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I can separate my family into three groups. First up are my siblings and my daddy. Daddy and my older sister will ask sometimes how I am doing, but I feel it is mostly like an obligation to them. My two older brothers never ask and I never bring it up. Next up are my in-laws. They always ask and th...

I was diagnosed in June 2019 having woken up with pins and needles in my hands in January. No previous symptoms. Pins and needles extended to whole body from chest down and I experienced MS hug a few times. After a couple of months things seemed more or less back to normal and although the pins and ...

Hello, So I got diagnosed with rrms last August, started on ocrevus in October. I was supposed to have the next infusion in March but it was cancelled because of coronavirus. My ms nurse rang me yesterday to say my treatment is happening next month- great! But due to covid19 I will have to isolate...

Daniel & Kevin are live on the Shift.ms Facebook page talking about diagnosis, MS and relationships. Tune in and ask them your questions here: https://www.facebook.com/shift.ms/videos/969374456852750/?v=969374456852750&notif_id=1590677836563640&notif_t=live_video

Only recently diagnosed (7 months ago) & I’d like opinions on my medication please. My MS nurse prescribed 10mg of Baclofen,one to be taken each night along with 30mg of Duloxetine,one at night for a week building up to two twice a day. I stopped both after a week as was experiencing such a mugg...

Hi guys, I have always wanted to be a paramedic (am currently an RN) but have recently been tentatively diagnosed with MS. I am wondering if anyone has successfully gained employment as a paramedic with a known diagnosis of MS or whether I need to put this dream to bed. Thank you :)

Hey there everyone, so I have recently been diagnosed and put on copaxone, with the medication arriving tomorrow. I also have the CSYNC autoinjector in my drawer, ready to go. If anyone is using, or has used it, I have a few questions. I did not get an appointment with the nurse to show me how to ...

https://www.instagram.com/p/CArz6I8gwTj/ Family Matters is a new short film series by Shift.ms that aims to capture the value of an MSer’s close support network and the impacts that diagnosis can have on relationships. When Daniel was 15 years-old he woke up one morning unable to see or walk. He wa...

Hello to everyone, I have just joined you. I was initially diagnosed in 2009 with ADEM & thought it was benign MS. I have had ongoing symptoms over recent years which led to a recent MRI showing multiple lesions. The Consultant has diagnosed MS and referred me to Queens Square in London. I ...

Hi even though I have multiple leisons on brain and spine the neurologist still will not diagnose, but she has suggested the GP prescribing Gabapentin for chronic pain. Was just wondering whether anyone else takes this and if so how effective is it?