quite well. What tripped her up were simple daily processes of life. She might put food in the oven to cook, but fail to turn it on after doing all the prep work. Also, she began to frequently misplace her keys and have trouble remembering where she put household items. She had been a very intelligent person with a lot of energy and had previously been involved in a lot of volunteer projects she helped run. Upon talking to her husband, it was learned that she had been having similar difficulties over the past two years. Driving was a big issue as well; she felt she could recall how, but still had trouble operating her vehicle. She also frequently got lost on routine trips, like to the grocery store. Additionally, she would forget whether she had eaten and had several extra meals in a day unless a helper or a family member was keeping

This can be true even at the onset of dementia, they can become disorientated and confused (Alzheimer's Association, 2015). This type of situation should therefore be anticipated, and the staff trained in what to do in the event it occurs: (1)carrying out a structured daily routine to minimize confusion, (2) identification of the most likely times of day that wandering can occur and planning activities during those times, (3) activities to reduce anxiety, agitation and restlessness,(4) reassurance scripting for when a person feels lost, abandoned, or disorientated, (5) the use of non-corrective dialog that is focused on exploration and validation when the patient starts talking about wanting to leave to “go home”, or “go to work” etc., (6) ensuring that all the patient’s basic needs are met-like food, drink, and toileting, and (7) avoiding busy hectic places like shopping malls and grocery stores during outings (Alzheimer's Association,

Alzheimer’s disease has many affects on the patient’s family. It’s important to determine what the family’s needs are, and what they need to be educated on as they watch the disease progress. Family members need to be aware of the numerous resources available for them and their loved one, especially for when their health deteriorates. Some available resources include: Home health services, respite care, long term care. We need to provide support to the families, and there are many local support groups that they can attend. Respite care should be offered to give the family members a break. Family members need to let their feelings out, we need to encourage them to be honest with themselves, and to not bottle anything inside. Adult day care

If your loved one has recently been diagnosed with Alzheimer's disease, learning everything you can about the common form of dementia is critical to getting the best care for him or her. Understanding the truth of common Alzheimer's myths can help you and your loved one understand the disease better.

     Alzheimer’s, the most common form of dementia, is a disease that afflicts more than 4 million older citizens in the US. Alzheimer's is a degenerative neurological disorder that leads to impairments in memory, thinking and reasoning. AD is the most common cause of dementia in older people, and mainly affects people 65 and over. Within the last few years, there have been drugs that can temporarily treat the patients, but it remains a form of dementia that is irreversible. The disease is very hard on both the person who receives the diagnosis and on his or her family and friends. Aside from medical help, those affected by the diagnosis may want to consider counseling and support groups to help them cope.