Monday, September 16, 2019

My Alzheimer's Journal #11

Yesterday I told my Sunday School class that after the three sermons I'm scheduled to preach in October and November, I'm going to have to stop preaching. It is just getting too hard to write a sermon. And today, for the first time, I let all of my Facebook and Liker friends know about my Alzheimer's with the following post:

I was diagnosed with MS when I was 38 and with Alzheimer's two years ago. As the Alzheimer's continues to ravish my brain, and the MS continues to make my legs more and more uncoordinated, I totally get the last sentence in Nouwen's first paragraph. I have spoken it to Connie and Pastor Cliff on several occasions. Please pray with me that as I continue to decline, I'll do a better job of living the second paragraph than the first.

Preparing for Death
Some people say they are afraid of death. Others say they are not. But most people are quite afraid of dying. The slow deterioration of mind and body, the pains of a growing cancer, the ravaging effects of AIDS, becoming a burden for your friends, losing control of your movements, being talked about or spoken to with half-truths, forgetting recent events and the names of visitors—all of that and much more is what we really fear. It’s not surprising that we sometimes say: “I hope it doesn’t last long. I hope I will die through a sudden heart attack and not after a long, painful illness."

But, whatever we think or hope, the way we will die is unpredictable and our worries about it quite fruitless. Still, we need to be prepared. Preparing ourselves for our deaths is the most important task of life, at least when we believe that death is not the total dissolution of our identity but the way to its fullest revelation. Death, as Jesus speaks about it, is that moment in which total defeat and total victory are one. The cross on which Jesus died is the sign of this oneness of defeat and victory. Jesus speaks about his death as being “lifted up” ()ohn 12:32-33).--Henri J. M. Nouwen 

Sunday, September 15, 2019

My Alzheimer's Journal #10

I officiated at my last wedding yesterday. I forgot to tell the audience that the families of the bride and groom were supposed to remain for pictures when I dismissed the crowd. Felt like an idiot when the mother of the bride finally told me what I had done. Feeling very sad that I messed up at what I knew would be my last wedding.

That is all for today.

Thursday, September 12, 2019

My Alzheimer's Journal #9

I'm feeling very depressed. A month ago I gave up teaching Sunday School because it took me 8 to 10 hours to prepare a lesson. And in class when everyone is talking I get confused and my wife tells me I don't respond appropriately to the members' comments or questions.

Then yesterday I had to tell my friend and mentor, Father Ken, that I can no longer do weddings for the God Squad, including the ones in just a few weeks that I told him earlier I thought I could still do. I no that puts a burden on him and I hate that because the God Squad has been so good to me over the past 18 years.

And I now realize that I'm going to have to tell Pastor Cliff that I can no longer preach for him when he is away.  It takes me up to 20 hours to write a sermon. It used to only take half that time. And I've been getting mixed up when I deliver the sermon. Connie tells me she doesn't think people notice yet, the just think I'm pausing for dramatic effect. But I notice. And I'm sure like everything else, it will get worse as time goes by. I have two sermons left to preach this year and thankfully I have them all written. But my last sermon in October will be my swan song.

All of these things I'm having to give up are things that defined me as a person. As I told Connie last night. I feel useless. And I hate that.

That's all for now.

Saturday, September 7, 2019

My Alzheimer's Journal #8

A friend asked me a few weeks ago what my symptoms where. He wanted to know how I suspected I had Alzheimer's before I went to the doctor. So I told him. When I'm standing at the kitchen counter fixing dinner and realize I need something from the refrigerator, I walk over to the fridge and open the door. Then I stare into the fridge trying to remember why I opened the door. When I'm in the bathroom getting ready for the day, it takes me forever because I'm constantly trying to remember if I'm standing at the sink because in need to apply deodorant, or shave, or brush my teeth. I often walk out without doing at least one of those. And when I wake up in the morning, I usually have no idea what day it and I have to look at my phone to see what the date is.

My friend, trying I think to console me, said, "But people our age often do those things." I responded, "You don't understand. I don't do those things often, I do them every damn time."

Enough for today.

Friday, September 6, 2019

My Alzheimer's Journal #7

Getting diagnosed with Multiple Sclerosis at age 38 was a bummer. Finding out my memory problems are the result of the onset of Alzheimer's was much worse. But last Friday I met a totally blind six to eight-year-old boy at St. Jude's Children's Hospital was balding from his chemo treatments and I decided I need to reflect a bit more on my many blessings.

I married well. My wonderful wife has stood by me through thick and thin and I love her more than words can express. We have three wonderful sons whom we adore. We also very much love our daughters-in-law, and we have been blessed with thirteen grandchildren who, like the kids in Lake Wobegone, are all above average.

I have enjoyed every job I've had and, for the most part, have had great bosses, colleagues, and mentors. Though I've had to cut back on things I used to enjoy like driving and officiating at weddings, I'm thankful that I'm still able to preach occasionally.

Connie and I love our doctor who is both a gerontologist and an intern. She is the doctor who diagnosed my Alzheimer's and unlike any other doctor we've ever had, I sure she would recognize us if she saw us outside of her office. She remembers things we tell her about our children and grandkids and she doesn't seem to rush through her time with us when we are in her office.

I'm thankful for our church. We get so many positive affirmations there. Though we could do better, I'm glad we worship in a multicultural church that seeks to serve "the least of these."

That's enough for now.

Monday, September 2, 2019

My Alzheimer's Journal #6

Don't have time to write much this morning. But just wanted to say that several people have asked me if my diagnosis of Alzheimer's has shaken my faith. As a pastor, I can understand the question because I have ministered to people whose faith was indeed shaken by a medical diagnosis.

But way back when I was 38 and first learned I had Multiple Sclerosis I actually felt my faith strengthened, and the same has happened now with my Alzheimer's diagnosis. Maybe the following quote will help explain it: 

"Jesus came to bring good news to the poor; not to those who serve the poor! I think we can only truly experience the presence of God, meet Jesus, receive the good news, in and through our own poverty, because the kingdom of God belongs to the poor, the poor in spirit, the poor who are crying out for love." -- Jean Vanier, founder of the L'Arche communities.

I found this quote in today's reading in "Common Prayer: A Liturgy for Ordinary Radicals>" After the quote above was this prayer:

"Lord, even the seraphim and cherubim hide their faces in your presence as they declare your praise. Help us mere mortals to humbly dethrone ourselves and bow before you, that in our weakness we might know your good news and forever sing your glory. Amen." 

Though I do complain about my memory loss to my wife, I somehow feel closer to God than ever before. Even with my lousy voice, I still sing God's glory.

Saturday, August 31, 2019

My Alzheimer's Journal #5

Alzheimer's is so weird. As I mentioned in a previous post I could not remember my oldest grandchild's name the other day. And, especially in the evening, I often get confused when Connie or someone else is trying to explain something to me. That happened last night, but then, just 30 minutes later I was able to complete a crossword puzzle in record time. Truly I don't understand how that's possible.

I can tell that at times Connie gets exasperated or frustrated with me when I forget something important or don't understand what she is trying to tell me. And that pains me. I can remember things that happened long ago. I remember our best friends at the time of our marriage telling me they were so glad Connie and I got together because they did not like the rich Boston doctor she was seeing before me. Sometimes now I wonder if Connie made the wrong choice.

I struggle with depression a lot now. Connie suggested I ask our PCP to give me some drug to deal with it but I don't think that would do any good. I'm pretty sure I don't have clinical depression. I'm just sad that my brain is wasting away. I'm not suicidal but I admit there are times that I am jealous of friends or acquaintances who get ill and die relatively quickly from some cancer or heart disease. It took my mom and my aunt years to die from Alzheimer's and the last several years they were so frightened and confused and such a burden to their loved ones. I feel like I'm already a bit of a burden to Connie and I hate that.

That's all for now.

Wednesday, August 28, 2019

My Alzheimer's Journal #4

Yesterday was a very depressing day for me. I came to the realization that I was making too many mistakes due to my memory loss in interacting with the brides and grooms whose weddings I would be officiating. So I contacted Father Ken to let him know that after November of this year, I would no longer be able to work with the God Squad Wedding Ministers. I've been with them for almost 20 years and it brought me so much joy and satisfaction. But I didn't want to embarrass them or my brides and grooms by doing something stupid or forgetting something important.

Then last night I saw a funny meme on facebook that involved a humorous pun. So I copied it and when to send it to my oldest grandson who is an expert punster, only to realize that I could not remember his name. That devastated me. I had to look on his mother's page to find his name. He comes to our house all the time. He used to cut our grass before we moved into an HOA community.
But I couldn't remember my own grandson's name. The experience made me remember when my father put pictures of my brothers and I and our spouses and kids on the wall with labels explaining who we were to help my mother remember before we came to visit. I guess I'm about at that point now in this horrible disease.

I remember after my dad died of a stroke thinking that I wanted to go out like him. Go quickly. I hoped not to die like my mom who was so frightened and disoriented in the last year of her life. She got to the point where she not only did not know any of us, she didn't even know her own name. And now, knowing that is my own fate, well... it's very depressing. I remember how much caring for her took out of my dad, even though they were living in an assisted living community. Connie is not in the best of health and I worry about being a burden to her when I lose more of my cognitive ability.

That's all for today.

Monday, August 26, 2019

My Alzheimer's #3

I'm pretty sure my hearing problem is making my Alzheimer's worse. We got back from our trip to see our grandson graduate from Army boot camp on Saturday and then yesterday hosted a welcome home party for him. We had 19 people in our little house and with so many people talking at the same time my hearing aids can't discriminate the words I want to hear from all the background noise. So I miss a lot of what is being said. And working hard at trying to understand what people are saying literally wears me out.

I have, however, discovered one good thing about Alzheimer's. When watching an Agatha Christie mystery I have seen once or twice before, the surprise ending is still a surprise.

One of my most aggravating symptoms is not being able to say a word that I want to say. A couple of times I've resorted to pantomiming the word. Connie almost always knows what I mean when I do that. Yesterday I was talking to Connie about our trip and I wanted to say our grandson's name, I know what his name is but I couldn't get the word out, so I saluted and since we had just come from his boot camp graduation, Connie knew I was talking about Zach.  Another thing I have noticed is that the word I can't get out is almost always a noun.

In a few minutes, Connie will drive me to church so that I can spend time with my Stephen Ministry care receiver. I'm still able to be a Stephen Minister because most of what that entails is just listening.

That's all for now.



Monday, August 19, 2019

My Alzheimer's Journal #2

Years ago, when our first granddaughter was very little, Connie and I were still in our late 50''s. But we were definitely feeling our age and had begun to discuss things like living wills, advance care directives, etc. In one conversation about our future, I remember Connie saying, "I want us to live long enough to dance at Sissy's wedding. Sissy just turned 16. If my disease progresses at the rate my mon's did and if I'm still alive, I doubt I'll even know who Connie and Sissy are.

It seems weird to me that I can remember a conversation with Connie that took place at least 15 years ago, but I need to check my smartphone each morning to know what day it is.

In a couple of days, Connie and I will be going to Missouri to attend our grandson's graduation from Army boot camp. This will be the first time we have gone on a long trip when I won't be driving. I used to love driving. It was relaxing for me to drive on a long trip. But now, especially late in the day, I get confused by lots of stimuli. So if the traffic is heavy and Connie is telling me what exit to look for and semis are whizzing by, I'm so inundated by stimuli that I don't know what to do. And that too makes me feel guilty because Connie has always hated driving in heavy traffic and now she has to or we have to stay home.

That's all for now.