My father, soon-to-be 97, has been with us seven years. We recently brought in hospice and that really gives me a break; however, he is doing quite well. I suppose the guilt comes in whereas I know he will die someday but not knowing when is so difficult. I know this sounds terrible but I am ready for him to go but he keeps going like the energizer bunny. At the same time, I know I will be devastated when the time comes. Does this make sense? I just want my life back and now that it seems my friends are nowhere to be found it makes it even harder. My husband and I now have a sitter who comes on Tuesdays and we get away for eight hours. I am trying to get back to the gym. I recently sent an email out to two friends telling them I have set aside Thurs evenings for movie/pool/get together if they are interested. Tonight is the first night and i have not heard from anyone. So, I will watch the movie and have my wine by myself I guess. Is this a problem with any other caregivers and how do you cope with it?
You are compassionate and caring. Some people are just more sensitive than others. Acceptance is key here, as no amount of worrying will change it. It may sound trite, but if you try to concentrate on the blessing of having her this long, and look at how well she's done up to this point, it may help. Then, know you'll be there for her as she gets more frail. When she is worn out, she'll probably be ready to go and you may find it easier to let go of her at that point. You will still feel the pain, but knowing she's lived a long life will help you cope, and you won’t want to see her suffer
Carol
bless your heart .
dont worry about ur siblings .
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Give the most comforting care you can to your loved one and also to yourself.
Carol
as for friends , they call and comes and vist me when they can, and its too bad i could never go to thier house and have a good time . i thought it was just a matter of time he be on his way out , well its been almost 3 years now , i honestly think he s going to live many more years . lol .. thats ok whatever dear good ole lord has plans for me i shall go down that path . wink
Carol
One thing that caregiving does is to help a caregiver like you and me recognize how time flies, even as the support we provide sometimes seems to be occuring in slow motion. Nothing lasts forever, though. Today, I am happy to be able to see my Mom's face every day. She has always been my best friend, even at 84.
I am fully understanding your situation about greater distance between you and your friends. It happens to many of us caregivers, for various reasons.
In my situation, I am only too happy for a social breather from too many evenings out, too many happy hours, just schedule overload when all I really needed was to slow down in order to become a better caregiver. In my case, I would say that caregiving has taught me that I prefer moments of simplicity and more, rather than less solitude and reflection, instead of the social rat race.
I have gladly chosen to refocus and created new friends in my community, and, enjoy morning coffee visits now and then with my new friends, including neighbors I never got to know when I was always either going to work, or working too late. I increasingly turn down the requests to meet for happy hours, lunch, etc., but that's just me. My heart and Spirit are now in a different place because I recognize that life is short and I don't want a full schedule; just a contented Spirit and simply abundant days.
If your former friends have since moved on, is there anyone in your community you might be able to introduce yourself to over a cup of coffee in your garden, maybe? I am not a church-goer, but if you are, if your husband stays home with your Dad every other Sunday, allowing you to go to your church, or visiting a new church may be a way to connect to others real-time, as much, or as little as you wish. Or, how about a concert, or inviting a neighbor to a play, or for ice cream, or for a drive?
It depends on how much and how badly you wish to reconnect.
Another thing you may wish to consider is hosting a mid-morning coffee get-together with a couple of your neighbors in your garden? I am all for coffee minutes these days, and, hot tea, or iced tea, only because I do not choose to spend my precious moments of respite preparing complex meals and elaborate place settings, etc. Coffee and end-of-workday wine get-togethers on my deck require no preparation on my part, just getting comfortably dressed.
How much socializing are you wanting to do? Maybe host a movie night with popcorn and soft drinks only? Once a month? Every 2 weeks? There are always things to do; just depends on scale and scope of what you want, and, how involved you wish to become. Also, look for local charity events if you are wanting more, rather than less social visibility. I choose less. Hope my musings help. You are not stuck. You just have to think outside-the-box. Hope you get to restoring your sense of social balance really soon! Hugs to you and your beloved Dad!
And to 1215: Congratulations! Happy dining! Hope it meets your needs and the desires of your heart. You're a great encourager to others. And, whoo hoo! on the upcoming vacation, too. Sounds dreamy.
When I read your post, I felt that I could have wrote it. My mom is almost 97 and has been living with me for the last 3 years. I am an only so I get to be the only caregiver......lucky me.
I feel exactly as you do about everything...saddness, anger, wanting my life back, etc. I always feel guilty about those feelings but they say it is normal. I forgot what normal is.I feel that when something good is happening in my life she steals all my enjoyment.
Next weekend my mom is going to respite for 3 days. We have a family wedding out of town so she has to go there. She says she doesn't mind but she really does not want to go. She keeps saying that she would never live there and that she is only going because she has to. The ALF said she might like it and want to stay. They don't know her the way we do. She will tell them it is a nice place but will call me every minute to ask when I am coming to get her. I still feel that something will happen and we won't be able to get away.
I let you know if it works out.
I also tired to find a support group in my area. Found one and went once. The counsler wasn't very supportive.......just told me to send her to daycare/nursing home. Told her that was not an option. She wasn't too helpful after that.
Thank God for this site........just to know that we are not alone helps me get thru the day sometimes.
I just keep praying that this ends soon(she does have chronic pain)........I think my mom will bury me first!!!!
onenandonly
I love Carol's post. You are truly an encourager!
My heart goes out to 1215, marylee, and others. Caregiving is not for sissies!
Take care, all.
I can so relate to you. My mom in law moved in with us just over a year ago and just as our grown children were moving away. I had looked forward to travel time with my husband and starting my own new career that I had looked forward to for some time. I had NO idea how involved I would have to become in the caregiving with her. She is 83 and mid-stage AD. No one understands, even my own family does not really know what the day to day 5 day a week job is like. My sister in law commented to me the other day that she has to do her shopping on one of the two days that she has her mother and it's a nightmare. I said "tell me about it!" she said, "oh no, YOU have no idea!" and I said, "oh YES I do!" and she said, "yeah, but I have to work all week and then deal with her too!" Can you imagine? At that point, I totally knew that she felt that my caring for her mom all week was not considered a "job" in her mind. It really makes you feel isolated and without hope. There are lots of AD sites on Facebook where you can relate to others and talk in a forum such as this one, but truthfully, I believe that the only way to get back to normal is to get outside help for the caregiving. My MIL's attorney wants to look into assisted living so that we can return to normal as a family within 6 months. I dont think this is going to go over well with her but the reason she lives with us is because I have been so against nursing care. But ALF's really offer interaction and activities for them that I really can't provide and she may have more fun there. As her disease progresses, they have professionals to handle that whereas I am not a nurse and may not be as helpful or knowledgeable. If income/money is an issue, I have learned there are many ways to seek funding an a good Elder Care Atty can help with that. Look into it. You do need your life back. You have to look at it as you are doing your dad a favor by re-connecting him to others like himself and allowing him that social interaction as well. keep in touch :)
You will miss him when he's gone. You will grieve. But you are grieving his eventual passing now, as well as grieving your former life. Your life will be slow to come back but please keep making advances. As former friends (if you want them) or new friends learn you are available, you will find your life slowly become more normal. Meanwhile, a support group is a good idea.
Please, please everyone. If you have every watched this long slow death and just wanted it over, you are not bad. You are human. You are compassionate toward your loved one who is suffering, and toward yourself. Don't sink into guilt over human thoughts.
Take care of yourself and do keep trying. Maybe you'll find some new friends at the gym.
Carol