Living at home, my mother’s multiple sclerosis (MS) and dependency on her family, made her miserable. Her family was tired of waiting on her, and she knew it. When my mother informed me that she planned to divorce my father and move to a nursing home, I felt my...
November has been deemed the month we openly celebrate National Family Caregivers according to the Caregiver Action Network. This annual celebration of those that assume this role begin 1994. The theme chosen this year by the Caregiver Action Network is “Caregiving...
After my mother’s multiple sclerosis (MS) crippled her to the point of dependency on a wheelchair, one of the things she desired was supernatural healing. My father shared his plight with a few of his customers (he owned a retail business) and came upon one with...
We usually don’t use the words humor and caregiving in the same sentence. One could easily argue that caregiving is not very funny. However, humor can be a secret and wonderful coping mechanism to rely on at times when laughter does not seem like an option. I was my...
After a day of classes at a nearby college, I rode the city bus home to where I lived with my parents. I turned the key in the lock and walked through the front door, clutching my books. Mom’s authoritative voice rang from the living room, “Will you bring me a razor...
Being a caregiver for someone who has a memory deficit can be extremely challenging. It becomes even more difficult when that person is unaware of their dementia or any other limitations associated with it. Dementia can directly impact a person’s ability to follow...