Alzheimer's Support Groups

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

Caregivers play a crucial role in the care of dementia patients. Providing care for dementia patients results in stress related health impacts to the caregiver. The caregivers go through a journey with the dementia patient and need a strong support system. The best approach to dementia care is for health care providers to provide information to and monitor the caregiver, in addition to the dementia patient, encourage the caregiver to take care of themselves, to seek support, and to work as a team to provide the best care for the dementia patient.

Everyday more and more people are effected by dementia. This disease is taking over the lives of innocent people around the world. The U.S. Department of Health and Human Resources have designed The National Plan to Address Alzheimer’ Disease. This plan focuses on many important areas greatly affected by this irreversible disease and concentrates on the struggles one faces during its presence. I found three areas to be very important to the future of Alzheimer’s and other dementias; Expand research aimed to identify and treat Alzheimer’s, Educate and support people with Alzheimer’s and their families upon diagnosis, and Enable family caregivers to continue to provide care while maintaining their own health and well-being.

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:

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,

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

It is a complex disease people often times do not know how to care for. Although a decline in memory and bouts of more forgetfulness are more common as one ages, spotting the difference between normal age-related symptoms and Alzheimer’s is important for families so that they can get their loved one the best care available. Even with proper care though, caregivers can misunderstand the symptoms of those afflicted, leading to an improper treatment of the patient. There are an estimated between 2.4 and 3.1. million AD caregivers in the United States, a majority of which are family members, who may not know proper care techniques or may be of older age themselves, as they could be caring for a spouse (Schulz and O’Brien1, 185-94). In fact, in a study of caregivers of those to patients with a memory ailment including Alzheimer’s or Dementia found that spouses have consistently been found to be more depressed than other relatives caring for a family member with a cognitive impairment (Schulz and O’Brien2, 771-91). To help in awareness, there are many new classes being offered in schools that can better prepare caregivers. The U.S. Department of Health and Human Service’s (DHHS) National Plan to Address Alzheimer’s Disease dedicated a major goal to “Enhance Care Quality and Efficiency,” with major strategies including building a workforce with the skills to provide high quality care, explore

In the book, Surviving Alzheimer’s: Practical tips and soul-saving wisdom for caregivers, the writer, Paula Spencer Scott, gives insightful advice in regards to caring for someone that suffers from the unfortunate neurological disorder, Alzheimer’s. Scott does not hesitate to share multiple ideas, experiences about trying these ideas, and even included professional advice from geriatric specialist

Alzheimer’s is a degenerate disease of the brain. There are an estimated four million Americans that live with Alzheimer’s, it is believed that the disease accounts anywhere from 50 to 70 percent of all cases of dementia (UCSF medical center). The vast amount of cases leads me to believe that we would not need to look very far to find either a friend or family member distant or close that has had a personal or familial experience with this disease.

Dementia can have a detrimental impact on takes a devastating toll on carers, affecting both their physiological and psychological wellbeing. According to the a poll, administered by the Alzheimer’s Association (2016) in the US, which questioned 3,102 adults in America about their attitudes, knowledge and experiences related to Alzheimer’s disease –, about 60 percent of carers of people with dementia carers rated their emotional stress of caring as high or very high, nearly 40 percent said they suffer from depression Aand approximately 74 percent said they are "somewhat" to "very" concerned about maintaining their own health .

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

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.

Alzheimer’s disease is one of the most prominent health issue in older adults. In fact, more than 35 million people are diagnosed with Alzheimer’s disease worldwide. (D’Aoust, Brewster, & Rowe, 2013) Of these individuals, a good portion are taken care of by at home caregivers. These caregivers can described by husbands, wives, mothers, and fathers. “Alzheimer’s disease (AD) is a chronic, progressive illness characterized by impaired cognition, loss of ability in instrumental and basic activities of daily living (aDL), reduced global functioning, and behavioral and psychological symptoms” (Haro, Kahle-Wrobleski, Belger, Agnello, Jones, Reed, Vellas, Wimo, & Argimon, Pg. 677, 2014) As the amount of patients with Alzheimer’s disease

In the pamphlet Basics of Alzheimer’s Disease, the Alzheimer’s Association adds late onset, traditionally known simply as Alzheimer’s, targets primarily people 65 and older. The disease follows a series of steps from mild decline with little noticed changes to very severe cognitive decline where the final stage of the disease is in progress (Basic 19-21). Throughout the stages, independence becomes lost and family members will become care takers and in the later stages nursing homes or hospice may be needed. One book encourages the care giver to communicate through body language, tone, and written instructions to help alleviate as much stress as possible for those living with Alzheimer’s (Living 47). The book further adds when caring for a person with Alzheimer’s remember to maintain patience and to show respect .

The authors opines that due to the advances in medicine our life expectancy is likely to extend and many of us will be called upon to be caregivers for someone in our family who requires special care. This book guides and educates readers on what can be done from a caregiver's standpoint to be better equipped to nurture people living with Alzheimer's disease. This book is authoritative as it packed with tips and techniques from five authorities in the field, and provides insights such as: What caregiving style will suit me best? What skills are likely to remain as Alzheimer's disease progresses? How do I balance my needs with the needs of the person I'm caring for? And much more! The most important tenet of this book is that we can better care