Working with Neuropathy?
Do any of you still work? I'm 68, I was working until last year. I retired because I hurt too much. Doctors diagnosed neuropathy.
Interested in more discussions like this? Go to the Neuropathy Support Group.
Do any of you still work? I'm 68, I was working until last year. I retired because I hurt too much. Doctors diagnosed neuropathy.
Interested in more discussions like this? Go to the Neuropathy Support Group.
Hello @pfbacon
While I do not have neuropathy, I do have other health problems that resulted in my retirement when I reached my full retirement age. It is important after retirement to find physical and mental activities that will keep you moving and that will help you enjoy life. As @johnbishop mentioned, do you have hobbies, crafts or other activities that will help you? Also, a lot of communities have senior citizens centers where you can find some activities to keep your mind and body active.
I found a work-at-home job which is quite nice. It gives me an activity that I enjoy and keeps me busy. Do you think that your previous job provided you with skills that you could use in a work-at-home position?
Often AARP has information about these types of positions.
Sounds like you've got a LOT going on in your life. With so many challenges, I am really grateful that you are here for us 🙂
BTW - It is very common for people with DTD to panic when they become disoriented - ESPECIALLY when driving. I've described it by saying 'How would you feel if someone picked you up and dropped you into a completely foreign environment?' Truth is - one moment you are comfortable - know where you are - and the next minute nothing looks familiar. I thought I was losing my mind!
My husband has dyslexia. When I finally had the courage to tell his about my disorientation issues (undiagnosed at that point), he immediately said that it sounded like a form of geographical or environmental dyslexia. Thank God - he is extremely patient with me.
@iceblue
That's an interesting observation - the connection between dyslexia and disorientation, environmental dyslexia.
When I retired we lived 130 miles from anywhere. It was a 3 hour drive each way, so after a long day of shopping and doctor appointment, it was usually well after midnight when we got home. One night, at around 11, I came to the turnoff toward home - and home was 100 miles away. All of a sudden something weird happened to me, and I couldn't go any further. I know now that I was having a panic attack. We had to turn around and get a motel room. (We crossed that motel off our list of places to stay - disgusting.)
I don't think I was disoriented. I just shut down. It was a really strange feeling.
Being suddenly disoriented is disconcerting, even frightening. I'd never heard a name for it - DTD. In the past ten years I've experienced it numerous times and I hate admitting to my wife that I'm having a brain freeze, and not the kind I get from eating ice cream too fast.
Another way I experience brain freeze is when I'm playing the piano at church. I'll forget what key I'm playing in, or I will jump to the wrong verse (I lead the music service on Sunday evenings). A couple of times I had to stop and start over. My major in college was music with a focus on piano, so that kind of thing shouldn't happen. I wonder sometimes if it's because of a medication, but it's not something new. I warn the people about my brain glitches. It's embarrassing. It could fit under the label of dyslexia, I guess.
Jim
Hi, @iceblue - thanks for sharing about the developmental topographical disorientation (DTD). This abstract of a journal article published in Trends in Cognitive Sciences offers more information on this condition and a link to the full journal text, if you're interested https://www.ncbi.nlm.nih.gov/m/pubmed/27450709/#. Sounds like this is a more newly described condition.
@iceblue - DTD would be a great topic of discussion in the Connect Brain & Nervous System group, https://connect.mayoclinic.org/group/brain-and-nerve-diseases/, if you'd consider starting it. I think others may also have this condition and benefit from finding support. Directions for starting a new discussion are found in the Get Started on Connect section at the bottom of every Connect page https://connect.mayoclinic.org/get-started-on-connect/.
Thank you Lisa 🙂 I will check out the info on starting a new topic. I just know that for years (decades), I knew something was wrong, but couldn't quite put my finger on what it was. And it does make for a pretty lonely life because you are limited in where you can go...
FYI:
https://www.ncbi.nlm.nih.gov/m/pubmed/20431873/?i=2&from=/27450709/related
* Dr. Iaria, the author of this article is the Researcher at the University of Calgary where I went through my testing. I have not actually met him, but have interacted with him via e-mail.
https://www.ncbi.nlm.nih.gov/m/pubmed/27923326/?i=3&from=/27450709/related
* This is the published study my sister and I were included in. I have also exchanged e-mails with the author (Stacey Barclay)
Good morning, @iceblue, My memory check tells me you have a medical appointment today. Was this the one with your GP for pain management? Please let us know the results. I will be watching for your post. I hope today is free of suffering for you. Chris
Thanks for the follow up Chris! I saw my doctor on Friday, and he has given me a 3 month prescription of Gabapentin that indicates I can take up to 600 mg/day. I have been taking 400 mg/day for the past week, and will stay on that for at least one more week before considering an increase in my dosage. My feet are still very painful, but I have noticed that the pain in my hands, arms, and calves has settled down. I am supplementing with T1's a couple of times a day, and although I'm disappointed to be taking those again, it will only be until I land on the right dosage of Gabapentin....
I am 57y/o and currently undiagnosed but the symptoms are present going on 3 months. I work full time at a desk. I was wondering if working has been a problem for anyone?