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Oh and this ms is PANTS

Spoke to my MS Nurse and consultant and they think I am mad and dismiss me I tried the lowest dose, but after a week, still really bad headaches. Stopped again, and my head is fine and I can function again Just interested to know if anyone else has this problem ? Thanks : )

The pain, stiffness and loss of power in my legs has been so bad lately that I have just been avoiding going anywhere at all. I was doing so well up until the middle of April and I thought I'd turned a corner, but one day everything just deteriorated and I'm not improving at all. Even just taking th...

I thought I’d post something, that when I was originally diagnosed, would have definitely helped me dealing with the whole sh*t show that is life with MS, and how to at least make it at least a little bit easier. Don’t get me wrong I’m no MS suffering martin lewis (the irony been by nature Im very...

We’ve just launched Shift.ms polls! Take part in the first poll below👇 *Bonus points if you can leave a comment and let me know: are you happy with how long it took?

In one in four cases of Multiple Sclerosis, the first noticeable symptom is a problem with one of your eyes. MS can affect vision in different ways including optic neuritis, uncontrolled eye movements, and double vision. Kirsty shares the experience of her first symptom in our latest Animated Sympto...

Hi everyone, I've just joined this forum as I don't have a clue where to start! Sorry for the long post... 3 years ago, I suffered severe jaw pain on holiday. The pain then went to my sinus and head. After a year of suffering, I was told they were migraines. Which confused me as my jaw and mouth w...

As the title suggests, I was officially diagnosed last year with RRMS after one big hit of vision, headaches and balance loss. i have suffered from these symptoms and others on and off pre-diagnosis which now make sense with the MS diagnosis. These things from diagnosis have stayed, but I have slo...

I am so fatigued after a days work that my evenings and weekends are just turning into me being in bed. My neurologist says i need to choose where i “spend” my energy, as i should i be depleting it at work or should i save it for my family life? The best option would be to retire early (I’m only 5...

Well, I've finally gotten a cold for the first time since my diagnosis. I'm currently on kesimpta as my dmt and am just wondering if any of you lovely people have had any differences in getting sick since your immune system has been suppressed? Any advice for not getting worse? Thanks!