September 5th, 2005. We had all been together out at the house in London on the 5th-it was Labor Day and we had gathered as a family to celebrate my nephew Sam's 16th birthday as well as our 6th anniversary. Dad had been diagnosed with ALS almost a year prior to this day and while he was deteriorating pretty rapidly, we had no idea the end was near. We had had a discussion with him about 3 days prior about his need for a catheter and getting a hospital bed in the house because physically, we just couldn't get him in and out of bed anymore. He wasn't happy about that but we really had no choice other than have him go to a nursing care facility and none of us wanted that. He wanted to be at home. He had started to have some respiratory issues (he used a BiPap machine) and trouble swallowing but he had made it clear in his medical directive that he did not want to be trached/vented nor did he want a feeding tube. Anyhow, we said our goodbyes on the 5th and I told him I loved him and that I'd see him tomorrow. I was going to pick Evan up from preschool and come out and help my mom with him that afternoon. Nothing out of the ordinary. I went to bed not knowing just how much my world would change the next morning.
September 6, 2005. The phone rang about 6:15 a.m. and Mike jumped out of bed to answer it. I got up as well and as he hung up the phone, he turned to me and said, he's gone. It took me a second to realize what he was talking about because, while ALS was ravaging his body, he was not near death. We were told we needed to get out there as soon as possible if we wanted to see him before the funeral home came. We got Evan up and told him and I think that was the hardest thing I've had to do yet. He adored my dad. He was 4 1/2 and getting ready that day to start his last year of preschool-that's why Sept. 6th was supposed to be a monumental day in our house that year, not the death of Grandpa.
When we arrived in London, I went into the living room where his body was. I felt a sense of comfort immediately when I looked at him because I knew Dad was in heaven. The body before me was just that. Dad's soul and spirit was elsewhere. I kissed his head and told him I loved him and that he was no longer suffering. It turned out to be a beautiful blue sky day, just as Dad would have loved.
We all gathered at the big dining room table where we all sat for quite awhile, alternating between laughter and tears. Cathy and Mike went out for Krispy Kreme doughnuts and Egg McMuffins-I will never forget that! People stopped by all day and new tears would start again along with more laughter. Food was brought, flowers were dropped off. It was overwhelming to see how much he meant to people not only in the church but in the town of London. It sounds kind of strange to actually say this out loud, but it was kind of a fun day, one I didn't want to end. Yes, we were emotionally and physically exhausted but the gathering of people at his home was something Dad loved. And gathered they did!
Now to today. I have been thinking a lot about these past 10 years. I don't feel as though much as changed in my life, although I hadn't been working at the hospital when he died. I like to think he'd be proud of the work I've done these past 8 years in the place where Evan's journey began. I've run a half marathon and I've gotten myself in pretty good shape but other than that, I've just gotten older (I'm 52-yikes!). What strikes me the most is how much his grandsons have changed in these past 10 years. Jack was 19, Sam 16 and Evan 4. A lot happens when you are young and 10 years go by. Jack is now happily married with an almost 4 month old baby boy who was named after my dad. Sam, as of last week, is now happily married as well. Both hard working, respectable young men. Sweet and caring too. Evan went from a small boy in preschool to a 5'9" high school freshman. So many milestones have been reached by these three and my dad was not there to witness them. That's when it hits me that he's really been gone 10 years.
ALS is a cruel and ugly disease. It was so hard to watch my dad's body fail him when his mind was still so sharp. That's what this disease does to people. We had decided to participate in our first Walk to Defeat ALS before he died and had hoped to walk in his honor but instead, three weeks after his death, walked in him memory. We have walked every year ever since. We will continue to walk until there is a cure.
To be continued.......
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| His last day |
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| This is how I think of him |














