Small fiber neuropathy?
I never had a biopsy to dx it. I’m wondering if I have the biopsy does it make a difference in the therapies? A year ago I was dx’d with severe chronic nerve damage in lumbar and cspine: polyradiculopathy.
I have severe pain and spasms in lumbosacral back, legs and feet since 2021.
In the summer of 2023 I started (an continue having) get spasms in the trapezeous muscles on the right.
I’m currently flaring with bad pains to both shoulder that is crippling then after a long while it disappears. I developed lightning like pains to the bottoms of my feet and toes. The only thing that seemingly helps the surface pain is the lidocaine cream I apply. So far…
The neuromuscular doctor said last year no long fiber neuropathy per the nerve conduction study. She said I’d need a biopsy to determine if i have sfn.
An old nerve doctor said I had demyelination in left leg she thought secondary to diabetes. WEll, the diabetes hasnt climbed to damaging enough numbers to put me in flair much less cause the demyelination.
The foot dr last week gave referral for feet, for neuropathy and balance. So this confuses me. It all does.
I’d like to know if SNF can move around the body and cause the tingling in forarms and fingers and can the pain in SNF affect the very surface of the skin?
If someone can make sense of what Ive written I’d appreciate any help insight or feedback.
I have not received a diagnosis regarding the polyradiculopathy. I’m going to press the doctors for answers now because it’s really out of control.
Interested in more discussions like this? Go to the Neuropathy Support Group.
Thank you Art. When it affects the heart and blood pressure, do the two happen simultaneously? Or can you have low 50;s. To 60’shr (from high heart rate 90’s for a year and then have the blood pressure go to 107/75 where it is usually higher. Not saying there is a link but I don’t understand why there is a change. When do you tell the neurologist about a strange heart rate? I am on blood pressure meds, same ones for long time. Don’t want to overthink it but don’t want to ignore what might be important signs. Thank you.
One thing that immediately reduced my foot and hand tingling, and the burning sensation, was eliminating all processed sugar from my diet. You could try that for a day or two and see if it helps. I eat fruit, but not fruit juices or items with lots of natural sugar.
Here is a DMSO link. //www.healthline.com/health/what-is-dmso#What-is-DMSO? As to the spinal stimulator, that is my question, too. My doctor wants me try it so I'm looking for experiences to help me decide.
I have been told by several doctors that SFN is life altering but not life threatening and have read pretty much the same. May I ask where you got your information? Thanks.
Is your SFN from diabetes? My labs come back negative for diabetes. In the 5+ years I 've had SFN no cause can be found.
I hard arrhythmias first.. Scared me. I have a son with congenital heart disease that almost died from tachycardia. My heart started jumping in my sleep. It would stop and when it started back up it would jump and wake me up. I was afraid to go back to sleep. I had a one month holter monitor test showed the bradycardia and tachycardia. I was sent to a electrophysiologist that diagnosed with cardiac autonomic neuropathy. Being a RN I told him he was lying. I went to the neurologist and had the biopsies. Within the
last six months my BP has been high. 159/99. The arrhythmias have started back up so the cardiologist and electrophysiologist decided to do another one month holter monitor on me. We will see what happens from here. The BP medication made me nauseous and throwing up so we stopped it.
No diabetes. Right now it’s idiopathic sfn. Sugar is apparently a trigger for inflammation, causing symptoms….
Before it went high it was always low.
I’m so sorry for what you’re enduring. I hope they find answers that can help you. 🤗
I developed nerve damage in my feet as a result of my high immunity kicking in to protect my feet from the foot operation I had to remove a neuroma. My immune system went in to protect my feet but instead attacked the nerves in my feet. Hence the serious damage. Fortunately it can be reversed. Doesn’t happen often apparently. USA has far more advanced methods of working out what nerve damage has occurred than where I live so it was in the USA that type of damage was assessed and then treatment could be started. I’m very fortunate.