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2,506 total results

Comments (2,285)

Thank you! Why mess with what works?! I don’t and have never abused my meds. I...

https://connect.mayoclinic.org/comment/849042/

first post about being diagnosed with MS

Discussion: How am I going to manage getting cut off my Valium after years ?!

Support Group: Mental Health

Posted: Apr 25, 2023

Hi again Betty. My doctor doesn't know the cause. We ruled out ALS and MS, ruled...

https://connect.mayoclinic.org/comment/903964/

We ruled out ALS and MS, ruled out autoimmune

Discussion: Shingrix and peripheral neuropathy

Support Group: Neuropathy

Posted: Jul 29, 2023

Thank you for your posts about the TG6 test. I, too, saw the webinar with the...

https://connect.mayoclinic.org/comment/996679/

I seem to be ruled out for MS and Lupus

Discussion: Anti-tranglutaminase-6 antibody test - Gluten Sensitivity Test

Support Group: Digestive Health

Posted: Jan 13 2:04pm

Yes I use it and have been for a few months. With great success actually. I...

https://connect.mayoclinic.org/comment/1032824/

I have MS (Multiple Sclerosis) and my

Discussion: Anyone tried Accelera SR 100 device? Or Walkasins?

Support Group: Neuropathy

Posted: Mar 13 10:58am

I also a very disappointed that Mayo isn’t taking any new neurology patients. I have been...

https://connect.mayoclinic.org/comment/1117638/

Nothing helped my symptoms, and MS was

Discussion: I have a neurological illness that has puzzled doctors.

Support Group: Brain & Nervous System

Posted: Aug 4 10:46am

I have had Trigeminal-Neuralgia since 2005. It started small. Which it came on short shocks. Then...

https://connect.mayoclinic.org/comment/818479/

And then all my other MS problems I

Discussion: Multiple Sclerosis (MS) - please introduce yourself

Support Group: Brain & Nervous System

Posted: Feb 28, 2023

Another update. It has now been almost three weeks since my last treatment. My pain continues...

https://connect.mayoclinic.org/comment/757018/

every bra recommended by people with MS

Discussion: Has anyone tried Scrambler Therapy for neuropathy or for pain?

Support Group: Neuropathy

Posted: Oct 4, 2022

Hi Barbara Rene' (@barbararene) - Think happy thoughts about PMR going into remission. My first occurance...

https://connect.mayoclinic.org/comment/137601/

significantly improve the symptoms of her MS

Discussion: How to address PMR pain while decreasing prednisone

Support Group: Polymyalgia Rheumatica (PMR)

Posted: Feb 24, 2017

To not require pre-approval by your insurance providers for your clonazepam especially since you’re taking MS...

https://connect.mayoclinic.org/comment/286154/

clonazepam especially since you’re taking MS

Discussion: My clonazepam story: More regulation seems to be coming

Support Group: Addiction & Recovery

Posted: Oct 24, 2020

The left side of my face is numb. I had an MRI to check for acoustic...

https://connect.mayoclinic.org/comment/868434/

ps it can be a sign of MS but I don&

Discussion: Small Fiber Neuropathy and Face?

Support Group: Neuropathy

Posted: May 29, 2023

Oh my gosh, I'm so sorry you're going thru all of this and that those doctors...

https://connect.mayoclinic.org/comment/247339/

movements and am wondering if it's MS

Discussion: GI Disorder and Internal Shaking

Support Group: Digestive Health

Posted: Aug 11, 2019

Hello @sbrokenshire. that is certainly a lot of symptoms and potential diagnoses to be thinking about...

https://connect.mayoclinic.org/comment/244233/

connect.mayoclinic.org/discussion/multiple-sclerosis-ms-please-introduce-yourself

Discussion: I just need answers.

Support Group: Just Want to Talk

Posted: Feb 3, 2019

Ronc, I also was a caregiver for my wife who had MS and was quadriplegic for...

https://connect.mayoclinic.org/comment/985454/

was a caregiver for my wife who had MS

Discussion: Where to draw the line between active surveillance, removal, radiation

Support Group: Prostate Cancer

Posted: Dec 23, 2023

I didn't have a brain biopsy. My lesions are deep in the pons and both my...

https://connect.mayoclinic.org/comment/706808/

confirm that it's CLIPPERS and not MS

Discussion: CLIPPERS: Looking to connect with others

Support Group: Autoimmune Diseases

Posted: May 9, 2022

I didn't even know I had the seizure until the next day, my husband thought I...

https://connect.mayoclinic.org/comment/184217/

thought I was having symptoms related to ms

Discussion: Watching a Meningioma Brain Tumor

Support Group: Brain Tumor

Posted: Feb 28, 2019

I was diagnosed with Achalasia in early 2009, and was operated on at the age of...

https://connect.mayoclinic.org/comment/49862/

Oddly enough, he was living in MS at

Discussion: Achalasia

Support Group: Digestive Health

Posted: Jan 5, 2012

Hello @nmo2016 Welcome to Connect. Neuromyelitis optica (Devic’s disease) is complex, and care for it is...

https://connect.mayoclinic.org/comment/211192/

misdiagnosed as multiple sclerosis (MS

Discussion: Neuromyelitis optica (NMO)

Support Group: Autoimmune Diseases

Posted: Aug 7, 2018

My internal vibrating or shakiness started spring of last year and has only gotten worse since....

https://connect.mayoclinic.org/comment/214481/

I don't have Parkinson's, MS

Discussion: Monthly shaking episodes that continue to progress

Support Group: Brain & Nervous System

Posted: Dec 12, 2018

I gave Buprenorphine a try for over a year, hoping I could switch to that from...

https://connect.mayoclinic.org/comment/1028407/

hoping I could switch to that from the MS

Discussion: Chronic Pain members - Welcome, please introduce yourself

Support Group: Chronic Pain

Posted: Mar 6 4:11am

Since I was diagnosed with sfpn or CIDP, I've seen neurologists, pain specialists, a pain therapist...

https://connect.mayoclinic.org/comment/966206/

dose Naltrexone before I go back to MS

Discussion: What type of doctor do you get your PN care from?

Support Group: Neuropathy

Posted: Nov 17, 2023