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@gmag44 

EditedLast reply

gmag44

How long do Solumedrol 1000 infusion benefits last?

Tomorrow will be my last day getting infusions and then I take the medicine in pill form for a week and then I start on Zeposia. Can anyone tell me what to expect moving forward?
First posted on the Shift.ms app
11

Animated Symptoms | Spasm

Shift.ms Series

Animated Symptoms | Spasm

@don162 

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don162

Dating

Is dating hard with this disease?
First posted on the Shift.ms app
17

@Swannie 

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Swannie

New job.

I’m looking for a new job and I’m wondering when and how do you tell your new employers about your condition. I found out about my RRMS whilst working at my current job so they know. But how to explain myself to people at a new workplace? Thanks.
First posted on the Shift.ms app
22

@Jessicaannlang 

Edited

Jessicaannlang

Just being curious

Does anyone have a night when your wanting to go to the toilet constantly and then when you get into bed your knees start to hurt so you can’t get comfortable no matter what position you lie in?…
First posted on the Shift.ms app

@sahil 

Last reply

sahil

Treatment

Anyone have vison lost problem? And it's recovered or not? I recently diagnosed the MS and have lost my left eye vision. It's recover now. But not fully recovered. Dr said we are not sure. But they are trying full recover can take 6-12 months medicine. But I don't trust bcz it seems recover is stopp...
First posted on the Shift.ms app
14

@bpapi22 

Last reply

bpapi22

Social Anxiety

I was diagnosed in 2006 with PPMS. Tysabri & Gamunex-c not work last 3 yrs. The past 14 mths it hit hard, I barely able word form, speak and walk with cane/walker. I have bad social anxiety, especially around others I know. What y’all found help calm that? I’m find I hide out alone to not feel it.
First posted on the Shift.ms app
10

Do I Really Need Accessible?

Shift.ms Blogs

Do I Really Need Accessible?

@JSanchez 

Last reply

JSanchez

HSCT

Hey has anyone tried or thinking about the stem cell transplant treatment yet? Considering this option and was hoping to hear some people's experience with it. Some have said they are no longer on a DMT but I suspect it's not the same for everyone?
, United Kingdom
First posted on the Shift.ms app
10

@asultana 

EditedLast reply

asultana

HELP!! Looking for advice/opinions.

So I was diagnosed with MS 2023. I had my first consultation with the Neuro today after 2yrs (I know very long time). I had 2 relapses in 2023 (pins/needles & numbness in 2 different areas). But I have had no relapses ever since then. Just on and off fatigue. I am otherwise very well & fit in myse...
First posted on the Shift.ms app
30

@ktdolly 

Last reply

ktdolly

Oral surgery question

Hi everyone. I’m new here and am looking at a probable MS diagnosis. I have some additional testing to get done, but everything is pointing in that direction. In addition to that, I am scheduled for a gum grafting procedure next week. My neurologist said it’s fine to have it done, but I’m anxious ...
First posted on the Shift.ms app
10

@Laura_Borg 

Last reply

Laura_Borg

Medication

Does everyone take medication as I did a couple of years ago but found it made my ms worse so haven’t started anything new as I’m worried it will have same effect , I don’t even take paracetamol as not very trusting , does anyone else feel like this ?
First posted on the Shift.ms app
7

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