One of my favorite bloggers recently wrote a very funny post about her husband using too many pronouns http://bagladyinwaiting.blogspot.com/2016/06/bag-lady-report-conversations-with.html I had to laugh when I read it, because Jim has often done that over the years. However lately it is more than just trying to figure out who he is talking about. It is often what he is talking about that keeps me guessing.
We went for a lovely walk today around a small lake. Temperatures in the low 70's, sunny, light breeze. Just a beautiful day. Stopping for ice cream on the way home made it all the more special. While driving home, out of the blue, Jim said "maybe we should go there".
Me: "Go where?"
Jim: "you know....." (long pause, I could see he was desperately trying to retrieve the correct words).
Me: (searching my brain for any inkling of what he might be trying to say) "go to the store?"
Jim: "no, up here" (pointing straight ahead).
Me: (finally figuring out this was a reference to a conversation we had yesterday) "you mean the Jazz Fest?"
Jim: "Yes!"
I cannot imagine how frustrating this must be for him. Things like this happen several times a day, where he struggles to find the words he wants to say.
We went to a men's store to buy him a new suit for an upcoming wedding. He picked out a very nice suit. While he was changing back into his street clothes, the salesman and I picked out 4 ties that would go nicely with the suit. Jim comes out of the dressing room, and I ask him if he likes any of the ties we picked out. He quickly pointed to one and said "this is OK". We're at the register cashing out and the salesperson puts the tie into a bag. I'm finalizing the payment, and Jim suddenly says "wait, what about a tie?" The salesman quickly says "you picked one out; it's in this bag!" Jim clearly does not remember this and tells the salesman "no I didn't!"
I hate situations like this. It leaves everyone feeling bad. To make the best of it, I pulled the tie out of the bag and said "maybe you would like to look at other ties to see which one you like". This worked well, and he picked out a beautiful tie that goes well with the suit.
When we got home he fretted over the next two days about alterations that are being done on the suit. He was convinced that the tailor did not know that the legs needed to be tapered a bit and hemmed. I just kept reassuring him that the tailor pinned the pants so that the fit would be just right for him. Fortunately he believed me, and he did not call the tailor.
On our return from Florida this spring, we discovered a pine tree that had fallen during high winds. We had a local landscaper remove the tree and replace it with another, smaller one. In normal conditions the new tree would not need too much attention, but this has been a very dry, hot month and the tree is starting to show some damage from the heat and dryness. In retrospect, it should have been watered by us. But I have never paid attention to these kinds of things, because Jim did all of the landscaping work, and loved it. Times have changed.
Jim pointed out the brown areas on the tree and angrily said he was going to call Pete and ask him what he was going to do about it. Jim had the details all wrong. He insisted that this occurred 3 years ago and that it cost $1200. (It was only $350). And it wasn't Pete; Pete was the builder who built our house 11 years ago. Oh my goodness.
Realizing that the damage to the tree was our fault because we did not properly water it, I knew I had to intervene. Otherwise he would have called the wrong guy demanding that he replace the tree. I gently tried to relay the facts. At first he insisted that my memory on the facts was incorrect. Fortunately I keep track of everything! I was able to pull out my expense sheet from May of this year to show him the details of who, when, and what happened. It worked.
Mental gymnastics is what I am calling it these days. When things are said that are not accurate, I do not correct unless it is important to do so. Can you imagine what it would be like to have someone correcting you all day long? Not good.
So I put on my "caregiver filter" as I call it. This filter helps me to try to understand what he is saying, helping him to fill in the gaps when needed. I try to handle situations in ways that do not hurt his feelings. I'm not perfect, and never will be, but I am definitely getting better at it.
Saturday, July 2, 2016
Thursday, June 23, 2016
Memory for 2
We went to Philadelphia last weekend. We both enjoy this city, rich in history. We stayed downtown and used the Phlash bus to get around. The Phlash bus runs a continuous route that takes you to all the different historic sites. We did a LOT of walking as well. We had a wonderful dinner with friends of our's on Sunday night. A good time was had by all.
I did all of the driving down, and most of the driving to go home. Jim didn't seem to mind, thank goodness. Even with our GPS and with me helping to navigate, it would have been too much for him. He does OK driving locally, but anything new and different causes anxiety, frustration, and generally makes for a miserable time for both of us.
Being in a different city brought to the surface the many limitations he has when he is out of his element. I heard him ask with amazement many, many times "how do you know that?" The funny thing is, he does not view it as a deficit that he has, but rather he sees me as being very smart.
The last few times we have traveled he has forgotten to pack some pretty obvious things; socks, favorite sneakers etc. On this trip I surreptitiously checked his bags prior to leaving and was then able to casually say "did you remember to pack your ..."
I planned our activities so that we would enjoy the best that Philly has to offer. We managed to check everything off our list! Jim struggled with the details of our plans; I just focused on telling him that we were OK. He responded well to reassurances that we were on the right bus, at the right location, etc.
There are different descriptions for the stages of dementia. Based on this one http://www.alzheimers.net/stages-of-alzheimers-disease/ I would say that Jim is in stage 4; moderate decline. I'm guessing that it is not an exact science and that there are probably variations that don't hold true to the description. Plus, some days are better than others. And some are worse.
I am learning a LOT about home maintenance. Jim has always maintained a list of resources for any house related problems. I never really paid any attention to it before, but now I absolutely need to. He is not really capable of handling a phone conversation with any complexity in it. He gets confused, forgets what the issues are, leaves out critical information etc. So now it's up to me. I'm getting used to it.
From what I have read, denial is fairly common in Alzheimer's dementia. It is not necessarily an intentional denial, but rather a lack of insight. I've also been reading about doctors who are not forthcoming with patients in giving them a diagnosis of dementia. Reasons for this include fear of damaging their relationship, concern the patient is too fragile to handle the diagnosis, trying to protect the patient. It must be frustrating for physicians, as there is no cure, no fix. Doctors will sometimes prescribe cholinesterase inhibitors (such as Aricept). But this is often done at the request of the patient or family. Research shows that while the medicine may improve cognitive functioning for a year or so, it does NOT stop the progression of the disease. How sad.
Our next trip is in August for a wedding. Travel plans are underway, and I'm anticipating a wonderful weekend celebrating with friends.
Memory for 2. I'm ready for the challenge!
I did all of the driving down, and most of the driving to go home. Jim didn't seem to mind, thank goodness. Even with our GPS and with me helping to navigate, it would have been too much for him. He does OK driving locally, but anything new and different causes anxiety, frustration, and generally makes for a miserable time for both of us.
Being in a different city brought to the surface the many limitations he has when he is out of his element. I heard him ask with amazement many, many times "how do you know that?" The funny thing is, he does not view it as a deficit that he has, but rather he sees me as being very smart.
The last few times we have traveled he has forgotten to pack some pretty obvious things; socks, favorite sneakers etc. On this trip I surreptitiously checked his bags prior to leaving and was then able to casually say "did you remember to pack your ..."
I planned our activities so that we would enjoy the best that Philly has to offer. We managed to check everything off our list! Jim struggled with the details of our plans; I just focused on telling him that we were OK. He responded well to reassurances that we were on the right bus, at the right location, etc.
There are different descriptions for the stages of dementia. Based on this one http://www.alzheimers.net/stages-of-alzheimers-disease/ I would say that Jim is in stage 4; moderate decline. I'm guessing that it is not an exact science and that there are probably variations that don't hold true to the description. Plus, some days are better than others. And some are worse.
I am learning a LOT about home maintenance. Jim has always maintained a list of resources for any house related problems. I never really paid any attention to it before, but now I absolutely need to. He is not really capable of handling a phone conversation with any complexity in it. He gets confused, forgets what the issues are, leaves out critical information etc. So now it's up to me. I'm getting used to it.
From what I have read, denial is fairly common in Alzheimer's dementia. It is not necessarily an intentional denial, but rather a lack of insight. I've also been reading about doctors who are not forthcoming with patients in giving them a diagnosis of dementia. Reasons for this include fear of damaging their relationship, concern the patient is too fragile to handle the diagnosis, trying to protect the patient. It must be frustrating for physicians, as there is no cure, no fix. Doctors will sometimes prescribe cholinesterase inhibitors (such as Aricept). But this is often done at the request of the patient or family. Research shows that while the medicine may improve cognitive functioning for a year or so, it does NOT stop the progression of the disease. How sad.
Our next trip is in August for a wedding. Travel plans are underway, and I'm anticipating a wonderful weekend celebrating with friends.
Memory for 2. I'm ready for the challenge!
Saturday, June 11, 2016
Planning for an Uncertain Future
I remind myself frequently that we are still early in this journey. I read other blogs, and realize that others have many more challenges than Jim and I do. It helps me to appreciate what we have now, knowing that greater challenges are sure to follow.
Shortly after I retired, I arranged for us to meet with an attorney so that we could do our wills and get our health care proxies and living wills written. We also did power of attorney for each other. POA is a very powerful thing to do, not to be taken lightly. We both agreed that we wanted this set in place so that we could act on the other's behalf, should the need arise. Of course when we did the POA, I was thinking ahead to the day when I might need it because of Jim's further cognitive decline. It's funny, but the other day Jim said to me "shouldn't we do a will or something?" I reminded him that we had already done it, including the POA and health care proxy. His comment back was "well, as long as you know where it is." I assured him I did!
We decided against long term care insurance quite a few years ago. Working in the health care field, I saw patients who were put through the wringer when the time came that help was needed. Fighting the insurance company for the financial benefits promised is a stressor that older folks don't need. Long term care insurance companies are able to raise the premiums at will. If they raise them to the point where it is cost prohibitive, you are out of luck, and there is no return on the money you have already spent for this insurance. Some long term care insurance companies simply get out of the business, leaving the people who paid all of these premiums high and dry. I'm sure there are reputable companies out there, but we decided to self-insure. In other words, money that we would have paid in premiums we put into our investments. Another option for funding elder care is the reverse mortgage. This is not without pitfalls as well. No perfect solution, and I think it also depends on individual circumstances.
We've always managed our household so well together. I know that finances can be a strain for many couples. Not so for us. It was an area that we loved planning and talking about. We shared financial goals and it was always easy for us to agree on how we saved and how we budgeted our money. It still is, except that now it is me, alone, who is following the investments, rebalancing our portfolio, doing the spreadsheets, and paying the bills. We used to love to do this together, but now it is painfully frustrating for him to be a part of it. So I just do it, and he is happy he doesn't have to be involved. We both have investments from employer based savings plans. The POA will allow me to access the funds that are in his name alone when the time comes that I need to do this. By having the POA in place now, it saves a lot of hassles and headaches that would occur at some future date when the funds are needed.
As far as housing, for the last few years I've gone back and forth on whether we should downsize further. Should we give up home ownership and just rent? Or should we sell this home and buy something smaller? For now, the answer seems to be just to wait and see. I love our home, our neighborhood. And I love it when we can say goodbye to winter and head south to FL.
Jim is still able to do a lot of the outside maintenance. He is very fussy about the lawn, and it always looks impeccable. We hire for the big jobs, such as painting the house, tree removal. Our house is new enough so that mechanically and structurally it is pretty sound. But I can look into the future and see a time where we will want to live more simply. Just not yet.
Well, when I started this post I wasn't sure what I wanted to say. But when I started typing, the words just seemed to flow. As always, it feels good to be able to share my thoughts with all of you. Thanks for listening!
Thursday, June 2, 2016
It's Late; 11:35 PM To Be Exact
It is 11:35 PM, which is late for me to still be awake. My mind doesn't seem to want to rest tonight. I usually have no problem falling asleep, but I seem to have a lot on my mind. I'm hoping if I write about it, perhaps I can put things to rest.
We have a wedding to go to this weekend. It is about 2 hours away in unfamiliar territory. We will pick up my mother, and then head out to the wedding. I know that I need to be the one driving. Jim does best with short, familiar trips. Will he agree to me being the driver this time? We'll take my car because it is larger and can easily hold all of us. Usually if I say something like "I'd really like to drive today" he is pretty agreeable. Especially because we will be driving my car and not his. Fingers crossed this all goes smoothly.
Then there is the wedding itself. Will people notice? I always wonder. A lot of the things that I notice are things that perhaps others would not. They might give it a brief thought, but then just move on. A lot of times the things I notice are not off a lot, just "half a step off", as I like to say. I often times find myself helping to explain, offer a minor correction, filling in an obvious gap when we are in public.
The more obvious evidence of cognitive loss are seldom displayed in public. Maybe on some level he does know that he has limitations. Maybe he chooses to cover it up as best he can in public, and feels safe to ask/say these things to me in private.
We are having our house painted by someone we know who does this for a living. Jim became focused on the chargers that the painter left plugged in to outlets in our garage overnight. (I'm not very handy, but I think the chargers are for power tools that the painter uses.) After the painter left, Jim obsessed about how it was dangerous to leave them plugged in overnight. I tried to reassure him to no avail. He called the painter to question him about it. This is after the painter put in a very long day of hard work. I listened to the message that he left on voice mail. I can't even imagine what the painter thought when he listened to that message. I am embarrassed. I admit it. The painter never called back (no surprise to me). Jim insisted that we unplug the chargers while we sleep tonight. I sure hope they have enough charge in them for tomorrow's work.
The brother whom I am closest to is the only person who has asked me about Jim and his cognitive changes. It is a relief to have someone know, someone I can talk to. Is he the only person to notice, or is he the only person to have the courage/nerve to say something to me?
It always feels good to put my thoughts in writing. I think I'll do one of my Ken-Ken math puzzles and see if that tires out my brain enough to induce sleep.
********************************************************************************
Addendum: Things always look better in the morning :-) The chargers are plugged back in and look to be fully charged. I plan on buying lunch for the work crew today. Then headed out to get my car serviced. Life is good. Hope this finds your day filled with warmth and sunshine.
We have a wedding to go to this weekend. It is about 2 hours away in unfamiliar territory. We will pick up my mother, and then head out to the wedding. I know that I need to be the one driving. Jim does best with short, familiar trips. Will he agree to me being the driver this time? We'll take my car because it is larger and can easily hold all of us. Usually if I say something like "I'd really like to drive today" he is pretty agreeable. Especially because we will be driving my car and not his. Fingers crossed this all goes smoothly.
Then there is the wedding itself. Will people notice? I always wonder. A lot of the things that I notice are things that perhaps others would not. They might give it a brief thought, but then just move on. A lot of times the things I notice are not off a lot, just "half a step off", as I like to say. I often times find myself helping to explain, offer a minor correction, filling in an obvious gap when we are in public.
The more obvious evidence of cognitive loss are seldom displayed in public. Maybe on some level he does know that he has limitations. Maybe he chooses to cover it up as best he can in public, and feels safe to ask/say these things to me in private.
We are having our house painted by someone we know who does this for a living. Jim became focused on the chargers that the painter left plugged in to outlets in our garage overnight. (I'm not very handy, but I think the chargers are for power tools that the painter uses.) After the painter left, Jim obsessed about how it was dangerous to leave them plugged in overnight. I tried to reassure him to no avail. He called the painter to question him about it. This is after the painter put in a very long day of hard work. I listened to the message that he left on voice mail. I can't even imagine what the painter thought when he listened to that message. I am embarrassed. I admit it. The painter never called back (no surprise to me). Jim insisted that we unplug the chargers while we sleep tonight. I sure hope they have enough charge in them for tomorrow's work.
The brother whom I am closest to is the only person who has asked me about Jim and his cognitive changes. It is a relief to have someone know, someone I can talk to. Is he the only person to notice, or is he the only person to have the courage/nerve to say something to me?
It always feels good to put my thoughts in writing. I think I'll do one of my Ken-Ken math puzzles and see if that tires out my brain enough to induce sleep.
********************************************************************************
Addendum: Things always look better in the morning :-) The chargers are plugged back in and look to be fully charged. I plan on buying lunch for the work crew today. Then headed out to get my car serviced. Life is good. Hope this finds your day filled with warmth and sunshine.
Wednesday, May 25, 2016
Pretty Good Week
Jim's riding lawnmower essentially died, requiring the purchase of a new one. I was busy this past week and weekend getting ready for and co-hosting a wedding shower for one of my nieces, as well as helping my elderly mother. Normally I would have accompanied him to Lowe's, just to be in a supportive role. But circumstances did not allow for this.
I knew something was slightly amiss when he called me with the question of which credit card he should use. Told him it was OK to use either one. He replied "I didn't know if we had enough left on the cards". I didn't really understand what he meant by that, but it seemed like he was looking for direction, so I told him to use the blue American Express card.
Jim and I have never carried any debt, other than a mortgage. We have always paid our credit card bills in full every month. He knows this, at least he used to know this. I've been doing all the finances, including managing our investments for the past several years. I always discuss updates with him to make sure he feels like he is still in the loop. But honestly, I don't think he would ask if I didn't bring it up.
When we connected at home later in the day, he attempted to articulate some problem with making the purchase of the lawnmower. It was so unclear to me what he was explaining, that I just kind of listened, and reminded myself of why I need to go with him for these kinds of purchases. The next morning I heard him on the phone engaged in a confusing conversation with someone from Lowe's. I'm guessing that sales people must run into this time to time. In the end it all worked out. Two days later the new lawnmower was delivered.
One of my favorite bloggers recently wrote about the uncertainty of knowing exactly where her husband is in his progression of dementia. https://aliceinmemoryland.com/2016/05/23/so-how-is-ralph-doing/ I relate to that; the need to know where we are at, what does the future look like, how will this play out, and how will it all end. But that is not how life works, of course.
Jim actually seems stable at the moment. Will he stay this way for a long time? I hope so, because this seems doable. I am getting better at knowing how to respond and how to make things less stressful. For both of us! Life is good.
Friday, May 13, 2016
"What is My Birthdate?"
It seemed like such a simple question, but it was so sad to hear him ask it. Jim approached me last night with his driver's license in hand. The following conversation ensued:
Jim: "When is my birthdate?"
Me :"January 20, 1949"
Jim: "No, when is my birthdate?"
Me: "Your birthdate is January 20, 1949."
Jim: "No...(long pause) I mean....(long pause)"
Me: "You mean how old are you?"
Jim: "Yes! That's what I asked!"
Me: "You are 67."
He struggles with finding the right words. Not always, but sometimes. Sometimes he will say something brilliant! He cannot handle phone conversations that involve any kind of complexity. Yesterday he asked me to call to change the date and time of a Dr. appointment.
He can no longer operate the thermostat, cannot operate our new washer and dryer; the list goes on.
The other day he was struggling with the TV remote and asked for my help. After I helped him he said "My brain! What would I do without you!" But these moments of insight are rare.
The other night we were waiting in a restaurant for our takeout order. He blew me an air-kiss (goofy lovey-dovey thing we do at home). I said "I think the waitress just saw you do that." He said "do what?" I said"blow me an air-kiss". He said" I didn't just do that!" I let it drop, because what is the point. He doesn't remember. Less than 10 seconds ago. So sad.
Since we have been back from FL, I think he actually functions a little better. I have read that it is important to keep everything as consistent as possible. It makes me seriously rethink all our plans to travel. Kind of hoping for a Northern California this fall and London next spring. Just don't know if I have it in me to handle all the stress it will generate for him.
I'm getting good at NOT saying "don't you remember...?" because obviously he doesn't! I also am good at not showing shock when he can't remember his age, phone #, address etc.
He trusts me, and that is everything. He is so appreciative of everything I help him with.
Life is still good, and I am grateful for his love.
Jim: "When is my birthdate?"
Me :"January 20, 1949"
Jim: "No, when is my birthdate?"
Me: "Your birthdate is January 20, 1949."
Jim: "No...(long pause) I mean....(long pause)"
Me: "You mean how old are you?"
Jim: "Yes! That's what I asked!"
Me: "You are 67."
He struggles with finding the right words. Not always, but sometimes. Sometimes he will say something brilliant! He cannot handle phone conversations that involve any kind of complexity. Yesterday he asked me to call to change the date and time of a Dr. appointment.
He can no longer operate the thermostat, cannot operate our new washer and dryer; the list goes on.
The other day he was struggling with the TV remote and asked for my help. After I helped him he said "My brain! What would I do without you!" But these moments of insight are rare.
The other night we were waiting in a restaurant for our takeout order. He blew me an air-kiss (goofy lovey-dovey thing we do at home). I said "I think the waitress just saw you do that." He said "do what?" I said"blow me an air-kiss". He said" I didn't just do that!" I let it drop, because what is the point. He doesn't remember. Less than 10 seconds ago. So sad.
Since we have been back from FL, I think he actually functions a little better. I have read that it is important to keep everything as consistent as possible. It makes me seriously rethink all our plans to travel. Kind of hoping for a Northern California this fall and London next spring. Just don't know if I have it in me to handle all the stress it will generate for him.
I'm getting good at NOT saying "don't you remember...?" because obviously he doesn't! I also am good at not showing shock when he can't remember his age, phone #, address etc.
He trusts me, and that is everything. He is so appreciative of everything I help him with.
Life is still good, and I am grateful for his love.
Tuesday, May 3, 2016
Police at Our House!
Last summer we decided to put in a security system to monitor our home while we are away during the winter months. It seemed like a good idea; we could monitor the thermostat remotely to make sure the furnace was working and the security system would alert if someone entered via door or window, or if motion detectors were tripped. We actually live in a very safe neighborhood, but being gone for 3 months seemed like a long time to rely on friends/neighbors to check on our house periodically.
We use the system at night as well, putting it in the "arm stay" mode. This turns off the motion detector, but will alarm if doors or windows are opened.
I realized last fall that Jim is not able to arm or disarm the system without looking at a very short list of instructions. It's pretty basic; 3 steps for arming and 2 steps for disarming. (Example: disarming requires touching the red bar and then entering our password.) Our password is one that we have used for years for our garage door opener. Every morning and every evening I always ask him if he wants to arm/disarm, or if I should do it. He always says, I'll do it, but you watch me. He faithfully puts on his reading glasses and pulls out the instructions, and proceeds to do it under my watch.
Well, the other morning he awoke before I did, and according to him, he saw "a lot of smoke" outside. He opened an outside door to check it out, and you guessed it, the alarm went off. (The smoke he saw was simply the vent for our gas furnace to the outside.)
Meanwhile, I awaken. I am still not quite awake, but Jim starts to tell me that "the smoke alarm went off" (it didn't) and "I went outside to check out the smoke I saw". Next thing I know the police are knocking at our door. I'm still fuzzy trying to figure out what had happened (after all, it is only 6:00AM). The police were very nice, said don't worry, these things happen. Sigh.
I finally figured out that what Jim thought was the smoke alarm was actually the security alarm that went off when he opened the outside door. He felt bad afterwards. I tried to make light of it so he wouldn't worry about it. I think it really made a huge impression on him, with the police showing up. The next day he was still talking about it, and saying he would from now on make sure that the alarm system was off before he opened any doors in the morning. I encouraged him to wake me up, if I was still sleeping so that we could "do it together". He liked that idea :-)
More and more I am filtering almost everything, trying to evaluate how decisions will impact Jim. I'm getting better at it, I think. It's not just for Jim's sake, but for mine as well. Easy does it, one day at a time, keep your cool. So cliche, but so true.
We use the system at night as well, putting it in the "arm stay" mode. This turns off the motion detector, but will alarm if doors or windows are opened.
I realized last fall that Jim is not able to arm or disarm the system without looking at a very short list of instructions. It's pretty basic; 3 steps for arming and 2 steps for disarming. (Example: disarming requires touching the red bar and then entering our password.) Our password is one that we have used for years for our garage door opener. Every morning and every evening I always ask him if he wants to arm/disarm, or if I should do it. He always says, I'll do it, but you watch me. He faithfully puts on his reading glasses and pulls out the instructions, and proceeds to do it under my watch.
Well, the other morning he awoke before I did, and according to him, he saw "a lot of smoke" outside. He opened an outside door to check it out, and you guessed it, the alarm went off. (The smoke he saw was simply the vent for our gas furnace to the outside.)
Meanwhile, I awaken. I am still not quite awake, but Jim starts to tell me that "the smoke alarm went off" (it didn't) and "I went outside to check out the smoke I saw". Next thing I know the police are knocking at our door. I'm still fuzzy trying to figure out what had happened (after all, it is only 6:00AM). The police were very nice, said don't worry, these things happen. Sigh.
I finally figured out that what Jim thought was the smoke alarm was actually the security alarm that went off when he opened the outside door. He felt bad afterwards. I tried to make light of it so he wouldn't worry about it. I think it really made a huge impression on him, with the police showing up. The next day he was still talking about it, and saying he would from now on make sure that the alarm system was off before he opened any doors in the morning. I encouraged him to wake me up, if I was still sleeping so that we could "do it together". He liked that idea :-)
More and more I am filtering almost everything, trying to evaluate how decisions will impact Jim. I'm getting better at it, I think. It's not just for Jim's sake, but for mine as well. Easy does it, one day at a time, keep your cool. So cliche, but so true.
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