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1,064 total results

Comments (969)

@artemis1886 How are you being treated for your CAN? How were you diagnosed with severe axonal...

https://connect.mayoclinic.org/comment/1068153/

diagnosed with severe axonal sensorimotor polyneuropathy

Discussion: Has anyone had a tilt table test or examination?

Support Group: Autoimmune Diseases

Posted: May 15 6:48am

I developed B6 Toxicity from ingesting 100 MG B Complex for 4 months. My primary symptom...

https://connect.mayoclinic.org/comment/1065841/

are others caused by the Small Fiber Polyneuropathy

Discussion: Neuropathy: What works and what are scams?

Support Group: Neuropathy

Posted: May 11 8:01am

Hey @10987654321. I'm reading your posts yet do not understand if you are working with a...

https://connect.mayoclinic.org/comment/319309/

recipient of Small Fiber Peripheral Polyneuropathy

Discussion: Neuropathy arms legs 27 yrs old progressing brain confusion

Support Group: Brain & Nervous System

Posted: Aug 24, 2020

I take Tegretol for small fiber polyneuropathy. It diminishes the burning pain and has few side...

https://connect.mayoclinic.org/comment/995536/

I take Tegretol for small fiber polyneuropathy

Discussion: Does anyone take Tegritol for burning mouth syndrome

Support Group: Chronic Pain

Posted: Jan 11 10:56am

My husband also a big drinker had his legs give out. He was also given a...

https://connect.mayoclinic.org/comment/744546/

chronic inflammatory demyelinating polyneuropathy

Discussion: Falling for no apparent reason: Any ideas?

Support Group: Brain & Nervous System

Posted: Sep 2, 2022

Hi Rags, Recently as ordered by my pain management doctor I had an EMG and nerve...

https://connect.mayoclinic.org/comment/258784/

testing showed severe sensorymotor polyneuropathy

Discussion: CRPS or Peripheral Neuropathy

Support Group: Brain & Nervous System

Posted: Apr 19, 2019

Thanks, John. I've had hundreds of labs, nerve conduction studies/EMGs repeatedly, and nerve biopsy, PET, MRIs,...

https://connect.mayoclinic.org/comment/194222/

biopsy, PET, MRIs, CAT scans, and the polyneuropathy

Discussion: Zero appetite, not getting adequate nutrition

Support Group: Autoimmune Diseases

Posted: Mar 28, 2018

Yes, some of the supplements are for various types of neuropathy. Also, sometimes, it's really for...

https://connect.mayoclinic.org/comment/1132253/

Also, sometimes, it's really for polyneuropathy

Discussion: Neuropathy Supplements - are they for all types of neuropathy?

Support Group: Neuropathy

Posted: Aug 28 9:58am

@helennicola @avmcbellar Helen, just FYI, 4 days ago @hazelnut posted this: "I had a ultra sound...

https://connect.mayoclinic.org/comment/243907/

The neurologist believes it also polyneuropathy

Discussion: Shingrix and peripheral neuropathy

Support Group: Neuropathy

Posted: Sep 17, 2020

My experience with standing and not moving, even for only a matter of minutes, is similar,...

https://connect.mayoclinic.org/comment/1005931/

diagnosis is idiopathic axonal large fiber polyneuropathy

Discussion: Feet and legs tingle and shake when standing for less than a minute

Support Group: Neuropathy

Posted: Jan 29 12:35pm

I ended up being diagnosed with fibromyalgia in 2002 secondary to the bacterial spinal meningitis. The...

https://connect.mayoclinic.org/comment/1096585/

have also severe axonal sensorimotor polyneuropathy

Discussion: Chronic painful muscle knots, widespread

Support Group: Bones, Joints & Muscles

Posted: Jun 30 12:49am

EMG/nerve conduction test Small fiber neuropathy is Two to three skin biopsies One doctor did three...

https://connect.mayoclinic.org/comment/1112204/

Severe axonal sensorimotor peripheral polyneuropathy

Discussion: Question: What testing have you had for neuropathy?

Support Group: Neuropathy

Posted: Jul 26 10:29am

Welcome @mrsmary, You mentioned your neuropathy started shortly after taking Anastrozole and then you switched to...

https://connect.mayoclinic.org/comment/707769/

Inhibitors Cause Sjogren’s Syndrome and Polyneuropathy

Discussion: Shingrix and peripheral neuropathy

Support Group: Neuropathy

Posted: May 13, 2022

Hi @hertz, Welcome to Connect. The best thing you can do to help yourself is learn...

https://connect.mayoclinic.org/comment/157769/

discussion to meet others discussing polyneuropathy

Discussion: Living with Neuropathy - Welcome to the group

Support Group: Neuropathy

Posted: Sep 2, 2019

@sparshall I have idiopathic small fiber peripheral polyneuropathy. I'm not familiar with the implication of the...

https://connect.mayoclinic.org/comment/93004/

idiopathic small fiber peripheral polyneuropathy

Discussion: Anyone here dealing with peripheral neuropathy?

Support Group: Neuropathy

Posted: Jan 15, 2020

I haven't had IV1g influsions. Are her kidney function tests good? IV1g can impact kidneys. My...

https://connect.mayoclinic.org/comment/897170/

My polyneuropathy is still early and

Discussion: IVIg Infusions for autoimmune neuropathy

Support Group: Autoimmune Diseases

Posted: Jul 17, 2023

My posts are always about my husband. Just fyi. His handwriting used to be beautiful and...

https://connect.mayoclinic.org/comment/915994/

tremor most of his adult life but the polyneuropathy

Discussion: PN and penmanship …

Support Group: Neuropathy

Posted: Aug 20, 2023

I was diagnosed with Idiopathic Axonal sensorimotor polyneuropathy 4-1/2 years ago. My doctor offered no treatment...

https://connect.mayoclinic.org/comment/922092/

with Idiopathic Axonal sensorimotor polyneuropathy

Discussion: Questions on IVIg treatment for what I have: Axonal sensory-motor

Support Group: Neuropathy

Posted: Aug 31, 2023

Not after covid, maybe because I already have a collection of autoimmune diseases. After catching H1N1...

https://connect.mayoclinic.org/comment/1011680/

The polyneuropathy and collagenous colitis

Discussion: Has anyone been diagnosed with an autoimmune disease after covid?

Support Group: Post-COVID Recovery & COVID-19

Posted: Feb 8 7:28am

Generally, the doctor will order blood tests every few months (60 mo. interval for me). I...

https://connect.mayoclinic.org/comment/1123341/

I was diagnosed with polyneuropathy

Discussion: MGUS diet: Any tips on food to enjoy or prevent progression?

Support Group: Blood Cancers & Disorders

Posted: Aug 14 7:08am