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Well still waiting for appointment neurologist..my left leg been numb since January..so my mobility has got worse but yesterday I woke to find my right leg too is going numb! Toes been numb weeks but it's lower leg it's creeping in too now. I've still been ok till today to get up stairs steadily..bu...

<p>My 14 month old granddaughter lives with us (along with her parents) plus my other sons. 2 are mental health key workers, my daughter in law is a nursery nurse key worker (currently furloughed) and my youngest at uni is earning money working part time as a key worker in Farmfoods frozen food shop...</p>

<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>

<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>

<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>

<p>Hi,</p> <p>I just had my latest infusion of Rituxan (after a COVID delay), and I always feel terrible afterward, but I’ve heard people say they feel better after treatment. Is this a case of “no two the same,” because of different DMTs, a combo? Just curious as I sit here in my post-infusion blah...</p>

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Hi After 4 years on alemtuzumab I was due to move to Ocrevus (following breakthrough activity) in April. Bad timing. I'm treated at the National Hospital for Neurology and Neurosurgery, and was told yesterday that infusions the new patients might not be available until September/October. A huge cau...