Shift.ms

@amandalynn96

2 Jun 2025 02:06Last reply 2 Jun 2025 05:27

Can anyone else’s hand itch so bad and you can’t seem to get it to stop?

First posted on the Shift.ms app

@Mike9

1 Jun 2025 17:26Last reply 2 Jun 2025 04:56

I’ve started a YouTube vlog

It’s called myelin and me. First video uploaded just now. Have a look if you don’t mind :-)

First posted on the Shift.ms app

@TheRRMSLife

1 Jun 2025 13:26Last reply 2 Jun 2025 00:39

Yay for a Shower!

Yay for Safely Managing a Shower today Before the Thunder Storms rolled in. Its çalling for Severe oʻne today. So my joìnts are gonna Love Me in a few hours.

First posted on the Shift.ms app

@EleanorAdmin

18 Dec 2024 13:10Last reply 1 Jun 2025 23:07

We don't blame you. When you apply for a Buddy, you're taking an active step to get support that will guide you along your MS journey. Interested? Of course you are! Look out for this button when your scrolling through our app feed... PS. New matches will be made in January as the Shift.ms team t...

@Johnwayne

1 Jun 2025 06:47Last reply 1 Jun 2025 20:34

Question for anyone with MS or this symptom.... DOES ANYONE HAVE PROBLEMS WITH EXTREME BRAIN ZAPPERS THAT FEEL LIKE LIVE ELECTRICAL WIRES FOR HOURS, to the point that you feel like you're going out of your mind..... Also when talking the brain zappers intensify

First posted on the Shift.ms app

@elliemb

1 Jun 2025 14:39Last reply 1 Jun 2025 15:17

Hello! Got my diagnosis last month for RRMS and I'm deciding on treatment options at the minute. I'm very prone to cold sores and UTI's and I've been suggested Kesimpta or mavenclad. I know they both have increased risk of oral herpes and uti's so confused as to which to go for. Any advice would be appreciated. Thank you :)

First posted on the Shift.ms app

@Sheilamarie26

30 May 2025 14:59Last reply 1 Jun 2025 14:50

Where are you from?

I'm located in the US in the state of North Carolina

First posted on the Shift.ms app

@Katiecosworth

14 May 2025 16:26Last reply 1 Jun 2025 13:08

How often do you get an MRI of your spine?

Just wondering how often you get an MRI of your spine done? I still don’t have a diagnosis of MS but as the years go on, new symptoms seem to appear. I had an MRI of my full spine back in 2021 but didn’t have any lesions there, only my brain. That was prior to my leg becoming as weak as it is now....

First posted on the Shift.ms app

@mooniecrush

1 Jun 2025 02:28 EditedLast reply 1 Jun 2025 09:17

what has been your experience with the latest trestments? What can i expect from the future?

I felt numbness and pain in my hand, turns out it was ms. This was a few days ago. I have been told by my doctor that these days people can live relatively normal lives and that I don’t have to necessarily loose my mobility or cognitive functions. Still, I wanted to ask, what has been your experienc...

First posted on the Shift.ms app

@RoseRivera1214

1 Jun 2025 03:03Last reply 1 Jun 2025 07:24

What to do?? Hi, my name is Rose. I’m new to this app. I was diagnosed with Ms back in 2016. Since than I’ve tried two dmts. Gilenya and mavenclad since than. Gilenya gave me horrible rashes for four years before my neuro switched me to mavenclad. That medication was the absolute worst. I lost about half of my hair and had frequent heart palpitations to where I needed a heart monitor twice. I only did the first year round 1 and never followed up for my second because of fear. I am meeting with my neuro within the next month about starting a new medication. What is some options that he could give me? And what is your personal experience with those DMTS?

First posted on the Shift.ms app

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