#faith - Shift.ms

Forum

We are a charity and rely on donations

Charity Number: 1117194 (England and Wales)

Registered Company: 06000961

Registered address:
Shift.ms, Platform, New Station Street, LS1 4JB, United Kingdom

London office:
Shift.ms, Somerset House, Strand, West Goods Entrance, London WC2R 1LA, United Kingdom

©2025 Shift.ms

Sort 247 results by

8 Sep 2025 03:38Last reply 8 Sep 2025 03:39

Do therapy two times a week and gym two times a week still walk with a cane how hard I’m trying, but hopefully we get this right this time and overcome trying really hard to get rid of my cane and have a balance to walk again as like my dream… But it’ll happen my faith is strong…

First posted on the Shift.ms app

25 Jan 2025 20:21Last reply 8 Jun 2025 18:29

Hello everyone 😊. A little about myself. I was diagnosed with MS (after experiencing a few different symptoms (🤔maybe in a period of 3 months or so 🤷🏼‍♀️). This happened November 2008 at the age of 30. After being discharged from the hospital, I went to see a neurologist who started me on daily injections. I don’t recall too much, however I remember the Dr telling me newly diagnosed patients will have a relapse in about 2 years. I was on injections (which injections 🤷🏼‍♀️) less than a year (due to insurance). About 2-3 years later, I again have insurance. I recall hearing anything you take or do to yourself can trigger your “MS”. So because of that, I refused to be back on meds/injections. My way of thinking (maybe not the healthiest) was “It’s been close to 4 years and I haven’t had a relapse or suffered from it. Fast forward ➡️, almost 16 years later I have never experienced anything to do with MS since the time I was diagnosed. I’ve doubted (and still do) of my diagnostic was correct. A few years ago I had some tests done on me and according to Dr- I still show cloudy patches bla bla bla. I’m very thankful and blessed with myself but I’ve also wished and prayed MS didn’t exist. I wish everyone the best, NEVER lose hope or faith and always be thankful you don’t have it worse 🥰.

First posted on the Shift.ms app

9 May 2025 02:51Last reply 10 May 2025 14:16

I'm suppose to start Mavenclad this weekend, what can I expect in terms of side effects, risk for infection and overall performance of this drug. I'm kinda faithfull/hopefully with a little sprinkle of fear of the unknown.

First posted on the Shift.ms app

Unpublished

13 Feb 2025 05:02 EditedLast reply 13 Feb 2025 06:27

Believe and have faith!!!!

What do you think 🤔. About Trump region?

First posted on the Shift.ms app

27 Dec 2024 14:34Last reply 31 Dec 2024 19:28

I’ve been dealing with an unbearable amount of anxiety and stress lately because of my new diagnosis and the medications. Some days I feel hopeful about my future and believe I can get through this but then I’m slapped with an unexpected panic attacks that is usually caused by new symptoms or fear of the unknown (my future). I don’t know how to cope with it. I’m trying everything possible: leaning onto my faith, venting, deep breathing, listening to music, etc. but nothing’s working. I’m really trying to remain hopeful but some times it can be so hard and unbearable. I’m only 17. Why does this have to happen to me at such a young age?

First posted on the Shift.ms app

27 Dec 2024 10:01Last reply 31 Dec 2024 15:32

I’m curious, are there any Catholic Christians here? My faith in God has been one of the most important sources of strength for me as I face the challenges of living with MS. I’m wondering if anyone else has used their faith to navigate their journey with MS, and if so, how has it helped you? 💞

First posted on the Shift.ms app

6 Feb 2020 21:57Last reply 9 Feb 2020 09:29

Walk by FAITH not by sight🙏🏽🙏🏽🙏🏽

Through all the pain, confusion and worry I realized I serve a MIGHTY good God and he has NEVER left my side and he NEVER will. At the end of the day God has the last say so its nothing I can do is pray and believe.

19 Nov 2018 05:21

Keep the Faith

God iss with all of us we are wrapped in his arms of love

28 Jan 2017 11:27Last reply 29 Jan 2017 07:51

Lost all faith

Visit with the Neurologist was extremely strained. She says while those MULTIPLE large white spots on the MRI have not changed in a year, she doesnt believe I have MS. I did get emotional-not that I want to be diagnosed with yet another auto immmune assasingator, but I have no answers. Its been t...

8 Aug 2025 16:29Last reply 8 Aug 2025 19:54

Have you ever sacked your MS team, and can you?

Hello, This is my first time here, although I was diagnosed with MS in 2016. I have rarely seen my neurologist - just twice in 7 years - and I have lost faith in their ability to help. I feel that my relationship is so poor with the MS team that I am thinking about leaving their care, such as it i...