Can someone help me? I’ve searched the web and all the MS sites and can’t find the answer.
I would like to hear from someone who has symptoms daily that come and go. Like everyday. For instance I permanently have numb feet but sometimes in the day it travels up to my knees then goes away back to jus...
He says, "I am interested to know if any of you who have COVID-19 are suffering from a persistent loss of smell and taste and how has it affected your life? Please let us know if smell training makes a difference."
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Here is the full post: https://multiple-sclerosis-research.org/2020/06/mscovid19-lo...
How much of your immune system do you think is not suppressed? If you know about some research or info I'd love to read.
Perhaps 20-40% I'd guess is active seeing as treatment is labeled as causing a low immune system.
Wow. When I posted my first post I didn't even notice the search option. 198 results on foot drop lol. Well, my question this time is if you exercise your head off (foot drop-specific exercises), can you make up for years of not knowing what was going on?Or I don't stand a chance?
Finding a way to get the human nervous system to grow back the myelin, the nerve covering that MS attacks and causes the symptoms, be they minor or major, we all experience is the next huge hurdle.
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I link to a total science paper here: https://www.cell.com/cell-reports/pdf/S2211-1247(20)30611-2.pd...
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...
<p>Afternoon all,<br>
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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>
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MS Stuff<br>
R...</p>