Small Fiber Neuropathy: What helps?

Posted by lisadog33 @lisadog33, Mar 28, 2017

I have been diagnosed with Small Fiber Neuropathy. My problem is this. Since before they diagnosed me, I was having other symptoms that I thought were not related including loss of appetite/weight loss, bladder control, bowel control, problem with eyesight at times, tremors, sleep issues among some other things. I was told by my Neurologist that those things are not related to small fiber neuropathy but when I look it up, it says it can affect your autonomic nervous system. What is the truth. I am having a heck of a time with bladder and bowel issues as well as either sleeping through the alarm or not sleeping at all. I hope someone can shed some light on this for me. Thank you.

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Profile picture for unclefreddy @unclefreddy

Did the magnesium help?

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The magnesium did help with the severe foot cramps. Now the epsom salts seems to be helping with feeling in my toes

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Profile picture for madison2023 @madison2023

I take 200mg of magnesium before bed and 1000 B12 and vitamin D in the morning. According to my neurologist, magnesium is a supplement that can help but not hurt you. You should not take it on an empty stomach though.

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Magnesium glycimate is most absorbable. Vit Bs in a neuropathy natural supplement is safest. Many Bs are synthetic including the shots and are not absorbable and float in blood causing blood tests to be high.

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Is there a particular Vitamin B supplement brand that you recommend?

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Hello!

I also have a whole host of symptoms going on that were diagnosed as Peripheral Neuropathy caused by the Moderna Vaccine. That was in May of 2021.

I was just diagnosed with small fiber neuropathy and I am in hell! Ugh! I am having a spinal stimulator put in next Friday. I will update you guys a couple weeks after my surgery to let you know how it is helping.

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Profile picture for katee @katee

I believe that neuropathy is all about the nerve system. Read some more on it. Maybe also check if you have something else like fibromyalgia, have a read up on it. It can be diagnosed by a muscular skeletal physician.

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It is. You are exactly right.

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Profile picture for John, Volunteer Mentor @johnbishop

Welcome @tb01, I'm not sure @kfrenc04 saw your reply so I thought I would respond. Ugg boots are just a brand of boots that some folks find warm and comfortable. I've never had them before but have friends that like them. Here's a link to see what's available:
https://www.ugg.com/boots/.
Have you been diagnosed with neuropathy?

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Check out the uggcloset.com That is their outlet.

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I have idiopathic small fiber neuropathy. I do not have the bladder and bowel control issues. It’s mainly my toes - numbness and bluish/purple in shower and sometimes other times. PRP helped with those symptoms for almost 2 years. It’s starting to come back again. They weren’t sure how long it would help.

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Thanks to all about supplements! Progressive Labs in Irving, TX sells pharmacy strength supplements and I have been buying from them for over 25 years. I have an account through my nutritionist but I think that now they sell directly to the public. 800-527-9512 CST http://www.progressivelabs.com

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Profile picture for John, Volunteer Mentor @johnbishop

Hi @ashlely, Welcome to Mayo Connect. I also have non diebetic peripheral neuropathy and only have numbness but without pain in the feet and ankles. Thank you for sharing your tip about taking care of the feet - it's really important for those of us with PN of any diagnosis. I wear socks to bed after rubbing my feet together one night a few years ago and tearing open a blood vein near the surface of the ankle during the night. I woke up to go to the bathroom and felt the bed was wet near my feet but didn't realize it was blood. Then when in the bathroom I looked at my feet and noticed blood spray coming out of my ankle. The paramedics were able to stop the bleeding but took me to the ER anyway. Moral of my story is to keep the toenails trimmed and wear socks if you like to rub your feet together.

John

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John: I came across a special diet for neuropathy, but lost connection to my cell provider when traveling. Would you have a link to this diet ?

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Profile picture for pfszakacs @pfszakacs

John: I came across a special diet for neuropathy, but lost connection to my cell provider when traveling. Would you have a link to this diet ?

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I'm not sure I've seen a special diet but have seen a lot of nutritional food listings for people with neuropathy. The Foundation for Peripheral Neuropathy has a lot of information on their site on the topic - https://www.foundationforpn.org/living-well/lifestyle/nutrition/. They also have a webinar on the topic that might be helpful - https://www.foundationforpn.org/webinar-nutrition-for-patients-with-peripheral-neuropathy/.

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