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@sunshine44 

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sunshine44

Nighttime jolts? Spasm? Nor sure

Hi guys :) Since being diagnosed with RR MS end of last year I've had these weird night time jerk movement happenings. I'm woken up by it feeling like my bed is collapsing beneath me. Woke myself up last night and my left arm was jolting (if that's a word) down to my hand into my pillow. No pain...

@DeSelby 

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DeSelby

Sleep paralysis

Anybody else have to deal with this? What a joyous experience, waking up completely paralysed head to toe and unable to breathe. Brain and nerve damage, the gifts that just keep giving 😅 Guess 🤣 it could be worse, I once spent about an hour in an MRI with Heart Radio playing and no way to stop it ...

@Flores_Doramis_Jr_ 

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Flores_Doramis_Jr_

Diagnosis

How old Where are you when you were diagnosed me 12

@MsinAround 

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MsinAround

Scared of the future

Things seem to be getting worse, maybe? Yesterday I had to use a power scooter when I was shopping. I have a cane now. Two weeks ago I ended up in a wheelchair. I can’t keep up with my home. My husband is in the NVARNG (Army NG) and keeps getting activated for weeks at a time for these awful wildfi...

@cmc85 

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cmc85

Holidaying

Is it just me that finds going on holiday a daunting task? I am single so I'll be on my own. Malta being an island means taking a plane or ship. What im worried most is taking all the meds and supplements with me, And carrying the luggage. Exploring this new place is out of the w question now. S...

@jenandthezoo 

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jenandthezoo

Weird vision symptom

Does anyone else have vision issues that make you feel like you’re on psychedelics? I don’t know how else to explain it lol. It’s not blurred or double vision like I hear people commonly describe. It’s often triggered by moving my head or looking to the side or straining to see far away. It feels li...

@Miss420 

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Miss420

Tattoos...

I have quite a few tattoos but I have been getting open like sores either in or around them and I was wondering if any of you have experienced this or if i should look into a dermatologist? T.I.A.!🧡

@laurapacino 

Last reply

laurapacino

Mayzent/siponimod

Had rrms for 25 years now diagnosed with spms. Due to start mayzent/siponimod after being on Tysabri for 20 years. Anyone gone through something similar? And what’s been your experience?

@Mal26 

Last reply

Mal26

who else overthinks?

when i overthink, my MS symptoms come on so quickly...