The Wrong Diagnosis

Life with Mom

—-This is a story of a shared life with Mom after her diagnosis of Alzheimer’s Disease.—

For a while now, my mother has had an inkling that she may have Parkinson’s. She thought her father had it (undiagnosed), and knew for sure that his sister had it. Looking at her at the time she brought it up, I couldn’t tell, but something had her concerned.

We saw the Neurology Nurse Practitioner in December and requested that Mom be assessed for this. Alice, the NP, put her through a battery of movement tests and thought that there wasn’t enough evidence for this diagnosis. We let it go and forgot about it.

In March, I did a double take one day when I saw my mother’s left arm shaking quite significantly while she was holding her pocketbook. I asked her if she knew she had developed a tremor. She said she did. Her next appointment with Neurology wasn’t until June, so we decided to wait until then to request further testing. She was scheduled to see the MD this time. She hadn’t seen the Doctor since the original diagnosis of Alzheimer’s two and a half years ago.

We went through the routine cognitive testing where my mother answered questions and did some simple paper and movement exercises, while I answered several questions from a care-givers perspective about how I think she’s doing. We then mentioned our concern for the newly developed tremors and requested the Doctor’s opinion.

She shared with us that my mother did better on the cognitive testing than she did two and a half years ago, and after some more testing and questioning, agreed that she either has Parkinson’s or Lewy Body Dementia, which are both movement disorders, and both can have a dementia component . She added that these diagnoses are more treatable than Alzheimer’s, and the best ones to have as far as the many neurological problems people can have. Both the Parkinson’s and the Lewy Body are progressive, but manageable with medication and the old stand-bys of healthy living, which includes healthy diet, rest, and staying physically active.

I recall the doctor telling us two and a half years ago that they have a record of being 97% correct with their Alzheimer’s diagnoses. I’m glad to say that we…my mother, are in the minority this time.

The three-percenters are an elite and unique group, and we’re looking for more members.

IMG_0433

 

Advertisements
This entry was posted in Life with Mom and tagged , , . Bookmark the permalink.

6 Responses to The Wrong Diagnosis

  1. Ann mckinley says:

    Diane,I’m so happy your Mom’s Alzheimers diagnosis was a false alarm. Now,you can focus on what’s really happening and help her even more. All The Best to you and your precious Mom. ♡

    • Diane Fiore says:

      Yes, Ann, we’re happy to know the real diagnosis. When we thought it was Alzheimer’s, we embraced that too and went with it. Now we will shift and do our best in this new arena. So nice to hear from you. Hope you and your family are well.

  2. Glynny Schiavoni says:

    Wow! Talk about getting your head around that u turn! I’ve been thinking about you and wondering if things were o.k. since you haven’t written anything in what seems like a very long time. Glad to hear that maybe things are less dismal with Mom, but would like to know how you and Brian are holding up.
    Love you,
    Glynny

    • Diane Fiore says:

      We’re doing great, Glynny. Enjoying the summer and trying so hard to slow time down. We’re happy about the new diagnosis. And my mother always seems to take things in stride. Hope you and Mr. S are well. I think of you often and am sending you good wishes and love. Diane

  3. Nancy says:

    Diane, both you and Brian are angels in disguise. It’s wonderful how you, Brian and your mom go more with the flow of things rather than dwell on the unknown. That is a blessing. Our thoughts and prayers are with you that God will continue to watch over all of you, guide you and keep you in His loving care. Sending our love and hugs.

    • Diane Fiore says:

      Nancy, I cherish your sweet thoughts more than you could ever know. It’s the support of family and friends that keep any of us going. Our love and admiration to you and your family, always.

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s