Non-Length Dependent Small Fiber Neuropathy
there is much discussion of PN but seldom is much said about non-length dependent neuropathy. I guess it must be relatively rare. The condition affects all different parts of the body. I think it is usually idiopathic as is mine is. I was diagnosed with it more than 10 years ago. I’d like to hear from others with this type of small fiber neuropathy.
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Care to elaborate on what you can't take since you are on Eliquis? I'm in the same kettle of fish.
Thank you, kathleen123. If you are willing to share, what treatments are taking?
Hi, John. First I want to thank you for being so diligent and responsive on the forum. You are great.
Mine did not start out with my feet. It started with left side of my face tingling and my left arm and hand. Then it traveled to my feet and my right arm and hand within a month. I have tingling and "stabbing needles" sensation. My tongue started tingling as well. I also have internal "buzzing" sensation especially at night. Went through extensive testing to rule out MS, multiple myeloma, etc.
Right now, my symptoms are not that bad. I am on 300mg gabapentin once per day. I am trying to minimize drugs as much as possible. I've been getting acupuncture which seems to help especially my face. I am worried about how fast this can progress or if there is a possibility it can go away on its own.
Yes, my tongue and the roof of the tongue tingle which comes and goes throughout the day. My face (left side especially) feels tingling and "off". Lately, I also feel pressure (I can't really describe it as I've never felt this before) on the right cheekbone and near the right ear. I am a newbie to this diagnosis. I am on 300mg gabapentin once per day. I also take magnesium, r-lipoic acid and B12. I've been getting acupuncture (7 sessions so far) and it seems to help especially my face tingling. Of course, I am not sure if this is 100% attributable to acupuncture but I will take any improvement I can get. There seems to be very little information out there on progression. If anyone can share their experience, I'd really appreciate it.
@sf2021 I'm pretty sure I would have the same concerns as you do if I had the same symptoms. You mentioned that you've had extensive tests to rule out a few conditions like MS and multiple myeloma. I read in your other post that you have lately felt pressure on the right cheekbone near the ear. Have you discussed the new symptoms with your doctor? Just wondering if it may be providing more information to help with a diagnosis.
What to know about pressure in the head: https://www.medicalnewstoday.com/articles/326531#causes-and-other-symptoms
Thanks, do you have a formal diagnosis or is it "idiopathic"? I'm on a lot more gab than you and I don't take mag. because of that.
Hi
I have idiopathic neuropathy & it is progressive. I am not a diabetic. Is there any way they can find out why I have it? I did have abdominal surgery at the Mayo Clinic in 2018 & it was a difficult surgery so I am wondering if that had anything to do with it or was it the car accident I was in in 2007. I guess I will never know but the gabapentin does not help but when I forget to take a pill, I suffer terribly so you just don't know what to do. I have had this going on 2 years now & i just don't want to end up i a wheel chair.
Thank you for all your feed back. I lean a lot.
God Bless
Genie
I’ve not really found anything that helps the tingling, numbness type symptoms except good sleep and exercise. Because I have leg problems I can’t walk except for short distances around the house but I can really get my heart rate up with some of the chair exercises on YouTube.
I have not yet discussed with the neurologist as this is pretty new. I will do so if I continue to have the symptoms. Strangely, it does not feel like any type of a headache.
Idiopathic, I wish I knew what is causing it. I am most concerned about timeline and severity of progression.