I have been taking care of my Mothers needs for about a year now. She is 89 and physically in good health but mentally not so good. My problem is how to make the family members understand that I need a break - even though my Mother can take care of herself physically I need a mental break from her. She just talks about the same stuff over and over and over. It gets exhausting. When my brother or sister comes to give me a break my Mother cannot understand that I am leaving during "family time." So what has happened is the family comes over to "give me a break" and I just end up cooking for everyone and hanging around listening to my Mother say the same things that I have heard ad nauseam for the past 2 weeks. Has anyone else ever experienced this?? It is like I do not have a life separate from my Mothers life. So my sister comes over yesterday and I just sat her down and told her that I "visit" with my Mother 24/7 and they need to spend quality time with her apart from me. I then went to the movies which was lovely. What hurts is my brother and sister get to go home and have their lives. Their bi-weekly visits are getting shorter and shorter. The saddest part of all this is my relationship with my sister has suffered. We were very close but not anymore. It is practically impossible to just hang out together like we used to because my Mother does not understand why she is not invited and I do not wish to hurt her feelings. Anyone out there who has experienced this before?? Why do the other family members get so selfish?? I accept that I will be the caregiver to my Mother but the lack of help from others has left me very cynical toward my other family members.
I have to admit I didn't read all responses but the ones I did have the same answers---- CALL and get parent to Adult Day Care, CALL Home Care and have evaluation for services, so you can then figure out how to pay them. DO THIS! DO THAT! etc., etc., etc.,... This is why we caregivers with absent siblings are frustrated.. We are so tired of doing it all.. Most times it's so tiring getting it all organized that you can't even mentally enjoy yourself when you leave the house!
I know that at this stage in my Mom's progression of dementia not one of my absent siblings could stay with her an extended time.. The effects of the inconsistent schedule would be only a giant a** ache for me when I returned! It's just not worth it..I have enough stress now!! I don't need to "rock the boat"..
You are right, that you may not survive him. What are the plans for him, then? (It happened in my family, so I speak from experience.) Please do what is best for you.
For your sake, for your husband's sake, and for the sake of your children (in that order) do what you have to do for your own health NOW.
From my own experience, many medical professionals are either clueless or not concerned about the major stresses on the caregiving spouse. (Obviously this is a generalization, but I know I'm not the only one who observes this.) You can't count on them to take the initiative to see that you get treatment and health guidance. Your doctor says to avoid stress. Is he or she a standup comedian on the weekends, because that is very funny, isn't it? HOW do you avoid stress? What resources can you contact? What suggestions do you have, Dr. Funny? Where can I go to find respite care?
I am very glad to see that you've already tried one thing that could help you -- adult day program. Your husband didn't like it. Maybe it is time to insist that he attend this 2 days a week. Maybe your local Alzheimer Association would have some other suggestions for you. Maybe you need to place him in a care center for respite while you address your health issues.
You could hold a family meeting to explain your needs to your children. (I included the adult grandchildren in our family meetings.) You don't apologize or get defensive, you just lay it out for them. Perhaps you ask for their suggestions but you make it clear that you are in charge of the decisions.
I would try to avoid getting hung up on the diagnosis. Focus on the symptoms you observe and what is stressful to you. It doesn't really matter if he has Alzheimer's or Syndrome XYZ. You are not stressed out because there is a label in his medical file, but by his behavior.
The airlines say put your own oxygen mask on first before you try to help a companion.
It is time to reach for the oxygen, flowerangel.
Come back and let us know how this progresses.
What I do not know is when do I put my health problems before his. Then, how do I get my adult kids to understand that my health must come before his health at sometime or else the stress will cause a majorly bad effect on me. Two kids seem sympathetic, but live out of town. The in town one also doesn't totally believe in the diagnosis of the doctor for his father(we live with him by the way).
this is a condensed version of our life.
I know that Alzheimer's is a very individual problem in people, but there must be some guides for when the caregiver is physically as bad as I am and the patient is not. Am I a walking bomb waiting to have a heart attack in my situation? My doctors tell me to avoid additional stress. They do not seem to understand the stress his condition places on me. His doctor knows some of my medical problems, but he is my husband's doctor and his patient. What are other caregivers doing in my type of a situation? Thank you.
Nothing surprises me anymore. I live with and take care of my 97 yr old father.
He can be very difficult. The whole family, my brother, nieces, nephews, my kids are all adults and know this. I don't get any help from any of them. I talk to my sons and daughters-in-law about it. They listen but I know they're busy with working and their familes. My oldest son suggested that I get a Call Alert device so when I go out I can go and not worry. He means well, but all I really want is for them to invite my father to dinner, for a ride, to a diner for a sandwich. No one offers to take him for a week or even a day. I get the feeling when I start to tell them what is happening witlh him they just do not want to hear it. It's like "here she goes again." Yesterday I went to a early evening picnic. My father was busy all day poking around in the garage and yard. When I told him I was going he asked what time. When I was ready to leave I went into the den where he was sitting. He had his head back, glasses off looking forlorn. I told him I was leaving and he grunted. He's done this before, just enough to put the damper and guilt on me for leaving. I need to be with friends and laugh. I call it my therapy. So for your siblings to call you irresponsible is irresponsible on their part. Hang in there--------
He once told me "you love looking after mum". How I didn't smash his face in I'll never know. I was so stunned by his callous disregard for the actual facts that I was rendered speechless.
The sickener is, his wife had her granfather living with her (and her mother) years ago and she understands how hard it is, but even she doesn't seem inclined to help out!
Thankfully for me the System actually got it's act together a year ago and d'mother now goes to Daycare once a week and Respite every 6 weeks. But even at that I still find caring for her a grind.
You have my sympathies hadenough ((hugs))
What I have found is that friends and family are truly scared of the situation. And it is not like a babysitter/children. There is no joy n growth in it and they are afraid of the what if's (things that can go wrong) and also Honestly alot just really don't care. It takes a special kind of person to give selflessly as we do!! Your best option is to find paid help...if you ,can afford it. I cant but thru this site i have found renewed strength to push n research options to help me out....dont have much time to do it so havent found much yet but I feel empowered now! Just dont give up and follow any lead given to you here!! A good one that is sortof helping is to ask for other tasks that are not so intimidating that will lighten your load in other departments. Like mowing the lawn, doing some laundry, pick up RX's or groceries, etc.....just TRY everything, be creative and pro active. Dont get in a hole like me by waiting way to long to scream for help. We are not superhumans!! Good luck to you and press forward in positive ways!
Do you belong to a church does your Mom? Are their any neighbors who you trust to come sit with her for a hour or two?
What kind of insurance does she have that you may be able to get home care?
Can she go to a adult daycare? I take my motherinlaw two days a week from 9-4 an it helps. I don't let go of the repsonsibility but she is somewhere else and can interact with people her own age.
Can your Mom go to a Biblestudy, out to lunch with friends or family?
It isn't fair for just one sibling or daughterinlaw to take care of Mom. It just isn't.
Your have a sister close by ours are in another state.... there are a few phone calls and so we do it all for the most part.
You may just have to leave and find someone to stay with her once a week.
You have to go walk, excerise, be with your friends and do things for you.... even just go to walmart and just walk around the store.....
Take a long shower, read a book, go for a drive anything that will help you to mentally rejuvenate.
I didn't like the person I was becoming sarcastic, angryier if that is possible and resentful.
I have fallen apart three times begging my husband that I don't want to do it anymore.....I do not want this responsibility...... he tries to help where he can since he works full time..... but this is his Mother...who has lived with us for about 11 years...... I have been caring for her the past 10 months like this..... since her stroke......
We argue about doing her excerises, eating, drinking enough water, taking a bath, watching to much television, and so on....it is tiring....
My mind never stops thinking about what I have to do for her or with her.
I have my own physical issues, the house, grandkids and so on too...........
I understand....... please call your agency on aging or whoever works with senior adults and see what they have to offer....
check your local churches or assited living homes to see if they offer any classes for support...... we had one here locally for 6 weeks....and I loved it....I got out of the house...Mom stayed downstairs and one of the staff would watch her for me so I could attend the group.
Don't be afraid to ask for help especially if someone has offered like a neighbor.............
I tell my husband I may just put myself in a insane asylum....hhahahahhahahahahh
I love this website......I can vent and hear others stories, encourage and support them too....
Honey don't give up.....
Ask your sister what could she do to help you.? Could she watch Mom for two hours on Friday so you could go workout.
Sat for the afternoon so you could go run errands since it is easier without her and you could get more done.
Ask her from your heart what could she do what is her schedule like on such and such day. Would she be willing to do blank for you?
I always pray first and let God go before me....... and tell God what you need.....
After 10 long months of caring for my motherinlaw we got a card from a family member saying thank you....... WOW that means alot..... because they have no idea and live so far away that we do it all..........they have their lives and families.
My marriage has suffered,their is no privacy, intimacy, space even though she has her own room, we hear everything...... 11 years now...... we have been married for 13.......
Well I have vented too it seems..... I just understand..... it is like having a child.....
it is a process to get her up, dressed, fed and out the door.
She forgets thinks I tell her like we have a Dr appt..... and so on. ugh.
ok...... we need to get ready for the diabetic nurse to come so take care.....
Do not give up........
Frustrated2012