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An MS relapse, attack, flare-up or exacerbation (whatever your chosen description) causes new symptoms or the worsening of old symptoms for people with relapsing remitting multiple sclerosis. It differs from person to person and can be relatively mild, or severe enough to interfere with someone’s ability to function at home or work.Find out how others manage their relapses, ask a question, or share your own relapse experience.

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Recent activityNewest posts

@avic 

23 Jun 2025 15:56Last reply 23 Jun 2025 21:32

avic

When do you mark the anniversary?

For those of you that mark the anniversary of your MS, do you count your official diagnosis date or go from your first symptoms? I had my first relapse last year in July, I was initially told it could be MS then, but later told by a neurologist it was unlikely until I had a few more relapses and ...
Broomfield, United Kingdom
First posted on the Shift.ms app
15

@AlexanderM 

18 Jun 2025 22:16 EditedLast reply 19 Jun 2025 14:14

AlexanderM

Scared of disease progression even with DMT (long read)

I’m relatively new to this whole MS thing having gotten recently diagnosed and I haven’t had enough time to process this given that I’ve been distracting myself with work so much. To my detriment at times. My diagnosis has been a bit weird and quite dramatic but I’ll just vent here and hopefully s...
First posted on the Shift.ms app
10

@TanjaS 

17 Jun 2025 16:46

TanjaS

Kesimpta and infections

Hi, since October 24 I’m using Kesimpta. It’s doing a great job, IB had any relapses since then. But because kesimpta wekens my immune system, I catches a cold. Since last October I suffer from a runny nose and a blockage in my ear canal. This causes me to always be short of breath, I smell and tas...
Utrecht, Nederland
First posted on the Shift.ms app

@Dellkan 

14 Jun 2025 19:08Last reply 17 Jun 2025 14:50

Dellkan

Might need a new MS DMT

Hi all, I was diagnosed with MS in 2020, and started Ocrevus shortly after. However, after 5 successful years on the drugs (no relapses!), I was diagnosed with very early stage breast cancer. Thankfully, we caught it early and post-mastectomy, I don’t need chemo. Still, my MS neurologist is strongl...
First posted on the Shift.ms app
23

@martinemonique 

9 Jun 2025 18:00Last reply 9 Jun 2025 20:33

martinemonique

Is anyone taking Kesimpta and how are you finding it?

Hi everyone it’s nice to meet you all, I’m new to thins site. I was diagnosed with RRMS in December after experiencing symptoms since 2023. I’ve had 5 relapses since then and I’m getting ready to start medication. I’m a little nervous for this and was just wondering on other peoples experiences? Th...
First posted on the Shift.ms app
9

@AlexanderM 

7 Jun 2025 22:22 EditedLast reply 8 Jun 2025 17:45

AlexanderM

Does it ever get better?(mini rant)

I’ve recently been diagnosed with RRMS. It’s been a rough couple of months that led to my diagnosis and it has taken every ounce in me and more to just hold it together and not let my life fall apart. According to my neuro I’ve had like three relapses in less than three months and have a lot of inf...
First posted on the Shift.ms app
8

@WelshFijian 

31 May 2025 11:55Last reply 13 Jun 2025 13:12

WelshFijian

Relapses lasting 7 months

I’m newly diagnosed with RRMS and my flair up has lasted 7 months already. I had my first dose of Tysabri last week and I’m just wondering if anyone’s relapse has improved and severe symptoms have got better? I feel like I’m fighting a losing battle at the moment.
First posted on the Shift.ms app
18

@Tianna 

29 May 2025 12:37Last reply 29 May 2025 13:57

Tianna

Remission and Relapses

I was diagnosed at 21, been 10 years now, I’ve been in remission for about 7 years now, and I’ve only ever had relapse while not on treatmen, so I am glad to say my treatment (Ocrevus) is working! What is the longest you guys have been in remission? I do occasionally have fears of relapses but ...
First posted on the Shift.ms app
4

@Mrsjenks78 

12 May 2025 16:55Last reply 12 May 2025 23:09

Mrsjenks78

MRI Results

Finally got my results, the MS is stable. I haven’t had any relapses since I started my meds a couple of years ago. However, I still feel terrible. The fatigue, the anxiety and the cog-fog is out of control. My body doesn’t feel right, something is off. I’m currently on a heart monitor to rule out a...
First posted on the Shift.ms app
4

@Sophieee 

11 May 2025 23:41Last reply 12 May 2025 06:32

Sophieee

A relapse query

Hello! I’m sophs, I am 19 years old! And have been suffering with RRMS since I was 14. I was diagnosed with MS 2 years ago after I went blind in my left eye. In 2020 I was screwed over by Covid, i suffered my first relapse, I was 14 during this time. I selfishly went paralysed in my right hand. Whe...
First posted on the Shift.ms app
4
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