Mental Health and Depression Feed

...No rest for the caregiver. I climbed back in the car and fought my way through the streets to Mom. It wasn’t another false alarm. Mom really had fallen, and as usually happens after a fall, I couldn’t get her up off the floor by myself. I had to call the EMTs — again. Thankfully, this time she wasn’t seriously hurt. Hours later, once I’d settled Mom in her bed, I forced my way back through the still unplowed streets toward home, hoping for a couple of hours of sleep before morning, when I had to take my uncle to his neurology appointment for a post-stroke checkup. Read more →


Dear Candid Caregiver: My parents are both in their late 70s and doing quite well but I see that the need for making decisions about their futures, or at least gathering information, is closing in. We live in the same community, so my husband and I have been helping with some minor things around their home, but they are very independent and hire out the most difficult jobs. However, with time, I know that more help from us will be necessary. When do I consider myself their caregiver? How do I begin? What do I need to know? – Potential Newbie Read more →


When the average person thinks of dementia, generally Alzheimer’s disease comes to mind. At the same time, the person will likely think of memory loss. Both of these conclusions are understandable since Alzheimer’s is the most common form of dementia and memory issues are often, though not always, the first symptom of that disease. Surprising then, to many people, is the fact that there may be earlier indicators of potential Alzheimer’s disease or other types of dementia than frequent memory lapses. Read more →


For years, the push to do something about Alzheimer’s disease focused almost entirely on drug development. Find a cure. Develop a vaccine to prevent the disease. Develop a drug to “manage” people who live with Alzheimer’s and other types of dementia. What many people weren’t noticing, however, was that in tandem with this effort was a quiet revolution doggedly moving forward.  Long championed by Dr. Bill Thomas of Changing Aging among others, the thinking behind this movement has always been to recognize that people living with Alzheimer’s and other dementia were first and foremost people. Read more →


The question that travels hand in hand with these studies is who should start these drugs if they do prove to be effective? It’s not prudent to simply give the drugs to the whole aging population. We may soon have an answer to that question. A new study that shows differences in biological aging vs. chronological aging could help us find a way to differentiate between those for whom early treatment should be considered and those who aren’t likely to require the drugs. Read more →


Stress has long been considered a major risk for developing Alzheimer’s, but there hasn’t been any real understanding as to why this is so. Now, researchers at the Center for Translational Research in Neurodegenerative Disease at the University of Florida think that they’ve come closer to discovering the connection. Dr. Todd Golde, director of the Center, and his team have found how a hormone released by the brain in response to the body’s stress increases production of a protein associated with Alzheimer's development. Read more →


A report by the Mental Health Foundation (UK) is calling for dementia to be treated as a disability. They said, correctly, that dementia is seen as a disease like many others in that it should be curable. Tragically, only when dementia is caused by medications, infections or some rare, operable situation is it curable. Instead, it is a relentlessly progressive, destructive disease with which the affected must live until they eventually die. The Foundation says that it is also crucial that people with dementia have their rights respected and upheld.  Read more →


Increasingly, stress is considered a risk factor for dementia, particularly Alzheimer’s. Stress is also a risk factor for stroke and heart attack as well as a trigger for many diseases from arthritis to psoriasis. Obviously, limiting stress in our lives is a good idea. But how? Simply living what we call modern life seems to make stress the norm.  Read more →


Can people find happiness – even joy – while living with dementia? That depends, of course, on one’s definition of happiness and joy. But I do believe that there can be satisfying moments for people with dementia and their caregivers. World War II left my dad with a brain injury. He was in a coma for six weeks and had to learn to walk and talk again. This he did. He went on to live a successful life, at least until he was in his 70s and fluid started building up behind the scar tissue in his brain. Read more →


There are countless positive aspects to long-term caregiving, but those who’ve done it know that there are also negative effects, many lifelong. While some effects have been well studied during this last decade, there are changes that occur within most caregiver’s lives that are hard to measure. Some are nearly universal to caregivers, some perhaps more unique to the individual. Below is a short list from my personal experience when it comes to negative effects of caregiving. You, the reader, may have additions and subtractions if you were to make your own list. Read more →