My Boo Radley entered my life three summers ago. It was a hot summer day, and a lady I didn't recognize knocked on my door. My mom opened the door. I listened to their conversation from the alcove in the kitchen where I can conveniently spy without being seen. The woman's name was Elizabeth, and her mother had Alzheimer's disease. Elizabeth explained that she lived far away, and was worried about her mom, K's health. She wanted to make sure she was getting a balanced meal at night. I wasn't sure where I came in; but I soon found out. I was to walk over on Sunday nights and heat up dinner in the microwave. It was that easy. She was going to pay me, too. I was excited to meet this woman, but I was also confused. At 11, I had no idea why a person could be physically unable to press three buttons on a microwave oven. I assumed that the woman was probably just frail, and didn't like to leave her chair. That was exactly the case at first. I walked over every Sunday and had fantastic conversations with a witty, cheerful old woman. Having young grandparents, it was fun and interesting to be able to talk to someone who was older than anyone I had known before. We became friends and we talked a lot. She knew so much. Over time, however, things changed.
It began with changes that went almost unnoticed. She would misplace things, or try to eat soup with a fork. These were things that we could laugh about together, but would catch in my mind and worry me. Later, we would play games. She would always win. My worries would then be assuaged, and I would forget about the odd happenings that had caused me alarm. As her Alzheimer's Disease progressed, things went downhill too quickly. She couldn't think of words, and her sentences were left unfinished. She would get frustrated and break down, angry at herself for not being able to think clearly. She had to wear Depends, which embarrased her. She even forgot people's names. She always remembered me, but she probably couldn't have told me what I was called. All of these things reminded me that I was losing my friend to a disease. I wish I would have enjoyed that time, for the worst was yet to come.
About nine months after K was diagnosed with Alzheimer's, her daughter called me and asked that check on K more often. She was no longer capable of taking care of herself. Only in the almost constant company of others was she able to remain in her own home. I began walking there almost every day to make her dinner or visit. I knew that those were the a few of the last days that she would be able to communicate. We could no longer play games, because she never remembered how. Stories were difficult, for she lost her train of thought halfway through. Most days, we sat and watched the ocean together. I think that she loved that. She didn't have to feel pressured to speak, but she could enjoy being with other people.
11 months after her diagnosis, K began to scare me. I went to her house every day, and every day something was eerily wrong. She was usually in her pajamas late in the day, staring at a wall. Sometimes, she would have frozen, smiling expressions on her face that reminded me of a malevolent clown. Once, I let myself into her house and found the kitchen filled with thick smoke. I began frantically fanning and pouring water on the stove, which was on fire. A charred, microwavable meal was smoking on the stove burner. I put out the fire and then looked around for K. I finally saw her sitting in a chair, trying to call 911 on the TV remote.
I stopped wanting to go over there. It was creepy, and I did not like it. Her whole house smelled like urine, and she said things that didn't make sense. She would tell me that she was talking to her long-deceased mother; and would force me to talk to her, too. My own mother was having to make me go to K's when I was supposed to. I hated to go, and sometimes I would cry. I didn't like to see my friend like that, and going over to her house made me feel sad and terrified at the same time. I didn't understand how someone so lively could transform into a person so vapid. She was losing her memories, and I didn't understand why.
K moved to an assisted living facility when she became too dependant on others to live at home. I write to her every month. She probably has no idea who I am or why I write, but I don't care. I did a project on Alzheimer's disease, and I now understand what was happening to her. Many diseases can kill, but Alzheimer's is the worst. Alzheimer's disease blocks neuron communication, causing loss of memory. It contorts and ruins your mind, then kills you. Patients die after having been humiliated without even knowing what is happening. They die alone and scared. I hope that people find a cure one day.
I am so lucky to have met such a wonderful person who has shaped my childhood so dramatically. This experience is similar to Scout's because her experience included mystery and fear, but also realization that what she feared wasn't frightening at all.