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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: 1067

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@shiftms-polls

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Opinion check; Should HCPs discuss progression at diagnosis?

Are you the type of person who wants to know all of the facts about progression as early as possible, or would you rather cross that bridge when you get to it? There can be a lot of disparity surrounding the topic of progression, so let us know your thoughts down below 👇 Sharing your opinions c...

Should healthcare professionals discuss progression at diagnosis?

Total answers: 53

@Bigzbe34

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One day post infusion

Slept so hard when I got home from my infusion. Took the day after off just in case I need more rest which I do but I’m looking forward to feeling better I’m thankful for this page and the people on it when I’m feeling depressed and alone it’s nice knowing I’m not alone. I am trying to feed the wolf...

Odessa, TX, USA

@TaraMO

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Treatment in Ireland

Hey all! I’m currently living in London and 4 months into my treatment which is Kesimpta. Recently I’ve been thinking about moving back home to Dublin but this is really dependant on what treatments available and the cost / HSE. Can anyone shed any light on it? Ideally I want to stay on Kesimpta. Th...

London, United Kingdom

@shiftms-polls

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Poll: Has Shift.ms helped you to connect with like-minded people?

Almost 15 years ago, Shift.ms was founded because of a lack in vital social and emotional support for MSers. Today, we're still trying to make the best community for you. Fill out our poll to let us know whether Shift.ms has helped you ⬇️ PS. Click the link to fill out our annual impact survey an...

Has Shift.ms helped you to connect with like-minded people to speak about your MS?

Total answers: 63

@Msfighternadia

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Hate my life

Suffering from depression due too ms. People are mean and dont understand what i go through, going on dates ends up being ignored, friends turning their backs on me and co worker thinking i am just using my ms as an excuse too not lift heavy😞

@KingCorbs24

Dating someone with MS.

Hello, I recently went on a date with a person who after the second date told me about their MS diagnosis. She is 36 and I'm 33. As soon as I found out I started doing my research. I've spent hours on Google and YouTube. Trying to learn as much as I can about it. My only experience previously wit...

Los Angeles, United States

@Croft239

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Ms hug??

I keep feeling like I need to take a deep breath and yawn. My chest doesn’t hurt. But I just have this strange feeling like I need to do this deep breath all the time. Is this a symptom?? Thanks

Maidenhead, United Kingdom

Symptoms

@Yorete

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Your MS patient pack - I got your back 😄

Hello my fellow MSers, I thought it would be useful to do a MS patient pack. You know my experience has been the NHS leaving me to die and then bully me. No one bullies me & Londrina! So check this out- Listen you are disabled, you have MS and depression lives with us please deny it BUT you are ...

London, United Kingdom

@Madonna1

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Hello to all ms users

Hi all, it's been a few months since I was last on this site. There is no excuse, no reason but all the same I am still on Kensimpta and the walking hasn't really improved. My memory is still a blur and understanding of others is not always clear. There are options but it is taking the right one kno...

South Yorkshire, UK