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You can feel
sorrow
grief
anger (at the disease, not at mom)
helpless
You can know that you have done a good job caring for mom. Part of doing a good job is knowing when you can no longer do it safely either safely for you or her.
When you visit I am sure she is picking up on your feelings and that is why she cries when you leave.
Next time you visit before you leave get her involved with an activity, or if it is mealtime bring her to the table.
Make your good bye very low key. A hug, "I'll see you later" or "I'll be back" don't say "goodbye"
You ARE taking care of her by making sure she is safe and cared for.
You are not rambling everyone has these thoughts. It means you care.
I hope this doesn’t sound bad but be sure to fill your cup up with doing things for yourself. It will help you focus on the positive in your life, and I’m sure your mama would want that for you.
I feel a lot of guilt too for my mom being in a SNF. The other day I wrote and meditated on the affirmation: “I do what I can to help my mom.” I felt like a weight was lifted off my shoulders.
And for anyone whose parent really would prefer their adult child to sacrifice their own life and happiness for years on end- that’s a totally unfair, selfish, unrealistic, hurtful, unhealthy, and damaging expectation to put on your child. It should not be honored. Imagine if your friend told you this. What would you advise your friend to do?
I struggle with all this too. Therapy has helped. Reading comments like one below also helps. Regardless of how long my mom lives (she is nearly 80 now) I want to make it to my own old age knowing I have done the things I want for myself — including vacations, friends, hobbies, other family— not sacrificed it all for her old age. That doesn’t mean I don’t love her or that I’m not a good daughter. She may not be able to tell me “one or two visits per week is perfect, don’t worry, I’m just fine.” I have to set limits myself. Pretty much everyone does.
I don’t know how old your mom is, but let’s say she lives another 10-15 years like this, going very slowly downhill, then dies. Imagine yourself 10-15 years from now. Do you want to be able to say “I spent every waking hour with her for 10 years so she would not cry when I I left, forgoing all the pleasures I might have had in that time. Now I too am old and can’t do many of the things I hoped one day to do.” I hope not.
Bottom line — the decline and death of a beloved parent is hard no matter what you do. Choose the path where you do not sacrifice yourself as well as lose them.
It might help to put your own life first. Cut down your visits, and ramp up your outside interests. You will have more (and more cheerful) things to talk to M about, on your new regime of weekly or bi-weekly visits. M will have fewer crying jags to live through.
You might be someone who gets help by talking to a therapist. This isn’t a good way for you to spend the rest of your life, and it clearly isn’t solving any problems for M. Where will you be when she passes? Where would she want you to be? - and I hope that she is not like some really awful parents who don’t care at all about that. Where would she be if you pass first, which sometimes happens?
Please look after yourself, as well as M. And it may be that OP can look at you, see themselves in you, and realise the benefits of this approach for you - and for them.
I agree with those who say that you are doing the right thing by getting your mum the 24 hour help she needs and that you cannot provide. With the best will in the world, you can only do so much. Being an advocate and giving your mum your love, time and attention is enough.
I know the feelings of guilt can be overwhelming, but consider whether you can be the best advocate and company for your mum if you are overwhelmed. The answer will be "no", so you need to reframe your thinking and ditch the guilt. It isn't serving any useful purpose.
As others have said, counselling can help, as can cognitive behaviour therapy, which you can also learn to do on your own, if it's not easy to get a CBT counsellor.
One thing I think you should reconsider is your worry about the calming meds. Having recently witnessed my mum in distress, I thank all that is good for midazolam.
It helped Mum to feel calm and enabled her to have a peaceful death, which is the best any of us can hope for. But, yes, it did make mum sleep in her last days. I just thank goodness that she wasn't suffering.
When we interviewed Memory Cares for my dad the director said, we have a staff of people who each work 8 hour shifts and have two days off a week. One person can’t care for someone 24/7.
You are grieving - what I consider - one of the most difficult life experiences 'grief in slow motion.' And experiencing a loved one, your mom, slipping away in from you.
My only heartfelt support is somewhat Buddhist inspired "be present fully with your feelings" (whatever they are). It hurts, it feels awful, it is heart wrenching.
I agree with another here, get into therapy. I did and it really helps.
Take care of yourself as you can - put yourself first:
1. Be with supportive friends (who listen, not give advice unless you ask for it);
2. Be alone, with music or meditate, as you need / want;
3. Read, go to a museum, the park - whatever will help you 'be' with your broken heart. Exercise: yoga, jogging - get that energy out.
4. Reach out to whoever and whenever you need to: here, church, network support, friends.
As I said to my therapist, grief is like mercury. You can't get a hold of it. Its mentally, psychological, and emotionally discombobulating.
I think: What would I do if in your situation with your mom, crying as you leave.
1) as you did, go back and give her a hug. Look her in her eyes, smile, and say "i'll be back very soon." Depending on the degree of dementia, you could say that you need to go to the store and will be back in a few minutes. She may not understand and/or she may forget.
You might be able to intervene with the medication given. Ask. Assert yourself. Ask your own MD or another / discuss your concerns.
2) Get her a mechanical cat or dog to pet. Of course, this isn't a replacement of you although it is a distraction and gives her something to focus on, care for, pet, be a mother to some'one' that needs her.
* If my mom, I would definitely leave her in AL for reasons you mention. She will get 24/7 care that she needs.
* I don't know when you placed her in AL although it does take a person a while to adjust. Give her time (could be 2-3-4 weeks). Some facilities say to not visit until loved one is adjusted; it is an individual decision.
* Medication mgmt can be tricky - trying out what works. Do you think / know if staff / manager is confident in how / what they are giving her? Is it stabilized aside from specific situations when she gets 'too emotional' (or what?)
* Be real with your mom. If YOU feel like crying w/ or in front of her, do it. I've learned that people with advanced dementia 'get it' when responding to them both non-verbally and emotionally. (Smiling, tone of voice, eye contact).
I know you are asking about guilt. For me, a person who has worked on my inner self for over five decades, it is / has been one of the hardest 'feelings' to deal with - no matter how much I did / do ... that guilt of the "I should ... I should have... all the while fighting with how exhausted I felt. There needs to be a balance of 'pushing through' and knowing when to stop / rest / renew. And, frankly, realize that guilt feels like s---t or crap. It just does. Running away from it doesn't help.
While it may sound like a contradiction, I reiterate: Be present w/how you feel - own it (don't push it away) and at the same time, give yourself distractions / refocus your attention (gardening, walking, listening to music - whatever feels healing).
While no substitute for you, consider finding / hiring people to socialize with your mom. Perhaps ask church or local volunteer organization to arrange volunteers to visit. (I did this for my friend-companion.). He had THE BEST volunteers, who loved him, and were faithful weekly visitors for close to two years.
Your mom will likely 'do' better with individual attention and arranging for others to visit - and she'll get to know them, will likely help her feel included, loved, cared about.
I am sorry that your husband left you, whatever the circumstances. Therapy will help you - with the right therapist. Screen them; it is not a one size fits all.
Gena / Touch Matters
My thoughts are, if you are able and up to the care, take her home. I would take mine home but my house is too small for two elderly with walkers and dementia. My father wanders and can’t find the bathroom, therefore he urinates anywhere.
I pray you make the decision that gives you the most peace.
You CAN mourn it, and accept that she will mourn it. But taking on responsibility for it, for her happiness, simply isn't going to work. You are a human being with limitations; you need to accept that. Do feel free to share her tears and tell her you are so sorry for them. Continue to do what you can.
It is terribly difficult to stand witness to the losses of our loved ones, but it is wrong to take on responsibility that isn't ours.
So sorry about your husband.
If she has memory impairment she won't even remember that you just visited her. This is how it is with my own MIL, in LTC with memory impairment. She just got off the phone talking to one of her sons ("Glen"). I asked how is Glen doing? And she said, "I don't know... I haven't heard from him in a long time." Literally not 1 minute had passed.
Do not feel guilt -- because guilt is for when you do something that is immoral, illegal, unethical or selfish. You can think of your feeling as grief, which is what it is. When we leave my MIL we try to make sure it coincides with an activity or event at the facility. We wheel here there so that she has a distraction as we say goodbye. Then the staff takes it from there.
Make your next goodbye when you visit very short. Get her involved in an activity then quietly leave. If she says anything when you get up just say "I have to go to the bathroom" or "I will be back". I think she may be picking up on your feelings.
You are taking care of your mom. You said yourself that she is getting good care that even with hired caregivers you could not manage that level of care at home.
Be very grateful that you have found a place where she is well taken care of.
Get rid of the "G" word..guilt. You can feel sorrow, grief, anger at the disease but you have nothing to feel guilty for or about.
If you are concerned that she is "alone and sad" when you are not there ask the staff if she is alone and sad when you are not there. Is she involved in activities? Is she sad?
Eg 1. "not taking care of them.."
You ARE taking care of Mom by having her live with support 24/7.
Eg 2. ".. when they are so alone and sad."
Mom is NOT alone. She is living with many others, residents & staff. Sad? Maybe at that moment as you leave, yes. But probably not all day every day. She may well have a smile & a laugh with other people during her day.
When you visit you can bring EXTRA joy to her life. Your familiar face, your warm hug, both enjoy that lovely connection for the visit.