Hello world! Please change me in Site Preferences -> This Category/Section -> Lower Description Bar

A Shot of B12 or a Shot of Whiskey?

Posted by / in Blog, Mild Stage / 2 comments

Thank you for sharing

Your loved one is repeating the same things over and over, misplacing items or getting lost in familiar places.  You know something isn’t right.  Instinctively, you know they should see a doctor.

For us, that was about 4 months into Mom’s  beginning stage of MCI, or Mild Cognitive Impairment.  The first appointment wasn’t easy.  I told Mom gently that she needed to see her doctor.   I made the appointment, drove her there making small talk in the car, and she was wondering why I was taking her to the doctor when she felt fine.

We walked into the reception room, signed in, and Mom was still wondering why we were there.  We were both ushered in to the exam room.  The doctor came in, smiled and said, “Well Helen, how are you?  What seems to be the problem?”  Before Mom could answer “I have no idea,”  I braced myself and said we are having some memory issues.  I got a big stare.  From both of them.

There must be a better way.

After a short conversation with Mom’s doctor, he ordered blood tests to measure her vitamin B12 levels and her thyroid.  Believe it or not, low levels of B12 or thyroid hormone can result in a form of dementia.  He gave no mention of Alzheimer’s disease , but it would have been really awkward if he had.  I wasn’t ready to say it out loud and apparently he wasn’t either, especially in front of Mom.  Since Mom was still grieving over the loss of her husband, the doctor prescribed an antidepressant.

Later, the receptionist called and the results of the tests came back fine.  No shots of B12 were necessary and since she didn’t drink,  no whiskey either.  For me, there were days that whiskey might have helped.

I received no guidance whatsoever about what to do next.  The receptionist said something about a relative of hers who had memory problems, and I imagined her head shaking back and forth.  Back to the drawing board.

No mention of seeing a neurologist.  No mention of a brain scan, a memory test, Aricept or Namenda.

That was 2005.  Fortunately, it seems that more and more doctors are knowledgeable about Alzheimer’s but generally, society has a long way to go.  The stigma is less now, but I think one of the biggest problems is that there isn’t a lot the doctor can do.  At least dialogs can start.  The drugs that are on the market now may slow the decline, but there is no cure or sure way of prevention.

I learned on my own that a visit to a neurologist was in our future.  More on that later.

Suggestion:  After Mom had experienced symptoms for several years, I began to understand the best way to prepare for her doctor appointments.  I suggest that you give a written note with details of the symptoms to the receptionist BEFORE meeting with the doctor.   It prevents a lot of embarrassing moments during the exam for all concerned.

Please select the social network you want to share this page with:

We like you too :)

Lorem ipsum dolor sit amet, consectetur adipiscing elit. Donec tincidunt dapibus dui, necimas condimentum ante auctor vitae. Praesent id magna eget libero consequat mollis.

I had a nine year journey with my Mom who suffered with Alzheimer’s disease. I wish to share what I learned about caring for a loved one who has Alzheimer’s and also provide a website with information and helpful resources.

  • ron kays

    January 19, 2015, am31 11:17 AM

    Talk about being on the edge of the frontier where contextual experience is virtually non-existent! Add to that the human propensity to deny what which we cannot understand or “fix” right away and you’ve got the recipe for agony, which you detail in “Shot of Whiskey”.

    This is precisely why you’ve got to keep writing about Helen and the SImpson experience with Alzheimer’s. Even though it’s 2015 and “we’re not in Kansas anymore”, figuratively speaking, there are people who have not seen, will not look, or simply are too overwhelmed to find the “path” to a workable “solution”.

    Painful to recall as a family friend isolated from the nitty-gritty of the day-to-day struggle you all experienced. But, I thank God that you’re sharing this difference-making information with folks entering the Alzheimer’s wilderness. They need the map and compass you–and Helen–are offering.

    • Virginia Naeve

      January 19, 2015, am31 10:13 AM

      Thank you, Ron. I’m very touched by your thoughtful comment. I promise you, I will keep writing. As long as Mom and I can help at least a few people out there, this project will continue. Thanks and God bless.

    Enter the Discussion and post your Comment