Hey, is there anyway to beat the fatigue. I'm really struggling to have energy or stay awake atm.
It's making me feel depressed and I just wanna cry all the time. X
Im finding it difficult to keep working with my fatigue. My job involves lots of online meetings and fast turn around of things. Im a project manager. I work remotely/ home based. I would love to quit my job, dont enjoy it anymore. My MS has now taken over. I didn’t really feel it before, only the p...
As we all experience MS a little differently and as our symptoms remit or evolve i'm curious as to what the most common affliction fatigue feels like to you?
At the start i would have an hour or two of dense brain fog (usually in the early afternoon) which i combated by shifting my working hours ar...
My question is: would a walking stick make walking less fatiguing or is it just to help with balance?
After a recent flare, I find that fatigue is stopping me from getting out and about. I’ve rested for 3.5 weeks taking just 10 min walks five times but otherwise staying in the house (I’m a girl w...
My daughter was diagnosed with MS Last August and seems to be coping she’s been on Plegridy. She gets fatigue at times and says her legs feel heavy is this a common side effect of this condition?
Has anyone successfully learned how to take breaks before you think you need them? 😅
The past few weeks, I find myself able to work and do activities for 3-5 hours and then by 2 PM, I am usually so fatigued – clouded with brain fog and physically drained of energy that I cannot do anything but lay...
Hello all,
I’m newly diagnosed and my MS is very active. I have a question about how to navigate wheelchair/mobility aid use: I’m an elementary teacher and I’m working through fatigue management, energy conservation, and heavy/weak limbs (on top of several other symptoms). By lunchtime I feel ill an...
Hi all,
I've just had Covid and although the virus wasn't that bad, it's caused a bit of a flare up of old symptoms, which I guess is to be expected. But the main one is my old friend fatigue (yay!).
I know rest is obviously important while I recover, but I usually exercise a lot and having spen...
Hello all
Has anyone else had a core body temperature that has been hard to regulate? I have always had Uthoffs and worse symptoms in heat, but this is totally different. Just sat on my sofa at home for the last 6weeks my temperature is yo-yoing from one end of normal range to the other.
I have e...
Hiya looking for advice.. Really struggling with fatigue currently. And my hours were Increased in work. So.find myself exhausted. Have you found anything to help.
I was only recently diagnosed - back in May last year - and through all different symptoms, fatigue and achiness seem to be particularly insistent. I was wondering if anybody had some advice for dealing with any of them?
I was diagnosed in 2001 with RRMS and found in a MS magazine my saviour!
Holland & Barret Guarana Tablets 1000mg !!! They got me through all my years of being a single Mum and working too ! Still have one a day now. They work a treat and have been a life saver xxx
Hi friends. How do you cope with MS fatigue? I have battled this for 20 years. It seems to be getting worse and worse. I need to pull myself out of it somehow. Feeling like all I do is lay in bed and sleep. That’s no way of life. I know I can get some sense of strength back. I would love to hear al...
Happy New Year to you all.
I was diagnosed with RRMS in October 2020. I have told my close family and a few friends about my MS but don't like sharing too much with them as I know it upsets them as they can't relate. This past month life has just been a challenge with one thing and another and it'...