Neuropathy in feet and limited toe movement?
Just curious as I was diagnosed with peripheral neuropathy in the beginning of this year but have yet to see a neurologist about it (postponed till end of June due to COVID19). I have constant pins and needles, numbness, pain in both my feet. It's gotten worse over the years (been dealing with it for ~10 years and never went to a doctor about it due to lack of insurance) and now I can no longer even bend my big toes at all and even bending any other toes are rather difficult. Just wondering is this common...anyone else have this?
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Hah! Love this John! So creative and what a wonderful nostalgic memory for you. 👍🏻😁
Cant believe it goes back to 1927!
I have the same neuropathy issues as you. Numbness in my feet, especially my toes. Can't bend my toes. Spasms and tingling are almost constant. Mine appears to be genetic as my mother, grandmother, brothers, uncles and cousins have similar symptoms. I went to a doctor at Stony Brook Neurology who's specialty is peripheral neuropathy last Monday and had a genetics test done. Simple saliva test, much like the Ancestry and Hereditary tests you've probably heard about. Results should be back in two weeks. The doctor suspects CMT or HSN but also tested me for MS, Parkinsons and ALS. She doesn't suspect those conditions but wants to rule them out. She said this test will show if any genes known to cause periphrtal neuropathy have mutated. She also wants to do a MRI of my neck. She said that peripherals neuropathy of the lower extremities can sometimes be caused by a pinched nerve in the neck. She mentioned C1/C2 so I assume that's the lowest disk in your neck. But she wants to wait for the results of the resgenetics test before going to plan B given my family history.
Yup, I believe you are right. It's all connected to this nerve illness. You know, for your posts oday I looked for an emoji with a thumbs down and I can't believe there isn't one. Do people think every reaction one has deserves a thumbs up? Crazy.
Have you ever listed out every bad health symptom you have, every single one? It would first of all be interesting to see how many you come up with and secondly whether they might all be related to neuropathy, or if any seem not to be. Just a thought.
I remember those John. Between reading those and looking and counting for "cats eyes" (59 Chevy's) we made the time pass in the back seat.
Hi @mjpm2406 I am sorry to hear about your issues, the spasms and tingling sound awful. I had not heard of testing genes specifically related to neuropathy. I didn't know there were genes for neuropathy, but it makes sense if its hereditary, i.e. multiple family members have it. And your doc thinks that some of the manifestations of your problems might be related to mutations of such neuropathy genes? Very interesting. Sounds like a good doctor, very inquisitive, you must feel lucky to have her. Best, Hank
@jesfactsmon Sadly, yes I have. It's an ongoing list which I have sent to Mayo for my file. Here it is in all its messy glory.
A few things have settled or shifted since supplementing B12, taking Lyrica and the supplement protocol, but mostly I seem to be stuck with lasting problems. However, I continue to work on them everyday between PT, mild walking and body movement as tolerated and mindset. My PT was waiting until after Mayo to start an occupational therapy regimen, as now he only performs myofacial release once a week and rotates body parts to where the pain is at it worst. I cant wait until October for that. I've been waiting long enough. So, last week he gave me 4 mild, beginner exercises to start for my back. He had wanted to work off of Mayos designed plan for me. But, time is a wasting!
OK, firstly I believe you've got mindset down. Secondly, YIKES! That is some list! I have to look it over. I'll get back to you in a couple days. (Now where's that thumbs down thingy!)
You make me smile 😁
@rwinney Rachel, Oh Rachel, Oh Rachel!!!! What you are enduring!!!! This list is unbearable. Brutal. You so clearly have autonomic problems along with your small fiber problems. I am so overwhelmed reading this. I suggest that you prioritize your top 3 or 4 problems, so that the doctors have focus. But actually, your descriptions are variations of the same problems hurting various parts of your body. I still would start your final copy with the top 4, right on top. You obviously need testing for the autonomic stuff, too. I do too, actually, as I suffer from getting overheated and totally sweaty, out of the blue. I also feel like my feet are soaked, when they are not. I wish I could wave a magic wand and POOF!!!! All of us are better. By the way, this has nothing to do with sickness; my son also works in pharmaceuticals. He sells the high end cancer drugs to docs, hospitals, etc. One pill can be over one thousand bucks. Is there something wrong with that, or what??? And BIG PHARMA laughs! My son's sales goal for last year was 6 million dollars. Ha! Love you, Rachel Lori