Tag Archives: feelings

Feelings

This is another entry about the feelings my husband who is weighed down with dementia feels. He’s not alone, for this is a two-person journey from beginning to end. What I’ve seen in Bill is the sadness of losing each skill, each thought, each piece of him to oblivion. I’m not morose, or a negative person, but this is a sad condition of the mind. Dementia is a condition of the mind that two people have to deal with. Each must adjust and help one another cope with the stages that must take place.

My mother had Alzheimer’s and I watched her go downhill for 16 years. I took care of her every need for those years. She did not have to be alone going through the process of memory loss alone either. When she was sick and dying, Bill was diagnosed with Dementia. Sometimes I forget what really is happening to the person within. When you are with a person with such a condition, perhaps every day, you don’t see the gradual change. Others do see the larger picture and see the downhill slide.

To those who take care of these ones, it seems as if all of a sudden that ugly monster has shown its’ face and this decline appears so sudden that it takes your breath away. To me it feels as if it has been sudden that his thoughts and speech have trouble coming together, if at all. I remember the thoughts of his heart wanting to come out, but they were stuck. The thoughts were there, the memories are there, but the words are not.  

He struggles to get the thoughts out and it hurts me to the point of my heart breaking in two. As he tries to form the words or remember his thought, the look of desire in his eyes I know that he has something important to say to me. The unwillingness of his mouth to form the words that have already gone into obscurity and as the thought itself entered the doors of extinction, we look at each other helplessly. I can only hug him, tell Bill that I love him, and it’s not his fault it’s the monster attacking again. Then nothingness fills the void of silence.

 Sometime in Jan or Feb of this year, his son called us. I do not remember what the objection was, but JR was mad at me and he told me that he was very angry with me. He thinks that his dad should be down there with him where he could care for him properly and he could see his grandchildren. I started to cry, and I told him that he has a right to be angry and it was OK to be angry with me. His dad found his voice, grabbed the phone and let him know a few things that his son was not aware of. Bill reminded him that I was his wife and JR had no business getting me upset.

That was only one small thing that we have to work with. Bill has to remember that his son has not had to deal with older people and never with Alzheimer’s and Dementia. It is a shock for him to see his dad like this, and he doesn’t see it as bad as it really is at this time. 

Thankfully, there is no one else on bill’s side of the family that we have to hold their hand and deal with this too. When you look at this, it comes down to the importance of the relationship that Bill and I have built over the years that is getting us through this. My sister said it all when she said that when you get old, all you have is your family to take care of you.

That’s the truth isn’t it? As for us, we’re just plugging along like everyone else is and taking it one day at a time.

 

There also was a sparkle, and I loved it. That’s for another blog,

 

Remember

The word “Remember” can invoke many thoughts to each of us. You may even wonder where to begin. I’m sure that each of us could write a book on our own memories. I’m only thinking of the first thing that this precious word makes me want to write.

I remember the reason I fell in love with my husband. We lived in Colorado at the time and I remember the first conversation I heard him have with his mother. (His end of course.) The gentle tone in which he spoke to his mother reminded me how children are supposed to obey their parents. It made me remember that the reason we obey is because we love and respect them. He’d laugh each time she spoke of what “Muffin” (her dog and only companion) did that amused her that week. She talked about any visitors she had that week.

He spoke with deep concern about how she was doing and what needed to be done to her house. It was older and was in need of much attention. Bill’s two brothers helped as much as they could. They talked for about an hour and sometimes longer. This impressed me as them having a close relationship. This might spark a flavor of “mama’s boy” to some, but he was no “mama’s boy.”

One brother lived in Germany at this time. He was in the army. He and his wife lived on the base for a while, and then moved off base. They flew home at least couple of times each year. At those times, they visited each of their parents and took care of the needs that were a little more expensive.

The other brother lived about an hour and a half away from her and visited as much as he could. He also did what he could to visit and if she needed shopping done, he would do it for her. He visited her on a regular basis. He was a policeman in that town he lived. From Fairbury to Grand Island was the shortest distance of the three brothers to their mother’s.

We lived in Denver, about a six hour drive, but Bill made that drive when he could, and did physical work on the house and the yard. When I began to go with him I would make meals for her. I’d put them in containers, and then in the freezer so she could just take out one for her, and heat it in the microwave. I also did housework for her that she was unable to do for herself. Their mom had arthritis, and was pretty well crippled with the disease.

For a year I listened to him call her every week without fail. He spoke to her in that same mild and caring tone each and every week. How could you not fall in love with a man such as this? He treated me with the same caring tone and respectful manner. The sincerity in his voice and mannerisms spoke volumes as to what kind of man Bill was.

As the year went along, I heard conversations with his two boys in California also. This was the same manner as he spoke with his mom. Those conversations didn’t last quite as long, but the attitude, love, and respect was shown to them as well.

What can I say? After a year, he asked me to marry him. We got married and here it is 28 years later. He still takes care of me in the way only a husband can take care of a wife; loving, caring, and sometimes even crying together. I still care for him as only a wife can; listening, laughing together, sharing a sunset, or even a simple meal are still pleasurable to us. We tolerate his dementia, and we tolerate my physical and emotional problems. We try to keep them in their place and go on enjoying the love and respect we have always had for each other.

Mom’s Alzheimer’s

When mom started doing strange things, we sort of laughed at her, as she herself did along with us. She was living with my brother in his house at this time. However, things didn’t stay funny, they got worse, and things had to change. It was up to my sister and me to do something.

Let’s go back to when we started noticing things that we all thought were funny. We would find her keys in the refrigerator, an item that she misplaced we found in the back of a closet. That day she may have driven 3 or 4 blocks out of her way and didn’t know why. She forgot to pay bills so Lynn and I started doing her shopping

Then things got worse. She was going to a friend’s house that was close to mine. The nursery at the corner called me and said that my mother drove in a ditch in front of the nursery. Being concerned, I told them I would be right over to get her. They told me the forklift got her out and she seemed dazed. I asked to speak to her and they told me that she’s not there, she was gone. NO…NO…NO I thought to myself why did you let her leave I wanted to say but didn’t. Instead, I got in my car and went looking for her myself. When I couldn’t see her on any road, I went home and started calling her on the phone. It took her three hours to get home. We only lived 30 minutes to her house.

The second incident put her in far more danger than the first one. She went to NH to visit her sister and spread dad’s ashes at his former college. I got a call at midnight from my aunt Margie in NH. She further told me that when she had called and didn’t know where for sure Margie told her to ask someone and then mom said that she was in some town on the shoreline which was 200 miles out of the way. Mom said that she was going to stay at the B&B she was at and would drive to her house in the morning. Mom got there the next day after noon. She had been a long way from Alstead.

Definitely, we knew that something was wrong and it was time to find out what. Lynn found an expert in geriatrics who was teaching classes in Alzheimer’s and Dementia at the University of Colorado which is where mom went for all her doctors. He asked if we could hang around for part of his lecture so he could show an example of an Alzheimer’s patient. My sister and I agreed. When he introduced her, he mentioned a couple of symptoms. Did he have to point out that she looked a little lost and scared?

Then my brother had us all over for a picnic. He asked my mom to go get the broom for him. She got to the top of the stairs and began to get that lost look on her face. Meanwhile, I went upstairs to get something for my brother and my mother was standing in the middle of the small hallway at the entrance muttering that she was afraid to ask Ronny what she was supposed to get. I yelled down at him to find out what mom was supposed to get. Ronny said impatiently that he already told her 3 times a broom and I pointed to where it was. In the meantime, I had gone and got what Ronny wanted. So here, our mother was handing Ronny a bag for trash. Ronny told me that she was deliberately trying to make him crazy. I tried to tell him it was the Alzheimer’s and she couldn’t help her forgetfulness and wasn’t trying to make him crazy.  He said that Lynn and I had to move her out of his house and that he couldn’t take anymore of her pretending. Again, I tried to explain that she can’t help that she forgets. It’s not a game or trying to make you nuts, but if you really want her out, we will move her.

Lynn and I started looking for a place for her to live and I (for lack of anyone wanting the job) got to be her POA. Lynn found one right away which was a new place. It was a one-bedroom senior’s only apartment building. The manager told us straight up that this was not assisted living and there’s not always someone there so she has to get things done and if she gets a lot worse, she will need assisted living arrangements. Therefore, the long road begins. In 1999, Bill and I decided to move to Missouri. Somewhere quiet and settle down there. You know, someplace with a couple of acres. We had bought a 4plex in Joplin and the first floor was empty. Until we sold our house in CO, we had nowhere to go, so we stayed on the first floor of our 4plex.

We had been out here for 6 months and Lynn called and said that she wanted mom to come out here. Lynn insisted that she didn’t want to take care of her anymore. Therefore, I went back to Denver got mom and brought her out here. The first place I looked was perfect for her. The staff was wonderful, the administrator involved with the patients, and the food just like mom cooked. The décor was classy.

Each and every day I went to see mom and spent four to five hours with her. We’d read, put puzzles together, and talked. I got to know mom as an adult instead of a mother. Getting to know her as an adult was a privilege that showed me why people loved her so much.

Then in 2008, I fell and broke my shoulder, had to put mom in the nursing home, and Bill had already been diagnosed with dementia and so begins the long journey …

Difficult Apology

There’s a program here that gives a prompt. That is to help writers get their thoughts running again. Now, you may use these single words for that purpose,  just for practice, or you may do them  for fun.

I wrote a daily prompt a while ago that was on the word apology. I began by saying that an apology that consists of a short statement such as “Oh, sorry ’bout that” is an unacceptable apology. When an offense is committed against a person it becomes a personal offense. A personal offense deserves a personal apology. Sometimes an offender doesn’t realize that they have offended or hurt someone.

After 20 years, my personal offense against my family has become a painful realization of just how deeply that one act hurt them. I never dreamed that my actions would hurt anyone but myself. Seeing that it does, apologies are long over due. After I wrote and posted my apologies online, thoughts of my own attempt ran through my mind again. Slow motion flashbacks kept me awake night after night. This was a very sensitive subject to me and to my family. Once believing that my children, my stepson(s), our granddaughter, and my parents would not suffer any pangs from that act, but now I knew that it did. I removed the post. Unfortunately, I hastily destroyed it and wish I hadn’t.

A comment on one of my posts was a cry for help so, I had to write this post. I have to do this for my family because it has taken me more than 20 years to realize the unimaginable agony I caused the ones closest to me. Unexpectedly, I found myself needing to apologize to a number of people. That one comment made me imagine what happens to each family member when someone commits suicide. Jess, there was a day you revealed to me you remember the day of musical chairs. Then you asked where that was. I had to tell you that it was at the hospital for people who needed help.

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This act would have hurt you in a way different from all the others. If you had known that when it happened, you would have realized by the time you were in grade school that your grandma would have been there in your life to watch you grow up. Had I succeeded, you would have realized this was my fault that I wasn’t there.

Your years of growing up were some of the happiest years of grandma and grandpa’s lives. The visits, the overnights, the talks, and the vacations we took together, we always tried to do things that your parents didn’t do with you. I would have missed all those things.

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When someone commits suicide they don’t really want to die, they want to stop the pain. I remember wanting to die way back when I was a child, but I didn’t know why or how to do it.

He never saw any of the promises the recruiters made. He was in Afghanistan but a couple of months and they sent him home. He was in Bethesda Hospital for a while and as soon as he got out, he waited for a train on the deck and threw himself onto the tracks in front of the train.

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To everyone that felt the sting of my actions, I truly believed at that time, I was only hurting myself. I truly believed that it would affect no one but me. Anyone who thinks that way needs help right now. I knew I was in trouble and headed for more, but I didn’t know how to stop it. Owing everyone in the family an apology, I am going to try to do that now.

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My husband and I had a long talk along with my apology to him. This was the most difficult person I have ever had to apology to. When I realized how deeply my husband loved me, how much he depended on me to care for the family and all that had to be carried out. If he had me no longer, and had to take care of all the affairs, and how much this would have devastated Bill. I could see it then. He would not have been able to bear this happening to him. He had already lost so much in his life; this would have deadened his emotions to the point of physical and emotional paralysis.

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JR, although you are grown now, you were young at that time. If I am correct, I believe you were 13. Words will never be enough and there are not enough words to apologize to you. I know that this did hurt you in ways I don’t know how, still to this day. You saw what was happening to me and I sincerely apologize for the unhappiness and uncertainty I caused in your life at that time. It was more difficult for you than any of the kids. You were at the age that you needed a mother figure in your life, and I let you down. In the younger years of yours and Jason’s lives we did have many good memories, but I am aware of the bad ones too. There were too many and I feel badly about those days too. Sometimes I still cry about those days, and I cry even more over the selfish act of suicide. We’ve never talked about it, so I don’t know exactly how you felt, how much you knew, or what damage I did to you.

Jason is not here for me to apologize to. It’s too bad that he was hurting so badly that he needed to make the pain go away the only way he knew how. (His girls were loved so much by him and they loved him too. He might have been able to put the brakes on and she would not be so wild.) I know that this hurt him at that time in ways I don’t know either. My attempt affected him somehow but I won’t know until the resurrection. He was a difficult child to get to know what he was thinking. It may not seem like it, but at times I felt as if he were my own too. He tried to reach out for help, but I was not able to cope with him at that time. Many times you saw me help him when he needed it no matter what. I know that your father didn’t know what to do to help either of you. He’s a good man and loves both of you. I do look forward to seeing him again. We both did the best we could at that time.

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Now I turn to my own 2 daughters. Tammie, I know you were and still are very upset with me and there isn’t anything I can do about that. You only stayed with us a couple of months. When your father changed the lock on the door without your knowledge and you didn’t want to come back to us, I just figured that you didn’t love me, so I let you go. I didn’t order the police to put you on a plane back to us.

I don’t know how my actions affected you, if it did at all. You are further away from me than words. All I can do is apologize. I truly am sorry for my act of selfishness.

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Lauralee, You were around when this happened and I’m so sorry that it hurt you; some day I would like to sit down and talk about that. I hate now what I did years ago. Our relationship has always been rocky at best. I know we laughed about that before, but it isn’t really funny. I am sorry that I don’t recognize how this affected you since we are not very close. I would like to talk to you about it someday soon. My deep apologies for not being there. Thank you for the amount of time that you let Jess visit us and spend so much time with us while she was growing up. I feel bad that we didn’t have time to have lunch when I was in Denver. I’m sure Jess told you I got pretty sick in Laramie. I won’t be back to CO again. The altitude I can no longer tolerate. The doctor said that once you leave, you can’t go back if you have lung issues.

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This is for my parents who were thankfully busy with their own lives. My dad was sick and my mother was trying to take care of him and work at the same time. Now they are both gone, so I cannot apologize to either.

Underestimate

Why would you want to do that?

I underestimated myself all the time until I took a good look at the word and then a good look at myself. Using the thesaurus, I found the first word listed was “under value”

I didn’t know myself at all. Here I was plugging along and just going through the motions of life. I never stopped to think that I had any value at all. Until I got off  “my little pity pot” and took an honest look at myself.

  1. Yes, I had faults, so does every one
  2. I just had no energy and I didn’t care if I made a difference in anybody else’s life
  3. I’ve never felt I was worth anything at all. OK I told myself.. 

It’s time to get off the pity pot and get some positive juices going. The reasons above are now things of the past. First of all, I am a person who is a giving person, I love people and it makes me happy to give to others. I know that I make them happy because they always tell me how glad they are when I stopped in and visit them, or bring them something to eat when they’re sick.

Then there are all those years that I contributed to society by working, paying taxes Then there is the fact that I have talent in some things. I love photography, and I have a knack for writing. It doesn’t matter, stories, diaries, resumes, etc. I found that when I looked at life through the eyes of an objective person, I have a lot of worth.

So, let’s all get off of our “little pity pots” and take a good look at ourselves. I will never underestimate myself again and I bet you won’t either.

Dance, Dance, Dance

Dance? Why, Thank You Sir

When I saw a flyer sitting on the counter at the nursing station one day while I was waiting for Bill to get ready, I just knew this would be something Bill and I would be interested in going to. There was going to be a shindig at the nursing home. Everyone and their families were invited. There would be a Country Western Band from 2-4pm. A petting zoo would be set up between 4-6pm which consisted of a skunk, kangaroo, porcupine, camel, capybara, and some other more common animals to our part of the world.

Of course, there would also be hot dogs, soda, cotton candy, and a few other choices of usual carnival food items. We went to this as it was set up in the driveway of the nursing home. I didn’t get there until 3pm since my home care worker came that day and wasn’t done until 2:30.

When I got there, the band was playing in the main dining room and Bill was just being escorted back to his wing so I told the aide that we would like to go over and listen to the band. We walked back over to the main building and could hear the music coming from the dining area. I told Bill that I’d like to go and listen to them and we began to go down the hallway. The closer we got to the dining room, the louder the music. I suggested that we go listen to it in the visiting room in the front. Bill agreed and we started to walk back the way we came.

We hadn’t gotten very far; Bill stopped, took my cane, set it aside and said, “Let’s dance!” Just imagine my surprise at that since in our 29 years of marriage we had never danced. Not even at weddings would he dance! Now that I can’t keep my balance very well, hence the cane, he wanted to dance. “Okay, I replied let’s dance!”

There we were, just dancing our hearts out and both of us smiling from ear to ear oblivious as to what was going on around us. Occasionally I did notice the ones that could see down the hallway from the dining room were just watching us instead of the band and smiling too. Some of the family members made remarks such as, “Oh look, they’re dancing, isn’t that just adorable?” and, “Isn’t that precious?” Several stopped and watched for a few moments smiling then walked on. I thought to myself, “Yep, we’re old,” and once again turned my attention to dance with my husband. Bill grinned from ear to ear, and was oblivious as to anything going on around us. I just wanted to be in the moment with my husband while he was happy as he was before this monster overtook him.

I know it used to make me smile too when I’d see older people dancing or walking hand in hand down the sidewalk. It is smiling and worthy of an “Oh, isn’t that just precious?” The literal translation of those types of statements is, “Isn’t that nice an older couple is still close and intimate? They want to and can do things that they did when they were younger. We fit the bill, 29 years of marriage, and even through the dementia we giggle over a private moment while taking a walk. In marriage there is an intimacy that only those two people have. A look, a twinkle in the eyes, and a reach for the hand. Those days are much fewer now as the dementia has slipped into Alzheimer’s.

The next time you see an older couple dancing together as if they were one, ice skating as only a couple that has been married for years can do, walking hand in hand and talking, perhaps even giggling at a memory only they share, think to yourself, “Isn’t that precious, and isn’t that adorable?” Happy marriages filled with laughter, trust, love of a lifetime, intimacy, and gracefulness in old age.

Not every time I see him, will he smile and that new sparkle will be there. I am not fooled by this kind of behavior for I know the time will come when his eyes will be blank once again, his smile will fade away, and he finally will no longer remember me. This happens, day by unannounced day. For now, I will take these fine days while his eyes have a mischievous spark once in a while and his smile is sincere. I will take today and cherish it even after it all stops.

He is not smiling as much and is confused as to where he is moving. He is wandering and that is not good. He is now in a dangerous position. I know that when we go to the doctor he is going to put him into a nursing home.

A letter to my stepson

 

 

My dear Stepson,

From the first day you came to live with us when you were eight years old, and the cutest little boy I had ever seen. You looked like your father, walked like him, talked like him. You followed after him all the time. Your brother had come to live with us at the same time. I’ll have to admit, we had some issues settling in and thinking of us as a family. I’m not sure that either you or your brother ever did.

I know you remember the house we lived in when your dad and I were married. Remembering one instance still brings tears to my eyes, and that is when your brother got up on the roof to help your father repair some shingles. I was standing there when you asked if you could help too. Your father said “No you can’t, just your brother can.” I saw the tears welling up in your eyes as you looked at me with disappointment on your face. Do you remember what I said? I do.

I said, “That’s okay, I need you to help me shop, you are so good at finding coupons for me. I just can’t shop without you. You’re my little shopping  buddy.” So off we went. You were, content while we were shopping. You helped me a lot. You and I cooked together, you helped me with dishes, and sometimes you helped with cleaning. You helped me almost all the time.

That was just one instance and it may not even mean much to you. You do not have to be someone’s mother to see your stepson is hurting and try to sooth that big scrape. You do not have to be someone’s mother to feel your step child’s pain, see hurt in their eyes, and be there when he needs you.

I was the one who was there when you were in trouble, and it was me that talked to your teacher when he cursed. You don’t have to be a mother to watch your plays, and go on field trips with your class. Do you remember who cooked for the family, changed the sheets, cleaned the house, tucked you in and kissed you good night? Son, did you hate me back then?

I’ve stuck with your dad through each stage of dementia. With each skill he lost I’ve been here to cry for him. When a thought was lost because he couldn’t get the words out. I cried for him.  Every time he would get mad at himself who was there to calm him? I’ve been here all along. You haven’t seen him slip at all. You just come here and think he is fine because he is having a good day. You have not been here for anything he has been through.

Do you realize that if I had not called, you would not even know you father has dementia? I say that because you never call him. I’ve called you. Why? Because I think you should know about your dad even if you don’t think of him often. Yes, you visited us three or four times, but you wouldn’t spend time alone with your father. It was you who was telling me to get him involved to keep his mind active. I didn’t see you trying to do a thing for him.

When I told you he was coming in and out of Alzheimer’s now. You immediately wanted to move us to Phoenix. You must have thought that he was able to be moved without falling further into Alzheimer’s. Your father is 72 he needs to be in a nursing home, but I am still caring for him. I take care of his every need. I dress him, I bathe him, I comb his hair, I shave him, I brush his teeth; and I help him eat when he can’t. He doesn’t like it when he can’t see me, in fact, he panics. This goes on 24 hours a day, 7 days a week, 12 months a year.

Then just the other day I had to call you again because you don’t call your father. You would not even know that your dad was slipping in and out of Alzheimer’s. When I explained that your father and I talked about moving to Phoenix and neither one of us thought this was a good idea. He was worried about starting over again too.

When I told you about us not wanting to move down there, I knew you thought that I talked him out of it. You don’t really know your dad at all. I could hear it in your voice. I’ve heard that tone before. However, that Sunday your father could hardly talk. His head was on the arm of the chair, and random words ran together with no formed thought. Suddenly he snapped out of it when he was saying bye to his granddaughter. He joked with her, changed in an instant. I rejoice when he snaps out of it. That means I’ll have him with me one more day.

Saying good-bye to your father only and not just once, but several times. You made your feelings very clear when you did that. You’re not very subtle, you are very plain to read. You believe that I have not taken care of your dad very well. Let’s look at that. From the time he was in the nursing home to the day I texted you that he was slipping in and out of Alzheimer’s, how often did you even call to see how he was? I can recall the exact number of times. It is 0. Now when he is slipping away from me so fast that I will soon lose him, you think you can just move us down there and take care of him yourself. No, neither one of us wants to start over. Your dad and I have been married 29 years come the 23rd of July, and I want to have  your father with me as long as I can.

I am your step mother and once you love a child you don’t just stop because he is a step child. I have no idea when you started to hate me, perhaps it was the day you screamed at me about the nursing home. Oh, it doesn’t matter. My feelings are; I was thrust into that position and I became a mother to you. Never will I ever claim to be your mother and I never did. I did mother you for 8 years. Think about these things, because lately you have burdened me with your hatred on top of the burden of caring for your father. It is what it is. I just have no more to say. I’m worn out.

Your loving stepmother

End of phase

End of retirement phase

 

Along with dementia comes a loss of many things in our lives. When one party is sick, and the other has dementia, the medial bills stack up fast on the credit cards. With medical and bills piled up, something has to give.

Therefore, another phase of our lives ends after retirement. We had to sell our beautiful four-bedroom home on five acres. One reason was the medical bills that stacked up leading us to bankruptcy which put an end to our good credit we had at the time. Alzheimer’s had resided with my mother for 15 years by now. Dementia had been diagnosed in my husband Bill’s life. No more trips, no more dropping everything and going somewhere. Yes, the carefree phase of our lives had slammed the door quickly.

We had entered a new phase. It was one of high medical debt, and maxed out credit cards. There was no end in sight to this new phase either, especially after I fell and broke my shoulder. Necessity left me with five surgeries in the first year alone. My mother had to be moved to a nursing center and I still needed to be with my mom often. My mom needed me in these last of her days, even if she didn’t recognize me. I had to be sure that she still was taken care of properly. I had to take her laundry home and wash it because her clothes disappeared when they went to the laundry there. Dementia in the first stage was waiting at home for me.

It does sound like I’m whining, but I’m not. My mom died a few years ago. My husband’s dementia is in the second stages, but I don’t mind. Our bills are under control and we now live in a one-bedroom apartment. I wouldn’t say that life is good, but for me it is. I still have my husband home with me. I rejoice each day that we are able to communicate and be understood by each other. That is a joy in my life.

In the early years of our marriage, he had to care for me. He did it so lovingly and never complained. He was there for each medical emergency, and each surgery. Now it is my privilege to care for him. I hope that I can do that with the same love and gentleness that he has done for me all these years. So now begins the final phase of our lives and I will still thank our heavenly father for the Kingdom we pray for, the Kingdom that will rule over the entire earth, (Rev 21:4) and tells of no more death or tears.

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Retirement ends

End of retirement phase

 

Therefore, another phase of our lives ends after retirement. We had to sell our beautiful four-bedroom home on five acres. One reason was the medical bills that stacked up leading us to bankruptcy which put an end to our good credit we had at the time. Alzheimer’s had resided with my mother for 15 years by now. Dementia had been diagnosed in my husband Bill’s life. No more trips, no more dropping everything and going somewhere. Yes, the carefree phase of our lives had slammed the door quickly.

We had entered a new phase. It was one of high medical debt, and maxed out credit cards. There was no end in sight to this new phase either, especially after I fell and broke my shoulder. Necessity left me with five surgeries in the first year alone. My mother had to be moved to a nursing center and I still needed to be with my mom often. My mom needed me in these last of her days, even if she didn’t recognize me. I had to be sure that she still was taken care of properly. I had to take her laundry home and wash it because her clothes disappeared when they went to the laundry there. Dementia in the first stage was waiting at home for me.

It does sound like I’m whining, but I’m not. My mom died a few years ago. My husband’s dementia is in the second stages, but I don’t mind. Our bills are under control and we now live in a one-bedroom apartment. I wouldn’t say that life is good, but for me it is. I still have my husband home with me. I rejoice each day that we are able to communicate and be understood by each other. That is a joy in my life.

In the early years of our marriage, he had to care for me. He did it so lovingly and never complained. He was there for each medical emergency, and each surgery. Now it is my privilege to care for him. I hope that I can do that with the same love and gentleness that he has done for me all these years. So now begins the final phase of our lives and I will still thank our heavenly father for the Kingdom we pray for, the Kingdom that will rule over the entire earth, (Rev 21:4) and tells of no more death or tears.

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Dementia and/or Alzheimer’s?

Have you ever wondered if there is a difference between Alzheimer’s and Dementia? Does it even matter? Why should you care?

A few specialists say there are no distinctions and they utilize both Alzheimer’s and Dementia equally. Some specialist’s find there are a couple of contrasts yet say they all end up in the phase of Alzheimer’s so it doesn’t make a difference what it is called. In the two articles in Lifescript.com, and ALZ.org there are varying opinions.

Alzheimer’s sickness is the most widely recognized reason for extreme mental deterioration (dementia) in the elderly. It has been evaluated that 30% to half of individuals more than 85 years of age experience the ill effects of this condition.

Alzheimer’s starts with unobtrusive indications, for example, loss of memory, for names and late occasions. It advances from making the same inquiries again and again to trouble learning new facts. In this stage, they forget to pay the bills, and lose the worth of a dollar by being scammed. Further stages are a few eccentric behaviors some depression in varying degrees, they lose the concept of time; there is no recognition of that fact.  These steps are not always in this order and usually take years to just go through these stages mentioned. Through the span of the illness, the individual step by step loses the capacity to complete the exercises of regular daily existence. They have an inability to recognize their friends and even their seldom seen children are attributes of modestly extreme Alzheimer’s. In time, for all intents and purposes every single mental capacity comes up short.

See more at: http://www.lifescript.com/wellbeing/non-alzheimers_dementia . See more at: http://www.lifescript.com/wellbeing/a-z/elective treatments  http://www.lifescript.com/wellbeing/a-z/elective treatments. This data is from lifescript.com

Dementia-Symptoms: The very first thing Difficulty recollecting late discussions, names or occasions are regularly an early clinical indication; unresponsiveness and gloom are likewise frequently early manifestations. Later indications incorporate inhibited correspondence, misguided thinking, bewilderment, disarray, conduct changes and trouble talking, swallowing and walking.

Modified rules for diagnosing Alzheimer’s were distributed in 2011 prescribing that Alzheimer’s be viewed as a gradually dynamic cerebrum sickness that starts a long time before indications rise.

Mind changes: Hallmark variations from the norm are stores of the protein piece beta-amyloid (plaques) and bent strands of the protein tau (tangles) and additionally confirmation of nerve cell harm and passing in the cerebrum.

Take in more about Alzheimer’s http://www.alz.org/alzheimers_disease_what_is_alzheimers.asp  Alzheimer’s infection. Above is the utilization of the two utilized conversely? This data is taken from Alz.org

I watched my mother for 16 years go slowly downhill with Alzheimer’s. I took care of her, seeing to all of her needs. She did not live with us, but I watched her closely until the very end. Now, I watch my husband quickly slip from dementia into Alzheimer’s. So they both do end up in the same place but the ride is very different.

Alzheimer’s may seem dramatic at times to those who are the caretakers, it can be and I’ve dealt with that too. Each time there was a turn in my mom, it was a sad thing. She may have lost her friends names. It was embarrassing for her and she began to stay home more. I moved her from Denver to Carthage, MO and I placed her in a nice assisted living facility only a few miles from me so I could visit her daily and spend a few hours with her each day.

In dementia the distinctions are much more difficult, they are significantly heart wrenching. Dementia has a face that flies up repeatedly; it’s ugly, destructive and rears its head with more destruction than the last time. This malady may ransack your friends and family who are unfortunate victims of this vicious and destructive dementia. It steals their fundamental abilities one skill at a time. Understanding of words and communication disappear silently. Ability to follow instructions becomes impossible. They don’t recognize a common object even if they look at them and hold them in their hands there is no recognition. Dementia steals their lives and in the end, Alzheimer’s takes it.

The saddest day I had with my mother was the point at which she inquired as to whether she would forget me as well. I couldn’t remain there and mislead her. With tears in my eyes, I disclosed to her that she will, however I will feel it more than her since she won’t recollect me yet I’ll recall her.

The saddest typical day for a man with dementia, I can just figure. Each time Bill slips, it’s been more devastating than the last. From all out wood appearances it seems he struggles with all of life in general. He lives in a world that is upside down and this continues to be anything but comfortable; additionally this experience is something that he can’t control. Much the same as the specialists over, a few people accept there are no contrasts between the two conditions. If you would like to know the answer to that question, continue reading this series of “The face of dementia.” Whatever they lose, the caretaker will need to figure out how to manage it. Each time the appalling creature demonstrates its face; you have been innovative and figure out how to coexist with it.

So decide for yourself whether Dementia and Alzheimer’s words are interchangeable. Listen to my observations during my mother’s Alzheimer’s and my husband’s Dementia.

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