Latest California Healthline Stories
For Alzheimer’s patients and their caregivers, social and emotional isolation is a threat. But hundreds of “Memory Cafes” around the country offer them a chance to be with others who understand, and to receive social and cognitive stimulation in the process.
Harvard psychiatrist Arthur Kleinman shed his “veil of ignorance” during 11 years serving as the primary family caregiver for his wife, who had a rare form of early Alzheimer’s disease. In a new book, “The Soul of Care,” he offers suggestions for transforming health care ― just as caregiving transformed him.
Knowing when — and how — to limit a loved one’s access to digital devices is akin to taking their car keys.
A large public hospital in Los Angeles gets over 1,000 unidentified patients a year. Most are quickly identified, but some require considerable gumshoe work — a task that can be complicated by medical privacy laws.
As the number of Americans with dementia rises, health professionals grapple with how to talk to patients about gun safety at home.
Two leading experts on caring for people with Alzheimer’s offer ways to make life better for patients and their caregivers.
Only about half of the people with Alzheimer’s symptoms get a diagnosis, partly out of fear of an incurable decline, doctors suspect. But Jose Belardo says facing the future allows him to plan for it.
As the number of people with Alzheimer’s climbs, so does the number of loved ones caring for them. The health of 16 million unpaid U.S. caregivers has become a focus for Alzheimer’s advocacy groups.
As more Americans are diagnosed with dementia, families who have firearms struggle with ways to stay safe. A Kaiser Health News investigation uncovered dozens of cases of deaths and injuries.
Across the country, community groups, hospitals and government agencies are stepping in to support the estimated 42 million family caregivers. In California, that includes providing training and sometimes a dose of fun and relaxation.