to all of you that have sent emails to me lately, wondering about my whereabouts on this blog. Sorry I haven't written -- I'm here. Just having a problem getting my thoughts in order and typing them out. I seem to have a problem lately with getting my thoughts organized and out whether they are in written or verbal form. I went to the neurologist last week and he told me that he thought that I had gotten a little worse in my "delayed speech pattern". Which basically meant that I was having a hard time getting my words out. I told him I thought so too, but then he looked at me and said, "you know, there isn't anything I can do for you". Which although I know that is true, it's hard to hear sometimes.
It's frustrating for me when I can have whole conversations in my head that I want to have with someone, but I can't get the words out.
My husband has been gone for about a week. He's home today. I know I have said it before, that when he is away and I am home alone, it is so much easier on me. He knows this too so I'm not saying anything out of line. I am amazed at how much easier it is -- not from the physical things I usually do like cleaning, cooking and dishes, but mentally. I find that I can stay up longer at night because I'm not as mentally tired from having someone around all the time. And I get much more stressed when my husband is around, not sure what that is all about, but I would probably be stressed with anyone around --that isn't aimed at him! My husband doesn't talk much, but he is a pacer -- he paces all over the house during the day. I'll be in one room trying to "do my own thing" and he will come in there many many times during his pacing. Each time it interrupts what I am doing and although he says he doesn't want anything, it's still an interruption in my brain. It's amazing how these little things will get to me. And, of course, the noise is an issue -- which it gets worse and worse. I think I might have had the television set on a total of about 5 or 6 hours during the entire time he was gone. Counter that with the almost non-stop television set being on when he is home, it sure makes a difference. He is getting better about wearing earphones with the televsion set, but it is still bothersome. A friend of mine with AD, just had some custom made ear plugs made that he says blocks out all the noise except for conversations. He says he can ride in the car with his wife with the radio on and not hear the radio but he can hear her when she talks. I might look into that. We have finished converting my son's old bedroom into a "quiet room" for me and it has certainly been a great place for me to go to achieve some peach and quiet.
On another note, my friend Carol and I went to Macon last week to an Alzheimer's fundraiser with the band Diamond Rio. It was lots of fun to be away together and the concert was really nice. Thanks Carol -- for being my chaueffer and most of all my friend for all these years -- Sainthood might be up there for you too! Carol will certainly understand this.
Subscribe to:
Post Comments (Atom)
3 comments:
I'm having trouble getting my thoughts together and on the computer too. I have the opposite problem with the house though; our youngest has been on homebound school and not having the house to myself during the day is making me nuts. I like them all coming home each night, but its hard to have him around and now the eldest is home for summer. I look forward to them having their classes and jobs this summer. We get to go to the beach soon. That always recharges my batteries and centers our family. How are you boys?
Hi... I just found your blog. I am my mom's care giver, she has been diagnosed last year with mid-staged Alzheimer's.
I believe she has Lewy Bodies Dementia because of her wild hallucinations and her lucid moments. One minute she is able to talk, next minute she can't find the right words.
She is not on any pharma meds. She takes coconut oil and supplements that were prescribed by our Naturopath Doctor.
I've modified our diet. We cut out all wheat gluten, potato and all processed foods. She has better days when she eats real food.
Food is medicine. I've seen the healing power first hand. There's always hope.
Hello, I just found your blog this morning and couldn't stop reading. I was caregiver for my Mom with Alzheimer's. She passed away from other causes 2 years ago, but I wish I had read your blog then. Her hearing was awful and eventually she was deaf, yet she refused to wear her hearing aid. Your article helped me to understand why.
Would you mind if I posted a link to your blog on my own blog. It's a different perspective from caregiver and certainly interesting.
Take care, Sandy
http://free-alzheimers-support.com
Post a Comment