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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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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, 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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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, 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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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Yeah Austin she is, and granted she has her own health issues... but she will never go lay down for a little while when I am there, she won't let me do anything for her, she gets S to help her, so then she gets frustrated because he doesn't understand what she wants.... I go in anyway.... and send S to the other room.... I am getting to where I speak up when she gets on one of her rants.... all she does is sit in that chair and dictate.... there is a part of me that feels compassion for how miserable she is, but I also will stand up for S and myself when she gets going on one of her tirades....I have noticed bruises on his wrists , like someone was holding him too tight, and scratches on his eyelid and underneath... he may be doing this to himself somehow, but I ALWAYS show them to her, and ask her about them.... partly because I don't want her accusing me of anything..... she would in a heartbeat... it exhausts me covering my ass all day with her.... because if something goes wrong, it's me that did it.... like the Tv episode.... I was so angry I raised my voice to her..... so that is why I say often PAID caregivers are NOT ROBOTS.... and yes I love my little Sman.... but nothing I can do about the times I am not there.... very frustrating....
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Ladee, I was touched reading your comment about your dad. I wished at least one of my parents could have been loving. But, you can't change the past. I was so proud of you and how you handled it. Of course, I would have embarrassed him more and said to M to watch what she's saying, etc.then end up having a shouting match. I reflected what you did...and..I think I will need to work on my temper before I could ever remember to do what you did by taking S to the kitchen for TLC.

Although mom was very violent, she did have her docile side - very rare, though. We would give her a doll to calm her down. She would cradle it. I have a photo of her holding the doll and laughing, wearing a knitted cap made by older sis. Anyway, I keep that photo framed and hung in my bedroom wall. This is the mom that I want to remember - not the scary, violent one or the now unresponsive one.
I think out of my whole family, I'm the only one who have a framed photo of her.

But, back to the lucid moment that S displayed. Years after mom stopped talking, responding or looking at us, she always had this blank stare. One day at the hospital, we kids were all in her room surrounding her bed and just talking like sis/bros do. My bro had a shocked/scared look while staring at mom. We all looked at her. For the first time in Years, her eyes were Not Vague or unfocused. She had intelligence in those eyes and she was staring at my oldest brother.

See, I told you, even mom thought Dear Brother should be taking care of her. You see, he is her Favorite Son. The irony is that when I was in middle school, I had caught her looking at me with such hatred in her eyes. I'm now caring for her..while Dear Favorite Son who lives next door rarely visits - not even this past Mother's Day. I wonder if he had that look of fear because he knew he was suppose to be caring for her? Or something like that? Since then, like you said Ladee, there is Still the Person in There. So, I try to talk to her normally. Have to go now. Time to change pampers, clean tube and ...wash the few plates I didn't wash after dinner. Hugs...
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Ladee you are so good with S-I am sure he knows how good you are with him-and he was comfortable with you to express his feelings M sounds like a real bitch.
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lildeb, your fired!!!! I know that doesn't mean a thing, but thought you may still want to hear it....lol
I wanted to share why I feel it is so important to always allow an Alz charge their dignity.... S is in a serious decline as I have shared with ya'll and the other night he had two "wetting" accidents.... when M was going on and on about it, I looked at S's face. what I saw was embarrasement, he was hanging his head..... with my voice like stone, I said to M, IF he could do it different, he would.... then took S's hand we walked into the kitchen to get him some juice..... he held on to my hand and said, " thank you, I am so embarrassed....." I gave him a huge hug and told him how much I love him, how much fun I have with him, how I look forward to seeing him... so my point is, even when we may think they are on the final journey to what this damned disease can do to the human mind and body, there is STILL the person in there... S hasn't had a really lucid moment in a couple of weeks... but he knew he was feeling shame and embarrassement..... and he needed reassurance, to know he would do it different if he could, that no matter what he is loved and appreciated....
I HATE this disease, with a passion.......
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Lots of hugs to you Brandy... I am sorry things are so overwhelming and too many unanswered questions.... You have too much on your plate. Is anyone available to help you? Are you able to go be with your mom for tests, and what do you think is wrong, and who will stay with hubby? Sorry for all the questions and don't answer if you don't want to.... just worried about you.... prayers for answers for mom and hope you get a break soon... Let us know when you find out something... hugs and angels to you.....
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Stormy, I see I am not the only one that gets it all type up n then, 'kapooie,' it is all gone.

Burned, Good luck on the bath time. I had forgot all about the mnl Monday bath. Can I get fired? pretty please. ; )
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How am I doing? I am ready for the rubber room. Not sleeping well, shaky, in pain, not knowing what is going on with my mother and what will happen to her, going to the nearest big town for a medical test and being on pins and needles about the outcome of the test. Dealing with husband's dementia and also my mother's dementia. Today I just felt awful.
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I Need a second job 4 real but things have slowed down and i need some more ideas to generate some money and i also have an estore run by amazon called mommangamchile-20 feel free to look around...semi desperate for anything lol...tomorrow is hubby's appt so wish us luck i get to argue with him on having a bath tonight.
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Well, hell i lost my post that i was writing to all of ya'll and i don't have time to do it again so i will be posting to ya'll tonight. Thank you all for the congratulations to connor bug!!!! It was a special event for us all. Love all of ya'll. stormyyy
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JoJo, I am sorry your grandma is in her late stages of AD n I hope you r able to get some help with the Medicare website that Cattail talked about. Sending you a prayer to help give you n your mom strenght n remember you can only do so much n you need to live your own life. What a wonderful your grandma has for helping her through this disease.

Taytay52, welcome to this board for we all know how we can have difficult days, hours or even minuets yet also, we have some good ones too. Just try to remember that it is the illness n not the person. Even at the Caregiver conference spoke about how it is a very hard n challenging job n that we as caregivers have to take time out for ourselves even if it is only One hr a day. For when we n just like any other caregiver thats working at NH facilities can become 'Burn-outs' n then, what good r we to the person who has no control of the disease. Remember that 'Humor" can be very healthy for you n laughter too. Try to find some humor while taking care of someone. Most of all, we have to take care of ourselves first so that we can continue to give 'good' care for our love ones.

Seemeride, how r you holding up beside the money situation for the funeral? As for the money of one absentee paying, you may want to call n see if they r going to be able to help pay for the cost when they come up in July? If you think it will start a mess, I personally would let it go for its not worth the fuss between relatives n its not worth getting sick over. I would just say, "do what you think best for you only truly know your family situation." Good Luck n sorry for your lose.

Stormy, I bet you will be taking lots of pictures of Connor graduation n too bad u can post one for all of us to see. Give him a big ole hug from all of us n tell him we our proud of him too.
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Good morning! Welcome to new posters....hope you find a home here as there are some wonderful care givers with lots of information and support to share.

seeme.....if it were me when it came to sending the sibs their "share" I would withhold the cost of the flowers. Otherwise you won't get it. Either way it's probably going to cause some anger. I guess you could look at it that the money is no longer your mil's.....but I know...it's the principle of the thing. It's not like they couldn't ask the cost before ordering to make sure it was affordable. When my sibs pulled their little stunt when my mom passed away at least they were wise enough not to expect anything from me!

Today is the col's birthday......88 years young! Will go spend some time with her later. She will get to wear a birthday crown today and the NH will do something special for her.

Hope everyone has a day filled with something good and not just the burden of care giving.
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