@username
Please wait...
For a better experience get the Shift.ms app
Sort by

@Kevinogcurry 

Last reply

Kevinogcurry

Vaccine

As anyone on this group got MS after the covid vaccine,
Ireland

@madsr 

Last reply

madsr

Music lovers?

I’ve only recently been diagnosed, and have found throughout the journey that music has really helped me process, grieve and find strength. Do you have any songs that may have helped you, or mean a lot with your illness? I’d love to give them a listen! ☺️

@samanthad 

Last reply

samanthad

Just diagnosed yesterday, what to expect?

Hi, I got told by Neurologist yesterday I have MS. I’m feeling a bit lost and confused and worried about how different my life will look now I have this condition. I’d be grateful to know if there are any things people wish they knew when they were first diagnosed that may help? I’ve just finish...

@louisaanker 

Last reply

louisaanker

DMT

Has anyone swapped from Ocrevus to Kesimpta?

@Dustinclaire 

Last reply

Dustinclaire

The long road to getting an actual answer.

Getting diagnosed with MS is rarely a straight line. Half the battle is just fighting through the initial confusion, the wrong turns, and the endless "maybe it's this, maybe it's that" before you were finally given a clear answer. Looking back, that whole diagnostic process was a mental test all on ...

@ecnerolf 

EditedLast reply

ecnerolf

Ocrevus, vaccines etc

Can anyone describe the starting of Ocrevus treatments and timeline (the 10 min injection rather than infusion)? I'm newly diagnosed and currently in active relapse, have not had any steroids and just having new symptoms pop up, for 9-10 weeks now. I was told to get on my choice of DMT ASAP (chose ...

Recovery of internal muscle control

Does anyone have any tips for repairing the connections to internal muscles? I've managed to 95% regain control of my limbs and other exterior muscles, but I have no active control over my pelvic floor Has anyone gone through this and managed to repair control over it? The effects are not debilitat...

@SoniaG236 

Last reply

SoniaG236

Duration of MS

Is MS a long term condition like Parkinson's? I had thought that it was until I saw a few comments recently on here where people said that their Neurologist had said that their MS had gone. Is it to much to hope that it clears up after say 10/15 years? Or is it that MS treats everyone differently?