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Caregiver for spouse with MCI (Mild cognitive impairment)

Caregivers: Dementia | Last Active: 3 hours ago | Replies (81)
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@mablesmith

SusanEllen66: I'm in the same situation with MCI, diagnosed a year ago. Much advice for caregivers but often I feel so alone being on the "other" side.

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Replies to "SusanEllen66: I'm in the same situation with MCI, diagnosed a year ago. Much advice for caregivers..."
sillyblone | @sillyblone | 3 hours ago

So sorry you are feeling that way. You are just as important. I think that sometimes lots of us do not see hardly any comments from the person living with the condition. Whether it be MCI, Parkinsons or any other condition. Please let me be one of those whom says I see you and I cannot fathom your fear and the what ifs. I don't want to be a person who dismisses feelings of anyone. Take care and 🫂 🤗

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SusanEllen66 | @SusanEllen66 | 3 hours ago

@mablesmith We are not the only ones.

If you want to meet other people with MCI, or dementia
please go to http://www.daanow.org
DAA is Dementia Action Alliance. It’s for people with MCI, or any type of dementia. It is specifically organized for the person with the disease.
I have met people from all around the US, and Canada online via Zoom “activities” we have an arts group, music, literature, one meeting is Faith, Hope, and Love.

I really enjoy the others. There is no cost or obligation. You can attend or not…

Hope to connect with you there 🌵🌻

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