← Return to My anxiety about my husband's memory loss is pretty bad
DiscussionMy anxiety about my husband's memory loss is pretty bad
Caregivers: Dementia | Last Active: Feb 11 11:16am | Replies (45)Comment receiving replies
Replies to "Hello. I hear all of that loud and clear. Like you, I have plenty of stressors..."
Thanks for taking the time to write that reply. Acceptance is my goal right now. It comes in spurts, though. When I think I've reached real acceptance, I see there's still a ton more to go. Every time my husband displays another sign, I have to accept it all over again. I'll get better at it.
I love your idea about positive interactions regardless of how we as caregivers feel. That's a great plan and I'm trying it already. It seems to help him. Finally, it really does help to know I'm not alone and that my feelings aren't weird or wrong in some way. Thank you.
I have found that if possible to do a couple kind deeds both enriches the other person and ourselves in so much that we can face difficulties better ..what do you think?
I hear you. Fortunately years ago my hubby took long term insurance. However how long will this go on, am I going to have to put him in a home. That’s my last resort. He would never want this. He will be 80 in August but he is active. It’s his memory that is terrible. Diagnosed 2 years ago with MCI. I just retired in June from teaching so I’m home and more available for him. I have days or moments when I’m screaming inside how much more can I take. Then I think if those worse off. People who have this at very early ages. I’ve been blessed we traveled and married 30 years. We had a good run. I’ve gone back to church and this helps me alot. I’ve joined this group. I grieved for him. Who he has become is not who I married. I just wish that knot in my stomach would subside. I’d like to live and enjoy life. We do go out but it’s always a worry. I mostly try to think about people who have it worse to get me through this. Gif bless us all. I’m here if you need to vent.