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@bpapi22 

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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.

@DruBlue107 

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DruBlue107

@gagirl9986 

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gagirl9986

Back

Anyone ever have to get a spinal tap?

@Jessicaannlang 

EditedLast reply

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?…

@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?

@ktdolly 

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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 ...

@don162 

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don162

Dating

Is dating hard with this disease?

@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.

@sahil 

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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...

@JSanchez 

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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?

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