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Comments (1,172)

MGUS is considered asymptomatic and with a 1%/year risk of progressing to SMM or MM. However,...

https://connect.mayoclinic.org/comment/1238526/

MGUS 8 years as a follow up to my polyneuropathy

Discussion: MGUS and pain

Support Group: Blood Cancers & Disorders

Posted: Feb 16 4:52pm

This is what I found. On 3/12/21 it qas discontinued in the US. Most Recent Events...

https://connect.mayoclinic.org/comment/638056/

phase IIa trial for Distal sensory polyneuropathy

Discussion: Stage 2 Trials of Pirenzepine for Neuropathy

Support Group: Neuropathy

Posted: Sep 22, 2021

Hello @vradifegari -- I would like to add my welcome to Connect along with @gingerw and...

https://connect.mayoclinic.org/comment/266009/

Chronic Inflammatory Demyelinating Polyneuropathy ... Chronic-Inflammatory-Demyelinating-Polyneuropathy-CIDP-Information-Page

Discussion: Neuropathy and other strange symptoms

Support Group: Neuropathy

Posted: Jun 25, 2019

Hello John: First let me thank you very much for your timely reply and quantity of...

https://connect.mayoclinic.org/comment/219650/

Masquerading as Diabetic Autoimmune Polyneuropathy ... diagnosed with chronic axonal sensorimotor polyneuropathy

Discussion: In Search of Relief

Support Group: Neuropathy

Posted: Oct 12, 2018

Hi, I have a tens machine that came with slippers to hook up to little device...

https://connect.mayoclinic.org/comment/1381240/

that turns it on.I have idiopathic polyneuropathy

Discussion: I want to know more about TENS stimulation

Support Group: Neuropathy

Posted: Aug 28 11:24am

I have Sjogrens, SFN, Hashmotos, Ehlners Danlos, connective tissue disease, lupus, severe axonal sensorimotor peripheral polyneuropathy,...

https://connect.mayoclinic.org/comment/1278864/

severe axonal sensorimotor peripheral polyneuropathy

Discussion: Sjogren's and small fiber neuropathy: Seeing a rheumatologist

Support Group: Autoimmune Diseases

Posted: Apr 10 5:50pm

I have most of the same symptoms but I’m not dx’d with Fibromyalgia. I have Small...

https://connect.mayoclinic.org/comment/698646/

I have Small Nerve Fiber Polyneuropathy ... Small Nerve Fiber Polyneuropathy or

Discussion: How my Fibromyalgia started and the evolution of research

Support Group: Fibromyalgia

Posted: Apr 13, 2022

@vostie Its always good to hear LDN success stories. I’ve been on it for 10 years...

https://connect.mayoclinic.org/comment/1384983/

arthritis, fibromyalgia, and severe axonal Polyneuropathy

Discussion: Turning down invitations

Support Group: Post-COVID Recovery & COVID-19

Posted: Sep 2 11:18am

You are right there is no cure yet, but I just wanted to share with you,...

https://connect.mayoclinic.org/comment/735161/

diagnosis is severe axonal sensorimotor polyneuropathy

Discussion: Axonal peripheral neuropathy: Finally, a diagnosis!

Support Group: Neuropathy

Posted: Aug 8, 2022

@gretchie hi thanks for your reply. My fingers went into the “swan” position a few weeks...

https://connect.mayoclinic.org/comment/929608/

fibromyalgia, occipital neuralgia, polyneuropathy

Discussion: Sagittal Band Damage

Support Group: Bones, Joints & Muscles

Posted: Sep 13, 2023

Hi Dawn, I'm so happy to be in this group with others who know and feel...

https://connect.mayoclinic.org/comment/873791/

last week with bilateral peripheral polyneuropathy

Discussion: Living with Neuropathy - Welcome to the group

Support Group: Neuropathy

Posted: Jun 6, 2023

Just a suggestion on the shower comment - I have axonal polyneuropathy and balance is an...

https://connect.mayoclinic.org/comment/820093/

the shower comment - I have axonal polyneuropathy

Discussion: Axonal peripheral neuropathy: Finally, a diagnosis!

Support Group: Neuropathy

Posted: Mar 3, 2023

It’s interesting to read other people have the itch thing. In my case with Polyneuropathy I...

https://connect.mayoclinic.org/comment/626670/

In my case with Polyneuropathy I also

Discussion: Anyone here dealing with peripheral neuropathy?

Support Group: Neuropathy

Posted: Aug 15, 2021

I just wanted to share with you, that I also have had a lot of symptoms...

https://connect.mayoclinic.org/comment/700696/

diagnosis is severe axonal sensorimotor polyneuropathy

Discussion: Does anybody have experience with SANEXAS for neuropathy?

Support Group: Neuropathy

Posted: Apr 20, 2022

HI everyone my name is Jennifer I have been living with my neuropathy since 2014 since...

https://connect.mayoclinic.org/comment/683129/

everything that deals with the peripheral polyneuropathy

Discussion: Living with Neuropathy - Welcome to the group

Support Group: Neuropathy

Posted: Feb 21, 2022

@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, 2024

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, 2024

@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

@putsy it sounds to me like you are doing everything, and more to help yourself. Mayo...

https://connect.mayoclinic.org/comment/1376377/

I’ve had Polyneuropathy for 10 years

Discussion: Has anyone found a treatment that helps with peripheral neuropathy?

Support Group: Neuropathy

Posted: Aug 22 1:38am

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, 2024