shift.ms

Hi everyone, today I found out about the MS hug 😩 I thought I was having a big panic attack, it last just over an hour and the only way I can describe it is like an elephant is crushing my ribs and I was struggling to breathe, added with bad back pain and headache. So as a sufferer of anxiety I…

Hi all, I’m new to this site but am excited to be here. Im 28 and was diagnosed with RRMS 2 months ago after over a year of numbness, tingling, fatigue and changes in my sense of hot and cold. Doctors suspected I may have Lyme disease so although they found spinal cord lesions in my first mri my …

Hello fellow MS people! I joined up and have been loitering here for a couple of weeks now and have made a few friends… I wish I had found this forum years ago! I know this isn’t the first post on the subject, but this is my first post here and I would like to get some opinions and sugg…

Good morning everyone I was hoping I could ask for some advice please, I got diagnosed with MS back in December last year. Not sure what type. Have got another mri on Saturday but anyway yesterday and today I’ve felt terrible, my balance has gone, I’m more fatigued than normal, a can of…

So tmoz I will going to a beer b q. I don’t have to cook myself n clean up for a change. I’m gunna be waited on woo hoo. Burger 🍔 in one hand and a carling 🍺 in the other, watching the England 🏴󠁧󠁢󠁥󠁮󠁧󠁿 game ⚽️. My ideal day.

Hello people, I think I got a letter about me but meant for my Peterborough doctor from my Addenbrookes doctor. Strangely I liked it. I needed Google to understand the medical terminology regarding my MRI results. However I now know the severity of everything. But I’m a little naughty when th…

So my left index finger goes rigid it’s happened a few times now but today it was so painful made me cry. I’m wondering if it’s because I over did it yesterday… Hope everyone is well

Hi everyone, I’ve just joined here. I got the official diagnosis of RRMS in March and have been taking Tecfidera for about a month now. The main side effect I have is red hot flushes, which usually happens when I’m at work which can be irritating. I was wondering if there is anyway of …

Has anyone experienced really aching legs feel like they are going to cramp up all the time can be really uncomfortable and painful?

Hi – i I have SPMS & can still walk a bit. If I stand for a while I get muscular pain like I’ve just over exercised. This turns into neuropathic buzzing pain. I’m in the process of scaling up gabapentin. I just wondered if anyone else has experienced this & if medication has help…