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Support Group for Those of Us Living With Mild Dementia

Aging Well | Last Active: 2 hours ago | Replies (199)

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@rashida

@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. 🤷🏼‍♀️

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Replies to "@SusanEllen66 in Canada MRIs, EEGs, neurologist/specialist referrals are used as a last resort for anything. For..."

As far as I am aware, the only real insight an MRI will provide as it relates to Alzheimer's are fairly late term changes - like loss of cortical volume.

Cognitive testing by Neuropsychiatrists are how I prefer to trend progression over 12-18 month chunks of time.

Slowing that progression is the holy grail. I dont believe there are any meds that make a material difference. But I do believe that specific usage “exercise” can slow things down. Its about laying down new neuronal pathways. Function on a well used pathway may decline, but I try to develop new ones via new knowledge chains - in the hopes it will provide the equivalent of an alternate route for whatever I am asking my brain to do at that moment.

All that said to suggest that small concise bits of learning anything new should be helpful even if they dont seem useful. Can’t hurt is my view.