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Bookworm, simple misunderstanding, just want to clarify... S is my charge.... I am a paid caregiver.... I go to thier home everyday and help..... or take the blame as the case may be... and I am glad you have that pic of your mom... just shows me how no matter how you were and still are treated you have been blessed with an open mind and a very loving heart..... It really doesn't matter, in the end, if family recognizes what we do, there is a Higher Power that knows, and like minded caregivers that truly understand how we feel and do appreciate everything we do ...... I am so glad you are posting and sounds like you are feeling a little better..... this sight is a literal life saver for us..... keep coming back and letting us know how you are doing..... hugs across the miles to you...
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Ladee, as bad as it is for you, I do think about how much worse it could be for Sman if you weren't there, and I am comforted that you are there for him. Thank you. I appreciate what you do.

I am stuck in a vicious circle of in laws, paperwork and phone calls daily concerning mil's business. Had a talk with sil yesterday and told her I was pissed about the flowers. She apologized and said the check will be in the mail.....we'll see. We asked her to pick out the flooring to be replaced and she threw it back at me.........just sent her another email putting the ball back in her court. Don't ask to help if you can't make a decision. I don't sound very sympathetic, do I ???? I will next tell her that NO decision is the wrong one. I'm tired of walking on eggshells, but the walk just started and I can't give up yet. I can't wait till my puppies get here. Sometimes I just hate people.....oops, I guess someone woke up crabby today.............
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I haven't been able to keep up with this - where do you guys find the time?!

Yesterday sucked. Not from caregiving so much as other stuff. I'm sure you don't want details, but suffice to say I was very sad and depressed on top of that.
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You get to be crabby Seeme, would be different if you weren't trying to work with stupid and greedy people... and yes, don't walk on eggshells, doesn't accomplish anything in the long run, just makes us crazy.....I think we all need a pair of 'don't f*ck with me" boots.... try not anwering the phone for one day, just one... it can all wait, nothing is that important and yes it's time for the furbabies.... they aren't even my babies and I can hardly wait... for one thing I know how happy you will be... and if you're happy then so am I..... sorry the jackasses are wearing you down.... how is Mike??? You both are in my prayers every day.... love ya Seeme Sue..... my precious gift from God.....
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PCVS, we don't find the time , we make the time.... I would go insane or go postal if I didn't have the release of this thread and others on this sight... and yes we do want details... makes us all feel not so alone.... make the time, this sight is a life saver... hugs to you.....
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PCVS, yes, we want details........I need to get out of the hole I am in......it will make me get out of my own head for a while...................
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Ladee - kudos to you! I appreciate ALL paid caregivers - even if it's only for an hour. I have never wanted to be in the medical profession. Yes, I consider caregivers as medical professionals. I grit my teeth when well-wishers say that after "this", I can work as a nurse since I have all this experience in taking care of the bedridden. Nothing against your profession, but I would Never willingly take up this profession as a career.

I should have clicked on your name to get your backgroud...actually I did but I forgot. Lately, I've been very forgetful. It's driving me crazy. I microwave food, it dings, I open the refrigerator to take the food out. This have been happening a lot lately. Sometimes, I just stand there staring into space because I forgot what I was going to do. I sure hope it's not Alz but just a Lot of Stress and lack of sleep.

And to all of us caregivers, kudos to us! We don't get appreciated or rewarded enough. I'm feeling a bit better today. Some days I feel down and just don't want to associate with anyone. So, I just surf the site and see what's up.

Respite Social worker visited on Tuesday. Dad's blood pressure went up. I told dad no more "lazy" meals. From now on, we cut back the amount of food, eat more veggies,fruits and less meat. He says his health is fine. So he can eat whatever he wants. Lately, he's been touching inside his pamper. It's frustrating because it's "the handwriting on the wall" that as he becomes more senile, he will be making Awful Messes. Twice, I told him to quit touching inside his pamper. He said he's not doing it. I show him the pamper with some of his pooh on the front top. He gets angry and said that he didn't do it. Someone else did it. I told him that it's night time, no-one's here to touch it but him. I dropped it because he was getting really angry that I'm accusing him Sigh...

I think I'm allergic to changing their pampers. If they're soaking, I will keep sneezing. My nose gets all stuffed up and I start sniveling. Too bad I can't quit this caregiving responsibility due to it being hazardous to my health...Later....
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Yes Im Here Ive been busy busy busy... Schools out Trying to divide my time. egually ha ha The BIL babysitter ran off with her boyfriend and left him high and dry so ex wife said she can watch them every other week he owns a home improvement construction so he asked if they can come here as needed there great kids ... BUT MIL thinks she is babysitting gets on nerves of all kids. She trys to act like she can walk and nothing wrong with her. I told dr, she gave her increase of deppresion meds and nerve pill now this week all MIL wants to do is sleep but dr. said might make her tired give it couple weeks my husband said he isnt complaining & probaly kids made her tired last week wait till next week before we think she is out of it. HE probaly is right....MISS YOU ALLL.......
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Hi all another busy night day..dad has diarrhea and vomited last night..poor guy finally got him up a little while ago..gave him some lomotil..maybe it will help. Talked to hospice nurse to ok..if it doesn't work will give phenergen..blahk...another worrisome day. At least he is alert today.
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Sorry to hear you had such a night with Dad......give him a hug! You might try Zofran for the nausea/vomiting. Beats the heck out of Phenergan.

tbailey.........enjoy the quiet while you can.........it never lasts....:)
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Omg what a start to the day sitting around waiting for transportation and then find out they had hubby on the wrong date so had to reschedule his appt for the 27th and got promised that we wouldn't be bill and by the time the medicab would arrive with handicap access today we would have missed the appt since we are two freaking hrs away from Phx...then i am tired as heck.
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Calgon take me away.....................
We still have not heard anything from the doctor, and now i am wondering if i heard sis wrong on what she said the other day. I thought she said that the dr would call us with the results of the thoracentesis. And i got to thinking that they have never called us with results of this before so i asked sis today if she had heard from the dr and she said no that he said that he would call with the new appt time. Do dr normally call with tests results? Should i try calling his nurse? This waiting around is for the birds.......... Love and hugs stormyyy
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UHM, Need to clarify, Jam, Seeme, ASG, Vickie Vic, Austin, Notlike, Beck, Stormy, and all of you are my gifts from God.... dont' want anyone to feel left out... it's because I know all Seeme's been thru here lately, I do love you all.... hugs..
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My grandmother doesn't have dementia or alzheimer's (that I know of) however she can be very hard to deal with. She was an environmentalist /antinuclear protester when she was younger and still is heavily interested in religious, political and health issues. Every day she wants to read me newspaper articles and express her strong opinions. I have had depression and anxiety all my life, so I don't want to hear about any other bad news. We argue often. Both of us get irritable. She is on high blood pressure medication and a tiny dose of Seroquel at bedtime. Her eyesight is bad, and she wants to read everything she can before her eyes get even worse. I hate that she is on an anti-psychotic, but without it, she can't sleep. If she doesn't sleep, neither can I. We live together, and she never had a drivers license, and I have driving fear. We are pretty isolated at home most days, except for radio, tv and internet. I'm 37, single, and rarely see or hear from friends. I worry about leaving my grandma alone for very long, so even getting groceries and running quick errands is stressful. I rarely get out to do anything for myself. I feel guilty that I can't take her out and find her some more entertainment or another companion that can stay with her. Home health nurses are not an option. Over the past 5 months, my grandma has developed head nodding, increased mouth movements like jaw biting, licking her lips, and rubbing her tongue over her teeth. When I sit near her, I can hear lip smacking noise and it drives me crazy. We just got digital cable and she can't figure out the new remote so she gets frustrated. I wish there were someone else that could sit with her to give me a break once in a while, but her friends are all older and in declining health also. I am tired and feel like crying every day, and when she sees me sad, it makes her feel bad too.
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Musiclover, are you on any meds for your depression and anxiety??? If not check into it as soon as you can... meds are not the answer to everything, but they do help... possibly if you weren't so anxious and stressed, you could handle the situation a little better, and feel more like getting out once in awhile... and why are paid caregivers not an option.... it would do both of you some good... someone to read to her and let you out of the house once in awhile.... let us know how you are doing... come back and talk to us... we're here to help if we can... hugs to you and it took courage to post.....
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I'm not on any medication...don't want to be sleepy or have side effects that could keep me from helping my grandma if she needs me or if there is an emergency. (I've tried medicine in the past.) We had a few $125 home health nurse visits after she got out of the hospital, but they only stop by for a few minutes, & check BP. My grandma doesn't want any more outside help. (She can do some things on her own.) We have some transportation services here, but they have to be scheduled well in advance for a ride. We have one friend that stops by once a month to take us out to eat, but she stays very busy. When I leave her alone, or even go to another room for a while, she re-reads religious books, old political clippings and things she wrote years ago, and it gets her worked up. She wants to write letters again and voice her opinion to others, even to service / repair people who come into our house. If you try to restrict her from reading or hearing news, she can get angry. My fear is that she could have another highly emotional outburst or episode like she has had in the past year, but so far, in the past few months she has been manageable. Thanks for responding, I don't have an outlet for my feelings other than websites.
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Musiclover, then blast away here... why don't you let her write letters to the editors... and she may have some great insight that needs to be shared .. how frustrating for her to be so active and now unable to do so many things she loves.... let her write to whoever she wants.... what are they going to do... and you don't have to mail them or would she know?..... Find her a political chat room.. as long as she doesn't come across as a terrorist, then it's all good..... does she use the computer.... but we are here for YOU... come back again and again. make some friends, and we even laugh here.... we get so silly sometimes,, beat the hell out of going insane.. and sorry to hear you are unable to take meds... there are many on the market now that do not make you sleepy... just wish you would check in to it just to give you more energy... anxiety takes a trememdous amount of energy..... hugs to you.. let us know how you are....
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My grandma is 87 & doesn't use the computer. She would know if her letters weren't mailed, but the local paper may not want to print them anymore. Sometimes she lets me read them, and if it's too emotional or doesn't make sense, I try to revise them before any get mailed out. She has a few good points, but can express them in a strange way.
As far as things to help me, I take vitamins and supplements. We eat fruits and vegetables as often as we can. It helps somewhat. Thanks for the hugs.
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Musiclover, for me a couple hundred mg of 5 hydroxy-tryptophan controls the worst of my severe chronic depression. Does your state have an Area Agency on Aging? They might be able to advise you so that you can get some help.

Today was better for me than yesterday, but I'm exhausted now. I can't seem to get on here til end of day when I'm wiped out. I know my mother is going downhill and I seem to be suffering from "anticipatory grief" but my worries are about me. As in, "how can I manage when no one is buying my art?!" (I'm a self-representing artist). How am I going to keep us in the house, fed, clothed, heated in the winter, etc, etc, etc.

I am lucky though that my mother is still a sweet person and never gets abusive. Only occasionally cranky and very rarely stubborn. But who of us does not? And besides, I know everything must be so frightening for her now.
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Busy day for most here...hugs and angels to you all. And welcome to the new posters. Glad you found us.
Ladee - we love you! And you can call me anything you want, except late for dinner! LOL
So very tired. Work has been really busy, and going to the gym is fun but makes me tired, too. I am glad I'm able to get there though, and have some time to myself.
Mom thinks she has a UTI. She made herself an appointment for tomorrow. I'm glad she is able to do things for herself, but I think it will just be that much harder when she can't anymore. It's a fine line going between doing for her and letting her do for herself. At least she told me about it.
Stormy - call the nurse. At least she can tell you how to get the results. Hugs.
Vic-I'm thinking of you and sending good thoughts. I know it's hard to keep on doing what you're doing, and watching your Dad decline. You are so important to your parents, and a good example to me. Bless you!
My Rebel dog gets worse each day. Now he won't take treats except for Barkin Bacon, and would barely eat the ice cubes Mom crushed up for him. I don't think it will be too much longer. But he has this sweet look on his face, like he's amused with us. I hope he is remembering happier days.
Goodnight, and better tomorrows.
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Notlike- I called the nurse and of course that got me nowhere. She said that the results had not come in yet and that they still have it down for his next appt is june 28th. I wouldn't be surprised if they didn't change his appt to a sooner date. Wait, wait and wait some more that's all we do. Can u tell patience isn't my strong suit...
I am so sorry about your dog being sick; they are like part of the family. Hugs.
Vic and lil deb- hope you both are doing ok. Thanks again for congratulating connor on his graduation the other night. He is my lil man. I love him to pieces.
Ladee- Love you girlie. So you want to be a auntie or a granny???? lol.
Cattails- thank you for your post the other day. Connor is definitely a blessing to me. He is the reason i am still here and not completely insane, YET.......... He is my lil rock. Sis did go to his graduation the other night. I'm glad she went to see him in all his glory.lol I think back on 2 years ago how things were so different between me and her. We are still close but it is different somehow, maybe not as close. I know that she made a decision a long time ago to step up and take care of mom or dad which ever one needed it. But i think she thought it would be mom because she was the one with the congestive heart failure. But mom was active and was able to look after her self and then she died very suddenly. I think my sister just never thought that we would be looking after dad and i didn't either. I know this sounds terrible but i am ready to get on with my life with my family without having to be consumed by caregiving. Don't get me wrong, i love my dad and i hate that he is going through all of this and i see that his breathing is getting worse and will probably continue to get worse. Sis i know is tired of this she has got to be, plus her not being able to go home but once a week. She will be the worse one out of the three of us if dad dies. I will be there for her to help her through the grief. I still believe she is living in a fantasy world that dad is not getting better. I think she would be content not to know the results of dads tests because she is in denial and doesn't want to face it. Well i better get to bed, thanks again Love and Hugs to you stormyy
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Stormy: Whatever your sister is feeling, you have to honor it. She needs to know that she did the best she could for your dad. That doesn't mean that you have to do the same. It just means that she needs to hear you say that your dad lived a better life because of her care. I so agree with your comments about your sister's denial. That only makes it more difficult for her. I'm so grateful that you have Connor and can bask in the wonderful light and love that he casts on your life. So many parents are so busy when their children are little and they miss so much. This is your time with Connor so continue to make it the best years of your life.

I think your dad will likely pass soon. The test results will come, but the writing is pretty much on the wall. His quality of life seems so limited. I pray for his peaceful passing. I hope your sis can get into some counseling after your dad is gone. She is going to need help stepping back into a life of her own. Be prepared that she may have some anger and difficultly with the transition. Don't take it personal and try to relieve her sadness by acknowledging her dedication. You will probably need to do this often because she will need it, but then you can turn your gaze to Conner and let the light flood into your life. It will be a good balance.

Wanted to say more to others, but Dad needs to use the bathroom so got to go for now. Hugs to all, Cattails
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Back from the potty break.

Notlike: I just wanted to say how sorry I am about Rebel. I love, love, love my dogs and I have lost 2 very special ones. Both were like my soul mates although they were night and day from each other. Still, they had a lot in common. A love and loyalty; a way of making you feel whole when you felt you were in pieces. They would make my heart swell with love for them. I miss them both so much, but I am so grateful I got to have them in my life. What a blessing they were. I often hear people say that losing their pet was so painful that they could never have another. My Kate was with me for almost 11 years. When she passed away it was the worst. My husband and I were heart sick. But then I met a friend for lunch one day. She was big time into dog rescue and was up to her eyeballs in foster dogs. She had this one, cattle dog, border collie mix, sitting in the front seat of her car when we met for lunch. It was recovering from leg surgery and it went home with me that day. That was my Sky dog. She was so amazing. She was 5 when we got her and passed away last September from cancer. She was 10 years old at the time and I felt so cheated. She was so strong and I would thought she would have made it to 15 years for sure. We lost her a month before we brought my dad home from rehab to live with us. I don't feel I've ever really had a chance to grieve loosing her as it has been night and day with my dad since last July.

Anyway, I don't mean to go on about our pets, but they are such special members of the family. Please give Rebel a hug and kiss for me. He'll be in good company in the afterlife.

Hugs, Cattails
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Darn..lost the post! Oh well prayers and happy thoughts for everyone. Dad had a decent day and night ..
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My 75 yr old mother with dementia is always talking about leaving and I heard of elderly gps. Does anyone have experiance with this or prices or know how to go about getting one? I seen some on line but I don't know who to trust. Thanks.
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bekwalk, at the top of the page there is a section called Elder Care, click on it and then go to Safety... there is a monitoring device there, hope this helps....
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ladee, you r so right that paid caregivers r NOT robots. Just because someone may receive a paycheck or cash don't mean they r not human. You do really great with the two n sound like a very careing & compassion person so, if u feel u need to do an ourburst SHOUT go outside n give it all u got! Okay, maybe in the backyard for neighbors may wander if you r going bonkers. % ) Can you make a few minuets of your time to do 'tense & release' muscle stretches that can help you relief some tension before getting around the M? I do my shoulders at the table sometimes by pulling from one side then the other n it helps somewhat. (somewhat to me is better than none.)
Just a thought with Sman n M that, she may be getting frustrated or jealous n she may be causing some of the bruising like on his wrist n he may be doing himself on the face out of frustration?
btw, That felt very good for a moment to be fired, thanks. ; )

We had to bury grandma kitty yesterday for she was probable in her 90's in human life. I had to get hubby to get her from underneath the car for she is mostly an outdoor cat. She had ants on her, this was before she passed. I tried to get her take water twice from eye dropper n she wasn't having it. I then got the little pest ass ants off her about 10 of them damn thangs! I wrap her up n brought her inside out of the heat n wipe her with a cool wet rag n put her in a huge dog cage. She was not in any pain, just I guess it was her time to go any day. I hesitated to tell mnl but she had already saw her. Hubby didn't won't his mom back their but I felt she needed to say her good-byes for it was part her cat. That cat would walk with her across the street when the mnl live over in the other house. She even walk with her down the street like a little dog when mnl use to walk up the block with no complaints. So, I let her go back to say her goodbyes. I done what I thought was best for even though she has moderate AD she is a Human being n has Feelings too. I explained it to hubby n not sure if he understood or if he was worry she going to flip out. I wouldn't had done it if I even thought that would happen. Mnl did very good back their n cried as I cried with her n I told her she was not in any pain that it was just her time to go for she is a very old kitty. She understood n I took her out of the room. Hubby n I would check on her n I would continue to wet a little rag on her n had a fan going lightly n some shaded area if she needed it. Took mnl out of the house to get her mind off of her old kitty n when we got back she was gone to pet- heaven. Neither one of us said anything to her n I am not unless she asked abour her, for she said her good bye's yesterdayn I don't won't to upset the mnl too much. We buried her in backyard with her little blankey without mnl even knowning late yesterday. She lived a great life n she was not in any pain n now she is in kitty heaven.
Well, I got to go give my two indoor kitty's some big hugs n remember to appreciate every day you have for nothing last forever.
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lildeb, sorry about the kitty, but getting to say goddbye was a good thing for mil.
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Sorry to hear about the kitty lildeb.........and so glad you had mil say her goodbye. I'm still sad for my blind doggie.....will miss her forever. The spot on the floor where she had her bed still is empty. The other dogs don't get in it like they did when she was still alive.....they're probably thinking it makes puppies disappear if you get in there!
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Caregiver: That word should weigh more than others on a page, sag it down a bit and wrinkle it, because the simple-sounding job frazzles as it consumes and depletes. Not that it's only gloomy. Caregiving offers many fringe benefits, including the sheer sensory delight of nourishing and grooming, sharing and playing. There's something uniquely fulfilling about being a lodestar, feeling so deeply needed, and it's fun finding creative ways to gladden a loved one's life. But caregiving does buttonhole you, you're stitched in one place.
-Diane Ackerman
"One Hundred Names for Love: A Stroke, A Marriage, and the Language of Healing", 2011
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