#msworriors - Shift.ms

28 May 2025 11:05Last reply 28 May 2025 13:49

13 years ago today I was officially diagnosed . . .

13 years ago today I was officially diagnosed with MS. I acknowledge this day every year for two reasons. The first is so I can say a massive thank you to the friends and family who have been there since the beginning (or joined me on the way) in supporting me on my journey living with this disease....

First posted on the Shift.ms app

4

@Redvariant

18 Aug 2024 11:19Last reply 18 Aug 2024 15:37

Motivation

If you’re struggling, just remember we are at civil war with our ms, so don’t let your ms win!! #mswarriors

First posted on the Shift.ms app

2

@Marz

2 Nov 2022 12:58

Grateful

Hi everyone, I’ve had RRMS for over 20 years. I was diagnosed during a time when Australian TV was flooded with commercials of young women with MS in wheelchairs. So, when I was diagnosed naturally I assumed this was what my future held. Thankfully, I had a tribe of supporters who would not allow ...

@RobbiHall

24 Oct 2020 15:01Last reply 25 Oct 2020 02:25

#MultipleSuperbness God's Way

40 years singing & telling story songs about NOUNS. Over 1 Million students, in schools, communities, languages, locations resulted inmy showing up. Quite a few folks with MS in the "entertainment" industries overcome like Montel, Terri Garr, Selma Blair, Annette Funnicello & Pryor stressed & miffe...

Portland, United States

1

@PaulGriffiths

19 May 2019 05:07Last reply 22 May 2019 16:15

Your opinions please

Hi guys and dolls, having RRMS at an advanced stage my disabilities are quite severe although my sense of humour and fun and love of life drive me thankfully. I've recently started a website called, www.mswarriorsandtalkmatters.com where I like to post info on my own experiences and relevant informa...

4

@MrWash

6 Dec 2024 07:45Last reply 6 Dec 2024 22:09

Iron sharpens Iron

I accepted the diagnosis in 2021, I processed all the whirlwinds of emotions, prayed to God, then jumped into the gym to craft my body for the ongoing WAR! What the mind commands the body shall follow! As the great CT Fletcher says “I COMMAND YOU TO GROW” #MSWARRIOR

First posted on the Shift.ms app

5

@LuLuu

31 Jul 2024 15:40Last reply 1 Nov 2024 06:38

MS Warriors🤩

Hey everyone! 🌟 Just wanted to share a little bit about my journey with MS. Despite the challenges, I've come to see it as my very own superpower. It's a reminder that staying positive and resilient can truly make a difference. Let's keep pushing forward, supporting each other, and spreading hope. ...

First posted on the Shift.ms app

7

Deleted

@Mwsurviver

13 May 2023 14:44

Instagram

Follow me on Instagram, for us people with ms. https://instagram.com/mswarrior2023?igshid=ZGUzMzM3NWJiOQ==

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@Mwsurviver

12 May 2023 15:10 Edited

Follow me on Instagram

I have created an Instagram, just for us with multiple sclerosis, https://instagram.com/mswarrior2023?igshid=ZGUzMzM3NWJiOQ== Thank you! 🎗🧡 We are Warriors

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@wxrmthinthesun

28 Feb 2023 14:31 EditedLast reply 2 Mar 2023 18:34

How do you live with your MS?

I'm just sharing some thoughts here and I'm curious about other people's opinions! So, we may all know that Christina Applegate did a red carpet in the past couple days with a cane that had "FUMS" all over it. Which I respect but it's not for me. The "MSWarrior/Fighter" and the " FUMS" mentality isn...

Scotland, UK

12

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