Alzheimer's Care Benefits

There are many community services out there to aid dementia patients these may include community nursing, meals on wheels, homecare, home modification, Alzheimer’s Australia, commonwealth centerlink centres, carers association, counselling, ACAT and respite care.

There is a limited number of family members and medical staff for the growing Alzheimer’s population. An important goal that we have included in our Outcome Goals is to identify, educate and increase the number of volunteers at facilities such as the Rosener House. This will increase the positive human contact for these residents and increase the time the medical staff has to address specific health needs of the elderly Alzheimer’s residents.

From the obvious and widely-reported physical benefits to the researched, studied, and documented healing powers, and mental and emotional benefits. So, when we look to yoga's effects, especially on the brain, it's not exactly surprising to find that there's benefits there, too.

Alzheimer’s disease is not only life-changing for those who are diagnosed but also for their loved ones. Caring for someone with Alzheimer's disease or a related dementia is a difficult, stressful, and deeply emotional journey. Support groups are an essential part of that journey, whether it is for caregivers, family members, or those close to someone diagnosed with a dementia-causing illness.

(Beattie, 2002) An individual’s rate of progress through the stages varies, and symptoms are unique to the person, making it difficult for families to know what to anticipate, but if they are properly educated it may help them be aware of the different course of the disease, potential causes of behaviors, interventions and various treatment that may be used, making the outcome of care be more effective for the family and the patient. (Osborn&Vaughn, 2010)

One of my main questions was whether I could do anything emotionally to cope with Alzheimer’s and with that search I had better luck. One of my favorite pieces of information I found was to face your feelings head on “think of all emotions...positive and negative...be as sad as you want...work through anger and frustration...these are healthy feelings...it’s common to feel love and anger at the same time” Taken from a paper published on (“Alzheimer’s Association website”). The next thing I found that helped me personally was how to deal with guilt, personally I’ve experienced feeling guilty when taking a break or not being there for my grandma when she needed me, as well as regretting things I had done before knowing about the illness. Something interesting I found that I would’ve never thought of was to continue to participate in as many activities as possible.(“Alzheimer’s Association” pg. ) I also found that a good way to keep an emotional connection longer is to personally connect with the sufferer. A few ways to do that is to keep eye contact with throughout the conversation, to always refer to them by name when talking, continue the conversation as long as possible because is makes the person with AD feel better about themselves, and be aware of the body language you’re presenting (“Grief and loss as Alzheimer’s progresses” pg. ). I would say the most essential piece of information I learned was the best thing I can do is just comfort the person with AD and make their time left as easy as

The impact that Alzheimer’s disease has on the patient’s family and caregivers is really devastating. It must be very hard for the patient’s family to see what their loved one is going through. They may feel grief and lose. It is a very unfortunate thing for both the patient and the family to live life with the loss of memory. They may have had so many good memories in the past but due to this disease patient may lose all those memories. It is very hard for family and caregivers to see the patient struggling with doing daily activities due to memory impairment. Sometimes it can be overwhelming for family members and caregiver to manage time because they have to give extra attention and dedication. They need to make sure that the patient is

Knowledge can empower you when it comes to being a caregiver, just as it can in most other areas. There are many online resources designed specifically for caregivers including those provided by the Alzheimer's

According to the Alzheimer’s Association (AA) (2016), it is estimated that in 2015 nearly 5.3 million Americans have Alzheimer’s disease and of those citizens, 5.1 million were 65 years old or older (“Alzheimer’s Disease Facts and Figures,” 2016). This non-curable form of dementia, a general term for a group of symptoms of declining mental abilities that interfere with daily life, effects and kills 1 in 3 people in the geriatric population (AA: “Alzheimer’s Disease Facts and Figures,” 2016). It is important for nurses to be aware and knowledgeable of this disease because of the huge prevalence of Alzheimer’s in the American population. Nurses should be educated on treating and battling the

Overall the best option for the patient is a nursing home . Family members can hire full time nurses to take care of their ill loved one in their own home. Even though it sounds like a better option than a nursing home it can be more expensive than a nursing home . According to Planning for Care Cost “$20 per hour for a home health aide ,$68 per day for adult day services’ (Care Cost 1 ). These are some of the cost for having a nurse take care of an alzheimer patient , it doesn’t cover the medicine and other expenses they might need

Alzheimer’s disease, the most common form of dementia, is a progressive neurological disease afflicting 24.3 million people worldwide. 4.5 million people in the United States are diagnosed with this illness annually (Leifer, 2009). Victims of Alzheimer’s disease reach a stage when they are no longer self-sufficient. Those with severe symptoms or lacking family support systems are relegated to nursing homes. Although scientific studies indicate that Alzheimer’s disease leads to a loss of memory and independence, researchers have proven that caregivers are also affected both physically and emotionally. Research is currently being conducted in finding ways to treat Alzheimer’s and helping their caregivers in the process.

There is a growing epidemic in the United States that makes life for senior citizens fraught with danger and uncertainty. The current state in which millions of senior citizens live is frightening. Since 2015, there is an estimated five million people who are dealing with the effects of the Alzheimer’s disease and around 83,000 who die from it each year. Although doctors have some methods of treating Alzheimer's disease, these methods are quite inadequate. Even if family were to use the current Alzheimer’s disease treatment methods, it would only minimally delay the effects of Alzheimer's disease. Additionally, the treatments for Alzheimer's disease is often too expensive for family to cover the cost. With all of this in mind, it is necessary

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

Since people with Alzheimer’s have problems in doing daily tasks, the caregiver plays a significant role to take care of them. The caregiver center launched by the Alzheimer’s Association offers online guidance to help people become a caregiver step by step.

Living with dementia and Alzheimer’s can be very difficult. Especially if the patient lives alone it can be quite difficult. Things that were once easily done are now harder to do. Making meals can turn dangerous very quickly, Taking medication with no one around can be more than difficult because that patient may not remember to take that vital medication, Or another scenerio is that the patient may forget that they have already taken their medication and take more than their supposed to. Both are dangerous situations.