Idiopathic Polyneuropathy: My endless journey to a near-diagnosis …
Hello!
I have been here before. Several times each time posting under what seemed to be the correct topic at the time, such has been my maze-like journey to a diagnosis. I'm not there yet (that 100% positive diagnosis), but I'm closer. Only yesterday, I met with my neurologist, and he came as close as he dared come at the moment, calling my ongoing balance problem idiopathic polyneuropathy. Since I also have some cervical stenosis and am already scheduled for an MRI in two weeks, my neurologist suggested we plan to talk next after he has had a chance to look over the results of the MRI. This journey to a diagnosis has been a long one. I'm curious to know if others have had a similar experience. And what was the outcome? I'm doing PT for balance and taking B-12 and alpha lipoic acid (the neurologist's recommendation). But are there other things I might try at this point, something I might ask my neurologist about? I believe others' experiences with this condition would be of immense help.
Ray (@ray666)
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Good morning, Ed (@njed)
I couldn't agree more! It is too easy to say "no" to opportunities to be with friends, all because of a fear of some mishap. Of course, mishaps can happen, but after years of practicing how to manage our various neuropathies, we should have developed a bag of tricks to keep ourselves reasonably safe. I believe I have. It's too easy to become a person who always says "no" to opportunities. I intend to try my darnedest not to become that sort of person.
Ray (@ray666)
Good morning, Debbie (@dbeshears1)
I can still remember the day I completed my first marathon. I'd been working in LA at the time, but flew back to Denver specially to run in that event. Frank Shorter had just won the Olympic marathon and I was still young enough (and crazy enough!) to think, Heck, if he can do it, I can do it. I didn't run my best, but I can still remember how I wept running the final hundred yards to the finish line. It was a very special experience, one I'll never forget.
Ray (@ray666)
Deb - that feeling you got after the marathon is exactly what we with PN need to experience. OK, so now it isn't a 5K which I too did into my mid 50's. It can be a small walk and the next day a block longer. I am in PT and for insurance to pay, there has to be improvement. Each time I can stand with eyes closed for 2 seconds longer without holding on, that 5K feeling is what I feel.
Wow, thank you everyone, I love reading these posts! I'm in the early stages of "giving up things I don't want to give up," but I've been dealing with this pain for 7 years. Vertigo and balance, too, but I think they're unrelated (I get a rare kind of migraine and my neurologist says the vertigo I get is a type of migraine or are migraine-related, but when I get a "vertigo spate," it lasts for days). Right now I am struggling with a family wedding in Sri Lanka my sister desperately wants me to attend. I am in the US. That'd be over 22 hours of travel minimum, with 2 flights (18 hours of flying time). My pain is localized to the backs of my thighs--sitting and especially standing up is excruciating for about 2 minutes each time I do it, especially if I've been sitting for a while. I have been struggling with how to make that trip... maybe if I fly first class and can lie down I can be comfortable, but that's $20K. My son has been home with me this weekend (I'm 62, he's 35) and he has convinced me that it is 100% unreasonable to consider attending that wedding, and maybe I needed someone's absolution or something, but now I feel more comfortable telling my sister "no." It's not marathon shopping, but honestly... when I back up to 30,000 feet and look at it, it's a completely insane thing to consider.
It has been very helpful reading everyone's comments about things they've had to sacrifice in the name of frustrating idiopathic undiagnosable crippling damn pain.
Also, FWIW, I've seen a neurologist, a pain specialist, a physical therapist, and have been on a course of pregabalin (Lyrica) up to 800 mg/day (divided dose), with nothing but side effects to show for it. I also tried numbing cream, LOL. This sucks, but it's nice to know I have a tribe. Thank you, everyone.
Good morning, Libbie (@libbiehyman)
I enjoyed reading your post and would like to say I totally understand your dilemma. You may have read mine where I mention being unsure about going to a local coffee shop (uneven sidewalks, long sitting, an unfamiliar path to the restroom, etc.) –– a far cry from a flight to Sri Lanka! I believe there's an art to knowing which challenges are important to take on, to avoid becoming a total stay-at-home, from those challenges that are simply "too much." I work every day on practicing the art of being about to tell one kind of challenge from the other. Good luck to you!
Ray (@ray666)
Thank you, Ray. These are such wonderful, supportive posts to read. I am definitely "choosing my accessibility battles." I was just diagnosed with severe osteoporosis, which really pissed me off. I joined a gym and am weight training and I go to a yoga class once a week, where I struggle clumsily in a class of people who can bend over while standing on one leg. I talked to the yoga teacher who was sweet and kind, and she said "set your mat up over by the barre. Use the barre to pull yourself up or to hold onto for stability if you need it." Well, THAT improved yoga 100% for me! So I'll drive 5 miles to a yoga class where I can stagger around like a newborn giraffe and clamp onto a barre for dear life, but I feel a whole lot more confidant saying "no" to a wedding 22 hours and 3 flights away, and less guilty about it after talking to my son and reading about what other people have had to sacrifice and how they've felt about having to say "no" to others. You guys are the best! THANK YOU!
libbiehyman | @libbiehyman
You have a wonderful sense of humor, Libbie! And a sense of humor is essential when dealing with our various infirmities. I have a dinner party this evening I'll soon need to get ready for. After reading your post, I find myself hoping that the hosts have a barre leading from their dinner table to their bathroom. LOL
Ray (@ray666)
Tell your hosts you'll come if they set their party up in a dance studio with your chair near the wall. Acquire some tulips or something and a passable bottle of wine and you'll be all set!
Regarding the vertigo and migraines, you might want to read up on Dysautonomia. My occasional dizziness that had developed over the past year has now changed to a distinct pattern. I didn’t realize this immediately. I was seen by a Dysautonomia specialist in February, and run through a gamut of tests. Turns out my blood pressure and heart rate fluctuate very little under testing (tilt table, etc). I’m starting to think that this specific pattern of dizziness is neurological (by that I mean a type of seizure) - something I plan to share with my neurologist this week. I have small fiber neuropathy, misdiagnosed as fibromyalgia until a year ago. All these other seemingly unrelated physical issues are most likely related to some weird diagnosis - my sister has the same symptoms.
I used to shy away from people because of inappropriate shoes for events. There is only one shoe that works for my brain, feet, safety, etc, and they’re not very dressy and look weird with shorts. I am so happy that I got to the point of not caring what other people think and how they might judge. People can’t help what they don’t know or understand. It’s all taught me a lot about compassion and relevance.