I just realized that it was 10 years ago, 2014, that I started this blog. It has been four years since I wrote anything in it. My, how time does pass quickly.
In February of 2022 I had a stroke, brought on by A-fibrillation. I had A-fib for several years, but my primary doctor said there was nothing that could be done to diagnose me unless I saw a him during an episode. Since he was not worried, I was not worried.
I trained for a marathon with A-fib, but never had an episode for a medical professional to diagnose me during my training. It became part of my life. Run. Heart palpitations. Rest for awhile. Repeat. For years.
In February 2021 I had an episode that lasts for three days. We were in a pandemic and emergency rooms were not a place to be, but I needed to have someone listen to my heart. An emergency room nurse checked my heart and heard A-fib rhythm. 155 beats a minute. Then the episode began to diminish. I was down to 96 beats a minute when the emergency room doctor saw me. He diagnosed me with cardiac A-fibrillation, gave me to prescriptions, and sent me home. The next day I had a stroke.
My husband noticed that my speech and words were not right. He said I needed to go to the doctor. Why? I did not notice a difference in my speech. He nagged me for three more days until I finally agreed to go to the ED. I do not remember that he told me I was not making sense when I talked. I finally did stop talking by the time he convinced me to go to the ED. I also had a consistent headache.
My husband could not go into the ED due to COVID precautions. Somehow the nurse understood what I needed and got me into the treatment part of the ED where a doctor saw me immediately. I understood what he was saying and had no physical symptoms of a stroke, other than my garbled language. CT scan, MRI, more doctors. They said they found an “unusual mass” in my brain. Another MRI. I wanted my husband! They finally determined that I had a stroke, all of it focused in the language center of my brain. (The language center of my brain is where most of the injury was from a fall and concussion two years before this diagnosis.) I heard myself as speaking clearly, those listening heard gibberish.
I was admitted to the stroke unit. I do not remember much past them telling me I had a mass in my brain. One of my daughters asserted her strong personality and was allowed in to visit me. I don’t know if I was still speaking gibberish or if she could understand me. She brought me a toothbrush, a hair brush, and my iPad. I do not remember much, but I do remember that she was my strong advocate. I am forever grateful to her.
I was evaluated by speech, physical, and occupational therapists. On day three they let me go home and directed me to work with a speech therapist. My language was returning, but my written words did not make sense. I told my boss I would be out of work for a week or two. I was incorrect. I was out of work for three months!
The speech therapist was wonderful. She had experience with people who have “high functioning” speech disorders. Word games and physically hand writing were key to my recovery.
Now, over three years post-stroke, I still have deficits. Most people can’t tell, but some slight changes are noticeable to my family and my work team. I placed a great deal of stress on myself to return to who I was before the stroke. In January 2024 I retired from my leadership position at a not-for-profit organization. The day I told my boss I was retiring is the day a massive emotional load was lifted from me.
What next? I continue to play word games. I play memory games. If I have a writing issue I switch from technology to handwriting. I stress over my written words and I am restarting this blog.


