Husband With Slow Cognitive Decline: So sad & confused
About 11 years ago at age 55, my husband became very ill with a high fever, was admitted to hospital but not treated with any ABX (until too late), so became delirious. He had developed severe pneumonia in both lobes. When he was discharged he was a different person, with pretty profound short term memory loss. I blame the hospital for their negligence which allowed the delirium to develop. Eventually, after seeing every kind of dr under the son, he was diagnosed with MCI. We are now retired (he was a computer engineer) and I’m struggling with my fears about the future. He drives safely (uses the GPS almost always), takes care of his own personal hygiene, does yard work when he needs to, helps around the house, and helps with our two grandsons on the two babysitting days. He does many “normal” things, he just can’t remember anything - which is very NOT normal. There are other cognitive issues too. I don’t want to keep going on and on because there’s just so much to talk about, but I’m wondering if anyone else is in a similar normal/not normal at all type situation. I feel like I’m always waiting for some awful event that will propel him into something more advanced like dementia. I’m also reluctant to get him into another round of neuropsych testing. The first round about 3.5 yrs ago wasn’t particularly helpful but could it be now if things have changed? How?Also, 3.5 yrs ago his MRI showed no sign of Alzheimer’s. In a fairly recent discussion with a neurologist, he suggested maybe/probably vascular. I do take care of all appts and bill paying but then again I pretty much always have. I just don’t know what to do next. I don’t sleep well and am depressed and sad that my life has become this all encompassing thing, and I’m disappearing. Sorry for the novel, just so sad and confused.
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I am still hanging in there, which is good as husband has severe issues. We did update all the paperwork a few months ago. Our issue is having no family in touch and so signed a testamentary trust for the house and contents--they will clear the house, sell it and give remaining funds to sons. It might be academic anyways as Medicaid for long term care may be our only option when funds run out.
You did a great service tactfully for yourself and for her!! Way to go! It can be very challenging to be find creative solutions!
My husband has CIDP he started having issues. We went through years of falls fractured bones. He finally got a diagnosis of CIDP but he was unable to walk by the.He now gets IVIG therapy. He fell and had a fractured hip after his surgery he was so confused he did not recognize me or our son. Anesthesia seems to really add to memory issues. Fortunately we are home safe and doing pretty well. But he has to have help with daily hygiene. Some days are better than others we just are taking one day at a time. It’s hard to see the ones that we love decline. The golden year are not easy sometimes
It’s ironic that commercials show seniors out dancing at high end resorts, active and laughing and smiling. Is that reality? If it is I’m definitely doing something wrong. Golden years have been rough!….David
Our situation sounds very similar to yours. My husband has had all the tests and is on medicine which is not helping. No definitive diagnosis except early stages of Dementia. He is 85. He has lost a lot of weight and I cook heavy meals. He asks the same questions constantly and the other things you reported. It’s really wearing me down !
Amen! Had I knew that my husband would have got sick we would have traveled more. Now it’s hard to walk we don’t travel except to the doctor appointments. Hindsight is always clear…Jane
Hang in there and if you don’t think the medicine is helping call your doctor and tell them. You live with him 24/7 and you know him. I would recommend getting him a protein shake to add calories.If he has diabetes Sam’s Club sells Premire Protein and it’s low carbohydrates. I have watched many Utube videos on caregivers and dementia. Might try it to get pointers on dealing with the repeat questions. Dementia Careblazers . Good luck Jane
Don’t be sorry for the long post you are not alone in the journey. And I bet you felt better releasing the tears. Sometimes I go downstairs to do laundry or take a shower when I need a good cry. There’s nothing wrong with it ! I’m sure your son needs to understand what is going on as well. Not easy seeing it unfold….Jane
Thank you. It’s been a very hard week and I realize I have to make a lot changes. Feeling old and tired .
He does not like Ensure. Will try the shakes …I will look for u tubes ….so tired…thanks so much ….m
What you are feeling about losing yourself is so true...it’s something I’ve experienced with my mom as she approaches seven years of her diagnosis. It’s easy to say make time for yourself and sometimes hard to do. I thought I was doing OK but it became overwhelming even as I made time for myself. I now have caregiving three days a week and it helps so much. Still this journey is a hard one. Courage.