As a writer, words are important to me. Consequently, I will often invest a lot of time searching the dictionary, thesaurus and Google, trying to find the very best, most accurate, articulate, and precise word to describe an emotion, thought, event, or person. Seven years ago when I was diagnosed with Mild Cognitive Impairment, I…
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A moment of serenity
Last week I wrote in my journal this spontaneous and uncensored entry: “I’m grateful for good days, calm days full of peace and acceptance, and for seeing life as beautiful, just as it is.” What a gift this entry was to me. Re-reading it conjures up the way I felt when I wrote it, and…
An absurd question {written by Beth}
This is a guest post written by a new voice and perspective on the topic of memory decline—my daughter Beth. She will write about what she experiences as a caregiver, a loving daughter, and as a woman who has excellent medical instincts. Since this is a new experiment, I would appreciate getting your feedback. Are…
To be told or not to be told
Our family values and embraces being honest and forthright. Topics of religion, politics and sex are fair game at any family gathering, and differences of opinion have been encouraged, accepted and honored. So it seemed only natural to be open with my children regarding my diagnosis of Mild Cognitive Impairment. From the onset I have…
Family reunion
It has been almost a month since I’ve last posted on my website; the longest I’ve been silent since I started my blog. My excuse is I have been busy preparing for and hosting a family gathering at our home. I’ll briefly relate the affair as it is pertinent to my journey with MCI: How…
Acceptance
I just returned from five wonderful days with my dear, dear college friends of fifty years now. We’ve stayed in touch over all these years; initially through a chain letter, then email, and now we see and talk to each other through messenger. However, our most important communication is when we meet in person. At…