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Caregiver..hope job comes through!
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thanks everyone, but unfortunately it requires a move of a few hundres miles away and I am in no position financial or otherwise, and I prefer to work from home, however, on a brighter note they did tell me of a position coming up in October I might fit into .... they also said if they start hiring from home in that department I'll be hearing from them....I have a job I like but better pay and benefits is a good draw for me away from it
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Well, Saturday was a good day. I did nothing related to caregiving. I know I'm lucky to still get a day like that once in awhile. It won't last, but I make the most of it while I can. I did what I wanted, when I wanted.
Of course, I paid for it. Last night, instead of being at the gym, I ran their errands...picked Dad up at the tire place, dropped off library books, bought buttons for Mom that she thought were on sale but aren't until Friday - but I had to run right over and get them before they ran out. Oh, back to real life.
Dad is not really better. He is only having one BM a day, which is an improvement. But it's still mostly liquid. It's been 4 days without his meds, and I expected to see more improvement if that's the cause. I think the going less is only because of the new pill they started him on. I'm going to email the doc tomorrow if things don't improve and make an appointment at the GI clinic. I'm also waiting for the C-pap people to call me back. he's lost so much weight, his mask doesn't fit right anymore. When it rains....
Cat-Good to see your Dad was out and about in his wheel chair. He seems to be settling in pretty well. Hugs.
Wanda-poohey on the broken car! My parents' van has been broken, too. It sucks. Hugs.
Caregiver - I was LMAO about the placement of the dead bug! Hope you do find a better job closer to you. Hugs.
Mary - blessings to you! Enjoy your normal life. Your family will be so happy to have you home. Hugs.
Vic-Glad you got some stable days. Any kind of normal is nice. Relax a bit when hubby gets home - I know you need it. Hugs.
Hope everyone is having a decent day, and if not, may angels hold you up.
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Caregiver,
great news. Take the job!!!!!! These past few years have been very hard on many of us - getting back to your former income level is a great opportunity.
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Notlike... How awesome for you!!!!! That was a MUCH needed break for you, and of course no one could tend to all those tedious details like you can.... they were just waiting for the SUPER CAREGIVER to return.... sorry, M does the same thing to me... she has two other women working for her now, but I get to do this silly stuff..... aren't we SPECIAL...
M said no on the lady that interviewed yesterday, and I'm glad.. wasn't my decision tho the daughter did ask me what I thought...... oh Lord, what a question to ask ME... of course I told her what I thought.... that I didn't feel like the lady really wanted to work, that she may have thought it was just setting around watching TV and maybe fixing a meal.....but M is the one that said NO, so another girl coming in tomorrow.... either way, I get my long weekend... YeEEeEE Haaaaaaaa !!!! love ya'll
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How is this for a turn of events:
As said before, I am leaving my Moms house to go back home to my family.
Mom wanted me to be her caregiver, a position I do not believe I can, or want to do.
Today, told Mom I was leaving, she said some mean things and told me to leave and never come back.
Well, Mom called me a little while ago, apologized, talked like the Mom I knew, but still got angry when I said I could not care for her properly at home.
Then she said it would be helpful if I could find her long-term care paperwork so they can pay for another 30 days in the nursing home.........................
.
So, deep down she knows she shouldn't be home yet, but was bullying me to give in.
I tried to be very nice during the conversation, but you know, I do not like bullies.
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Hang in their Mary. Your sibs can help her with the paperwork if needed before you go. You need to be home with your family. Hugs, Cat
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One more day, then a glorious four days of not hearing... would you, could you, can you, did you, by the way, oh I forgot, when are you, why didn't you, you should have, when you have time, is it, well, I don't know about that, I need you to, and on and on.... so going to train new girl today, watch her with S, and take my little check to the bank, come home and SLEEP..... love ya'll, hugs across the miles...
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Mary-Good for you for holding your ground. At least your Mom realizes she needs care.
Ladee-A wonderful long weekend to you! That's awesome. Let's see how many naps you can get :)
Got home last night and their van was in the driveway with the flashers on and the hood up. yippee. Dad was cleaning it out and must have turned the headlights on by accident. So the battery was dead. Big emergency, don't ya know...needed to go to Walmart for Polident. It' never as funny while it's happening as it is the next day :)
Good day to everyone.
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Hi Jam! Hi everyone! New to the forums. Doing ok today, but again it's still early. Taking care of my 89 year old father in law with progressive dementia. He seems to be on the same dementia stage your Mom is Jam. Some days are not that bad but others we feel like we're going to lose our minds with his. Right now we're battling his urge to migrate back home. He used to be a snowbird for many years until about 8 months ago when he had some strokes that affected his memory even more. He forgets and / or refuses to use his walker often... we're lucky last time he felt was on fathers day. The other day he sneaked out of the house to go for a "walk"... but a worker on the street told us he was asking for a ride. His VA nurse just brought us some door alarms we need to install as soon as possible. Last night we watched 'Happy Feet' with him and he seemed to enjoy the music. We've only been living with him and watching him for about five months but already sometimes wonder for how long are we going to be able to live like this. My husband is a dialysis patient and my health is not that great either so sometimes it seem like too much to handle. *hugs all around*
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Welcome MariRosa, hope you find a 'home' here..... lots of great people on this thread, lots of love and encourgement... collectivly a lot of experiance... so hope to hear from you again.....

Notlike, what do you mean the new caregiver won't take care of S the same as me ?!?! Ya, uh huh she will !!!! Girl has a ton of energy.... want me to see if she'll hire out in other states??? She's going to do fine.... she's loud, won't take M long to squash that!!!! So, on my first long weekend in 8 months or longer... YE HAAAAAAAA.... More later, after my first nap..... love ya'lllllll
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New to this post - kindred spirits with funny, bittersweet, heartbreaking - strangely similar tales to share. Latest with my 81 year old Mom who lives with me is she seems to have forgotten how to take out her implanted dentures. Two nights now have been mega battles to get her to let me take them out and put them in the Efferdent. Trying to decide if I do it once a week is enough or if that will give her an awful infection under the full upper. Sometimes I feel I will go mad - nice to have a place to vent. I am looking forward to this Saturday - I am actually getting out to go with friends (not just to work). Sometimes it feels like I just work and take care of Mom... and this past weekend she forgot my name. She was fine 6 months ago except for the Arthritis. It is an incomprehensible disease! Miss her so and then all of the sudden she will tell me I look nice out of the blue - guess I better treasure those moments. An hour later she may tell me I am being mean when I tell her she needs to take her dentures out. Thanks for the sounding board.
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Well, dads bronchoscopy went alright. Dr said that he had a lot of secretions that he thought was coming from him aspirating drink and foods. He said that he didn't see anything for concern, no masses, and that he still did not have the ct scan back that they did yesterday. And dad has a appt with him again this monday at 11:30. Lord i hope sis can carry him to that. So as i told brother yesterday while we were up there at the hospital. THE SAGA CONTINUES.............. Like the Godfather movie. I told him i guess we will be starting on movie #6.............. Brother said, "Not the Saga". I had him cracking up, laughing. He said i told you they wouldn't find nothing wrong with him just like all the other drs. Then last night sis tells me that dad said that if the pain in his side (right lung) where the pleural effusion is didn't get any better then he was going to have to go somewhere. And sis just said that maybe he has got pleurisy. So who knows???? Well i gotta go pick up bil at the hospital and then connor from daycare. Chat with ya'll later. love and hugs stormyyy. P.S. To be continued just like the mini series...............
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My mom is having a colonoscopy tomorrow to make sure that she doesn't have colon cancer (super low risk) or anything other problems. She'll be home Friday morning, she says. I have to admit that I'm not at all thrilled. Not at all.

To top it off, my fiancé is going back home in a few days. I'm not thrilled about that either. It's like my life is going to suddenly just crumble all at once with his leaving and my mom's coming home. I'm terrified of the anxiety I'm going to feel once again with him gone. I have such fears of bad things happening to him, so much fear of being abandoned. All of that will come back in a matter of days, starting with his bus ride back home.

Well, I guess my break was good while it lasted. I didn't do much, hardly answered the phone (all my neighbors have been calling, probably wondering what's up since my mom's car has been gone so long), just sat on the couch watching scary movies and indulging in takeout.

Here's to my miserable life coming back.
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I care for my mom who has pulmonary fibrosis and severe arthritis. She can stay home with the help of myself and another caregiver. I am stressed out but am so grateful she doesn't have dementia or cancer. We are closer now than ever before. I never thought i would be able to say that. It is fulfilling most of the time but my fatigue is affecting my social life.
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Smitty, when was your mother diagnosed with pulmonary fibrosis?

My step-mother was diagnosed with that several years ago, but a few months back was told that she had less than 6 months left to live. All of this has taken its toll on my 87 year old dad who wishes she would agree to move to an assisted living together.

I wonder if your fatigue is not a warning sign saying that you need some extra help in taking care of your mother?
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Smitty~I have a brother with Usual Intrestital Pneumonia/Fibrosis and my sister was just diagnoses with Intrestial Lung Disease. Is your mother's pulmonary fibrosis a result of an autoimmunine disease? I ask because you mention she has arthritis. My brother is taking high doses of Prednisone to reduce the inflammation. My sister has not started a treatment yet still waiting for all the results to come in. I empathize with your not having a social life because of the fatigue. I hope you can get help either from family, friends, church, or home health care. Keep us informed!
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Ladee: Enjoy every minute of your very long overdue days off. I hope you can sleep in, putter around and just enjoy your the fact that you are alive.

Welcome to the new posters. It's late at night for me, so I'm going to bed, but I will reply to you. My heart goes out to all you are dealing with.

Sharynmarie: So glad to know your sis does not have lung cancer. I don't know what Intrestial Lung Disease is , but I will look it up. Sounds chronic, but I hope for the best.

Notlike: Enjoyed your post.

Hugs, Cattails
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Ladee: Enjoy every minute of your very long overdue days off. I hope you can sleep in, putter around and just enjoy your the fact that you are alive.

Welcome to the new posters. It's late at night for me, so I'm going to bed, but I will reply to you. My heart goes out to all you are dealing with.

Sharynmarie: So glad to know your sis does not have lung cancer. I don't know what Intrestial Lung Disease is , but I will look it up. Sounds chronic, but I hope for the best. Hey, I just looked it up, but all I could find was interstitial lung disease, which is essentially Pulmonary Fibrosis. Does that sound right to you? You know my mom had Pulmonary Fibrosis for years and years. God Bless her, it just came out of nowhere. She never smoked or was around 2nd hand smoke. No idea what caused it, but in so many cases that is true. Sending you and your sis white light and healing.

Notlike: Enjoyed your post.

Hugs, Cattails
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Good Morning to all and a big welcome to our new posters! I hope you feel comfortable here with us while on your care giving journey. I know it's been long and grueling for most, if not all, of you. I thought I should give an update to our new friends since I see there is no longer a date by the original post so you don't know when it was started. I began caring for my mother-in-law in Nov 2009, that was when we, my husband and I, moved her closer to us. She had been living alone in her home about 30 minutes from us, but due to falls, abuse of alcohol, and uncontrolled incontinence we knew she could no longer live alone. After 8 mo of declining mental status, trial and error to find workable meds, finding ways to keep her from killing herself......she liked to sneak outside and pull weeds and throw them over the edge of the pond which was a 20ft drop-off or cross a 2-lane BUSY highway to retrieve trash.....we brought in extra help. We also fenced the backyard to keep her corralled and then had to put a dead bolt on the front door to keep her from heading for the highway. Last Oct, after finding her on the floor with her face banged up, my husband made the decision to place her in a NH. There were a lot of other issues going on at the time.....incontinence to the point of wearing poop all over her if I didn't get to her in time, and yes she was in adult diapers. Things just progress to the point where you know "it's time". The home she is in consistently is rated a 4 star home, but she will call us once a week to let us know how "incarcerated" she is and those mean people won't let her come home, yet when we see her she can't say enough good things about it. Her mental capacity has all but disappeared; she can't hold a thought at all. Ask a question and her eyes glaze over and it's like I've never said a word. Placing her was a life saver for me as I have my own physical limitations to deal with and we both know that she is getting excellent care. She has recently developed a cardiac arrhythmia so we will see where that takes her.
All of you are in my thoughts and prayers today and everyday...........peace to you all!
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Cat~I am sure Pulmonary fibrosis is the same thing and yes a chronic condition. On line it says treatment is with steroids but in my sis's case don't know if that is possible since she is diabetic and steroids play havoc with blood sugar. Tomorrow I take her in for a colonoscopy to rule out colon cancer and next week we will have all the results with the course of treatments. She is quite relieved knowing it is not lung cancer. Thank you for sending the "spirit of healing" our direction♥!
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Some of you know me from other threads. Today I need to write here. My mom lives w me, 81, dementia, probably Lewey Body, experiencing period of rapid decline recently. She got me up at 6am (way early for her) very confused. She has been unable to get re-oriented. She has however, spoken clearly about being at the end of her life. She's tried to finish a knitting project that was ignored for months after being a big mess she could not fix. She wanted to call my brother to make sure he really knows she loves him (he has had many problems that have made him a challenge to all of us. She told me stayin with us has been the best part of her migrant that I was the best thing that ever happened in her life. She thanked me for loving her even though she knew she made it hard to stay in loving mode, and thanked me for taking care of her. She thought about what could be done to her ring to give us each a nice piece of jewelry. I am frazzled and raw. I so want to call my husband and weep, but I can not do that to him. His greatest work stress is when he doesn't have enough work to keep all of his workers on a job. That rarely happens but today he has to lay off some hard working employees w young families. I am going to finalize some financial papers for my mom-has to be done-and probably won't get back here until late tonight. If ever I needed your support here, it is now. I just want to ball my eyes out. But I will keep my chin up and go a step at a time, hopping my mom is not at the end of her life just yet. Thanks for being here and understanding in a way others can't. Until later tonight...kimbee.
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Kimbee: My heart goes out to you. I wish I could put my arms around you and hold you tight. You could cry all you wanted. I can't take away your pain or worry, but I can point out that the words your mom shared with you are amazing and so full of love and gratitude. I am so happy she could give you that gift.

You have been an amazing daughter and your mom has been blessed, as she said, to have you in her life and by her side during her last years. Even in these difficult times, with her dementia closing in, you both can still share the love you have for each other. I don't have words to express how very precious that is and what a comfort it must be to your mom. I know it is to you also.

You are a very wise and loving person, so I don't think there is anything I can tell you that you don't already know. Just take those moments with your mom and cherish them. When you love someone, losing them in very painful, but knowing that the love is shared and that you have made your mom's life better with your love, understanding and compassion is the true meaning of what life is all about.

Sending you love and comfort my dear friend, Cattails
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Kimbee- I am so sorry that all of this is happening to you and your mom. Caregiving is a tremendous job, but all of us know that already. But it seems like that you have had a loving relationship with your mom. I wish that i had that with my father, but i do not. I had that with my mom and it was priceless beyond belief. Take the memories and cherish them and be blessed in the knowledge that you had a wonderful relationship with your loving mother. Many prayers and hugs to you sweetie. Love, Stormyyy
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Vic, glad to head to both parents are doing okay n you having a back spasm can hurt big time, I feel for you girl. You have any muscle rub you can put on it? Let hubby do all the lifting n twisting stuff when he gets back home. Take care.

Mary, 13 hours is a lot. I don't understand Fl laws myself for I have heard other people telling me about their parent getting discharged from the hospital due to no insurance. I understand they need their money but these r human beings! They try to do my dad while I was down there too until I had a nasty fit n threating to get the news people out their for my dad was not physically fit to be sent home. So, they sent him to a Rehab center for that was what they had suppose had done in first place. Fl & GA both suppose to be having construction work but u have probable already passed it. Drive safely, crank up the music n take breaks. Enjoy yourself.
Caregiver, do what your gut tell you to do n I hope it is take that job n congratulations too. I hope you get the job.
Ladee, you know how to say the right things n Caregiver, we r all your family too n rooting for you n your job.
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This morning my mother decided she couldn't get out of bed properly and I found her lying sideways across the bed. I couldn't get her back into the bed, or out of the bed, she kept roaring that I was hurting her...
I ended up calling the doctor, who came out and helped me get her into bed (roaring her head off the whole time). Doc was worried in case she'd broken a hip, but she hasn't fallen in the last 48 hours, and there didn't appear to be anything wrong with her hip (she was able to move her leg around happily enough)
I reckon she's having us on because she knows she's going into Respite for two weeks next Tuesday.
So I've had a quiet day (she was asleep in bed!) watching the Olympics :-)
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I am caring for my mom who has dementia....I am doing it by myself.I am so tired all the time.There are days I want to give up but I cant its my mom...feel guilty for thinking about putting her in a nursing home.I cant even cry anymore its all gone....I just need someone to tell me...your doing a good job and what your doing is a good thing.
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Kim, you and mom are surrounded by angels... sometimes they know, and how awesome and a blessing you will never forget, the precious words she said to you.... and no we hope this is not the end either, but if in fact it is, then please stay in touch, we are here for this part too.... I wouldn't have gotten thru my lady Ruth's death without my friends on this sight...... sending you strength, sending you love, sending you comfort....... and all the kick ass hugs you can handle.... love ya

Blue, glad mom got untwisted.... and ya, it may be a little acting out before respite, but you take it anyway, regardless.... I woke up many mornings to find Ruth in some strange positions...one day one leg hanging off the bed the other one THRU the bed rail... still have no idea how she did that.... took awhile with her bellowing the whole time, but we got her untangled.. we either have to laugh or cry, depends on how tired we are I guess... hugs to you and enjoy your respite.....
Momof3, you ARE doing an excellant job... and raising three kids, is this the mom with triplets? Just that by itself is unbelievable , much less caring for your mom.... come back and talk to us.... vent until you feel better, this is a safe place to put it down..... and you might even get a suggestion or two to help you out, if not, then you'll get lots of love and support... no one else understands like another caregiver....

Hugs to everyone today.... more later......
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MariRosa, Those door alarms sound like a great idea and glad the VA nurse brought them to you. Another idea of what I have done is that, I put a sliding lock at the bottom of our door n I got it dark to match the door for mnl can't see it that much. Now, she cannot walk out the door if it is in the middle of the wee hours. They say at the bottom for they don't tend to look down because they are too busy grabbing the door knob. Sorry to hear that your husband is on dialysis. I was on it for two years. I hope he is doing okay. I know that has to be hard on you and now keeping an eye on the fil. I have not heard someone use that word in a long time, 'snowbirds.' Gosh, it would be so great to just go to the beach on a weekend without a freaking care in the world. I can just smell the salty air.
Notlikemom, so true for it is not as funny while it is happening. However, later it gotta give you a little crackle or you go crazy.
I forgot to mention about taking the mnl to get her lab work that I was behind on time so I had to rush her out the door withing 20mint. Yep, I knew we, hubby and I was in trouble with the 'fire-cracker-red-headed-wood-pecker- mnl.' I thought I had a whole hr before her appt until hubby ask me, while he still in bed n Im just sipping on my cup of coffee that, "did we just get back already?" Im like what???? Why? he said her appt was at 8:55 n for dumb ass reason I thought it was for 9:55 and her it was 8:35am. We r rushing n its a fasting lab n I didn't won't her to pee in toliet for then she wouldn't be able to go their with the lab. I'm dropping things, grabing my glucose meter, grabbing keys, running out the door n told hubby to get mom out of her room for she is trying to put on a freaking necklace n deciding what jacket to wear. Its 80ish degrees!! Necklace!! Please get in the car we r running late. that is what I was actually saying as I ran out to the car. I got to the car running honking the horn hopeing that will get her moving n I hear her yelling at hubby. I knew this rushing crap was heading for diaster. Yet, I knew last night her appt was 8:55am, I guess maybe I got some Alz going on? Dumb, dumb, dumb... anyway he finally gets her out n she arguing all the way cursing n we rush to get to the place. I still have to drive to get to the place too. We made it right on time-speedy just a tad. We sat a few every bit of 3 mint into anothe waiting room. I went ahead n got her a pee cup n it was stanky. I mention it to the nurse that suppose to draw her lab. In the process of collecting the foul smell pee, the mnl happens to wear half of it on her pants n part all over my hands due to all over the cup. The cup runner over. Well at least we can wash all that off n we got all tha done n I apologize to mnl for it was my fault not paying attention to the time. She said, "don't worry about for I don't know what I do without you." I was shocked that came out of her mouth, but thankful. Now, that made my day as a caregiver. Even if you can get a smile from them sometimes is very pleasing to know that we are doing the best we can n sometimes they do recgonize what we are doing or for at least now.
I hope everyone has a great day.
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Momofthreeboys, you've come to the right place. Everyone is here to support you, and let me say that you ARE doing a good job and a good thing. You're only human. No one expects you to be perfect. You're compassionate, generous, and caring. Anyone can see that. You're a wonderful person for taking care of your mom and for not giving up. Keep your chin up and come here to vent anytime you need to.
~~~~
My mom had her colonoscopy today. The biopsy results aren't in yet, but they said they didn't see anything that looked like cancer. They said her colon is pretty much a goner though. Looks like surgery is inevitable. She's a little worried about that, but seems hopeful since she spoke to the surgery. Apparently, the surgery won't be as bad as she thought and she won't even have to wear a colostomy bag the rest of her life, just for about two months. Plus, she'll never have to worry about getting colon cancer. Thank goodness for that.
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