I never did have a sense of direction. I can remember ending up on the wrong end of my high school building, not being able to find my car in a parking lot and heading downtown when I wanted to go uptown, It is SOO worse lately! I wonder if anyone has experienced this, or am I on the verge of Alzheimers?
No Sense of Direction: I never did have a... - My MSAA Community
No Sense of Direction
SueAB , I think some of us are more challenged with a sense of direction than others. I thought I had a pretty good sense of direction. But at the beginning of my relapse, I came out of a store and felt sure I had just come out of a different store. I felt disoriented and couldn't think where I'd parked my car. That was a frightening symptom that was a precursor to the real cognitive fog that came later. Fortunately, I haven't experienced that particular disorientation again, but I think it's wise to let our doctors know when we see a new symptom like that. I sure hope your cognitive issue is only temporary.
SueAB i was seeing a patient in a building that I was familiar with but when I left their room I couldn't remember whether to go left or right. I went left, sure that was correct and dead ended into a wall. It was a weird disorienting feeling (and I usually have a good sense of direction)
Lately my sense of direction has been pretty good, but when I was younger it was my son's job to remember where I parked the car. My husband, however, has an excellent sense of direction. But on leaving the grocery store a few months ago, we searched and searched the parking lot for our car only to finally remember we had driven my mother-in-laws car.
Thank goodness 😅 you remember that. I always look up at the building and if it has the store name I try to remember which letter/lane my car is in
But when I go to the hospital parking garage you know those little cards they have by the elevator that says what floor your on. I always take one you never know if you'll forget the floor your on. That would not be good.
SueAB My neuro has said that people with MS often have spatial relationship issuses, which is why we bump into things. Maybe a sense of direction is related to this.
Sometimes when I find myself opposite I think to myself.......find a reason and call it an act of GOD! I always find something where I'm at(not suppose to be) that makes it worth it then makes sense...its a gift....