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@Kelly88 

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Kelly88

Connections

Anyone from fife here? Would love to connect with others who are going through it all too
Fife, UK

@Jc06 

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Jc06

Kesimpta

Recently diagnosed with RRMS and had 3 issues (lapses)in 9 months and being advised Kesimpta. anyone advise how this has worked for them and how the injections to yourself have gone etc? Also any big issues with side effects? Or all gone ok for people?

@BillySmith 

EditedLast reply

BillySmith

How long did it take you to get diagnosed with MS?

We’ve just launched Shift.ms polls! Take part in the first poll below👇 *Bonus points if you can leave a comment and let me know: are you happy with how long it took?

How long did it take you to get diagnosed with MS?

Total answers: 2235

@05Kubann 

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05Kubann

Ocrevus side effects

Just looking for some advice. I've had my second dose of ocrevus and I've been constantly ill since the first. Covid, whopping cough that has stayed with me for 3 months now. I'm achy, fatigued and quite frankly miserable. They keep ignoring for me an MRI (I didn't even have a baseline before they t...

@MissWhy 

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MissWhy

50k in May challenge

Has anyone else signed up to take part in this challenge? Do it! I’ve already had over £200 in donations and I’m being realistic about how I can use the AlterG to help me walk 15k during May

@Alicja 

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Alicja

Can I change my job.

Hi Everyone, I'm thinking about my career. How far and what I have achieved for myself. And I keep thinking MS is holding me back. Got so many other things on my head and some, actually a lot of them I need help with. But still hoping I will one day I will change my qualifications. I'm administrato...

@KarriW 

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KarriW

How can you tell if your having a relapse?

Hi, I'm newly diagnosed, almost 3 months. How can you tell if you are having a relapse? I started having worsening pain on my weak side, a very painful headache, worsening dizziness which has led to nausea so bad I haven't been eating very well, general malaise, worsening fatigue... Everything just ...

@shiftms-polls 

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shiftms-polls

The emotional impact of your MS diagnosis

Cast your mind back to that moment when you were sitting opposite your doctor and told “it’s multiple sclerosis”. Three words that are nothing short of life changing. When we speak to MSers about their diagnosis appointment, it’s clear that how those three words are delivered, and the care that im...

MS & trauma. On a scale of 1 to 5, with 1 being not traumatic at all and 5 being extremely traumatic, how would you rate the emotional impact of your MS diagnosis?

Total answers: 1108

@Samah 

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Samah

What’s your experience been like?

Hey, so I’ve been neglected for years with my MS however I’m now hopefully on route to get it sorted… o just gave birth and I’m having some side effects (yaay) anyway we’re about to start Gabapentin at 100mg night time use - has anyone used it? What’s your experience? I’m also now reading I to DMD...