Polyneuropathy – search | You searched for comments

To narrow your search, try adding quotation marks around phrases.

Search tips

Search by keywords or complete phrases.
To narrow your search, try adding quotation marks around phrases.
Example: "predictable behavior" will narrow the search results to only include content that has the exact phrase "predictable behavior" in it.

1,064 total results

Comments (969)

@2dogman welcome! I also have severe polyneuropathy. My neurologist gave me Gabapentin, but I could not...

https://connect.mayoclinic.org/comment/961102/

I also have severe polyneuropathy.

Discussion: Psychological effects of living with neuropathy

Support Group: Neuropathy

Posted: Nov 8, 2023

My toxin was too much Vitamin B6. I thought I could help my neuropathy in my...

https://connect.mayoclinic.org/comment/1030899/

dehydrating event caused Small Fiber Polyneuropathy

Discussion: Neuropathy caused by toxins, poisons and chemicals

Support Group: Neuropathy

Posted: Mar 10 8:49am

@fred101 Fred, thanks for your willingness to put your life on the line back then. With...

https://connect.mayoclinic.org/comment/1110169/

I have Polyneuropathy .

Discussion: Living with Neuropathy - Welcome to the group

Support Group: Neuropathy

Posted: Jul 22 8:27pm

Hello. Old Karl here. Lots of issues. Probably AL amyloidosis, systemic, hereditary. Constant headache pain for...

https://connect.mayoclinic.org/comment/94815/

psoriatic arthritis, rheumatoid arthritis, polyneuropathy

Discussion: Chronic Pain members - Welcome, please introduce yourself

Support Group: Chronic Pain

Posted: Oct 5, 2016

Welcome new members @gratefulone @jazzy27 @lindy1956 and @suziep. I invite you to join this discussion about...

https://connect.mayoclinic.org/comment/81489/

(chronic inflammatory demylenating polyneuropathy

Discussion: Anyone been diagnosed with CIDP? It's very rare

Support Group: Autoimmune Diseases

Posted: Apr 11, 2017

Hi Ray, Here I thought ANS had another spoke to it's wheel, shorter weeks! Just experenced...

https://connect.mayoclinic.org/comment/1114085/

and could be like without Autonomic polyneuropathy

Discussion: PN and handwriting …

Support Group: Neuropathy

Posted: Jul 29 1:36pm

That’s the problem I ran into. I got my questions answered and she wrote my doctors...

https://connect.mayoclinic.org/comment/1140506/

severe axonal sensorimotor peripheral polyneuropathy ... Small fiber polyneuropathy dysautonomia

Discussion: Interview with SFN researcher, Dr. Lawrence Zeidman (Reddit)

Support Group: Neuropathy

Posted: Sep 12 2:19pm

@davidpn - As the expression goes, join the club! I have polyneuropathy and find walking very...

https://connect.mayoclinic.org/comment/897442/

I have polyneuropathy and find walking

Discussion: Fatigue from Walking

Support Group: Neuropathy

Posted: Jul 17, 2023

I have polyneuropathy and my feet are pretty much numb. I have been going back and...

https://connect.mayoclinic.org/comment/606558/

I have polyneuropathy and my feet are

Discussion: COVID vaccines and neuropathy

Support Group: Neuropathy

Posted: Jun 3, 2021

@sunnyflower and @lorirenee1. I have experienced occasional burning and aching around and just above my knees...

https://connect.mayoclinic.org/comment/316845/

Polyneuropathy is equal opportunity

Discussion: Update on my DRG stimulator Implant. Implanted 12 days ago.

Support Group: Neuropathy

Posted: Aug 26, 2020

Hello @aggie98. Welcome to Connect. I think you will find support here that will be helpful...

https://connect.mayoclinic.org/comment/99104/

Peripheral Neuropathy too (Small Fiber Polyneuropathy

Discussion: Chronic Pain members - Welcome, please introduce yourself

Support Group: Chronic Pain

Posted: Jul 16, 2020

I was diagnosed with sfn and sensory polyneuropathy in February of this year by an emg...

https://connect.mayoclinic.org/comment/1044807/

was diagnosed with sfn and sensory polyneuropathy

Discussion: Treatment options that have worked for Small Fiber Neuropathy

Support Group: Neuropathy

Posted: Apr 3 12:59pm

Hello @helenwheels, Welcome to Connect. There are a few other discussions you may be interested in...

https://connect.mayoclinic.org/comment/614753/

. -- Axonal Sensorimotor Polyneuropathy

Discussion: IS IT NEUROPATHY

Support Group: Neuropathy

Posted: Jul 7, 2021

I had one injection. Had Sharp pain during but went well after. About 4 months later...

https://connect.mayoclinic.org/comment/103470/

Axonal Neuropathy and small fiber polyneuropathy

Discussion: Arachnoiditis: Trying to find a specialist

Support Group: Spine Health

Posted: Apr 2, 2020

Toe twitching that kept me awake at night was the first symptom of my Pfizer vaccine...

https://connect.mayoclinic.org/comment/820757/

subsequently developed sensory and motor polyneuropathy

Discussion: Jittery feeling, toe twitching, involuntary leg movements and more

Support Group: Brain & Nervous System

Posted: Mar 4, 2023

If you missed the first one, the Foundation for Peripheral Neuropathy is having another webinar on...

https://connect.mayoclinic.org/comment/926908/

Understanding the Connection Between Polyneuropathy

Discussion: Amyloidosis. Diagnosis, treatment, frustration. AL, hATTR, etc.

Support Group: Autoimmune Diseases

Posted: Sep 9, 2023

Yes mee too, I have also that sensation of acid reflux and a lot of saliva...

https://connect.mayoclinic.org/comment/1012257/

My polyneuropathy affects also my sweat

Discussion: PN & Acid Reflux?

Support Group: Neuropathy

Posted: Feb 9 6:17am

I also fell suddenly…into a rose bush. It felt like I “missed a beat” when I...

https://connect.mayoclinic.org/comment/1188966/

found I had first stages of Idiopathic Polyneuropathy

Discussion: Falling for no apparent reason: Any ideas?

Support Group: Brain & Nervous System

Posted: 4 days ago

Hi, @sdswoboda53 - welcome to Mayo Clinic Connect. I'd be scared, too, if I began having...

https://connect.mayoclinic.org/comment/81513/

chronic inflammatory demyelinating polyneuropathy ... chronic-inflammatory-demyelinating-polyneuropathy

Discussion: Anyone been diagnosed with CIDP? It's very rare

Support Group: Autoimmune Diseases

Posted: Jan 29, 2019

@rdg063 I've very sorry to hear you've been misguided. Of course you may have neuropathy without...

https://connect.mayoclinic.org/comment/211000/

deficiency causing Small Fiber Peripheral Polyneuropathy

Discussion: Looking to connect with people who have non-diabetic neuropathy

Support Group: Neuropathy

Posted: Jul 7, 2020