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<p>Need some advice. I have had health issues half my life. First started when I was about 16. I’ve been trying to find answers for years. Just recently found out that Ms was put in my medical records 2 years ago, although the Dr never verbally told me this. I also have trigeminal, occipital a...</p>

HI, I have just written a piece on MS and assistance dogs on the Barts blog- and how they help hundreds of people with MS lead independent lives:https://multiple-sclerosis-research.org/2020/05/mscovid19-dogs-are-being-trained-to-sniff-out-covid-19/?utm_source=rss&amp;utm_medium=rss&amp;utm_campaign...

<p>I have been reading the posts about working as a nurse with MS, and have a quandary – I am a therapist, with RRMS, due to start Ocrevus post-lockdown.</p> <p>The MS does not interfere with my ability to work. A colleague (the only one who knows about the MS) is anxious as to whether my employers ...</p>

<p>Hi all i find im a morning person with my rr ms, by lunchtime my fatigue starts to set in and i feel like im done the day. Does anyone else feel like this?</p> <div class="i-support-link"> </div>

<p>Is it safe for someone with PPMS to holiday in Devon UK this July .. We are prepared to follow all the rules given out by the government. I know MS means a compromised immune system but not sure if MS is on the vulnerable list ?</p> <p>Thank You<br> Jenny </p> <div class="i-support-link"> &lt;...</div>

<div class="embed-wrapper video-embed-wrapper"></div> <p>L...</p>

<p>Afternoon all,<br> –<br> Not sure when I ought to drop the Covid-19 tag from the headline. I think it should last as long the lockdown lasts. We see the conversation subtly changing now to more of the looking ahead. You can’t panic forever.<br> ——<br> MS Stuff<br> R...</p>

<p>Hi all, just wondering if there are any other nurses out there?? </p> <p>Are you still going to work?? </p> <p>I was planning on carrying on going to work and just being extra careful and socially distancing myself in my personal life (aka not going to shops and restaurants etc) but then I spoke...</p>

<p>Hi guys,<br> As I said in my introduction, passive neurologists and lack of initiative on my part have led me to suffer a severe foot drop (or club foot), which makes me almost drag my right leg. Foot drop has also confused me, because I thought I didn’t have RRMS, but SPMS, but shortened...</p>