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Susan and Angel, it's so sad that your family has chosen to 'disappear' in your lives. I have a large family - half of my siblings in the states, the other half here on island. For decades my sibs in the states would either send special occasion cards or just call briefly on the major holidays like Thanksgiving and xmas and my parents' birthdays. Since mom passed away 3 years ago, I've noticed that they've slacked off. No special cards for dad. No phone calls to home. So, I was very surprised that atleast 3 out of 4 actually called home at xmas. My dad had a very difficult time conversing with them. I do know that for my 'baby' brother, it's his girlfriend who nags him to call (she tells me this.) I try to imagine having absolutely no contact from any of my family. I would feel hurt.

Susan, I've learned that if I want to keep up-to-date with my sibs/family, I just read their FaceBook posts. I try not to 'like' their posts or comment. I don't want them to know that I'm keeping up with their news. I think with my family, we want to 'pretend' that only our friends are reading our posts - and not our immediate family. I do Lots and Lots of saving of my family's latest pictures in FB. They don't send it to me by Messenger. So, I go to FB and scroll thru their posts for the latest photos. It's the only way. Again - I won't post. - but all their friends do.
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Angel, here on island, we have 2 programs that helps caregivers. One is based on your income (we're in the way low middle income bracket) and one is based on how badly you, the caregiver, needs respite. The 2nd one is the National Family Caregiver Support Program. Both are aimed for helping caregivers. The first one provides a total of 4 hours a week (we asked for 1 hour for 4 days - to spongebath dad.) The NFCSP was basically one hour but they provide monthly caregiver's support meeting, therapist (if you need one), provide information on exercising, legal assistance, etc.... I recommend that you check your area and take advantage of these programs.

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Almost midnight and dad's hungry. Sis already gave him one bottle of Glucerna shake. Yes, yes, I know that's for diabetics and not normal people. I'm just going to give him one bottle a day until his nutrition drink shipment comes in. I had bought a pigs-in-a-blanket for lunch. I didn't get to eat it. So, we snacked on that tonight. He told me that he doesn't like the meat (hot dog.) I told him that he needs meat in his diet for the protein. He wins. He left the meat on his side table.
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I really don't know what the dael with but for the past 3 weeks and this only seems to be on Friday and Saturday mornings and I do mean early about 5 to 7am. I end up waking up and hearing Dad walking about in the house and everytime I find a mess to clean up yet he doesnt know how the mess got there.. So I told him we have invisible dogs and cats now. There was a spill on the kitchen floor and so I had to go out in the cold to the utility room to get a mop to clean up. Geez.. dad is always in a foul mood. Well what about me? I am the one who has to clean up your messes and you couldn't give a flip whether it was cleaned up or not. Oh and I had to hear for the umpteenth time how he wishes he would die. Lord.. Are you listening? Because I get so sick and tired of hearing it.
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Dad insists he's not touching his poop. He's not stupid. That's DIRT not poop. And he carries this off with such indignant anger. Yet, I've seen him sneak peeks at me to see if I'm watching him. When I'm not, he proceeds to stick his hand into the pamper. Or after he succeeds in touching the mess, he starts wiping the 'evidence' on his leg pillows, on his pants, etc.... Yeah, he keeps saying he wishes to die... but when he quotes his favorite saying, it's the opposite: "Give me liberty or give me.... life." He always stumbles on the word 'death'. Deep down, I think he's afraid of dying. Or he doesn't want to die.
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So tell him to stop touching the DIRT!
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I'm edgy today for some reason. Sometimes I feel a bit guilty for posting because I have help. Dad is in AL, but I try to stay involved - resentfully (I'm Codependent and in a program).

The smallest things are getting on my nerves today. The repetition... UGH!!!! I've never been a really patient or diplomatic person, so caregiving REALLY isn't my strong suit... especially since I don't really WANT to do it. I've been caring for this man and the women he beat since I was six years old.

The technology thing is nerve racking. WHY CAN'T THE STUPID CABLE COMPANY KEEP THINGS SIMPLE FOR SENIORS?!?!? He's legally blind with dementia, so the remote is confusing. I glued a textured button to the Channel Up key on the biggest remote I can find, but he still gets confused because the AL has HD cable which means that he has about 100 channels to cycle through. Of course he doesn't have the patience to do that so he insists that someone has "messed up" the TV. I'm sick of hearing that story over and over again.

Sometimes I just want to scream... at him for essentially placing himself in some of this situation (COPD is self inflicted and studies show that excessive smoking is closely linked to dementia). Scream at him for being so dysfunctional and creating this H*LL for me (multiple women that he mistreated, lots of illegitimate children that he abandoned that have NOTHING to do with him). Scream at the other children for not helping (totally irrational). Scream at myself for being such a sour puss about the whole thing.

I feel like I'm trapped in a prison of my own making as well. I've learned to say "no" to more things, but sometimes the guilt creeps up.

I think I'm just hormonal today.... needed to vent
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tinyblu - whether you are caring in the home or from a distance with your dad in an AL doesn't matter. You are still a caregiver, and both situations come with their own challenges. Trust me, sometimes it seems it would be easier to have them at home where you could watch over them 24/7 than in a facility where things happen and you have no control over them or aren't told what's going on until you throw a fit with the staff and demand to be given the info you need to advocate for your loved one.

Vent away, we're here to listen. And we understand better than most would.
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Tinyblu, vent, vent, vent. So many things seem to cause dementia. Hereditary (my mom and her mom), high cholesterol (oh!oh!), diabetes, migraine headaches (darn had these since middle school), Longstanding constant Stress (us caregivers), etc.... With all these increases and new diseases worldwide, I blame Adam and Eve. Why oh Why did they touch the forbidden fruit?! 😳🙈😩😔
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Tinyblu, my mom's in AL and just as demanding as when she lived with me. Vent away all you want. We're all in dinghys, rowboats, cabin cruisers and yachts on the same body of water. The thing we have in common is we have all sprung a leak and none of us wants to drown, or see others drown. This site is our life preserver. No comment is too big or too small that someone hasn't experienced it here. Your concerns are valid, true and understandable.
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I haven't been here for awhile. It's been an awful several months. My dad died. bookluvr, I read about your dad putting his fingers in his depends; my dad did that. He also used to pull at his catheter. No more. I miss him but I don't miss that he was unhappy having to wear adult diapers and mess with the stupid catheter and be at the mercy of nurses and our sad attempts to make the end of his life any better. I wish he would forgive me. I think he has. Happy new year everyone. He was the dearest dad and that is who I lost last year. Now I know what it is to walk around with a piece of my heart missing. Not only that but will have a buffoon to deal with who is supposedly in charge of this great country of ours. I am so depressed.
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I'm so sorry to hear of your dad's passing, Genevieve.
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Genevieve, I'm sorry about your father. If you feel deep down that your father has forgiven you, then so be it. You were there for him when he needed help the most. Be at peace.

As I read your post about your father and the depends/catheter, my dad is also going through that too -with the catheter. He keeps trying to pull it out. I feel so bad because he would keep telling me that he needs to pee and he can't. In the meantime, his hand is trying to unzip his pants and to reach inside. I tell him to go ahead and pee because the pee will go into the bag. I'm just so glad that he's wearing slacks and not a hospital gown. Can you imagine the mess!? Night!
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Hi, bookluvr, when my dad had that sensation of needing to pee and not being able to, it meant his catheter was blocked and either needed to be irrigated or changed. I would call the nurse to check it out unless you are irrigating it yourself. I found it needed to be changed about once a month. --Gen
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The caregiver(me) is doing rotten today. Dad refuses again to take a bath or to shave. He told me I need to go on and leave and worry about myself. I told him I will not have filth in my house and if he decides he isn't going to try anymore then I will be going to a hospital first of next week to talk to someone about what I can do about my situation. He says I won't make him do anything but then again I told him.. now I know why Mom got fed up with him so easily and chewed him out because he is completely hopeless. Dear Lord: Please help that man find where he needs to go.
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Angel - if your father is a danger to himself due to self-neglect - such as not bathing, not eating or taking his meds properly, you can discuss the situation with your local agency on aging, adult protective services or social services and ask them to tell you how to get him help without you having to be too involved. If he is termed a "vulnerable edlerly", there should be some actions that can be taken. I would urge you to call them first thing Monday morning.
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SusanA43.. I plan on doing just that. Enough is enough. After all. I am a 43 year old female that can only do so much. I haven't even lived life yet because of this. Mom was never this much trouble. In spite of it all Mom has been my guardian angel and she will help me through all of this also.
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Genevieve, dad's catheter gets changed monthly. Depending on the home care nurse, she irrigates it on her visits. He has prostate problems way before he had his stroke. He absolutely refused then and now to go to the urinologist. Too bad on his last hospital stay, I was hoping they had him see one. But they don't have a urinologist.

Angel, your father might prefer non-family people to assist him in bathing. He might not give them a hard time. Plus I've seen them in action when my didn't want a sponge bath. They were able to calmly and cajole him to agree to it. They have more patience than me.

I don't know if anyone is going to be do a new year's bbq today on our place. They don't usually but SIL puzzled me with a comment about New Years. Yesterday, fave sis said her daughter was doing a bbq today and family was going to her house. I admit that I was hurt on not being invited by fave niece even if I can't go. My shift with dad is when I'm not at work. Oldest sister shift is Monday-Friday only. Fave sis knew I was hurt and kept inviting to the bbq today but it's not the same.... sis said that maybe I can order takeout from my favorite Chinese restaurant. I will do that. I checked my lunch and house money. Oldest sister surprised me last weekend and bought me several micro-dinners. So I have some spare 'house ' $$. Yes! I have enough to buy beef broccoli and oldest sis gave me $4.80 to buy her the walnut shrimp. Yummmm. I better get up. Dad's pamper and b-fast, laundry, etc....
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Urinologist?? Correction- urologist.
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So.. you are never going to believe this. I tried this approach. I already tried being nice,, I tried being a preacher...I even tried being a military sergeant to get points across to Dad. Today I became blunt and told him this is my house and I am your daughter, We keep clean around here and I keep this house totally clean. I know you want to give up on yourself but I am still trying and you need to clean up some a shave and a bath. He said it was too cold to do either. I said I have another option if you aren't going to try and let me tell you he didn't like the option. I told him I was going to get help. Help? He said, never! An hour later he decides to shave and he said he wanted a bath. I said OK. I will help you. NO! I don't need any help he said. I said I am going to get your stuff together and I am giving you a bath. Believe it or not he didn't fight me or hit me or cuss me out.. he finally let me. Yes I used a few more unsaid words but now I have tried a different character this time... He just experienced what it's like for me to have Super PMS and it isn't even that time of month.... I can't believe it..It's a New Year's Eve MIRACLE!
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Aha! You finally found the ticket, Angel! Good for you!

I had the same struggle with my mother. She was a large woman, and getting into and out of the tub was difficult for her, and she was frightened she would fall. I totally understood that, but when I moved in with her, she hadn't taken a full shower in MONTHS. There was literally about an inch of dust in the tub from not being used. I paid $800 to have the tub cut down so she could just step in and out of it, put her large bath chair in there so she could sit and shower. She did very well with that for the first few months, then the resistance kicked in. She was too tired. She'd do it later. After this tv program. After dinner. Tomorrow morning, she liked showering in the morning better. Later today, after lunch. Every excuse under the sun.

I finally had to do what you did. After cajoling, pleading, begging, BRIBING (yes, I even resorted to that), I finally had just had enough one day and got a little upset and raised my voice to her - something I never did - and told her, "Mom, there is a bad odor in the house, and it's because you are not showering. You are going to get an infection or skin breakdown in your skin folds, and have to go to the hospital - and guess who's going to be questioned by Adult Protective Services about your care - or lack of it?? ME. And I'm NOT letting that happen. So you are going to shower TODAY. RIGHT NOW. And that's all there is to it!"

She showered. I hated taking that step, but it became necessary, and there were times she still resisted it, but for the most part, she showered on a fairly regular basis at that point. But I had to use this tactic pretty much every time after that.

What you'll want to check on is if he's actually showering, too - one of the ways I realized that Mom's dementia was getting worse was that she would get into the shower and simply sit there, letting the water run over her. She wouldn't do anything, then she'd get out and say she was done. Except....she definitely wasn't. There'd be evidence all over the chair and all over her backside that she hadn't washed, and her hair was dry. A few times, she actually fell asleep in there. (She could fall asleep in a matter of seconds.) I finally had to start washing her and washing her hair for her.
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Oh...and a funny afterthought here....after Mom had to go into the NH, they only showered her once a week, which was definitely not enough. She was a large woman with deep skin folds around her abdomen and back, which can gather bacteria and cause skin breakdown and infections if not cleaned properly. So I insisted on at least 3 showers a week, with thorough cleaning of the folds plus daily bed baths or sponge baths to be sure we didn't have that issue.

She really fought them on it, because it was uncomfortable and cold for her to sit on the shower chair in the big shower room they had. Then they asked if she wanted to try the walk in tub - hallelujah! She loved it. She hadn't had a good soak in a tub in years - just showers.

When she told me she took a bath, I asked how she liked it - she laughed and pointed at her chest and said, "They FLOAT!!" LOL
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He wasn't getting away with just the water on him. I made sure I put plenty of soap on the rag and I put the soap on myself. It's funny how they want to fight and fight you and then once it was all done he says " Now I feel better" and I said " You should just look at that dirty water isn't it nice to feel clean"
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That's so funny, Angel - my mom did the same thing to me! She'd fight and fight me on the shower - giving every excuse under the sun, and at times, outright arguing with me until I'd get upset and tell her she was going to shower, and that was all there was to it. Then she'd shower, I'd help her get all clean, and she'd come out and say, "Oh, I feel so much better now!" ARGH!
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Genevieve7, Sorry about your dad. It must be lonely without him. I understand.

We try to keep things politically neutral here.
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Politics. There were several big to-dos here on Agingcare regarding this. Moi's comment was deleted along with the others. =)

Let's hope your dad continues to agree to the washings. I remember those times with no fondness at all. I remember the bribing, too. And the saying how he really smells and family will be visiting soon and smell him stinky. Those worked for a while and then .... it got to only him agreeing to shower from several times a week to every week to then bi-weekly. By the time he had his stroke, it was down to monthly. I am glad that this new strategy is working for you.

Now, who ever heard of salt and pepper pork chop - with the pork chop being BREADED?!?! I have eaten at several different Chinese restaurants, and I never had breaded salt n pepper pork chop. I don't even like breaded meat. Well... that's the last time I order that specific food from that specific restaurant.

Hmmm.. I keep thinking of getting a piece of that pumpkin pie I bought yesterday. I couldn't believe how much it cost to buy pumpkin pie. $10.75!!!! So, to make it last long, instead of cutting the pie into 8 pieces, I cut it into 12 pieces. Since I'm also craving cream cheesecake, I've been googling for a non-bake recipe. I don't have an oven, or a toaster oven.. Just the microwave and a hot plate/burner.
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Fave sis had gifted me this iPad Air about 2 or 3 years ago. The storage is getting full. So I deleted some photos. Helped a bit. Then the available storage shrank. So I deleted photos in my linked email address. That helped for a while. Then it shrank. So I deleted several ebooks from the IBooks. That helped for a while.... then deleted more ebooks in IBooks....

I downloaded more ebooks into the kindle app. Storage shrank. After googling yesterday, I deleted the Facebook and radio Apps. And then added these 2 websites onto the iPad desktop as an icon instead of an app. By doing this, it doesn't affect my storage at all. Yes! I can download more ebooks. \o/ \o/
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Book, You've now made me crave cheesecake! Darn it girl, I love that stuff! Marie Callendar frozen pies were on sale for $4.99 today, usually $8.99, so I picked up a Key Lime pie. That will have to do for now but that cheesecake idea will be there until it's fulfilled. :)

I know Jello has a great no-bake cheesecake recipe if you can get the Jello mix. Haven't made it in years but I remember it was yummy.

Hubby and I splurged last night and made pears wrapped with prosciutto ham, baked and then drizzled with balsamic vinegar, an Asian kale salad and then crab legs with garlic and lemon butter. Kind of all over the map but a good New Year's treat.

I know it's now a new year but we are all dealing with the same old struggles. I intended to come into it with a new and improved attitude. That lasted exactly 11 hours and ended when I saw mom today. She has now developed bedsores on her backside from sleeping in her recliner. Thankfully, the caregivers are on the ball and treating it with ointment. I told her medicare will pay for an airbed so she can get out of the recliner. She screamed at me that she is NOT going on hospice.

I am so very grateful that the visiting doctors program starts this week. She was so very angry at me signing her up for that, but otherwise they'd kick her out. It's state law to have a primary doc if you are in an AL. Some of this stuff will be out of my hands. It won't be up to me to make her go to a doctor (well, for the most part). They can prescribe pain meds and manage them for her back pain.

When they give her a physical I will leave them a private note to check the nickel sized melanomas on her back. It has to be what it is - raised, black and bumpy with blue and yellow in the middle. So bad looking, I think she's shot through with cancer, but at a doctor's office for her back/constipation issues she refuses to let them look at them. Maybe now we can get to the bottom of her pain.

Sorry to hear about the BBQ mess-up by fave niece and that your Chinese order was not what you were anticipating. Stinks to be excluded because you were caring for your dad doing the hard work they avoid. Sometimes I just shake my head. Big hugs sent your way, book, and that there is some ease in this madness for you in 2017.
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Windy, please keep us posted on your mom and the melanoma - those spots on her back sound very suspicious. You're right to have them checked.

Hard to believe I've been working from bed for a full month now - glad to hopefully see the end of it soon. The neck/shoulder pain is not as bad as it was at first, so the bed rest is helping, but it's definitely not 100% yet. I still can't sit upright at my desk to work for more than 15 minutes, walk for more than 20 minutes without having to sit down, or drive more than a few miles. Hoping my dr. appt. next week comes up with some solutions, or at least a start to a treatment program for this thing. I know one thing - I probably won't ever be a good "caree" for a caregiver, because I *hate* being stuck in bed!
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Book, do you use Amazon for ebooks? I have a TON of ebooks on my tablet from the freebies that are on Amazon every day. There are several ways to find them - I get emails every day listing the current freebies, because they change just about every day.
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Well, silly me - Book, you said you use the Kindle app, so of course you're using Amazon! LOL

If you are interested, let me know and I'll message you the names and links for the ebook freebie services. :-)
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