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Comments (2,285)

Thanks for posting this Nate...I enjoyed the link for the "squatty potty" link. May have to...

https://connect.mayoclinic.org/comment/104567/

research into nutrition and causes for MS

Discussion: Specific Carbohydrate Diet

Support Group: Digestive Health

Posted: Sep 9, 2016

I have an appt scheduled in early January but have requested an earlier appt. I'm on...

https://connect.mayoclinic.org/comment/660292/

an auto immune disorder (lupus or MS

Discussion: Want to hear from others who have Stage 4 Chronic Kidney Disease (CKD)

Support Group: Kidney & Bladder

Posted: Dec 7, 2021

I’m going through the same thing now Craig. As I read your post I was like,...

https://connect.mayoclinic.org/comment/335162/

hours searching for symptoms of ALS, MS

Discussion: Weakness, tingling, hand coordination, paresthesia

Support Group: Brain & Nervous System

Posted: Mar 2, 2021

Wow! I have the same symptoms. I slept about 8 hours last night and I woke...

https://connect.mayoclinic.org/comment/186052/

suspecting autoimmune disorders, like ms

Discussion: Adrenaline spikes: Med detective needed, award given

Support Group: Diabetes & Endocrine System

Posted: Dec 22, 2018

@jimhd first of all I hope things are going better . You are in my prayers....

https://connect.mayoclinic.org/comment/241380/

months, one who specialty is neuro with ms

Discussion: Small Fiber Neuropathy?

Support Group: Neuropathy

Posted: Oct 10, 2019

@lorirenee1 Thanks so much for inquiring, Lori. I hope you are still doing better. I’m fine,...

https://connect.mayoclinic.org/comment/290568/

s first step is always to rule out MS

Discussion: Testing for Neuropathy

Support Group: Neuropathy

Posted: Jan 18, 2020

I have severe back pain with similar symptoms, but it is not related to fibromyalgia. I...

https://connect.mayoclinic.org/comment/232519/

Ms & fibro, I have all.

Discussion: Entire spine hurts - Due to Fibromyalgia?

Support Group: Fibromyalgia

Posted: Dec 12, 2018

Hi, From what you report from your testing, the neuropathy seems to be associated with specific...

https://connect.mayoclinic.org/comment/1035370/

But it was not MS and certainly not

Discussion: How do doctors determine SFN is NOT ALS or MS?

Support Group: Neuropathy

Posted: Mar 17 5:34pm

How wonderful for your daughter!💝 Having read in a few posts about hair loss with Ocrevus,...

https://connect.mayoclinic.org/comment/1028992/

infused medication give her relief from MS

Discussion: Ocrevus or Kesimpta? Which treatment should I choose for MS?

Support Group: Brain & Nervous System

Posted: Mar 7 2:04am

I am so sorry to hear of your mother's condition! I do not know if this...

https://connect.mayoclinic.org/comment/1090846/

tested me over and over for Lyme, MS

Discussion: My mom can't walk, doctor's don't know why

Support Group: Autoimmune Diseases

Posted: Jun 21 7:19am

If the surgery is the primary treatment and you say you "will refuse surgery almost definitely",...

https://connect.mayoclinic.org/comment/798814/

dear wife who battles the damage of MS

Discussion: HPV P16 positive cancer

Support Group: Head & Neck Cancer

Posted: Jan 19, 2023

Actually NOTHING. The Gabapentin never really worked. I was at Stony Brook Neurology (Stony Brook University...

https://connect.mayoclinic.org/comment/57952/

genetic test is but I assume its for MS

Discussion: Essential thrombocythemia

Support Group: Blood Cancers & Disorders

Posted: Jul 17, 2020

I am 48 yrs old woman from Ontario Canada just diagnosed with arachnoid cyst on brain,...

https://connect.mayoclinic.org/comment/51745/

I had MS like symptoms (vertigo,headaches

Discussion: Arachnoid Cyst

Support Group: Spine Health

Posted: Oct 22, 2019

You are not alone! I’m so grateful for you sharing your story! I literally thought I...

https://connect.mayoclinic.org/comment/759658/

for carpal tunnel, spinal issues, MS

Discussion: Carpal tunnel like symptoms post COVID

Support Group: Post-COVID Recovery & COVID-19

Posted: Oct 11, 2022

Hi all, my daughter is now going through a tough period after her recent major operation....

https://connect.mayoclinic.org/comment/154098/

based medicine more commonly used for MS

Discussion: Pleomorphic xanthoastrocytoma tumor (Pxa): help

Support Group: Brain Tumor

Posted: Dec 10, 2018

Hi John. Thanks for all the info. I agree that supplements do help many things. I...

https://connect.mayoclinic.org/comment/91895/

She cured herself of MS.

Discussion: Anyone here dealing with peripheral neuropathy?

Support Group: Neuropathy

Posted: May 6, 2017

Hello I live in a small town and nit one doctor learned about my problem with...

https://connect.mayoclinic.org/comment/145787/

I live in ms.

Discussion: muscle joint pain

Support Group: Bones, Joints & Muscles

Posted: Apr 4, 2017

I have not been diagnosed but my experience may help: I am in Melbourne, Australia and...

https://connect.mayoclinic.org/comment/818437/

I had a brain MRI to see if I have MS

Discussion: COVID vaccines and neuropathy

Support Group: Neuropathy

Posted: Feb 27, 2023

The timing on some of these life events are just so unfair isn’t it? It’s like...

https://connect.mayoclinic.org/comment/816089/

Finding an MS specialist would be a

Discussion: Internal vibrations, not sleeping well, stressed out

Support Group: Brain & Nervous System

Posted: Feb 23, 2023

To Ethan, moderator: I've not found any other mics designed or sold to work with my...

https://connect.mayoclinic.org/comment/270011/

I do watch MS-NBC because it does have

Discussion: Microphones for friends in noisy spaces

Support Group: Hearing Loss

Posted: Dec 30, 2019