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Central Scotland meet

<p>Hi!</p> <p>Welcome to our wee friendly group! </p> <p>We’re having a virtual meet up tomorrow on Houseparty from 12pm. </p> <p>We usually meet up in either an ice cream parlour, pub / restaurant or tearoom locally and have either brunch or lunch or afternoon tea, depending on the time of da...</p>

@mser79 

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mser79

The restarting of Ocrevus after coronavirus delay

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...

The restarting of Ocrevus after coronavirus delay

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...

The restarting of Ocrevus after coronavirus delay

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...

@crockett32 

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crockett32

Life with severe foot drop

<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>

@Tanya_Trenholm 

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Tanya_Trenholm

Ocrevus: delaying v shielding

This is a long post, so I apologise in advance. I was due to have my first full dose of ocrevus at the end of March. Having made contact with my MS team in the weeks leading up to this to check that I should still go ahead in the current climate (Coronavirus), I repeatedly got the answer back that m...

A Vaccine is 12-18mo Away, At Best

I am not trying to be a party pooper here. Why would I? I wrote a bit about them here https://shift.ms/topic/doms-covid-diary-sat-25th-apr This is an excellent piece from a pharmaceutical market analyst. These folk really don't care about you or me, they are in it for the money. End of. Have a re...

Daily Briefing Covid-19 [Apr 20th &#039;20]

<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>

@JoyceG. 

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JoyceG.

No DMT at the moment...

Hi all! I was diagnosed very recently with MS, on Feb. 26th 2020. Feb. 12th, 13th, 14th '20 I had a Methylprednisolone cure for 3 days, which didn't help me out of my relapse. Complaints are getting worse and my neurologist says DMT is not an option right now because of the corona virus. He says "I...