#be - Shift.ms

Last reply

All of us ms'ers getting to know each other better:

Hello, I have a question here for anyone that reads it and is willing to answer, to get to know all of us better. Where are you from originally? I was born in Michigan and lived in New York for a large portion of my life. I went to high school in Virginia Beach and went to undergraduate in New York...

First posted on the Shift.ms app

124

@Spiffy

Last reply

Good Morning Beautiful People🙋🏻‍♀️😊

I'm new here. I've had ms for what feels like 6 days past forever. I've been extremely fortunate that my ms has stayed quiet for a long time. However, I had pneumonia in September and have been in a whirlwind of symptoms with this flare since and my brain is stuck in mode " blah🫤." I'm seeing my ne...

First posted on the Shift.ms app

7

@Tia

Just found:Recent research has uncovered a shocking connection between multiple sclerosis (MS) and parasitic infections. Autopsy studies of MS patients revealed that every single individual who died from the disease had parasites within their central nervous system. This has led experts to question the role that these parasites might play in triggering autoimmune diseases like MS.While MS is traditionally thought of as an autoimmune disorder, these findings suggest that other factors, such as infections or parasitic infestations, could contribute to the development and progression of the disease. Parasitic worms in the brain have been shown to interfere with the nervous system, causing symptoms that resemble those of MS. This discovery opens the door to further investigation into the relationship between parasites and neurological diseases.As we continue to explore the causes of MS and other autoimmune disorders, it’s essential to look at all potential contributing factors. Addressing parasitic infections in early stages could offer a new pathway for treatment and prevention. This emerging research highlights the importance of considering all aspects of health, not just the symptoms. 🧠⚠️

First posted on the Shift.ms app

@pepe92

I be in pain

Ms pain is not for me I just wanna check out

First posted on the Shift.ms app

@SugaBug1971

Last reply

I was under the assumption that being diagnosed with MS later in life like in your 50s is it just as progressive as to being diagnosed at a younger age

First posted on the Shift.ms app

19

@jamoranto

Between The Sheets then Badu ..what.

https://youtu.be/0NwQVwewUGE?si=JH_V9IgxWFpfC8Ya

@cmkn924

Last reply

Best treatment for RRMS

Hi. I have recently joined this group due to being diagnosed last week with RRMS as I have lesions in both my brain and spine and spinal fluid. My neurologist told me about treatment options of Tysabri, Briumvi, Ocrevus and Kesimpta and wants me to pick one and message him in the patient portal whic...

First posted on the Shift.ms app

28

@messy100

Last reply

Best advice?

What is the best advice you’ve received about MS? I’ll start. I was told by someone with MS to be careful picking a DMT that doesn’t make things worse if you go off it. They said that people often switch meds and some meds can make you relapse if you quit them in a hurry. I will never forget that.

First posted on the Shift.ms app

21

@sunshine5897

Last reply