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Comments (2,285)

spinal issues/ spinal cord damage Lyme disease EMF sensitivity MS Paresthesias, hyperesthesias, neuropathy etc. are terms...

https://connect.mayoclinic.org/comment/1138185/

damage Lyme disease EMF sensitivity MS

Discussion: What might be causing electric feelings in my body?

Support Group: Brain & Nervous System

Posted: Sep 8 8:39am

Hi @iceblue I'll answer your questions in order 1) Addiction and SFN really have nothing to...

https://connect.mayoclinic.org/comment/241374/

potential like opioids (e.g. vicodin, MS

Discussion: Small Fiber Neuropathy?

Support Group: Neuropathy

Posted: Oct 10, 2019

Hey all, MRI came back normal. Both good and bad-- good because I guess it means...

https://connect.mayoclinic.org/comment/247347/

I guess it means I don't have MS

Discussion: GI Disorder and Internal Shaking

Support Group: Digestive Health

Posted: Aug 19, 2019

Wow! Reading what you published here is like looking in the mirror! But I HAVE NOT...

https://connect.mayoclinic.org/comment/118391/

But I HAVE NOT been diagnosed with MS

Discussion: Multiple Sclerosis (MS) - please introduce yourself

Support Group: Brain & Nervous System

Posted: Aug 15, 2017

I got into my old neurologist office. She says at this time that my MS panel...

https://connect.mayoclinic.org/comment/118512/

She says at this time that my MS panel

Discussion: Multiple Sclerosis (MS) - please introduce yourself

Support Group: Brain & Nervous System

Posted: Jul 3, 2019

@sbraden1234 He knows, but I don't think he wants to admit to a result that is...

https://connect.mayoclinic.org/comment/1171442/

may be an inflammatory problem like MS

Discussion: MRI results and Pain symptoms not matching. Dr says nothing he can do.

Support Group: Spine Health

Posted: Nov 10 8:28pm

Hi! Wondering if you’ve had a punch biopsy? A punch biopsy can help determine whether you...

https://connect.mayoclinic.org/comment/747825/

spinal tap w/ results leading to a MS ... Though I’m not happy to have MS, I’m ... MS van have wide ranging symptoms …

Discussion: New to neuropathy, terrified and seeking advice from you guys

Support Group: Neuropathy

Posted: Sep 10, 2022

I do vegan keto for brain fog, because with MS I was suddenly reacting to sugar,...

https://connect.mayoclinic.org/comment/1140219/

vegan keto for brain fog, because with MS ... lemon juice ( I have liquid diet, MS

Discussion: anyone tried vortioxetine for the treatment of brain fog from autoimmu

Support Group: Autoimmune Diseases

Posted: Sep 12 7:36am

Thank you. I have reached out to Harriet who has kindly offered to talk with me....

https://connect.mayoclinic.org/comment/696758/

Her mother has MS and was diagnosed

Discussion: Grand Parents Raising Grandchild

Support Group: About Kids & Teens

Posted: Apr 7, 2022

Hi @disneyfan, How are your side effects tonight? Same, better, worse? I came across this article...

https://connect.mayoclinic.org/comment/118409/

I came across this article from MS News

Discussion: Multiple Sclerosis (MS) - please introduce yourself

Support Group: Brain & Nervous System

Posted: Aug 28, 2017

Hi @tigreyes2004 - Were you diagnosed with nephropathy or neuropathy? I started looking into nutrition to...

https://connect.mayoclinic.org/comment/157810/

amazing story of how she helped her MS

Discussion: Living with Neuropathy - Welcome to the group

Support Group: Neuropathy

Posted: Sep 6, 2019

Accuracy is important 😊 I just was hoping that auto immune could be treated better, Someone...

https://connect.mayoclinic.org/comment/1068487/

demylenation, but it's not called ms

Discussion: Lesions on the brain and autoimmune disease

Support Group: Autoimmune Diseases

Posted: May 15 2:09pm

Northwest GA is beautiful!-- & how amazing you were able to follow your dream. It sounds...

https://connect.mayoclinic.org/comment/1127031/

I have had MS for over 40 years &amp

Discussion: A question came to mind regarding hope.

Support Group: Aging Well

Posted: Aug 19 7:18pm

All good comments and experiences we can learn from. Including the anger - - just let...

https://connect.mayoclinic.org/comment/1128739/

My wife of 53 years had Progressive MS

Discussion: The ways others react to news of your prostate cancer

Support Group: Prostate Cancer

Posted: Aug 22 11:59am

@lcamino Lynn, I had little time this weekend and my devices were being ornery so I...

https://connect.mayoclinic.org/comment/138658/

after just eating a handful of M&Ms

Discussion: New Transplant Blog Posts

Support Group: Transplants

Posted: Aug 13, 2017

I got prosthetic teeth for the lower left after my mandiblectomy. I did not have tongue...

https://connect.mayoclinic.org/comment/956472/

As my wife who has MS in addition to

Discussion: Radiation side effects with H&N cancer. When will they ever end?

Support Group: Head & Neck Cancer

Posted: Oct 30, 2023

I agree w/cwal, airway clearance for me is HUGE. I use a nebulizer w/albuterol 2xs day,...

https://connect.mayoclinic.org/comment/1078815/

Have broncheactasis for 7 yrs, MS 40

Discussion: Newly Dx Advise, Tips Needed

Support Group: MAC & Bronchiectasis

Posted: Jun 1 8:04am

I am so Rory you have been put through so much. I don’t have pn but...

https://connect.mayoclinic.org/comment/1106313/

not enough markers, a little like ms

Discussion: Be aware

Support Group: Neuropathy

Posted: Jul 15 10:05pm

Yes, it is difficult to explain to people just how uncomfortable this feeling is. If you...

https://connect.mayoclinic.org/comment/729228/

Some people with MS have what is called ... MS Hug apparently. but I do not have ... MS.

Discussion: Rib cage tightness: Not sure what it might be

Support Group: Digestive Health

Posted: Jul 21, 2022

Thank you so much for responding. To answer your question, I just want to be his...

https://connect.mayoclinic.org/comment/836467/

that was where he was diagnosed with MS

Discussion: Hairy Cell Leukemia

Support Group: Blood Cancers & Disorders

Posted: Apr 2, 2023