Within a year of my husband receiving his dementia diagnosis, I had a classic case of caregiver burnout. I couldn’t concentrate at work and most of my time was taken up with worrying about my husband’s uncharacteristic and impulsive behavior. I was petrified and intimidated about the future…overwhelmed with basic day-to-day activities. Continue reading “Welcome Sisters Susan Kiser Scarff & Ann Kiser Zultner, Authors of Dementia: The Journey Ahead”
When I was a young girl I dreamed I would grow up and become a nurse. I seldom left home without my nurse’s kit filled with band-aides, cotton balls, and gum drop pills just in case my services were needed. It seemed so simple in those days to comfort and to heal, or at least that is what my Grandmother led me to believe each time she let me practice my skills on her. Continue reading ““Meet Me Where I am – An Alzheimer’s Care Guide” by Mary Ann Drummond”
Ah… the wonders I found living with my mother in Dementialand. It all started almost minutes after she was diagnosed with progressive dementia. The cause was meningitis encephalitis. There seemed to be no choice at the time. I had to leave my bohemian life in the art world in California to return to a Chicago suburb where my mom was living. I am a painter. This had all the markings of a disaster. Continue reading “Meet Suzka Collins, author of “Wonders in Dementialand””
By Peggy Bushy
When Lewy Body Dementia entered my home, the world as I knew it began to shift, and I found myself in a constant state of confusion. My sweet mother, who lived in our home, was hallucinating, her stories and behavior were becoming more and more bizarre, and I had no idea why – neither did any of the doctors I consulted. Lost and alone, I could feel myself becoming a little more unglued with every passing day while I watched the family rules fly out the window one by one. “Wait! I depend on those family rules.” They may not be the same as the neighbor’s rules but they’re mine, they’ve been mine forever, and I’m comfortable with them.
June is Alzheimer’s and Brain Awareness Month, and today, June 21st is The Longest Day. Sponsored by the Alzheimer’s Association, these important events increase awareness of Alzheimer’s, related dementias, and brain health. In recognition of these events, AlzAuthors has put together our very first eBook sale! Continue reading “AlzAuthors Alzheimer’s & Brain Awareness Month eBook Sale! “
By Karen B. Kaplan
Perhaps it is not often that you come across science fiction that is (1) gentle and not full of weapons and nasty robots, and (2) includes a character who is one of the first with dementia to get cured of the disease. There are so many other aspects of reality to ponder, such as how robots might help or hinder grievers, it is a wonder that science fiction writers have not provided more material on such things. Continue reading “Karen Kaplan is Back with a Sci-Fi Dementia Novel”
Before signing off the final proofs of my debut novel I read the manuscript for the first time in over a year and realised that it was not just laced, but saturated, with guilt.
Invisible Ink tells the story of Max Rivers, a young London lawyer who seems to have it all: a beautiful girlfriend, a burgeoning career, an enviable address – but he harbours a secret. Continue reading “Meet Pippa Kelly, author of “Invisible Ink””
Alzheimer’s is a cruel prison that held my dear mother-in-law in chains for approximately three years, taking her freedom and her mind until it finally took her body. I understood little about the disease before watching a once brilliant, witty, and loving lady wither before my eyes. Continue reading “Meet Cynthia Toney, author of “10 Steps to Girlfriend Status””
Why choose Alzheimer’s as the focus of my new family saga novel Brought To Our Senses?
It’s a fair question. After all, Alzheimer’s is argued to be the disease feared most of all. The mind-robbing illness has a bad reputation and a stigma-stifling discussion in mixed company. So why exactly would I tackle such a difficult subject, one so many avoid altogether or shrug off as hopeless? Continue reading “Meet Kathleen Wheeler, author of “Brought to Our Senses””
By Molly LeGrand
I’ve worked in Long Term Care as an Activities Assistant for ten years. This role has offered a unique perspective on Alzheimer’s as I typically will meet the person after a diagnosis. And just like I would with a new friend or colleague, I begin to get to know them, and I get to know them with Alzheimer’s. Continue reading “Meet Molly LeGrand, dementia advocate, caregiver and blogger”