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    An Unsung Hero…The Family Caregiver

    In 2004, my father was diagnosed with Parkinson’s-related dementia and a few months later, my mother with Alzheimer’s disease. That was the year I became a caregiver. While my parents didn’t reside with me, I was still intimately involved in their daily care for the next 4 and 5 years. Traveling down that rabbit hole of dementia with my parents was difficult and sad. I watched helplessly as this disease steadily and ruthlessly chipped away at their brains, one memory at a time. That said, it was also a time of considerable personal growth for me. I learned to parent my parents with patience and compassion, caring for them much…

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    AlzAuthors: Ending the Isolation of Alzheimer’s

    When coping with Alzheimer’s disease, it’s easy to feel alone. The disease can be isolating. Not talked about as often as other ailments, there’s a stigma associated with losing memories, a certain shame. There shouldn’t be. It’s as uncontrollable as cancer, and yet there’s a shroud of silence that surrounds it. This silence leads to a denial of symptoms. Which may be why, according to a 2006 study by the Alzheimer’s Foundation of America (AFA), a diagnosis of Alzheimer’s is delayed an average of 27.8 months after symptoms appear. Healing comes from eliminating this silence. Talking enables us to cope, helping us realize that our challenges are not unique. Our…

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