shift.ms

So here is my short video where I try to describe fatigue. …

Hi All So over the past few months i have felt life just a little struggle. I have tried to carry on as normal but started to feel i just cant. I feel like im slowly losing the get up and go and that my body is shutting down. All i can think is my mind is losing the plot and that i cant think…

Doubt anyone remembers me but I’ve posted on here since 2016. Long story short but got CIS diagnosis in January 2017 and started on Rebif until December. Taken off due to low wbc meaning I couldn’t have elective surgery. Plan then was for 6 monthly mri/appointments and close monitoring. My case…

Hi everyone, so apart from a year on tec I always try and manage my MS with lifestyle changes however this cold weather and flu has really hit me. Therefore I am considering trying another drug. I am very stubborn, so if I decide I don’t like something I will just stop taking it. So I have read a…

I’ve had quite a hard time on Avonex with the side effects. But I’ve stuck with it for 7 years as it’s doing its job and I’m OK MS-wise. It’s been getting to me recently though so I’ve been thinking about the alternatives. I was chuffed to discover that the same…

Morning all on this chilly day. I have not been on for a while as have felt pretty rubbish. I had my first round of Lemtrada 7 weeks ago and was expecting to feel rough for a few weeks but not like this. The fatigue is the worst i have ever had and im really struggling to get through the day. I am …

My experience of using cannabis as an alternative to using prescribed drugs to aid my MS symptoms. Having been diagnosed with Multiple Sclerosis in April 2004, I have gone through Relapsing Remitting (RRMS), Secondary Progressive (SPMS) and now for the past couple of years find myself at the Primar…

My wife has just been diagnosed with primary progressive MS ?

Question for people who were on Tecfidera and then started Lemtrada: How long were you off Tecfidera before you started Lemtrada? Did you have to wait for you lymphocytes to return to normal? I currently see 2 different MS Neurologists and I’ve been given 2 different answers – so I’m inte…