Lewy Body Dementia (LBD) is a disease that affects a person’s thinking and motor skills. Due to the illness, people with LBD may behave in ways that are different than the past. LBD causes people to absorb information more slowly, have problems with balance, have difficulty handling things, experience hallucinations and sleep more, among other symptoms.
It can be hard for friends and family to understand how someone with LBD feels—and even harder to know what to say or do. Members of the Ann Arbor Support Group for those with LBD have put together some suggestions.
I have Lewy Body Dementia (LBD). Please . . .
Give me some slack. It takes me a little longer to do things because my brain works more slowly, but I’ll get there. Just give me time.Continue reading →
It makes sense that after a night of poor sleep, we might not be thinking as clearly the following day. But what about engaging in poor sleep habits throughout our lifetime? Could that put us at risk for long-term cognitive impairments, such as dementia?
Even in people who don’t seem to be cognitively impaired, poor sleep seems to correlate with subtle changes in the same brain proteins that are used to diagnose Alzheimer’s disease and other dementias. The question is why.
There are several explanations, which are not mutually exclusive and could all be true:
Sleep is biologically important for reducing or clearing harmful neurodegenerative proteins from our brains. Exciting new studies in mice have suggested that sleep may clean the brain of amyloid beta, a protein linked to Alzheimer’s disease.
In partnership with a caregiver, Michigan Alzheimer’s Disease Center is offering support groups for people with Lewy body dementia and their caregivers.
Lewy body dementia (LBD) is the second most common form of degenerative dementia in the United States. LBD affects an estimated 1.4 million Americans. The symptoms of LBD are often mistaken for more well-known diseases like Alzheimer’s and Parkinson’s disease. They are so similar that only 30-50% of all LBD cases are accurately diagnosed.
What makes LBD different?
The presence of Lewy bodies—abnormal deposits of the protein alpha-synuclein that build up in the brain—distinguish LBD from other dementias. The Lewy bodies are tiny spherical structures that develop inside nerve cells. Their presence leads to the degeneration of brain tissue. Continue reading →
Studies in mice indicate that our brains may go through a process while we sleep that rids them of toxins that build up during the day
Did you ever wonder what happens to our brains at night? If recent studies in mice are any indication, our brains may go through a process that rids them of toxins that build up during the day.
The studies suggest that during sleep, there is an expansion of extracellular space within the brain that corresponds with increased fluid movement around and into the deep parts of the brain. This fluid movement is associated with a more robust exchange of small compounds into and out of the brain itself.
In mice studies, some of these compounds include toxic proteins—namely amyloid beta protein, which is implicated in the development of Alzheimer’s disease and other dementias. How external fluid moves into, within and out of the brain tissue still remains a mystery. Continue reading →
Well-being is at greater risk for care partners in dementia care primarily because it requires recognizing, identifying and responding to what can be an extremely insidious shift in roles, relationships and responsibilities. Emerging care partners are learning to respond to an illness that cannot be seen while being simultaneously assaulted by the stigma that often comes with a diagnosis of memory loss. Unlike other age-related illness, Alzheimer’s and other related dementias can result in enormous shifts in personal identity, in addition to how a couple and a family function privately and socially. Consider the following suggestions for cultivating well-being while care partnering:
ONE: Use the word care partner more; see how this impacts perception. Adults living with memory loss will thank you for it. You may thank you for it. Continue reading →
“A partner paradigm strengthens our interconnectedness and can bring more awareness to the kindness and support that is right under our nose.”
When do you realize you are a family caregiver? Responses in my experience range from the darkly humorous to the completely visceral, such as: “When my husband started calling me ‘mom.’” Emerging caregivers are often not new to caregiving at all, but rather isolated from the pack. This delays significant steps toward caregiver support and activities that contribute to well-being and caregiver identity, such as joining groups for information, support, stress reduction or counseling. There may also be significant resistance to the word “caregiver” and associated activities. It can feel one-sided and lonely; a loaded word fraught with fear, judgment from friends and comparisons to other family members who may have carried this title in the past.
Emerging as a caregiver can be an uncomfortable and vulnerable time, a trust free-fall. A sense of loss and disappointment is completely natural. Continue reading →
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