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Welcome to Shift.ms

Hello, I'm the Community Intern here at Shift.ms! I'm here to listen to your stories and share them across the site in the hope that they'll be helpful to other MSers. #MSstories Just testing the @ function by tagging @poleyjo :)
Leeds, England, United Kingdom

@Bobbij 

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Bobbij

Benign MS

I was just diagnosed with benign MS not quite sure about it as of yet, all I know is my symptoms with Tingling in the scalp, right arm, pain in those areas also plus right leg, are very real, but I guess will know more once I get to see the MS specialist

@daveserjeant 

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daveserjeant

Welcome to new MSers

I've recently been talking to someone at work who's newly diagnosed. He remarked about the support he's getting from other MSers Going to test an @ and # by saying @Sclerobro #ocrelizumab
Nottingham, United Kingdom

@Karen_Sue_Thacker 

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Karen_Sue_Thacker

Early signs and symptoms of MS

Can someone please elaborate what are some of the early signs and symptoms of the disease? How do I approach the subject with my physician?

What diet is best for ms

I'm recently diagnosed with rrms, I'm not on any treatment yet. Just wondering what diet is best to follow?

@Sue_Ashton 

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Sue_Ashton

New to group. Experienced with MS!

Hello there. I have just joined the group as I have MS. I was diagnosed in 1994 and it's been a rollercoaster journey since. I'm feeling a bit miserable at the moment as my memory has gone on a go slow. I thought that things would improve when the heat reduced but I'm so forgetful. I went to an opt...

@Sclerobro 

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Sclerobro

Brain fog n' dizzy times

Hello im new to the site, so, im sorry if this has been mentioned before, but i have recently been having some occaisional dizzy spells. Nothing major, like getting out of bed quickly type headrush that can last minutes and sometimes a couple of hours and also the same with sometimes spacing out and...

@DesN 

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DesN

Understanding!

Hey all 🙂 im hoping this is common with others suffering MS.... people just dont seem to understand anything about it or what you might be going through! Friends... family and work colleagues see you looking normal and presume everything is fine.... I never want to come across dramatic but sometime...

Newbie

Hi I'm new to this group, I was diagnosed June 2020. My first symptoms started 2hrs ago as Carmel tunnel syndrone. My right arm would go numb for a few minutes and I would shake it off. January 2020 I went to ER with symptoms of right sides numbness and when I bend my forward I feel an electric ting...