#msfamily - Shift.ms

8 Jun 2025 11:07 Edited

MS Society Fun Day!

🎉 JOIN US FOR A FAMILY FUN DAY IN SUPPORT OF MS SOCIETY UK! 💜 📍 Niagara Leisure Centre, Sheffield (S6) 📅 Saturday 19th July 🕛 12pm – 5pm 👉 https://facebook.com/events/s/ms-society-uk-fundraising-day-/838459067943410/ We’re excited to invite you to a fantastic Family Fun Day packed with fun, f...

MS Society UK Fundraising Day - Niagara Center Saturday 19th July 2025 12-5pm

Event in Sheffield, United Kingdom by Lottie Grace Smith on Saturday, July 19 20255 posts in the discussion.

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Sheffield, UK

@AlexanderM

7 Jun 2025 22:22 EditedLast reply 8 Jun 2025 17:45

Does it ever get better?(mini rant)

I’ve recently been diagnosed with RRMS. It’s been a rough couple of months that led to my diagnosis and it has taken every ounce in me and more to just hold it together and not let my life fall apart. According to my neuro I’ve had like three relapses in less than three months and have a lot of inf...

First posted on the Shift.ms app

@Leeb

7 Jun 2025 10:08Last reply 7 Jun 2025 23:18

MS and gut bacteria

Interesting article on the potential culpability of gut bacteria in causing MS: https://www.eurekalert.org/news-releases/1086404 The article notes that there are likely multiple factors that come together (genetic, environmental, disease exposure) though the twin studies minimise these. Doesn't real...

First posted on the Shift.ms app

@lizzie86

5 Jun 2025 15:45Last reply 6 Jun 2025 19:57

Hey all I’m new here.

Hi all I’m just wondering if anyone wants to be there to support me?? My family disowned me when I was diagnosed in 2016 and I have not 1 person I can trust to be there for me as support coz they all only care about themselves, I’ve always been the 1 that supports them when they need it no matter wh...

First posted on the Shift.ms app

@swabybaby

5 Jun 2025 09:34

Thank you all for my birthday wishes I had a good day with family Xx

First posted on the Shift.ms app

@FaeryMae

4 Jun 2025 11:42Last reply 4 Jun 2025 14:04

What should I expect?

Hi! I just got diagnosed exactly 20 days ago, and then a few days after was my 25th birthday where I had to break the news to my family. My neurologist was great for ordering tests and getting me diagnosed buuuttt not so much anymore. I just had my first infusion yesterday, another patient at the cl...

First posted on the Shift.ms app

@hiimedison

2 Jun 2025 16:58Last reply 4 Jun 2025 16:04

Am I an anomaly?

28M, Asian, no one in my family history has MS ? You're so young? ? You're Chinese? ? You're male? ? Anyone in your family history? Idk how I should feel, was diagnosed in the ER in Nov last year, still really hasn't hit me since I live in SoCal and I'm on disability but damn, someone tell me...

@kyrgyzkiwi

1 Jun 2025 03:44Last reply 3 Jun 2025 20:33

Hot Showers

Hi, i feel like the new kid on the block, having only received my MS diagnosis a couple of months back and am waiting for my first infusion. I’m in NZ and we’re heading into winter so I’m grateful for the cooler weather, and how it reduces the symptoms. Speaking of which i am finding that having...

First posted on the Shift.ms app

@LisaB2

31 May 2025 13:44Last reply 1 Jun 2025 20:30

Explaining DMT to friends and family

Hey has anyone else had problems with friends and family understanding the treatment. I’ve spent time with my friends and family explaining the treatment and truly thought they understood. I had my first full treatment of Ocrevus yesterday and a friend has texted asking when will the treatment start...

Wakefield, United Kingdom

First posted on the Shift.ms app

@littleMStish

31 May 2025 11:35 EditedLast reply 4 Jun 2025 11:34

Has anyone’s doctors tried to find the cause of their MS? I think it’s bazaar that nobody cares what caused this in me, in the first place. No family history.

First posted on the Shift.ms app

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MS Society UK Fundraising Day - Niagara Center Saturday 19th July 2025 12-5pm