
Dad and I just finished a morning walk. We headed down the slope of our driveway, then up a steep hill to the street above us. Starting uphill gets the hardest part over with and then we can settle in for more gradual inclines and downhill slopes as we make our way around two neighborhood blocks.
Today Dad is in his wheelchair which involves me pushing his 160 pounds along with the weight of the chair. He can still walk. Fast when his mind allows. Mostly he shuffles. He is not as steady on his feet and has developed a fear of falling. Even though I hold onto him and use a gate belt with multiple handles what once was a 20-minute walk takes about 45 minutes now. The wheelchair is a great next step in keeping him on his feet. Recently, I have him holding onto and pushing his wheelchair for a portion of our walk and he actually takes short steps, slow but much better than shuffling. And, if he gets tired he can just sit down.
When dad is in his wheelchair, he no longer keeps his feet on the footrests. To avoid injury to him, and a great deal of frustration for me, I found foot wraps that attach around his feet securing them to the footrests. He also wears a safety strap around his torso with a quick connection around the chair as he has been unexpectedly standing up and at times while the chair was moving.
Dad’s cognitive limitations keep him from moving the chair on his own or using a walker effectively. Although the wheelchair has been an adjustment, it does keep Dad from following strangers and helps him feel safer especially when he is disoriented with his surroundings or doesn’t recognize me. He is still quite strong so depending on his reality we prevent any resistance altogether and use the chair. We can attend crowded events if we wish, go for long distances, navigate elevators better, and get to appointments on time instead of stressing at shuffle speed.
I took a second walk today. My care partner stayed with Dad while I went to our favorite beach. It was the first time I have been able to get to the beach this season. Although I was there by myself, I was definitely not alone. Dad was there. I thought about how he collected only black rocks until his pockets were so full his shorts started to drop, waded barefoot in the surf even when the water was so cold our feet grew numb and turned red, and watched patiently while I photographed a bird or shell. We shared hours and miles at this beach. Now I can’t get him onto the sand here because this beach doesn’t have a paved entrance.
Instead, I sometimes take Dad to the sidewalk along the seawall and push him in his chair near the water. It is important to me to keep him on his feet as long as possible for our quality of life and level of care. Lewy Body Dementia is easier when we embrace change and do our best with what we have to work with. So, For now, we walk this way – and sometimes that way, while we take things in stride.
To see Dad’s progression from hiking to walking miles on the beach to his wheelchair walks, read blog posts The Beachcomber, Go West Young Man, and Grand Canyon Light and Laughter







