LBD: Lewybody Caregivers Share Their Personal Experiences

As with most types of dementia, family members are the primary caregivers by default, at least at the beginning of the disease. They are usually the people who notice that something is not right with their spouse or parent. Again, like Alzheimer’s and most other types of dementia, care needs escalate with time. This ongoing care can be physically arduous and emotionally demanding. Jeanne Gibbs, whose husband had LBD, illustrates her husband’s state of mind with the scenario below, which she handled like a pro: ... Read the full article about Lewy Body dementia on HealthCentral for insight from caregivers: Carol Bradley Bursack is the Candid Caregiver MedicareFAQ – Medicare Resource Center Support a caregiver or jump-start discussion in support groups with real stories - for bulk orders of Minding Our Elders e-mail Carol                  Related StoriesCommunicating with Someone Living with Dementia: Some IdeasWhen People Can't Articulate Pain Body Language is a Crucial ClueDementia Caregivers Carry Soul Deep Grief 
Source: Minding Our Elders - Category: Geriatrics Authors: Source Type: blogs
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