The home is on lockdown because of Covid-19 and so we have not seen each other for 5 weeks now. They tell me that as a couple they are definitely a couple and always together. I am intellectually trying to understand, but I am heartbroken and angry and feel betrayed and my kids are devastated! Help
I take care of my mother. She has her own phone. She's had it since she moved with me over 3 years.
She searches for men on Facebook in the people you may know.
She says they ask to be her friends.
BUT they do not.
We have had 5 scammed so far.
My mom wants companionship .
My husband and I are with her 24/7.
My daughter lives across the yard and comes everyday. So I know it's not because she lonely.
I found out by the way she talks to the men that she is the one that is going after them.
She is like a teenager.
Talks to them one day and telling them she loves them the next.
I asked her how can you love him you barely know him.
Oh no. She says we have been talking for a long time.
Its all in her mind.
Its not fun to see her act so foolish.
I hear thing that make me question at lot of thing while we were growing up.
People are still people even when we get old.
I hope you understand that their mind is not right.
Julie Christie's character says to her husband that the relationship she has with the man in care comforts her because "he doesn't expect anything from me." I thought that was particularly poignant. Our family celebrates like it's Christmas when our Alzheimer's patient has a clear moment. We call each other and say "She's still in there!" There is absolutely nothing wrong with that but Julie Christie's character's statement made me realize that we all bring almost a palpable hope that she will be "in" when we visit.
I hope you and your children are able to find comfort that your husband has found a way to feel a little more 'normal' and hopefully safer and attached in his new home. I'm certain that for you all it is one more hard loss in the line of hard losses we suffer when we love someone through this disease.
Facilities are not the optimal choice, but very frequently they are the only choice, so guilting someone because they have had to make that difficult choice is cruel and ranks right up there with emotional abuse.
I can only imagine how hard that news was to receive. I want to encourage you to remember that this is not your husband betraying you, this is his brain betraying him and everyone that loves him. He can't help what his reality is. Alzheimer's and dementia puts the person in the far past and the right now, that's the extent of their reality.
My grandmother had a series of strokes that left her in full blown dementia over a weekend. She too found a companion in her facility. I was young at the time and I remember that she was happy to have him, it helped her feel more secure? Normal? Who knows what she was really going through, but she was laughing and giggling like a school girl and she was non-verbal before. I personally am happy that she was able to have some joy in the midst of this terrible disease. My granddad on the other hand was livid and very unkind in his refusal to see this as her disease and not her unfaithful heart and bad character. Never once paying attention to the fact that she had steadily regressed until we weren't in her memory. I remember as a 10 year old seeing her lose her life, every single day she was further from the present and I watched as people she loved were erased by that regression, so I encourage you and your children to remember him and not the diseased him, love him in the moment because he can still feel the right now and know if it is a happy moment or not. Don't let this ruin your beautiful memories and the reality of the life that created those memories.
We must understand that at some point the patient doesn't have memories perhaps of being married, and are not with intent cheating on a spouse. but cannot register the significance of their behavior. Yes, it is sad for the spouse to be aware of such a situation that they and their kids are hurt.
I have had a big discussion with my DW and adult children saying when it is time for me to go in to LTC, put me in a facility 100 miles from where we live, so they don't feel like just dropping in everyday. I want them to get on with their lives. I refer to my adult children but I also have a 13 yr old daughter who has not been included yet in this discussion. I want for my DW of 24 yrs to go on and build a new life with another man if that is what she wants, or just feel free to date, and I don't want the kids giving her grief about it. My DW is 8yrs younger than me and she'll have many years ahead of her to enjoy.
About six weeks ago, I on my own chose to give up driving. Yes it has put an extra burden on the family, but I didn't feel safe on the road anymore. I've had the discussion about driving with my Neuro doctor who I've been a patient of since 2005 and every time I have an appointment I've brought the subject up and after she's examined me, we've talked and she's agreed that I could still drive. She told me I'm the first patient in 20 years to bring up the topic, and she believed I would be the first patient who would stop on their own. Tomorrow morning we have a Tele-Med appointment and I will tell her I've put the keys away. I haven't even had an inkling of wanting to drive.
I know I'm declining on a more downward trajectory. I've had a happy life with my DW and family. My hope with my postings over the last four years, as a patients perspective, will help other patients and their family in the way they deal with dementia.
Happy Easter to all.
Memory loss is a terrible disease for those watching it. Patient has no idea what they are doing is wrong. Family has to figure out how to watch their loved one decline. Perhaps the lady's family is feeling the same way you are. Broken brains cannot sort out the reality. Did he still recognize you before the lock down? Have you been to the facility to say hello through the window? Maybe a protected visit like this is called for to see what the decline really is. 5 weeks is a long time with dementia.
Would you consider moving him? If not, this may be the way it is now. Very hard to accept, but reality. Very sorry for the pain you are feeling.
People with Dementia don't know what they are doing ..... but companionship is important to them. Even just a friend. I don't think you should read into this too much, provided it is just a daytime "friendship". He might even confuse her with you, just for companionship. My mother (86 yrs) with Alzheimer's, was placed into memory care with my father (91 yrs) with Dementia, they shared a room. But she BELIEVED everybody else were her boyfriends at the Mrmory Care facility ..... ! ! ! ! She used to be a shy introvert ..... who would never say or think things like that when we were kids ...... but now she lives in the past ..... 60 yrs ago, in her mind she is still young and beautiful like before she got married (she had black hair & the Elizabeth Taylor looks). She kept on saying the attractive (middle aged) husband of the owner of the Memory Care facility, is hér boyfriend ....... (one sided of course), so we never took it seriously ...... until one day the owner told my Mom "he is actually mý husband" .... and then she saw a tear running down my mom's cheeck ...... then we really realized my Mom lived in her own dream world, really BELIEVING thát (the owner afterwards felt awfull for telling her that). She has a few other "boyfriends" at the home, but we know it is all innocent, as they hardly talk to each other (they don't know what to talk about), they would just sit together (in their own chairs) watching TV together in the communual Lounge, or sitting at the same table together. It is all about companionship ...... (But I must say she is in a very good and specialized Memory Care Home, in South Africa, there are less than 20 residents in the Home, and the staff ratio is 1:2 (one Staff Member for every 2 residents).
Get more info about this so called "girlfriend" relationship, it is most probably completely innocent. Hopefully ♡
My heart goes out to you but it also is temporary. I’ve watched this dynamic play out so many times. Remember, this too will pass. While you can’t be with him, be grateful, yes I said grateful that he is not alone.
MC should be familiar with this very common behavior. What was her real purpose in calling?
I have not seen my husband in seven weeks and when the time comes that I can get back in to see him, I will call ahead, as someone recommended below, and tell the supervisor to "get all the women out of the way" because I'm coming in and I'm not in a tolerant mood for nonsense.
When the supervisor called me I asked him to PLEASE discourage what was going on. He said he was already doing that--but he's not there 24/7. He was not happy about it. I asked, "Would you put this in the classification of 'girlfriends'?" He said, "No. But THEY think so!" He said my husband is "flirty". I've never known him to be that way.
Just more to deal with on top of everything else going on in our society right now. Life is upside down. What else Lord?????
P.S. I have stopped asking "What else?" because I don't want the answer!
I'm certain that nothing anyone of us could say to you is going to ease your heartache right now.
I would suggest you do a little research on dementia and how it affects sexuality. It might help you to understand a little.
Someone replied that he hasn't truly betrayed you. I agree with that whole heartedly!
Remember, his brain has betrayed him!! He's no longer(mentally) the man you married.
Sending prayers and hugs your way!
God bless!
the facility is probably required to report this to you.
I don’t mean to come across as rude, but why does it matter when they tell you. Hard to take no matter when.