Shift.ms

27 Mar 2025 18:09Last reply 30 Mar 2025 16:29

Cannabis

Maybe I'm not up to date on this app but I was scrolling through some posts about pain and I was surprised that cannabis is rarely mentioned for pain management, sleep and general wellbeing. Personally it's made a massive difference in my own battle over the years for the better and I'm just surpris...

First posted on the Shift.ms app

24

@josiej8

28 Jan 2025 02:52Last reply 28 Jan 2025 12:02

A possible MS diagnoses

Hey. I’ve recently had an MRI scan which showed central demyelination in my spinal cord and it’s most likely to be MS (still waiting for a confirmation and you know what waiting lists are like). I’m a little nervous as I already have chronic seizures, Fibromyalgia and FND so I was hoping to find a ...

First posted on the Shift.ms app

2

@AndreaG

6 Feb 2024 09:44

Treatments for progressive MS

Webcast being offered to discuss new treatments for progressive MS: https://www.msif.org/treatments-webcast/?utm_source=facebook&utm_medium=organic-post&utm_content=global-webcast&utm_campaign=2024m7202_8678&fbclid=IwAR2zSOjcwCnfMjPqniqYh1iDP9MRTpd-WRNNmc8zVzCFfAR3-A1TcmeX6Rk&cn-reloaded=1

Swanley, United Kingdom

@pureandsimple

19 Dec 2023 10:26 Edited

multiple scerlosis 360°

Hello everyone, since I personally imagine it to be very exhausting to constantly educate about MS, I want to refer to this website! https://zkn.ukdd.de/en/ms360 I found it and think it is easy to send it to relatives, so that I you don't have to answer the same questions over and over again, and o...

@watsoncraig

26 Jul 2023 16:32

WHO

https://www.msif.org/news/2023/07/25/whos-decision-brings-hope-to-people-with-ms-worldwide/

Falkirk, UK

@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

@HackMyMS

12 Sep 2022 19:54 Edited

New guide for choosing DMTs

So, I see a lot of questions on this board about choosing a DMT or switching. Given that there are over 20 different options right now, it can feel a lot like cramming for the final in Your Future Is at Stake 101. The good news? The Multiple Sclerosis Association of America just launched The MSAA Tr...

@shiftms-films

11 Jan 2022 11:07

#LightningTalks: MS Diagnosis Top Tips

“Don’t fear the internet but if things are stressing you out - just walk away." Kelsey gives her MS diagnosis tips. Especially filtering through scary MS info from Dr Google. Have you ever scared yourself with information overload? 💬 Check out Kelsey’s #LightningTalk above ⬆️ https://www.youtube...

@Nudetritionist

25 Dec 2021 04:56Last reply 27 Dec 2021 21:48

Answer: The BEST Diet for MS

What is the best diet for MS? I’m in a few MS groups. I was in a few dozen more, but there’s sadly a lot of misinformation, extremists, and negativity when it comes to MS nutrition. Some promote a carnivore diet. Some promote keto. Others promote a paleo approach. There’s also a group of people tha...

6

@Louise_Christie

16 Jul 2020 19:27Last reply 18 Jul 2020 02:01

‘You shouldn’t breed’

Anyone else get highly f*cked off when people spread misinformation about the genetic link in MS? Plus the idea that a parent with MS would be less than and is selfish for wanting to have children!? I have enjoyed my life, I am still enjoying my life at 29, 2 years post diagnosis. Had my parents ha...

10

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