As the symptoms of dementia seem to be progressing, the one thing that seems significant to me right now is my inability to keep up with a conversation, especially over the telephone as the visual clues are missing. It is easy for me to say yes or no reasonably appropriately, but not so easy to more fully discuss or respond to the other person/people. When in a group, my husband works overtime as my back up brain, stepping in when he sees me stalling, or watching for visual clues of distress or confusion. It feels like I am in a fog, or inside a Gravitron, an analogy I used earlier in 2012, or drowning.
During conversation in groups, I often ‘disappear’ or find other things I ‘have to do’, for example if having people for a meal or coffee at home, I might go and prepare something in the kitchen, or wash dishes, or go to the bathroom. On the telephone, I simply ‘wing it’ most of the time and feel much like the confused telephone in this clip art! Inside my mind, I am questioning everything, wondering what people mean, trying desperately to remember the events of people they are talking about, or sometimes even what they said at the beginning of the sentence.
For the person with dementia, communicating with others becomes more difficult, but as we so often ‘fake it’ and learn ways to appear as if all is okay, it must be hard for our friends and family, or carers, to even comprehend we are not really in a conversation. Admitting to ourselves is challenging enough, but allowing others to know our reality is almost unbearable.

I also find it difficult when there are a lot of people all talking at the same time because all the talking confuses me, even if i’m not listening to what everyone’s saying. I prefer to just talk one-on-one.
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I cannot begin to imagine how difficult this is for you. At times I got the feeling my dad was faking it. But he always said everything was fine. No matter what, everything was fine. I hated thinking he felt lonely or fearful of what was happening. I wanted to comfort him somehow. But he told us everything was fine.
I worry about posting this comment. I don’t want to say the wrong thing.
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Everything is fine… Is a common reply!! So much easier than admitting it is not, and then when you do, and someone tries to explain it for you, when you still can’t understand, it is worse. Don’t be afraid to comment, I really love hearing from almost everyone. 🙂
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OMG, that is simply no not simply but bloody horrendous for you darling kate,cannot imagine. hope we can have a catch up either on 18/or 19th jan will email you. to the moon and back and on and on. xxxx
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Thanks so much for sharing “how it feels” – Hopefully it helps the rest of us think twice and work to make life easier for people living with dementia – rather than twice as hard!
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