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📢 Calling all US-based MSers 📢 Do you live in the US? Fancy helping Shift.ms with something? We have a new volunteer role available that is based around the US MS community. If you're interested please email sophie@shift.ms today 📨 Thank you.

<p>Hi guys has anybody tried this patch it’s called Taipatch. I live in Wales and I believe this has come from USA. It is expensive just wanted to know if it’s any good.</p> <div class="i-support-link"> </div>

I've been on Tech for 4 years and I recently had a MRI scan which showed new lesions (sad and disappointed). Yesterday My Neurologist called to formal tell me of the results. However my brain switched off and I didn't fully listen to what the next step is.

<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>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>

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...

Hi I just wanted to say hello 👋

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...

Hi I just wanted to say hello 👋

Hi I just wanted to say hello 👋