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

@St1gzy 

Last reply

St1gzy

UFC, MS and Terrible Sleep Decisions 🥊😴

Any UFC fans on here staying up for McGregor vs Holloway? 🥊 For the Americans, this is just a normal evening of watching the fights. For us in the UK, it’s a carefully planned medical procedure involving caffeine, snacks, questionable sleep decisions and accepting that Sunday is now a write-off. ...

Botox injections

My doctor recommended this, cause of the nerve pain I keep having, I’m curious, does anyone or can anyone give me more info about it

@HollyB 

EditedLast reply

HollyB

Shift work (incl nights 😴)

Hi It's been a couple of years since I posted in here. For the most part, my MS has been well behaved. A couple of cheeky flare ups due to stress, but Ocrevus seems to be holding the disease at bay for now. For the last 3 yrs I have had an agreed working arrangement with my employer that I think has...

@Beiersdorf 

Last reply

Beiersdorf

AGE

Just curious, how old are y'all when you were first diagnosed???

@ruari 

Last reply

ruari

Non dairy people

Hey guys how do you make sure you get enough calcium when you don’t consume dairy products? I recently switched to an oat milk that tastes great with both tea and coffee (which is rare) but I realised it didn’t actually contain any calcium carbonate. I’m going to switch back to one that does. I ea...

@LookWoolly 

Last reply

LookWoolly

Itchy hands

I have just increased my dulloxetine to assist with fatigue and ever morning I take it, I seem to get very itchy hands. Not sure if they are connected neither are the nurses/pharmacist. Anyone else had this?

@ColettePage 

Last reply

ColettePage

Fampridine

Hi all! After 6 years, I’ve finally found a consultant who will prescribe Fampridine for me! I live Liverpool, UK where it is not available on the nhs so I’m paying privately! Don’t get me started on the postcode lottery of this!!!! Anyway, thankfully, other than the initial consultation fee I am ge...

@adavison 

Last reply

adavison

Dealing with heat

My husband has MS and is really struggling with the heat. Says he feels like he’s going to be sick and can’t feel his hands properly. Does anyone else experience these symptoms? And does anyone have any advice for dealing with the heat?

A Deep Dive into the Addictive World of Slope

In the vast landscape of online games, where intricate narratives and stunning graphics often take center stage, sometimes the most captivating experiences come from the simplest concepts. Enter Slope, a game that strips away the fluff and hones in on pure, unadulterated gameplay. If you've ever fou...

@DeSelby 

Last reply

DeSelby

Story about the start of my MS journey

I don't know if I'd call it a funny story, but it's certainly a bit odd. So I had my first relapse in 2012 (although I think I had symptoms predating that with hindsight). Anyway it's 2012, I'm on a year out from university, and when I'm not studying Physics in preparation for my final year I was r...