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@SherryCLE01 

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SherryCLE01

One little thing

What’s one little thing you do for yourself to find a bit of joy while managing MS? For me, it’s watching a funny movie or comedy special — laughing always lifts my spirits. I’d love to hear about your little joys.
South Euclid, United States

Blessings!!

Grand Risings 🌅 ❤️💛💚 Have a Blessed & Productive Day ‼️‼️

@pablo55 

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pablo55

Pain on my Left Quad

Good evening my fellow MSers. I trying to keep mobile but my I am having problems with my legs. At the end of the day I average 5000 steps a day. Normal after lunch I will nap. When I get up is I feel my legs all weak. Then the pain set in on my left quadricep. The gabapentin and baclofen work...

@Diedre78 

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Diedre78

Bladder / Bowel urgency

Hey. I am working with a practioner who suggested making friends with other MSers with either bowel or bladder urgencies (I seem to have both). Sharing stories. Normalise the topic. Understanding each other. And so on. Anyone?

@S_777 

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S_777

Disability badge

I was rejected AGAIN... I was rejected initially & I appealed with neuro & ms & dr letters! I even had a fall recently with bruising to knees& bled & I sent my neuro's new recent letter update about new lesion & a MRI & images following my fall... They still rejected me for the disability badge App...

@NeuroPulse 

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NeuroPulse

My SUPERHERO!! 💯

MYELIN MANN – EPISODE 1: THE SIGNAL Marcus was just an ordinary guy trying to make it through the day. Then one morning, his legs felt like concrete. His vision blurred. His body wasn’t listening. Doctors gave it a name: Multiple Sclerosis. But what they couldn’t see was the battle happening insi...

@NeuroPulse 

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NeuroPulse

Fitbit/Apple Watch = “Know your body.”* NeuroPulse = “Reconnect with your body.”

Everybody is talking about what their fitness tracker can count… Steps. Heart rate. Calories. Sleep. That’s great but what about the people whose biggest challenge isn’t counting movement… it’s getting movement back? Meet NeuroPulse. A wearable designed with a different mission: helping people ...

@alisoncameron20 

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alisoncameron20

Fatigue off the scale

Ten years on from diagnosis and fortunately annual MRI scans show condition is stable. The fatigue is getting worse though. Trying to motivate myself is an ongoing battle. Tired of explaining myself. The Oscar winning performance of putting on the smile, being positive and cheerful when all I want t...

Drop foot/foot calluses

Is it normal for me to have foot calluses? I told my mom and she said it’s because of the way I walk , since I drag one foot and put pressure on them? I didn’t know that was even possible