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Support Group for Those of Us Living With Mild Dementia

Aging Well | Last Active: 4 days ago | Replies (208)

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@SusanEllen66

Two years ago I told my doctor that I just didn’t feel like myself mentally. He told me to go to my neurologist.
I had MRI, EEG, and a 4 hour neuropsychologist administered test.
I was diagnosed with Mild Cognitive Impairment.

Over the last two years I’ve noticed other things happening. I’m in the middle of testing again.
They said my brain has shrunk more, and now I have Ataxia.

If I were you, I would get tested so you can get treatment ASAP.

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@SusanEllen66 in Canada MRIs, EEGs, neurologist/specialist referrals are used as a last resort for anything. For instance, if one has concern about dementia a doctor usually gives you that memory test and if you fail you are put on medication to delay dementia. I have seen two friends a good ten years younger than I being diagnosed this way, both went downhill and died within five years, so when I started forgetting I did see my doctor about fifteen years ago but I have resisted this diagnosis and treatment method. My mother had Alzheimer’s (she too probably was given that same test and put on the medication) and died at 86. I am just going to do my best to keep my brain active as long as I can by whatever means other than medication, for as long as I can. So far, at 78, I have managed to cope. Unless I get an MRI to prove I have dementia, I am going to live in denial, I guess. 🤷🏼‍♀️