For those living with MS or caregivers has NMES been helpful for managing spasticity, muscle fatigue, or mobility? Were there specific settings, devices, or guidance from PTs that made a difference?

I find it so annoying when people give unwelcomed advice -for example when having frequent UTIs- do you drink enough water? Yes- but not going to help with neurogenic bladder. My favourite- we all get tired. Just try to rest! Hmm.. if it were that simple

I used to feel bad saying no. I used to go above and beyond for others, even when I didn’t have the resources to take care of myself. Now, I don’t feel guilty, if I can’t or won’t show up to certain things, or if I need time away from constant communication. For me, that level of energy output is a ...

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Hi all, I thought Id share this for the foot drop sufferers. I much prefer my FES but this has a place. My neurologist said to avoid these if poss as they dont use your actual muscles to lift your foot up. However, if you're just taking the bin out or popping to the shop this is on in seconds and no...

It's been a while.. on Thanksgiving night was rushed to the hospital had trouble breathing with chest pain, scans were done ended up with pneumonia and with an enlarged heart. Seen a cardiologist had a CTA scan of heart .. 2 days ago I get a call from the cardiologist telling me he found a 4.5mm no...

I finally decided to start Ocrevus. A start date is TBD. I am aware of the blood work I need to give prior to starting this infusion. I understand day one is filled with observation after the infusion is given. I’m just curious how it went for others in the beginning? Side effects? I pray it’ll be...

My name is india I have RRMS I live oklahoma. I just had relapse last year in September. Im working on get better