#i - Shift.ms

@smallfoot

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First posted on the Shift.ms app

@jbharris1356

I found out that getting diagnosed with MS is worse than living with it. Anyone feel this way?

First posted on the Shift.ms app

@mharris72

I have found reading other people's stories.Knowing we aren't alone is a little comforting.

First posted on the Shift.ms app

@Pily

EditedLast reply

Hi how are yall doing? Ok this might sound kinda dumb question but I always get ask what stage of ms is at im like huh? I just no I have ms but no idea about stages or anything like that. I forget everything all the time. I no my neurologist ask me if I have any relapses so I say no thats another thing I have no idea what are they talking about.. yes I have ms for 6_7 years and still no idea what they trying to bask ne if anyone can help would be supernawesome

First posted on the Shift.ms app

@EleanorAdmin

Edited

"Only 24 hours left" (said in my most dramatic voice)

So this is it 🚨 We're 24 hours from the end of the Big Give campaign and we're 33% towards our target. At lunchtime tomorrow the double donation pot closes so this is a final call to arms: please donate now! I've said it before but I'll say it again, here's how big an impact your donation will ma...

@msmeekmurphy

EditedLast reply

THIS ISH IS CRAZY AND I AM NOT HERE FOR THIS😳

I’m a very kind, knowledgeable, God fearing, smart, hustling ((all the good things)) woman.I Did not make a profile on this app for men to try to connection with me with nothing to say but….NVM. I’m not here for this so please stop. Thank you, I would go on a dating app if that’s what I was looking ...

First posted on the Shift.ms app

@JenniferWoods

Last reply

I'm new here

Hello everyone! I'm new here I was diagnosed with MMS back in 2022 and progressed to RRMS and I've definitely had some eventful twists and turns through my MS journey so far but I'm glad to be able to find a community of people who are going through something similar to myself. I hope everyone is ...

First posted on the Shift.ms app