I haven't posted in quite a while




Every time I think about it, something else happens and I put it off. It's been eighteen months since my DH entered MC and I wish I could say I have adjusted to being alone. My life is full of activities but underneath is the sadness that never goes away. In the evenings, when I am alone, it hits full force and the tears start falling. I miss my husband so much and yet we've been on this journey for so long that I can barely remember the man he was before Alzheimer's. How many years can you grieve someone? When I visit him in MC, he is always happy to see me and he is loving and tells me he loves me. I love him too and that's what breaks my heart. He wants to come home and I dearly want to bring him home but there is no way I can do that. I'm not physically up to it. When he looks at me with such sadness in his eyes it's all I can do not to bundle him up and take him with me. I visit often and relish his hugs and the little bit of time we can spend together. Then I leave and feel so empty driving home. This is my life now. I know God has blessed us and is taking care of us and with His help I get through my days. Still, I am lonely and cry by myself.
Comments
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So sorry for you and your life you must endure now. Life goes on, time marches on and some day he will leave this life for a life beyond and so will you. Then, once again you will be reunited with the husband you married for a life eternal. Blessings to you and he. Enjoy your limited time together.
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I’m so sorry to hear of your troubles. I don’t think we can ever predict how we will react to the various things we go through with this disease. It’s such a LONG painful journey and a long slow goodbye. It will be over someday and you can move on but be comforted in knowing he is happy and loves you still.
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I'm there with you. The guilt is relentless. I'm not successful in curbing it, so there's not much advice I can offer. I want this journey to be over, but it just lingers on. Nothing the therapist has offered helped. I know that in the end it's our attitude, how we ourselves react to the situation. Well, easier said than done. It's a long waiting game for death to come. It's a terrible, morbid thought. But it's how I'm feeling.
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I understand perfectly. My DH is also in MC, and the sadness never leaves. I can't bring myself to watch TV alone, because it is something we always did together. I have tried, but I just end up crying. At night I read and go to bed too early because it is so empty in the apartment. When I see him, he is always glad to see me, but he has declined so dramatically it just breaks my heart every time. I want him to go peacefully and end this terrible suffering, but I can't imagine life without him at all. Such a terrible disease!
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My DH has now been in MC for only two weeks. When I visited him today he was very glad to see me and we had a nice breakfast together. But after breakfast our time together devolved into his wanting to figure out a way to escape and how he had nothing and couldn't go anywhere and his life was taken away. He doesn't blame me for being in MC but he can't figure out why he is there and has a number of delusions about how he got there….I have a hard time saying it's the illness, not me. He wasn't very happy at home lots of times, but we did have lovely times together hanging out, going to dinner, watching TV, holding hands and I just hate this other life. I know placing him was right but as everyone has said the guilt is so overwhelming and the desire to bundle him up and take him home is something I have to actively resist.
8 -
It has been 16 months since my wife moved to memory care and I stay relatively active but with things that seem mostly meaningless. I feel like I am stuck between two worlds one where my wife is here and alive but not living and one that she is not. I can't really move forward because I am still anchored to the past. These feeling come and go. I go along doing OK for a while then all of a sudden they come back. This journey is hard but I am slowly getting through it. All we can do is keep going never giving up on trying. The Jews wondered the desert for 40 years before they found their promised land. May God bless you.
t
3 -
I'm going through the same thing with my wife, except that she's nonverbal and I have no idea what she might be thinking or what she might want. Sometimes she's happy to see me and other times she barely responds to me. When she does, is it because it's me or would she respond to anyone else the same way? Then she shows no reaction when I'm leaving. She's only three miles away, so we'll do it all again the next day.
6 -
yes, sadness and guilt sums up the journey of dementia. We understand. Hugs. 💜
2 -
Every step of this journey is such a difficult challenge. Big hug.
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Commonly Used Abbreviations
DH = Dear Husband
DW= Dear Wife, Darling Wife
LO = Loved One
ES = Early Stage
EO = Early Onset
FTD = Frontotemporal Dementia
VD = Vascular Dementia
MC = Memory Care
AL = Assisted Living
POA = Power of Attorney
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