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2,506 total results

Comments (2,285)

I have MS and fibromyalgia. I've had excruciating pain running down my left butt cheek down...

https://connect.mayoclinic.org/comment/786778/

I have MS and fibromyalgia.

Discussion: Tarlov Cyst on the spine: Any advice?

Support Group: Spine Health

Posted: Dec 19, 2022

I worked for a major pharmaceutical company for over 30 years. Clinical trials obviously are necessary,...

https://connect.mayoclinic.org/comment/694257/

are large numbers of drugs to treat MS

Discussion: Idiopathic Small Fiber Neuropathy Research

Support Group: Neuropathy

Posted: Mar 29, 2022

I have fibro, ms, sjogrens, cfs, lupus, peripheral neuropathy-100 types of neuropathy. I would see a...

https://connect.mayoclinic.org/comment/211835/

I have fibro, ms, sjogrens, cfs, lupus

Discussion: Financial strain of having multiple autoimmune diseases

Support Group: Autoimmune Diseases

Posted: Oct 19, 2018

My rehabilitative and physical medicine specialist and my gynecologist refer me to pelvic floor PT. I...

https://connect.mayoclinic.org/comment/845983/

And my MS benefited for the same therapy

Discussion: Low Back Pain May Be Sacroiliac Joint Inflammation, Special Treatment

Support Group: Bones, Joints & Muscles

Posted: Apr 19, 2023

Hello Everyone, I have PN in feet and legs and restless leg as well. The Neurologist...

https://connect.mayoclinic.org/comment/91625/

livable again as the treatment helps MS

Discussion: Anyone here dealing with peripheral neuropathy?

Support Group: Neuropathy

Posted: Sep 18, 2016

I’ve had 13 bone marrow biopsies and from experience I’ve chosen to have mild sedation with...

https://connect.mayoclinic.org/comment/889996/

xfe0f; It’s good news to hear your MS

Discussion: Does anyone else have MGUS?

Support Group: Blood Cancers & Disorders

Posted: Jul 4, 2023

Don't know if this will help of not. My husband was diagnosed with transverse myelitis after...

https://connect.mayoclinic.org/comment/860743/

We were concerned about ALS and MS

Discussion: Need some insight. Cannot see neurologist for 7 months.

Support Group: Brain & Nervous System

Posted: May 16, 2023

I already see a Rheumatologist thank you for the feed back I was diagnosed with RA...

https://connect.mayoclinic.org/comment/872984/

with RA when I was a TEEN I have MS

Discussion: Autoimmune Diseases are relentless

Support Group: Autoimmune Diseases

Posted: Jun 5, 2023

Dear Serry. I am sorry to hear about the MS and your concerns. You need positive...

https://connect.mayoclinic.org/comment/960708/

I am sorry to hear about the MS and

Discussion: dent in leg

Support Group: Neuropathy

Posted: Nov 7, 2023

@kgitti I am waiting to be tested for MS and CIDP. The symptoms are terrible and...

https://connect.mayoclinic.org/comment/1045095/

kgitti I am waiting to be tested for MS

Discussion: Has anyone really gotten over CIDP?

Support Group: Autoimmune Diseases

Posted: Apr 4 7:20am

I am not a nonvaccine person. I simply had an allergic reaction that affected my nervous...

https://connect.mayoclinic.org/comment/960712/

When I am in remission I mimmic MS but

Discussion: COVID vaccines and neuropathy

Support Group: Neuropathy

Posted: Nov 7, 2023

Hello Ms. Merry, Thank you. Yes, I am hopeful that the take away is, while documents...

https://connect.mayoclinic.org/comment/698438/

Hello Ms. Merry, Thank you.

Discussion: It’s because I love you…

Support Group: Just Want to Talk

Posted: Apr 12, 2022

Hello @sophiageld and welcome to the Digestive Health support group on Mayo Connect. So many can...

https://connect.mayoclinic.org/comment/993643/

or a neurological disorder such as MS

Discussion: Do any of you have paralysis of muscles that move food from stomach to

Support Group: Digestive Health

Posted: Jan 8 8:42am

Look into multiple sclerosis or myasthenia gravis as possibilities. Try a different neurologist maybe at Mayo...

https://connect.mayoclinic.org/comment/1093882/

I was tested for suspected ALS, MS,

Discussion: Mabye ALS? Alot of weird symptoms...

Support Group: Neuropathy

Posted: Jun 25 10:33am

I’ve been on IVIG / SCIG since 2021 for CIDP and occasionally steroids too following viruses....

https://connect.mayoclinic.org/comment/1111338/

then slight improvement aided by PT (ms

Discussion: CIDP (Chronic Inflammatory Demyelinating Polyneuropathy)

Support Group: Autoimmune Diseases

Posted: Jul 24 10:55pm

Hi there, I am 76 with advanced MS. My lesions are all In my brain so...

https://connect.mayoclinic.org/comment/1114602/

Hi there, I am 76 with advanced MS.

Discussion: Choosing palliative care; what is your experience?

Support Group: Cancer: Managing Symptoms

Posted: Jul 30 11:42am

My husband has similar symptoms and it’s been frustrating. He has right side weakness that is...

https://connect.mayoclinic.org/comment/869704/

He was diagnosed with MS when he experienced ... worst pain for my husband over the MS

Discussion: need help

Support Group: Brain & Nervous System

Posted: May 31, 2023

I have a bit of a unique situation. Not long after the covid jab I started...

https://connect.mayoclinic.org/comment/1164661/

It ultimately turned into an MS diagnosis

Discussion: Pineal Cyst: What symptoms led to your diagnosis?

Support Group: Brain Tumor

Posted: Oct 29 11:51am

I have SFN and in November was given the diagnosis. I also have 3 small brain...

https://connect.mayoclinic.org/comment/224493/

MS thought it was all psychological. ... MS doc thinks it may be early stages ... of MS, but referred me to neuromuscular

Discussion: Does Small Fiber Neuropathy also cause muscle spasms?

Support Group: Neuropathy

Posted: Dec 15, 2020

Thanks for sharing💖... I'm so hesitant about trying medications due to my history of complicated and...

https://connect.mayoclinic.org/comment/1118165/

My MS Specialist neurologist (the one ... My lesions do not follow the MS norm ... taking med/injections prescribed for MS

Discussion: Brain Demyelinating diseases OTHER than MS

Support Group: Brain & Nervous System

Posted: Aug 5 8:57am