Archive for the ‘grieving’ Category

27 July

Life On Hold Begins Again

Dad’s memorial mass was today at 11 am. It was, as masses go, a good one. I carried the cremains to the front of the church at the beginning of services. My niece, Dad’s oldest grandchild, did one of the readings. My cousin, Julie, did the other reading. Someone I don’t know, my older brother’s boss, did the intercessions. Boy was greatly distressed several times. Bran and I comforted him as best we could.

There was the usual tea after the services where I got to meet people I’d not seen in a long time (cousins I’d not seen since Mom’s funeral – I don’t remember seeing them there but they say they were and I believe them), and others I don’t remember from Adam. Of course, there were those who I’d never met before as they became part of Dad’s life after Mom died.

Other than the funeral home arrangement, there were 4 floral arrangements from family and friends. Bran too photos of them and a photo will be sent to each person along with the thank you cards.

The house was cleaned up yesterday. I vacuumed. I wish the machine was better. The suction didn’t really exist so I ended up having to go over areas I could feel stuff on, but the machine didn’t pick up the first four or five times I passed over it. I also had to pick up bits and pieces of paper (we took outdated books apart for recycling) that were in the carpet. This increase in work load wore out my back. Despite that I did get the dusting done (I don’t think the house had been dusted since before Dad went into hospital). I also cleared off the coffee and end tables of the stuff they had on them, washed up the ceramics (Mom collected Blue Mountain stuff) and put them back out.

My brother, sister and niece worked on getting the food together for the family coming by after the tea and did the other necessary cleaning. Boy and Bran did the powder room off the master bedroom. This was used as a back-up bathroom.

I’m quite looking forward to getting back home. I’m thoroughly peopled out (though my niece, Bran and Boy don’t count in that). My sister, her husband and my brother all smoke, so both my and Boy’s allergies are playing up. That doesn’t even get into the smell.

I may not like my brother-in-law much, but he has done a lot of work in a short period of time to do some of the cosmetic stuff that needs to be done to the house. He got the bathtub area done up so it doesn’t leak, he fixed the powder room toilet so it fills properly, replaced the kitchen faucet and did spot painting that needed to be done on the exterior trim (the rest of the exterior is brick and stucco). He also replaced the locks and some of the worn out light switches. All that since Friday. He’s a person who can’t just sit, so it worked out for him.

Tomorrow my niece goes back to her husband and daughter and we head back to ‘Toon Town. I have a few things that I chose to take back. One is a needle point that Mom did. It used to hang over the living room couch. I’m also taking Mom and Dad’s wedding photo, a small knick-knack stand, Mom’s family ring and a few other small bits and bobs. Boy has inherited a sweater, afghan and letter opener that was made from one of the original rail spikes used on the trans-Canada railway (at least I think that’s what it is). We’ll also be going home with a pile of food. There is a lot left over from the tea and then there was the food that was prepared here.

This isn’t home any more. It hasn’t been for a very long time. I realized it when I was laying on the back lawn with my niece and we were talking. With Dad’s death, the spirit that made this place home departed. It’s time to become someone else’s home. What we kids don’t choose to take will be sold or donated. The house will be sold and the estate distributed according to Dad’s will. The estate will probably go into probate since there is property involved. I don’t know how long that will take, but at the end of it I hope to be able to put a down payment on a house of our own.

Needless to say, going through Dad’s bedroom was like opening a time capsule. Dad moved a lot of his stuff into Mom’s old dresser, but the memorabilia she collected was still there. There were old newspaper articles about awards my siblings won, letters and cards from friends and relatives – some long dead. We found the book that Dad’s mom (Granny) used to keep track of the money that her sons sent her each month to help support her. This was before the days of government pensions for widows. We also found a couple of post cards she had written to Dad in French. Our niece translated them (the handwriting was somewhat unclear). They were both mundane and very special. My sister found a picture of Granny’s brother, Xenon. I’d never seen it before.

Bran volunteered to be family archivist. He’ll scan all the photos in the albums Dad made over the years and then he’ll can the slides. This project will consist of several years of work on his part. But for him it’s a labour of love. It also means that there will be an archive of photos available to all of us instead of only one person getting all the photos, or breaking up the collection.

It’s been a stressful time for all of us. My sister’s dog, Bailey, helped break the atmosphere. Besides grief, there’s also anger and dislike. My sister has been walking a fine line between all of us and had done it with relative grace, though she does tend to micromanage some. That’s ok. She’s executor of the estate and wants to do a good job. Dad trusted her and she wants to live up to that trust.

That’s about it. I’m going to go hunt down a sandwich (there are a gabillion of them in the fridge).

21 July

Family Plot

Dad died in the night. I’m going to finish out my shift today, there’s a staff meeting I want to attend at the end of the day. Tomorrow will be filled with the business of getting ready to go out of town and getting someone to take care of Dutchess while we’re all away. We’ll be leaving on Friday morning.

Thanks to everyone for your support the past month. It’s helped ease the load.

Naomi

18 July

Time Speeds Up

I just got a call from my sister. Dad’s blood pressure has dropped (he’s been hypertensive for many years, so this is bad news) and his kidneys are failed again. Apparently they had them up and running for a few days but that’s ended. It was suggested to her that they could increase fluids to help with the kidneys but that would affect his heart. They wanted to know how aggressive they should be. She said not aggressive.

It sounds like he’ll be gone within a day or two.

Funny how the categories “Dad” and “Death” are right next to each other in my list.

14 July

And Home Again

We were down to see Dad on Monday and Tuesday. Things haven’t changed any since I wrote last. Dad is not eating though he did take a few spoons of porridge on Monday morning and ice cream on Monday and Tuesday evening. They are still using Seroquel to sedate him when they are able to get him to swallow anything. If they don’t sedate him then they’d have to restrain him. For most of the visit Dad was non-responsive. He was responsive for very short time periods (two to three minutes) in a day. When he became agitated he’d strip himself of bedding, bed clothes, endanger the IV by pulling it (the entire pole and mechanics) down and out of his arm.

He would point at things that weren’t there and try to talk. However, because he has been breathing through his mouth it was impossible to understand much of what he was saying. He did tell me he loved me after I said I loved him, asked me “where is she” and when I asked who the she was, he looked confused and said he didn’t know. Then after a couple of spoons of ice cream he said “that’s enough”. I know he was trying to say things, he would repeat sound patterns when I said I couldn’t understand. This was quite frustrating.

This was only for a short time last night. Monday evening he was non-responsive and unconscious. Now we just wait while his body slowly poisons itself because of his kidneys not working properly. They work some as he has some urine passing through his body (the catheter bag had urine in it), but not enough to properly detox his body. He’s also slowly starving to death since he refuses to eat except for a few spoons of food in a day.

I emailed work while I was out of town and updated them as to what was going on. This way when Dad does die, they’ll be semi-prepared. I’ll need to be gone somewhat longer because, as with the power of attorney, both my sister and I are named as executors of Dad’s estate. There will be business I’ll have to be out of town for.

The stay at home was painful and awkward. I don’t want to be around my older brother and wouldn’t be if it weren’t for Dad dying. Bran was having difficulty with this as well since what affects me, tends to affect him as well, especially with family stuff. The entire house reeked of cigarette smoke. It probably wouldn’t have repulsed me so much but for my distaste for being around that particular person.

Bran went through the house and looked at things that needed to be done in order to get it fixed up for sale. Most of the work is cosmetic (paint, new flooring, cleaning carpets) with the exception of needing to gut the main bathroom and update the master 1/2 bath.

I went through some of the stuff in the basement. You can tell that Mom and Dad were children of the 1930s and lived on a very limited budget for many years of their marriage. I found an amazing number of things that most everyone now-a-days would have thrown out. Mom saved things like aluminum take out containers and styrofoam plates from under meat (she washed them up and saved them for who knows what). There were also various plastic containers for condiments, peanut butter and other things saved. I don’t know how we’re going to work out things around the work needing to be done around the house. I know my brother can’t be there for much of it since a) it needs to have the house cleared and b) he smokes. Any renovations need to make the house smell fresh to make the house more saleable.

I’m glad to be home. II missed Boy a lot while we were gone. We left Dad’s at about 9:30 this morning and arrived home around noon. While we were gone Boy did a lot of work to have the kitchen mostly clean. When we got home he made us Lipton’s chicken noodle soup for lunch (he forgot to take bread out so couldn’t make us sandwiches) and then he washed up all the dishes he used to create and serve lunch. He’s a darling boy. I’m glad I’m home and he’s around me again.

I got home to the happy news of receiving my mail package from China. After lunch we all piled into the car (I let Boy sit in the front since Bran had also greatly missed Boy) and off we went to the Shoppers Drug Mart where the package depot is. I now have a couple of different styles and sizes of nickel free silver spacer beads (Tibetan style), a couple different styles and sizes of nickel free bead caps (Tibetan style), two different lengths (2 cm and 3 cm) eye pins, and 200 metres of nickel free jewelry chain. Yes, it was a heavy package. They didn’t send me one item that I ordered 2000 pieces of. So I sent them an email telling them.

Everything I got has been repackaged into labelled plastic containers from the zippered plastic bags except for the chain. I want to spool that onto dowels to keep it from getting all tangled. Right now that’s also in a plastic bag. I didn’t expect that. I expected it to come spooled.

Anyway, I’ll be looking at my beading stuff and seeing what needs to be redone. I want to make sure it’s all quite durable. I used super glue on some of the pieces and those ones need to be redone because of it. The super glue makes two weak spots in the wire at each side of the glue site. The closer is also a weak spot because the crimp bead might slip (for things like bracelets and necklaces). This is especially important for the bracelets since more people tend to wear bracelets more long term (days at a time) than they do necklaces.

So, guess what I’ll be doing for the next few days. Yeah, knitting. HAH!

11 July

And So We Wait

The decision of the family is unanimous. No heroic measures are going to be used to resuscitate Dad. We are also not going to have them do much in the way of other measures, including dialysis. There’s not much point to it really. The blood tests aren’t all back yet. They’re trying to find out if he has an infection that is caused his kidneys to shut down.

Dad does have basic responses, but none of them bode well. When the nurses attend to him, take his pulse/blood pressure or wash him, he fights it.This doesn’t mean that he is aware of what he’s doing. He can’t swallow and therefore hasn’t taken any meds since he was found unconscious on Friday afternoon/evening. He doesn’t respond to commands of any sort and doesn’t respond to my brother’s voice.

We’re going to let nature take its course. The nurses will keep him comfortable, that’s all.

So now we wait for the inevitable.

To help me Bran has taken me on two car rides to help settle me down. He did that when my dog died in 1985. He would’ve done it if we had a car when my Mom died in 1993. He did that tonight. We went and got snacks for all of us. Did you know that Chapman’s Ice Cream company makes a no-sugar added, lactose free ice cream? They do. Only 14 grams of carbs per 1/2 C serving. That’s better than regular ice cream.

We went through the real estate listings for town as well. It was something to occupy my mind with and do a little bit of dreaming. It was a nice distraction. While we did that Golden Eye played on the DVD player. Laundry tomorrow so that we have clean clothes to to down to see Dad on Monday with. I’ll be sorting through the stuff collected over the years of Mom and Dad’s lives together (including “treasures” given to them by us kids). I don’t know what to do with things like their letters to each other from before they were married, Mom’s nursing uniform (100% cotton that had to be ironed and starched), Mom’s wedding dress and Dad’s wedding suit, and a plethora of other bits and pieces of so much living.

Thank you all, those who commented and those who are just thinking of me and my family. Your support means more than I could possibly say.

9 July

Dad

I got a call from my sister tonight. Apparently when the nurses went in to check on Dad earlier today he was non-responsive. They did some tests and found that he is in renal failure. They called my sister to find out how heroic we wanted them to be if Dad worsens.

She didn’t want to make that decision on her own. So she called my two brothers. They weren’t home so she left a message. Then she called me.

I told her that I didn’t think that Dad would want to be the way he is, at least not the Dad I knew before all this. The Dad I knew was a vital, energetic, and intelligent man with a very wry sense of humour. I love Dad a lot, but the person I saw was a mere shell of the man he used to be. He was hesitant, confused and not really there.

I told my sister that they shouldn’t resuscitate him if the need arises. I think that palliative care is all that’s needed now. We just need to let him go.

I’ll be going up on Monday regardless of what happens over the weekend. I could go up tomorrow, but what is the point? I don’t want to be the one to comfort my brother. There’s no business that I can take care of on the weekend even if he does die.

So that’s how things are now.

22 June

The Technicalities and Such

Well, I’ve done some processing of my visit to see Dad this past weekend. I don’t like processing. It implies feelings and I don’t do them very well.

What it all boils down to is that Dad’s mental condition is such that he’s not going to go home again. His needs far outstrip my brother’s capability of caring for him. Dad needs 24/7 care. My brother would have to have someone come in and, in essence, babysit Dad just so that grocery shopping and the like could be done.

I think the most painful thing for me was to see Dad, in his moments of clarity (and there were few of them) didn’t realize the state he was in. It’s better for him, I know. I mean, it would break him to know the state he’s in. But it brought home to me just how bad he is if even in times of relative clarity, he can’t recognize things. The weirdest thing was he remembered Bran’s name. I’m not sure he remembered it more than a hand full of times since we’ve been married in 1986.

Dad’s short term memory is shot. If you leave the room and come back he’ll greet you like he’s not seen you for an age. His cognitive abilities are damaged. He can’t keep track of conversations. He regresses in his memory, thinking that the entire family is at home or remembering my sister or oldest brother as living in Saskatoon.

Physically he’s very feeble. This man, who used to walk upwards of 10 miles a day doing errands can’t walk 10 feet without losing balance. His strides are about 1 foot.

He’s totally preoccupied with his watch and time. When he first arrived at the hospital the nurses took it from him (as they do with all jewelry in ER) and it distressed him enough that they gave it back to him. He told them that he was a navigator in the war and precise time was very important to him.

The practicalities are taken care of thanks to him creating a power of attorney for my sister and I. He thought that was what was needed in case of his death. It’s a good thing he had it drawn up because now we don’t have to go to the work of a competency hearing and such. The down side is that neither my sister nor I live in Dad’s city. We’ll be doing things as a team. That’s how the power of attorney works. Anything that needs to be signed needs both our signatures.

Interestingly, a power of attorney ends at death, so it would have done no good then. The business of the decedent is handed over to the executors (again my sister and myself) to dissolve, pay taxes and distribute the estate. However, it’s a damn good thing it was made up to take care of things now.

So that’s how things are right now. My sister is mailing up some paperwork for me to take care of when I get back from Edmonton at the end of the week.

Speaking of Edmonton…I have to be at the office at 6:30 am. (0630 – for those on the 24 hour clock). I’ve got most of my stuff gathered together but not packed up. I’ll be doing my showering in the evening before we go anywhere (if we do) tomorrow evening and Thursday) I imagine the other 2 women will want to shower in the morning. This saves some congestion at the bathroom.

That’s about it.

Ta-Ra

20 June

I Came, I Saw, My Heart Broke

and we got a flat tire.

I need a bit of time to process yesterday’s trip to see Dad.

In the nonce, enjoy the new PR site (promos, give-aways and ratings) created by Smelly Anne It’s new so there’s not a lot there yet, but I’m sure there’s going to be a lot there to take advantage of given some time. It’s called Fishing and Wishing. Just click on the image on the right and you’ll be taken there right away.

18 June

On Getting Old

Writing has always been my chosen form of expression. When I get highly emotional talking, being able to form cogent sentences abandons me. However, I can write. Maybe it uses a different part of the brain.

Speaking of brains. Yeah. Dad’s in hospital and won’t likely be going home. He’ll probably go to a home, just not his own. Apparently in the past months (who knows really how long) Dad’s mind has been leaving him. Because of issues I have with my older brother I haven’t gone down to visit Dad. The last time I saw Dad was when my oldest brother (not the one I have issues with) was visiting him and was able to drive up here. That was several months ago. Dad didn’t want to drive 2.5 hours on his own. That was ok though. I was content with short monthly phone calls.

On Monday my sister phoned. Dad is in hospital she says. Dad probably has dementia she says. It sounded bad enough then when she hadn’t gotten much information but hearing back on the history of things, yeah, it’s worse.

Apparently Dad has been forgetting who people are, like not remembering my brother, who lives with Dad. He wanted to know where Mom was. She’s been dead 17 years. There’s more, lots more.

Today my sister called to say that Dad won’t be going home. Even if my brother were to take advantage of the EI program for caregivers (a year off with unemployment benefits similar to maternity leave but designed for people who are caregivers of elderly parents) he’d have to be alert and on duty 24/7. Dad’s a wanderer. The hospital had to put him in a restraining chair. Yeah. And Dad figured out how to get out of it. He’s always been able to figure things like that out. This time it wasn’t a good thing. He was found to be wandering from room to room in the hospital.

He doesn’t appear to be worried about going home, at least that’s not the impression I was getting from my sister. I hope that’s the case. I’d hate for him to be fretful about being surrounded by strangers (but even family is getting to be like that) and wanting to go home. I’d like for him to be ok wherever he is.

We’re going down tomorrow to see him. My sister is going to be on the bus from her home in Alberta tomorrow as well. She arrives there sometime around 9 pm. We might see her. It depends on sunset times. Bran doesn’t want to drive home facing into the sunset. The glare is difficult enough when the sun is behind.

So now I get to grieve losing Dad. His body will be there, but he might not. Or at least the Dad I’ve come to know as an adult might not be there. It’s possible that I might be looking into my own future where I don’t know my son, my husband.

Life has gotten more difficult all of a sudden.