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@skezz 

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skezz

In person meet ups Scotland

Does anyone know if there are still active meet ups in glasgow/Falkirk/Edinburgh? I think I feel quite lonely in person dealing with the new diagnosis, I’d love to see some people face to face who understand 😊

@edwardkime92 

Edited

edwardkime92

Advice/help needed :)

Hey everyone! I was diagnosed with RR MS in May of this year. Had the CT scans, MRI scans and lumbar puncture. My first relapse lasted 3 and a half months. In the first 3 & a half weeks I was paralysed from the stomach down. My right arm was also affected. Now I cannot feel my right hand properl...

@Katherineee 

EditedLast reply

Katherineee

Ocrevus Injection

Went for my infusion last month and there’s already talk around the hospital about ocrevus being given as an injection instead of an infusion. Not sure what I think yet 🤷🏼‍♀️has anyone spoken to their neurologist about this yet?

@Krissy87 

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Krissy87

New diagnosis

Iv been told i have secondart m.s Since last year my symtoms have got worse. Eyes legs ect Hiw do people cope with change im just plodding along like always but im feeling shit
Louth, United Kingdom

@DominicS 

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DominicS

Fermented foods - A double whammy of deliciousness

I bake bread regularly. I saw this when I was forced to watch bake-off last night. I am making it tomorrow. Need to get green onions/scallions today then we’re off to the races. https://whattomunch.com/gochujang-sourdough-with-roasted-garlic-and-green-onions/

Calling Plegridy DM Users - have you ever had a drug break?

Hi I have been on this drug for around seven years; I still do not endure the flu-like side affects and other symptoms after taking the bi-weekly drug. Despite its efficacy being relatively low I have been stable so who knows whether it is helping. My neuro has approved for me to take a two month to...

@Julesle0 

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Julesle0

Constipation and MS

Hello all, Ever since my last relapse I’ve been having issues with constipation. Does anyone have any suggestions that have helped them with this? I’ve been taking laxatives to help but I don’t think it’s a good long term solution, any help/ advice or information is much appreciated !!!
London, United Kingdom

@Bluebell2 

EditedLast reply

Bluebell2

Does Tysabri increase energy?

Hi, I’m currently going into my 7th week without my Tysabri infusion (usually 4 weekly soon to be 6 weekly but missed last infusion as had UTI and was on antibiotics so MS team advised I wasn’t allowed it). Does anyone feel that Tysabri increases their energy levels or reduces fatigue? I’m definite...